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description Publicationkeyboard_double_arrow_right Conference object , Other literature type 2019 GermanyHülstede, Julia; Schonvogel, Dana; Wagner, Peter; Dyck, Alexander; Wark, Michael;add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.eu0 citations 0 popularity Average influence Average impulse Average Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=od______1640::ef37089186b86c0fa2bd090ce3e7dcb7&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Conference object , Other literature type 2019 GermanyHülstede, Julia; Schonvogel, Dana; Wagner, Peter; Dyck, Alexander; Wark, Michael;add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=od______1640::ef37089186b86c0fa2bd090ce3e7dcb7&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu0 citations 0 popularity Average influence Average impulse Average Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=od______1640::ef37089186b86c0fa2bd090ce3e7dcb7&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Conference object , Other literature type 2023 GermanyPublisher:MDPI AG Authors: Schmies, Henrike; Bengen, Nina; Müller-Hülstede, Julia; Ibitowa, Olayinka Ahmed; +2 AuthorsSchmies, Henrike; Bengen, Nina; Müller-Hülstede, Julia; Ibitowa, Olayinka Ahmed; Wagner, Peter; Wark, Michael;Catalysts for the oxygen reduction reaction (ORR) in PEM fuel cells are commonly constituted of Pt-based nanoparticles and a carbon support originating from fossil resources. In order to employ a more sustainable carbon support, activated sawdust was chosen in this study. This was firstly steam-activated at 750 °C and then thermally treated at elevated temperatures up to 2800 °C and reducing conditions at 1100 °C. Various physical characterization methods were applied to systematically relate treatment parameters to surface and structural properties of the carbon material. Deposition of small Pt nanoparticles on the biochar-based supports yielded in ORR active catalysts which were analyzed by thin-film rotating disc electrode measurements. The activity and stability towards the ORR of these novel catalysts was compared to a commercial raw oil-based Pt/C and the influence of support modification on the ORR performance was discussed.
Catalysts arrow_drop_down CatalystsOther literature type . 2023License: CC BYFull-Text: http://www.mdpi.com/2073-4344/13/2/343/pdfData sources: Multidisciplinary Digital Publishing Instituteadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal13020343&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen gold 4 citations 4 popularity Average influence Average impulse Average Powered by BIP!
more_vert Catalysts arrow_drop_down CatalystsOther literature type . 2023License: CC BYFull-Text: http://www.mdpi.com/2073-4344/13/2/343/pdfData sources: Multidisciplinary Digital Publishing Instituteadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal13020343&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Conference object , Other literature type 2023 GermanyPublisher:MDPI AG Authors: Schmies, Henrike; Bengen, Nina; Müller-Hülstede, Julia; Ibitowa, Olayinka Ahmed; +2 AuthorsSchmies, Henrike; Bengen, Nina; Müller-Hülstede, Julia; Ibitowa, Olayinka Ahmed; Wagner, Peter; Wark, Michael;Catalysts for the oxygen reduction reaction (ORR) in PEM fuel cells are commonly constituted of Pt-based nanoparticles and a carbon support originating from fossil resources. In order to employ a more sustainable carbon support, activated sawdust was chosen in this study. This was firstly steam-activated at 750 °C and then thermally treated at elevated temperatures up to 2800 °C and reducing conditions at 1100 °C. Various physical characterization methods were applied to systematically relate treatment parameters to surface and structural properties of the carbon material. Deposition of small Pt nanoparticles on the biochar-based supports yielded in ORR active catalysts which were analyzed by thin-film rotating disc electrode measurements. The activity and stability towards the ORR of these novel catalysts was compared to a commercial raw oil-based Pt/C and the influence of support modification on the ORR performance was discussed.
Catalysts arrow_drop_down CatalystsOther literature type . 2023License: CC BYFull-Text: http://www.mdpi.com/2073-4344/13/2/343/pdfData sources: Multidisciplinary Digital Publishing Instituteadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal13020343&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen gold 4 citations 4 popularity Average influence Average impulse Average Powered by BIP!
more_vert Catalysts arrow_drop_down CatalystsOther literature type . 2023License: CC BYFull-Text: http://www.mdpi.com/2073-4344/13/2/343/pdfData sources: Multidisciplinary Digital Publishing Instituteadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal13020343&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal , Other literature type 2019 GermanyPublisher:Elsevier BV Yezerska, Khrystyna; Dushina, Anastasia; Liu, Fang; Rastedt, Maren; Wagner, Peter; Dyck, Alexander; Wark, Michael;Abstract Degradation caused by fuel starvation may be an important reason for limited fuel cell lifetimes. In this work, we present an analytical characterization of the high temperature polymer exchange membrane fuel cell (HT-PEM FC) behavior under cycled anode starvation and subsequent regeneration conditions to investigate the impact of degradation due to H2 starvation. Two membrane electrode assemblies (MEAs) with an active area of 21 cm2 were operated of up to 550 min, which included up to 14 starvation/regeneration cycles. Overall cell voltage as well as current density distribution (S++ unit) were measured simultaneously each minute during FC operation. The cyclicity of experiments was used to check the long term durability of the HT-PEM FC. After FC operation, micro-computed tomography (μ-CT) was applied to evaluate the influence of starvation on anode and cathode catalyst layer thicknesses. During starvation, cell voltage and current density distribution over the active area of the MEA significantly differed from nominal conditions. A significant drop in cell voltage from 0.6 to 0.1 V occurred after approx. 20 min for the first starvation step, and after 10 min for all subsequent starvation steps. By contrast, the voltage response is immediately stable at 0.6 V during every regeneration step. During each starvation, the local current density reached up to 0.3 A∙point−1 at the area near the gas inlet (9 cm2) while near the outlet it drops to 0.01 A∙point−1. The deviation from a balanced current density distribution occurred after 10 min for the first starvation step, and after ca. 2 min for the subsequent starvation steps. Hence, compared to the voltage drop, the deviation from a balanced current density distribution always starts earlier. This indicates that the local current density distribution is more sensitive to local changes in the MEA than overal cell voltage drop. This finding may help to prevent undesirable influences of the starvation process. The μ-CT images showed that H2 starvation lead to thickness decrease of ca. 20–30% in both anode and cathode catalyst layers compared to a fresh MEA. Despite of the 14 starvation steps and the thinning of the catalyst layers the MEA presents stable cell voltage during regeneration.
International Journa... arrow_drop_down International Journal of Hydrogen EnergyArticle . 2019 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1016/j.ijhydene.2019.05.114&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen bronze 11 citations 11 popularity Top 10% influence Average impulse Top 10% Powered by BIP!
more_vert International Journa... arrow_drop_down International Journal of Hydrogen EnergyArticle . 2019 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1016/j.ijhydene.2019.05.114&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal , Other literature type 2019 GermanyPublisher:Elsevier BV Yezerska, Khrystyna; Dushina, Anastasia; Liu, Fang; Rastedt, Maren; Wagner, Peter; Dyck, Alexander; Wark, Michael;Abstract Degradation caused by fuel starvation may be an important reason for limited fuel cell lifetimes. In this work, we present an analytical characterization of the high temperature polymer exchange membrane fuel cell (HT-PEM FC) behavior under cycled anode starvation and subsequent regeneration conditions to investigate the impact of degradation due to H2 starvation. Two membrane electrode assemblies (MEAs) with an active area of 21 cm2 were operated of up to 550 min, which included up to 14 starvation/regeneration cycles. Overall cell voltage as well as current density distribution (S++ unit) were measured simultaneously each minute during FC operation. The cyclicity of experiments was used to check the long term durability of the HT-PEM FC. After FC operation, micro-computed tomography (μ-CT) was applied to evaluate the influence of starvation on anode and cathode catalyst layer thicknesses. During starvation, cell voltage and current density distribution over the active area of the MEA significantly differed from nominal conditions. A significant drop in cell voltage from 0.6 to 0.1 V occurred after approx. 20 min for the first starvation step, and after 10 min for all subsequent starvation steps. By contrast, the voltage response is immediately stable at 0.6 V during every regeneration step. During each starvation, the local current density reached up to 0.3 A∙point−1 at the area near the gas inlet (9 cm2) while near the outlet it drops to 0.01 A∙point−1. The deviation from a balanced current density distribution occurred after 10 min for the first starvation step, and after ca. 2 min for the subsequent starvation steps. Hence, compared to the voltage drop, the deviation from a balanced current density distribution always starts earlier. This indicates that the local current density distribution is more sensitive to local changes in the MEA than overal cell voltage drop. This finding may help to prevent undesirable influences of the starvation process. The μ-CT images showed that H2 starvation lead to thickness decrease of ca. 20–30% in both anode and cathode catalyst layers compared to a fresh MEA. Despite of the 14 starvation steps and the thinning of the catalyst layers the MEA presents stable cell voltage during regeneration.
International Journa... arrow_drop_down International Journal of Hydrogen EnergyArticle . 2019 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1016/j.ijhydene.2019.05.114&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen bronze 11 citations 11 popularity Top 10% influence Average impulse Top 10% Powered by BIP!
more_vert International Journa... arrow_drop_down International Journal of Hydrogen EnergyArticle . 2019 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1016/j.ijhydene.2019.05.114&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type 2022 GermanyPublisher:Elsevier BV Yezerska, Khrystyna; Dushina, Anastasia; Sarabakha, Andriy; Wagner, Peter; Dyck, Alexander; Wark, Michael;International Journa... arrow_drop_down International Journal of Hydrogen EnergyArticle . 2022 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1016/j.ijhydene.2022.06.254&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu8 citations 8 popularity Top 10% influence Average impulse Top 10% Powered by BIP!
more_vert International Journa... arrow_drop_down International Journal of Hydrogen EnergyArticle . 2022 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1016/j.ijhydene.2022.06.254&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type 2022 GermanyPublisher:Elsevier BV Yezerska, Khrystyna; Dushina, Anastasia; Sarabakha, Andriy; Wagner, Peter; Dyck, Alexander; Wark, Michael;International Journa... arrow_drop_down International Journal of Hydrogen EnergyArticle . 2022 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1016/j.ijhydene.2022.06.254&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu8 citations 8 popularity Top 10% influence Average impulse Top 10% Powered by BIP!
more_vert International Journa... arrow_drop_down International Journal of Hydrogen EnergyArticle . 2022 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1016/j.ijhydene.2022.06.254&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article 2024 GermanyPublisher:The Electrochemical Society Zierdt, Tanja; Knake, Jonas; Müller-Hülstede, Julia; Schonvogel, Dana; Wagner, Peter; Wark, Michael; Friedrich, Andreas K.;The replacement of Pt-based catalysts by Fe-N-Cs in cathodes of high temperature polymer electrolyte membrane fuel cells (HT-PEMFC) can significantly reduce material costs.[1] In a previous study, we revealed the feasibility of Fe-N-C-based gas diffusion electrodes (GDEs) for oxygen reduction reaction under HT-PEMFC conditions (conc. H3PO4, 160 °C) and showed the demand for improving the catalyst layer (CL) morphology.[1] We discovered that Fe-N-C catalysts are feasible to maintain the cell performance within a wide range of PTFE contents from 20 to 50 wt% in the CL.[2] Non-ionic surfactants can enhance the wetting of the CL with electrolyte in HT-PEMFC, as Mack et al. revealed by a reduced break-in time of Triton™ complemented Pt/C electrodes.[3] Furthermore, Lee et al. reported improved dispersion of PTFE binder within the catalyst ink due to employed non-ionic surfactant and increased the HT-PEMFC performance of the Pt-based electrode.[4] Our actual study firstly reveals that the non-ionic surfactants Triton™ X-100 and as alternative the less-hazardous Tergitol™ 15-S-9 similarly affect the Fe-N-C ink sedimentation. Therefore, Fe-N-C-based (PMF-0011904, Pajarito Powder) GDEs are fabricated through ultrasonic spray coating with Tergitol™ contents of 0, 1, 20 and 50 wt% in the CL and a constant PTFE amount of 50 wt%. The H2O contact angle decreases with increasing Tergitol™ content in the Fe-N-C CL, revealing an increased wettability. Furthermore, contact angles with conc. H3PO4 are determined at room temperature (RT) and 160 °C. With this approach the wetting behaviors of the CL at HT-PEMFC conditions are imitated. The contact angle of H3PO4 of the 0 wt% Tergitol™ GDE unveils a decrease of 39 % from RT to 160 °C, for the 1 wt% Tergitol™ GDE by only 4 % and by 15 % for the 20 wt% Tergitol™ GDE. No significant change is observed for the 50 wt% Tergitol™ GDE. Tergitol™ provides a sufficiently wetted surface at RT, whereas without Tergitol™ the Fe-N-C CL must be moistened at higher temperatures. Furthermore, the GDE performance is accessed by hot pressing a polybenzimidazole-based membrane onto the CL and subsequent electrochemically characterization in a half-cell setup under HT-PEMFC condition at 160 °C in conc. H3PO4 electrolyte. Figure 1 reveals the effect of Tergitol™ on the GDE performance. A surfactant content above 1 wt% leads to electrode flooding by the electrolyte and thus a performance decay, as the surfactant increased the CL wetting. The results are complemented by detection of the iron content of the GDEs by inductively coupled plasma mass spectrometry (ICP-MS) and scanning electron microscopy coupled to energy-dispersive X-ray spectroscopy (SEM/EDS) to compare CL morphologies and compositions along all GDEs. References: [1] J. Müller-Hülstede, T. Zierdt, H. Schmies, D. Schonvogel, Q. Meyer, C. Zhao, P. Wagner, and M. Wark, J. Power Sources, 537 231529 (2022). [2] T. Zierdt, J. Müller‐Hülstede, H. Schmies, D. Schonvogel, P. Wagner, and K. A. Friedrich, ChemElectroChem, 11 e202300583 (2024). [3] F. Mack, T. Morawietz, R. Hiesgen, D. Kramer, V. Gogel, and R. Zeis, Int J Hydrogen Energy, 41 (18), 7475-7483 (2016). [4] W. J. Lee, J. S. Lee, H. Y. Park, H. S. Park, S. Y. Lee, K. H. Song, and H. J. Kim, Int J Hydrogen Energy, 45 (57), 32825-32833 (2020). Figure 1
DLR publication serv... arrow_drop_down ECS Meeting AbstractsArticle . 2024 . Peer-reviewedLicense: IOP Copyright PoliciesData sources: CrossrefECS TransactionsArticle . 2024 . Peer-reviewedLicense: IOP Copyright PoliciesData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1149/ma2024-02443040mtgabs&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen 1 citations 1 popularity Average influence Average impulse Average Powered by BIP!
more_vert DLR publication serv... arrow_drop_down ECS Meeting AbstractsArticle . 2024 . Peer-reviewedLicense: IOP Copyright PoliciesData sources: CrossrefECS TransactionsArticle . 2024 . Peer-reviewedLicense: IOP Copyright PoliciesData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1149/ma2024-02443040mtgabs&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article 2024 GermanyPublisher:The Electrochemical Society Zierdt, Tanja; Knake, Jonas; Müller-Hülstede, Julia; Schonvogel, Dana; Wagner, Peter; Wark, Michael; Friedrich, Andreas K.;The replacement of Pt-based catalysts by Fe-N-Cs in cathodes of high temperature polymer electrolyte membrane fuel cells (HT-PEMFC) can significantly reduce material costs.[1] In a previous study, we revealed the feasibility of Fe-N-C-based gas diffusion electrodes (GDEs) for oxygen reduction reaction under HT-PEMFC conditions (conc. H3PO4, 160 °C) and showed the demand for improving the catalyst layer (CL) morphology.[1] We discovered that Fe-N-C catalysts are feasible to maintain the cell performance within a wide range of PTFE contents from 20 to 50 wt% in the CL.[2] Non-ionic surfactants can enhance the wetting of the CL with electrolyte in HT-PEMFC, as Mack et al. revealed by a reduced break-in time of Triton™ complemented Pt/C electrodes.[3] Furthermore, Lee et al. reported improved dispersion of PTFE binder within the catalyst ink due to employed non-ionic surfactant and increased the HT-PEMFC performance of the Pt-based electrode.[4] Our actual study firstly reveals that the non-ionic surfactants Triton™ X-100 and as alternative the less-hazardous Tergitol™ 15-S-9 similarly affect the Fe-N-C ink sedimentation. Therefore, Fe-N-C-based (PMF-0011904, Pajarito Powder) GDEs are fabricated through ultrasonic spray coating with Tergitol™ contents of 0, 1, 20 and 50 wt% in the CL and a constant PTFE amount of 50 wt%. The H2O contact angle decreases with increasing Tergitol™ content in the Fe-N-C CL, revealing an increased wettability. Furthermore, contact angles with conc. H3PO4 are determined at room temperature (RT) and 160 °C. With this approach the wetting behaviors of the CL at HT-PEMFC conditions are imitated. The contact angle of H3PO4 of the 0 wt% Tergitol™ GDE unveils a decrease of 39 % from RT to 160 °C, for the 1 wt% Tergitol™ GDE by only 4 % and by 15 % for the 20 wt% Tergitol™ GDE. No significant change is observed for the 50 wt% Tergitol™ GDE. Tergitol™ provides a sufficiently wetted surface at RT, whereas without Tergitol™ the Fe-N-C CL must be moistened at higher temperatures. Furthermore, the GDE performance is accessed by hot pressing a polybenzimidazole-based membrane onto the CL and subsequent electrochemically characterization in a half-cell setup under HT-PEMFC condition at 160 °C in conc. H3PO4 electrolyte. Figure 1 reveals the effect of Tergitol™ on the GDE performance. A surfactant content above 1 wt% leads to electrode flooding by the electrolyte and thus a performance decay, as the surfactant increased the CL wetting. The results are complemented by detection of the iron content of the GDEs by inductively coupled plasma mass spectrometry (ICP-MS) and scanning electron microscopy coupled to energy-dispersive X-ray spectroscopy (SEM/EDS) to compare CL morphologies and compositions along all GDEs. References: [1] J. Müller-Hülstede, T. Zierdt, H. Schmies, D. Schonvogel, Q. Meyer, C. Zhao, P. Wagner, and M. Wark, J. Power Sources, 537 231529 (2022). [2] T. Zierdt, J. Müller‐Hülstede, H. Schmies, D. Schonvogel, P. Wagner, and K. A. Friedrich, ChemElectroChem, 11 e202300583 (2024). [3] F. Mack, T. Morawietz, R. Hiesgen, D. Kramer, V. Gogel, and R. Zeis, Int J Hydrogen Energy, 41 (18), 7475-7483 (2016). [4] W. J. Lee, J. S. Lee, H. Y. Park, H. S. Park, S. Y. Lee, K. H. Song, and H. J. Kim, Int J Hydrogen Energy, 45 (57), 32825-32833 (2020). Figure 1
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more_vert DLR publication serv... arrow_drop_down ECS Meeting AbstractsArticle . 2024 . Peer-reviewedLicense: IOP Copyright PoliciesData sources: CrossrefECS TransactionsArticle . 2024 . Peer-reviewedLicense: IOP Copyright PoliciesData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1149/ma2024-02443040mtgabs&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type 2019 GermanyPublisher:Wiley Schonvogel, Dana; Nowotny, Manuel; Woriescheck, Tim; Multhaupt, Hendrik; Wagner, Peter; Dyck, Alexander; Agert, Carsten; Wark, Michael;Pt catalysts in proton exchange membrane fuel cells (PEMFC) typically use carbon blacks like Vulcan® based on fossil sources. Thus, an important research task is using sustainable supports in PEMFCs. Hydrothermal carbonization (HTC) converts biomasses into chars, which are possible substitutes for fossil-based carbons. In this study, a Pt catalyst derived from HTC of coconut shells is developed for catalysis of O2 reduction in acidic media. Thermal activation enlarges the specific surface area by factor of 7 to 546 m2 g-1, and generates electrical conductivity making the material suitable for catalysis. 1.8±0.5 nm Pt particles are well-distributed on the activated carbon. Cyclic and CO stripping voltammetry show an electrochemical surface area (ECSA) of 69±21 m2 gPt -1, being almost identical to that of the commercial catalyst using Vulcan® (69±6 m2 gPt-1). Although ECSAs are highly comparable, the activity for O2 reduction is lower compared to the commercial catalyst. HTC derived carbon has a lower degree of graphitization, less functional oxygen groups on its surface and a lower electrical conductivity than Vulcan®. This suggests different Pt–support interactions.
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You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.eumore_vert DLR publication serv... arrow_drop_down add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=od______1640::5865aa1e25a425c226a06b7f53e80c85&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type 2019 GermanyPublisher:Wiley Schonvogel, Dana; Nowotny, Manuel; Woriescheck, Tim; Multhaupt, Hendrik; Wagner, Peter; Dyck, Alexander; Agert, Carsten; Wark, Michael;Pt catalysts in proton exchange membrane fuel cells (PEMFC) typically use carbon blacks like Vulcan® based on fossil sources. Thus, an important research task is using sustainable supports in PEMFCs. Hydrothermal carbonization (HTC) converts biomasses into chars, which are possible substitutes for fossil-based carbons. In this study, a Pt catalyst derived from HTC of coconut shells is developed for catalysis of O2 reduction in acidic media. Thermal activation enlarges the specific surface area by factor of 7 to 546 m2 g-1, and generates electrical conductivity making the material suitable for catalysis. 1.8±0.5 nm Pt particles are well-distributed on the activated carbon. Cyclic and CO stripping voltammetry show an electrochemical surface area (ECSA) of 69±21 m2 gPt -1, being almost identical to that of the commercial catalyst using Vulcan® (69±6 m2 gPt-1). Although ECSAs are highly comparable, the activity for O2 reduction is lower compared to the commercial catalyst. HTC derived carbon has a lower degree of graphitization, less functional oxygen groups on its surface and a lower electrical conductivity than Vulcan®. This suggests different Pt–support interactions.
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You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.eumore_vert DLR publication serv... arrow_drop_down add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Conference object , Other literature type 2022 GermanyBengen, Nina; Schonvogel, Dana; Müller-Hülstede, Julia; Schmies, Henrike; Wagner, Peter; Wark, Michael;add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=od______1640::39a620779985de7dec70a8ff312187ca&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu0 citations 0 popularity Average influence Average impulse Average Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Conference object , Other literature type 2022 GermanyBengen, Nina; Schonvogel, Dana; Müller-Hülstede, Julia; Schmies, Henrike; Wagner, Peter; Wark, Michael;add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=od______1640::39a620779985de7dec70a8ff312187ca&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu0 citations 0 popularity Average influence Average impulse Average Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=od______1640::39a620779985de7dec70a8ff312187ca&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Conference object , Other literature type 2022 GermanyPublisher:The Electrochemical Society Bengen, Nina; Schmies, Henrike; Müller-Hülstede, Julia; Schonvogel, Dana; Wagner, Peter; Wark, Michael;To improve the lifetime of polymer electrolyte membrane fuel cells (PEMFCs), optimization of the fuel cell components is necessary wherein one research focus is the stability of the platinum catalyst support. Due to the harsh conditions in PEMFCs, e.g. high potentials (≥ 0.85 VRHE) and low pH (≤ 2), the catalyst support, which commonly consists of a high surface area carbon, degrades.[1] This is mainly caused by carbon corrosion, which becomes significant at potentials above 1.1 VRHE.[2] Typically, commercially available and chemically derived raw oil based carbons are used as catalyst supports. The use of multi-walled carbon nanotubes (MWCNTs) as a more stable, graphitic catalyst support with high electrical conductivity is well known in literature.[3, 4] The production of MWCNTs is expensive, which makes upscaling difficult. However, a previous study of our group Schonvogel et al. showed low stability of biomass-based supports, which requires further optimization.[5] Therefore, an approach to increase the stability of the biomass-based carbon support is thermal graphitization to generate a stable and ordered carbon structure. This leads to an increased amount of sp2-hybridized carbon with increased crystallinity and increased graphitic degree. At this point, the use of activated biomasses as carbon support is a cheap and sustainable alternative to MWCNTs and commercially available carbon blacks, for example Vulcan XC-72®.[5, 6] In this work, novel composite supports using thermally treated activated sawdust and MWCNTs will be investigated as Pt-nanoparticle support towards their physical properties and electrochemical ORR activity and stability. Sawdust was steam activated at 750 °C for 1 h in nitrogen atmosphere to create a defined pore system. Afterwards, the activated sawdust (aSD) was mechanically mixed with 20 wt.% MWCNTs. The mixture was treated at high temperatures (1500, 1800 and 2100 °C, under Ar atmosphere) in a furnace. For comparison, MWCNTs only were thermally treated under the same conditions. Physical characterization of the supports was performed using low temperature nitrogen sorption for determination of surface properties and crystallinity powder x-ray diffractometry (PXRD) for analysis of the degree of graphitization. Next, these novel carbon materials were used as support for 40 wt.% platinum nanoparticles. The platinum content was determined using inductive coupled plasma with mass spectrometry (ICP-MS) and the platinum nanoparticle diameter was analyzed with transmission electron microcopy (TEM) resulting in mean diameters ≤ 2 nm. In order to evaluate the activity and stability of the synthesized platinum catalysts, electrochemical characterization was performed for most promising catalysts before and after an accelerated stress test (AST, 0.6 – 1.5 VRHE, 500 mV s-1, 5000 cycles). For electrochemical characterization a three-electrode setup with a rotating ring disc electrode (RRDE) was used. The electrochemical active surface area was obtained by hydrogen underpotential deposition (HUPD) and CO stripping method. In Figure 1 the ORR curves, mass activities (MA) determined at 0.9 VRHE and MA loss of Pt/gaSD_gMWCNTs_2100 and Pt/gMWCNTs_2100 before and after AST are shown. Our study reveals that the mixture of 20 wt.% MWCNTs with sustainable aSD and subsequent thermal treatment results in a catalyst with comparable MA and stability to Pt/MWCNTs_2100. Thus, the use of activated biomass as the main component in catalyst supports constitute a more sustainable and cheaper alternative to MWCNTs. Based on these results, thermal treatment at higher temperatures of ≥ 2500 °C and higher biomass content will be further investigated to increase the stability. [1] F. Ettingshausen, J. Kleemann, A. Marcu, G. Toth, H. Fuess, C. Roth, Fuel Cells 2011, 11, 238-245. [2] V. Bandlamudi, P. Bujlo, C. Sita, S. Pasupathi, Materials Today: Proceedings 2018, 5, 10602-10610. [3] V. N. Popov, Materials Science and Engineering: R: Reports 2004, 43, 61-102. [4] D. Schonvogel, J. Hülstede, P. Wagner, I. Kruusenberg, K. Tammeveski, A. Dyck, C. Agert, M. Wark, J. Electrochem. Soc. 2017, 164, F995-F1004. [5] D. Schonvogel, M. Nowotny, T. Woriescheck, H. Multhaupt, P. Wagner, A. Dyck, C. Agert, M. Wark, Energy Technology 2019, 7, 1900344. [6] M. Iwanow, T. Gartner, V. Sieber, B. Konig, Beilstein J Org Chem 2020, 16, 1188-1202. Figure 1
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You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.eu1 citations 1 popularity Average influence Average impulse Average Powered by BIP!
more_vert DLR publication serv... arrow_drop_down ECS Meeting AbstractsArticle . 2022 . Peer-reviewedLicense: IOP Copyright PoliciesData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1149/ma2022-02421556mtgabs&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Conference object , Other literature type 2022 GermanyPublisher:The Electrochemical Society Bengen, Nina; Schmies, Henrike; Müller-Hülstede, Julia; Schonvogel, Dana; Wagner, Peter; Wark, Michael;To improve the lifetime of polymer electrolyte membrane fuel cells (PEMFCs), optimization of the fuel cell components is necessary wherein one research focus is the stability of the platinum catalyst support. Due to the harsh conditions in PEMFCs, e.g. high potentials (≥ 0.85 VRHE) and low pH (≤ 2), the catalyst support, which commonly consists of a high surface area carbon, degrades.[1] This is mainly caused by carbon corrosion, which becomes significant at potentials above 1.1 VRHE.[2] Typically, commercially available and chemically derived raw oil based carbons are used as catalyst supports. The use of multi-walled carbon nanotubes (MWCNTs) as a more stable, graphitic catalyst support with high electrical conductivity is well known in literature.[3, 4] The production of MWCNTs is expensive, which makes upscaling difficult. However, a previous study of our group Schonvogel et al. showed low stability of biomass-based supports, which requires further optimization.[5] Therefore, an approach to increase the stability of the biomass-based carbon support is thermal graphitization to generate a stable and ordered carbon structure. This leads to an increased amount of sp2-hybridized carbon with increased crystallinity and increased graphitic degree. At this point, the use of activated biomasses as carbon support is a cheap and sustainable alternative to MWCNTs and commercially available carbon blacks, for example Vulcan XC-72®.[5, 6] In this work, novel composite supports using thermally treated activated sawdust and MWCNTs will be investigated as Pt-nanoparticle support towards their physical properties and electrochemical ORR activity and stability. Sawdust was steam activated at 750 °C for 1 h in nitrogen atmosphere to create a defined pore system. Afterwards, the activated sawdust (aSD) was mechanically mixed with 20 wt.% MWCNTs. The mixture was treated at high temperatures (1500, 1800 and 2100 °C, under Ar atmosphere) in a furnace. For comparison, MWCNTs only were thermally treated under the same conditions. Physical characterization of the supports was performed using low temperature nitrogen sorption for determination of surface properties and crystallinity powder x-ray diffractometry (PXRD) for analysis of the degree of graphitization. Next, these novel carbon materials were used as support for 40 wt.% platinum nanoparticles. The platinum content was determined using inductive coupled plasma with mass spectrometry (ICP-MS) and the platinum nanoparticle diameter was analyzed with transmission electron microcopy (TEM) resulting in mean diameters ≤ 2 nm. In order to evaluate the activity and stability of the synthesized platinum catalysts, electrochemical characterization was performed for most promising catalysts before and after an accelerated stress test (AST, 0.6 – 1.5 VRHE, 500 mV s-1, 5000 cycles). For electrochemical characterization a three-electrode setup with a rotating ring disc electrode (RRDE) was used. The electrochemical active surface area was obtained by hydrogen underpotential deposition (HUPD) and CO stripping method. In Figure 1 the ORR curves, mass activities (MA) determined at 0.9 VRHE and MA loss of Pt/gaSD_gMWCNTs_2100 and Pt/gMWCNTs_2100 before and after AST are shown. Our study reveals that the mixture of 20 wt.% MWCNTs with sustainable aSD and subsequent thermal treatment results in a catalyst with comparable MA and stability to Pt/MWCNTs_2100. Thus, the use of activated biomass as the main component in catalyst supports constitute a more sustainable and cheaper alternative to MWCNTs. Based on these results, thermal treatment at higher temperatures of ≥ 2500 °C and higher biomass content will be further investigated to increase the stability. [1] F. Ettingshausen, J. Kleemann, A. Marcu, G. Toth, H. Fuess, C. Roth, Fuel Cells 2011, 11, 238-245. [2] V. Bandlamudi, P. Bujlo, C. Sita, S. Pasupathi, Materials Today: Proceedings 2018, 5, 10602-10610. [3] V. N. Popov, Materials Science and Engineering: R: Reports 2004, 43, 61-102. [4] D. Schonvogel, J. Hülstede, P. Wagner, I. Kruusenberg, K. Tammeveski, A. Dyck, C. Agert, M. Wark, J. Electrochem. Soc. 2017, 164, F995-F1004. [5] D. Schonvogel, M. Nowotny, T. Woriescheck, H. Multhaupt, P. Wagner, A. Dyck, C. Agert, M. Wark, Energy Technology 2019, 7, 1900344. [6] M. Iwanow, T. Gartner, V. Sieber, B. Konig, Beilstein J Org Chem 2020, 16, 1188-1202. Figure 1
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For further information contact us at helpdesk@openaire.eu1 citations 1 popularity Average influence Average impulse Average Powered by BIP!
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For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article 2024 GermanyPublisher:Royal Society of Chemistry (RSC) Funded by:DFGDFGWartner, Garlef; Müller-Hülstede, Julia; Trzesniowski, Hanna; Wark, Michael; Wagner, Peter; Seidel, Robert;doi: 10.1039/d4se00342j
Novel biomass based Fe–N–C catalysts exhibit a higher density of FeNx type sites with different redox characteristics compared to carbon black based Fe–N–Cs. These different characteristics are influenced by heteroatom doping and undercoordination.
add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.euAccess RoutesGreen hybrid 0 citations 0 popularity Average influence Average impulse Average Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article 2024 GermanyPublisher:Royal Society of Chemistry (RSC) Funded by:DFGDFGWartner, Garlef; Müller-Hülstede, Julia; Trzesniowski, Hanna; Wark, Michael; Wagner, Peter; Seidel, Robert;doi: 10.1039/d4se00342j
Novel biomass based Fe–N–C catalysts exhibit a higher density of FeNx type sites with different redox characteristics compared to carbon black based Fe–N–Cs. These different characteristics are influenced by heteroatom doping and undercoordination.
add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1039/d4se00342j&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen hybrid 0 citations 0 popularity Average influence Average impulse Average Powered by BIP!
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description Publicationkeyboard_double_arrow_right Conference object , Other literature type 2019 GermanyHülstede, Julia; Schonvogel, Dana; Wagner, Peter; Dyck, Alexander; Wark, Michael;add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=od______1640::ef37089186b86c0fa2bd090ce3e7dcb7&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu0 citations 0 popularity Average influence Average impulse Average Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=od______1640::ef37089186b86c0fa2bd090ce3e7dcb7&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Conference object , Other literature type 2019 GermanyHülstede, Julia; Schonvogel, Dana; Wagner, Peter; Dyck, Alexander; Wark, Michael;add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=od______1640::ef37089186b86c0fa2bd090ce3e7dcb7&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu0 citations 0 popularity Average influence Average impulse Average Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=od______1640::ef37089186b86c0fa2bd090ce3e7dcb7&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Conference object , Other literature type 2023 GermanyPublisher:MDPI AG Authors: Schmies, Henrike; Bengen, Nina; Müller-Hülstede, Julia; Ibitowa, Olayinka Ahmed; +2 AuthorsSchmies, Henrike; Bengen, Nina; Müller-Hülstede, Julia; Ibitowa, Olayinka Ahmed; Wagner, Peter; Wark, Michael;Catalysts for the oxygen reduction reaction (ORR) in PEM fuel cells are commonly constituted of Pt-based nanoparticles and a carbon support originating from fossil resources. In order to employ a more sustainable carbon support, activated sawdust was chosen in this study. This was firstly steam-activated at 750 °C and then thermally treated at elevated temperatures up to 2800 °C and reducing conditions at 1100 °C. Various physical characterization methods were applied to systematically relate treatment parameters to surface and structural properties of the carbon material. Deposition of small Pt nanoparticles on the biochar-based supports yielded in ORR active catalysts which were analyzed by thin-film rotating disc electrode measurements. The activity and stability towards the ORR of these novel catalysts was compared to a commercial raw oil-based Pt/C and the influence of support modification on the ORR performance was discussed.
Catalysts arrow_drop_down CatalystsOther literature type . 2023License: CC BYFull-Text: http://www.mdpi.com/2073-4344/13/2/343/pdfData sources: Multidisciplinary Digital Publishing Instituteadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal13020343&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen gold 4 citations 4 popularity Average influence Average impulse Average Powered by BIP!
more_vert Catalysts arrow_drop_down CatalystsOther literature type . 2023License: CC BYFull-Text: http://www.mdpi.com/2073-4344/13/2/343/pdfData sources: Multidisciplinary Digital Publishing Instituteadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal13020343&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Conference object , Other literature type 2023 GermanyPublisher:MDPI AG Authors: Schmies, Henrike; Bengen, Nina; Müller-Hülstede, Julia; Ibitowa, Olayinka Ahmed; +2 AuthorsSchmies, Henrike; Bengen, Nina; Müller-Hülstede, Julia; Ibitowa, Olayinka Ahmed; Wagner, Peter; Wark, Michael;Catalysts for the oxygen reduction reaction (ORR) in PEM fuel cells are commonly constituted of Pt-based nanoparticles and a carbon support originating from fossil resources. In order to employ a more sustainable carbon support, activated sawdust was chosen in this study. This was firstly steam-activated at 750 °C and then thermally treated at elevated temperatures up to 2800 °C and reducing conditions at 1100 °C. Various physical characterization methods were applied to systematically relate treatment parameters to surface and structural properties of the carbon material. Deposition of small Pt nanoparticles on the biochar-based supports yielded in ORR active catalysts which were analyzed by thin-film rotating disc electrode measurements. The activity and stability towards the ORR of these novel catalysts was compared to a commercial raw oil-based Pt/C and the influence of support modification on the ORR performance was discussed.
Catalysts arrow_drop_down CatalystsOther literature type . 2023License: CC BYFull-Text: http://www.mdpi.com/2073-4344/13/2/343/pdfData sources: Multidisciplinary Digital Publishing Instituteadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal13020343&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen gold 4 citations 4 popularity Average influence Average impulse Average Powered by BIP!
more_vert Catalysts arrow_drop_down CatalystsOther literature type . 2023License: CC BYFull-Text: http://www.mdpi.com/2073-4344/13/2/343/pdfData sources: Multidisciplinary Digital Publishing Instituteadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/catal13020343&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal , Other literature type 2019 GermanyPublisher:Elsevier BV Yezerska, Khrystyna; Dushina, Anastasia; Liu, Fang; Rastedt, Maren; Wagner, Peter; Dyck, Alexander; Wark, Michael;Abstract Degradation caused by fuel starvation may be an important reason for limited fuel cell lifetimes. In this work, we present an analytical characterization of the high temperature polymer exchange membrane fuel cell (HT-PEM FC) behavior under cycled anode starvation and subsequent regeneration conditions to investigate the impact of degradation due to H2 starvation. Two membrane electrode assemblies (MEAs) with an active area of 21 cm2 were operated of up to 550 min, which included up to 14 starvation/regeneration cycles. Overall cell voltage as well as current density distribution (S++ unit) were measured simultaneously each minute during FC operation. The cyclicity of experiments was used to check the long term durability of the HT-PEM FC. After FC operation, micro-computed tomography (μ-CT) was applied to evaluate the influence of starvation on anode and cathode catalyst layer thicknesses. During starvation, cell voltage and current density distribution over the active area of the MEA significantly differed from nominal conditions. A significant drop in cell voltage from 0.6 to 0.1 V occurred after approx. 20 min for the first starvation step, and after 10 min for all subsequent starvation steps. By contrast, the voltage response is immediately stable at 0.6 V during every regeneration step. During each starvation, the local current density reached up to 0.3 A∙point−1 at the area near the gas inlet (9 cm2) while near the outlet it drops to 0.01 A∙point−1. The deviation from a balanced current density distribution occurred after 10 min for the first starvation step, and after ca. 2 min for the subsequent starvation steps. Hence, compared to the voltage drop, the deviation from a balanced current density distribution always starts earlier. This indicates that the local current density distribution is more sensitive to local changes in the MEA than overal cell voltage drop. This finding may help to prevent undesirable influences of the starvation process. The μ-CT images showed that H2 starvation lead to thickness decrease of ca. 20–30% in both anode and cathode catalyst layers compared to a fresh MEA. Despite of the 14 starvation steps and the thinning of the catalyst layers the MEA presents stable cell voltage during regeneration.
International Journa... arrow_drop_down International Journal of Hydrogen EnergyArticle . 2019 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1016/j.ijhydene.2019.05.114&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen bronze 11 citations 11 popularity Top 10% influence Average impulse Top 10% Powered by BIP!
more_vert International Journa... arrow_drop_down International Journal of Hydrogen EnergyArticle . 2019 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1016/j.ijhydene.2019.05.114&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal , Other literature type 2019 GermanyPublisher:Elsevier BV Yezerska, Khrystyna; Dushina, Anastasia; Liu, Fang; Rastedt, Maren; Wagner, Peter; Dyck, Alexander; Wark, Michael;Abstract Degradation caused by fuel starvation may be an important reason for limited fuel cell lifetimes. In this work, we present an analytical characterization of the high temperature polymer exchange membrane fuel cell (HT-PEM FC) behavior under cycled anode starvation and subsequent regeneration conditions to investigate the impact of degradation due to H2 starvation. Two membrane electrode assemblies (MEAs) with an active area of 21 cm2 were operated of up to 550 min, which included up to 14 starvation/regeneration cycles. Overall cell voltage as well as current density distribution (S++ unit) were measured simultaneously each minute during FC operation. The cyclicity of experiments was used to check the long term durability of the HT-PEM FC. After FC operation, micro-computed tomography (μ-CT) was applied to evaluate the influence of starvation on anode and cathode catalyst layer thicknesses. During starvation, cell voltage and current density distribution over the active area of the MEA significantly differed from nominal conditions. A significant drop in cell voltage from 0.6 to 0.1 V occurred after approx. 20 min for the first starvation step, and after 10 min for all subsequent starvation steps. By contrast, the voltage response is immediately stable at 0.6 V during every regeneration step. During each starvation, the local current density reached up to 0.3 A∙point−1 at the area near the gas inlet (9 cm2) while near the outlet it drops to 0.01 A∙point−1. The deviation from a balanced current density distribution occurred after 10 min for the first starvation step, and after ca. 2 min for the subsequent starvation steps. Hence, compared to the voltage drop, the deviation from a balanced current density distribution always starts earlier. This indicates that the local current density distribution is more sensitive to local changes in the MEA than overal cell voltage drop. This finding may help to prevent undesirable influences of the starvation process. The μ-CT images showed that H2 starvation lead to thickness decrease of ca. 20–30% in both anode and cathode catalyst layers compared to a fresh MEA. Despite of the 14 starvation steps and the thinning of the catalyst layers the MEA presents stable cell voltage during regeneration.
International Journa... arrow_drop_down International Journal of Hydrogen EnergyArticle . 2019 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1016/j.ijhydene.2019.05.114&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen bronze 11 citations 11 popularity Top 10% influence Average impulse Top 10% Powered by BIP!
more_vert International Journa... arrow_drop_down International Journal of Hydrogen EnergyArticle . 2019 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1016/j.ijhydene.2019.05.114&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type 2022 GermanyPublisher:Elsevier BV Yezerska, Khrystyna; Dushina, Anastasia; Sarabakha, Andriy; Wagner, Peter; Dyck, Alexander; Wark, Michael;International Journa... arrow_drop_down International Journal of Hydrogen EnergyArticle . 2022 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1016/j.ijhydene.2022.06.254&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu8 citations 8 popularity Top 10% influence Average impulse Top 10% Powered by BIP!
more_vert International Journa... arrow_drop_down International Journal of Hydrogen EnergyArticle . 2022 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1016/j.ijhydene.2022.06.254&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type 2022 GermanyPublisher:Elsevier BV Yezerska, Khrystyna; Dushina, Anastasia; Sarabakha, Andriy; Wagner, Peter; Dyck, Alexander; Wark, Michael;International Journa... arrow_drop_down International Journal of Hydrogen EnergyArticle . 2022 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1016/j.ijhydene.2022.06.254&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu8 citations 8 popularity Top 10% influence Average impulse Top 10% Powered by BIP!
more_vert International Journa... arrow_drop_down International Journal of Hydrogen EnergyArticle . 2022 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1016/j.ijhydene.2022.06.254&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article 2024 GermanyPublisher:The Electrochemical Society Zierdt, Tanja; Knake, Jonas; Müller-Hülstede, Julia; Schonvogel, Dana; Wagner, Peter; Wark, Michael; Friedrich, Andreas K.;The replacement of Pt-based catalysts by Fe-N-Cs in cathodes of high temperature polymer electrolyte membrane fuel cells (HT-PEMFC) can significantly reduce material costs.[1] In a previous study, we revealed the feasibility of Fe-N-C-based gas diffusion electrodes (GDEs) for oxygen reduction reaction under HT-PEMFC conditions (conc. H3PO4, 160 °C) and showed the demand for improving the catalyst layer (CL) morphology.[1] We discovered that Fe-N-C catalysts are feasible to maintain the cell performance within a wide range of PTFE contents from 20 to 50 wt% in the CL.[2] Non-ionic surfactants can enhance the wetting of the CL with electrolyte in HT-PEMFC, as Mack et al. revealed by a reduced break-in time of Triton™ complemented Pt/C electrodes.[3] Furthermore, Lee et al. reported improved dispersion of PTFE binder within the catalyst ink due to employed non-ionic surfactant and increased the HT-PEMFC performance of the Pt-based electrode.[4] Our actual study firstly reveals that the non-ionic surfactants Triton™ X-100 and as alternative the less-hazardous Tergitol™ 15-S-9 similarly affect the Fe-N-C ink sedimentation. Therefore, Fe-N-C-based (PMF-0011904, Pajarito Powder) GDEs are fabricated through ultrasonic spray coating with Tergitol™ contents of 0, 1, 20 and 50 wt% in the CL and a constant PTFE amount of 50 wt%. The H2O contact angle decreases with increasing Tergitol™ content in the Fe-N-C CL, revealing an increased wettability. Furthermore, contact angles with conc. H3PO4 are determined at room temperature (RT) and 160 °C. With this approach the wetting behaviors of the CL at HT-PEMFC conditions are imitated. The contact angle of H3PO4 of the 0 wt% Tergitol™ GDE unveils a decrease of 39 % from RT to 160 °C, for the 1 wt% Tergitol™ GDE by only 4 % and by 15 % for the 20 wt% Tergitol™ GDE. No significant change is observed for the 50 wt% Tergitol™ GDE. Tergitol™ provides a sufficiently wetted surface at RT, whereas without Tergitol™ the Fe-N-C CL must be moistened at higher temperatures. Furthermore, the GDE performance is accessed by hot pressing a polybenzimidazole-based membrane onto the CL and subsequent electrochemically characterization in a half-cell setup under HT-PEMFC condition at 160 °C in conc. H3PO4 electrolyte. Figure 1 reveals the effect of Tergitol™ on the GDE performance. A surfactant content above 1 wt% leads to electrode flooding by the electrolyte and thus a performance decay, as the surfactant increased the CL wetting. The results are complemented by detection of the iron content of the GDEs by inductively coupled plasma mass spectrometry (ICP-MS) and scanning electron microscopy coupled to energy-dispersive X-ray spectroscopy (SEM/EDS) to compare CL morphologies and compositions along all GDEs. References: [1] J. Müller-Hülstede, T. Zierdt, H. Schmies, D. Schonvogel, Q. Meyer, C. Zhao, P. Wagner, and M. Wark, J. Power Sources, 537 231529 (2022). [2] T. Zierdt, J. Müller‐Hülstede, H. Schmies, D. Schonvogel, P. Wagner, and K. A. Friedrich, ChemElectroChem, 11 e202300583 (2024). [3] F. Mack, T. Morawietz, R. Hiesgen, D. Kramer, V. Gogel, and R. Zeis, Int J Hydrogen Energy, 41 (18), 7475-7483 (2016). [4] W. J. Lee, J. S. Lee, H. Y. Park, H. S. Park, S. Y. Lee, K. H. Song, and H. J. Kim, Int J Hydrogen Energy, 45 (57), 32825-32833 (2020). Figure 1
DLR publication serv... arrow_drop_down ECS Meeting AbstractsArticle . 2024 . Peer-reviewedLicense: IOP Copyright PoliciesData sources: CrossrefECS TransactionsArticle . 2024 . Peer-reviewedLicense: IOP Copyright PoliciesData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1149/ma2024-02443040mtgabs&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen 1 citations 1 popularity Average influence Average impulse Average Powered by BIP!
more_vert DLR publication serv... arrow_drop_down ECS Meeting AbstractsArticle . 2024 . Peer-reviewedLicense: IOP Copyright PoliciesData sources: CrossrefECS TransactionsArticle . 2024 . Peer-reviewedLicense: IOP Copyright PoliciesData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article 2024 GermanyPublisher:The Electrochemical Society Zierdt, Tanja; Knake, Jonas; Müller-Hülstede, Julia; Schonvogel, Dana; Wagner, Peter; Wark, Michael; Friedrich, Andreas K.;The replacement of Pt-based catalysts by Fe-N-Cs in cathodes of high temperature polymer electrolyte membrane fuel cells (HT-PEMFC) can significantly reduce material costs.[1] In a previous study, we revealed the feasibility of Fe-N-C-based gas diffusion electrodes (GDEs) for oxygen reduction reaction under HT-PEMFC conditions (conc. H3PO4, 160 °C) and showed the demand for improving the catalyst layer (CL) morphology.[1] We discovered that Fe-N-C catalysts are feasible to maintain the cell performance within a wide range of PTFE contents from 20 to 50 wt% in the CL.[2] Non-ionic surfactants can enhance the wetting of the CL with electrolyte in HT-PEMFC, as Mack et al. revealed by a reduced break-in time of Triton™ complemented Pt/C electrodes.[3] Furthermore, Lee et al. reported improved dispersion of PTFE binder within the catalyst ink due to employed non-ionic surfactant and increased the HT-PEMFC performance of the Pt-based electrode.[4] Our actual study firstly reveals that the non-ionic surfactants Triton™ X-100 and as alternative the less-hazardous Tergitol™ 15-S-9 similarly affect the Fe-N-C ink sedimentation. Therefore, Fe-N-C-based (PMF-0011904, Pajarito Powder) GDEs are fabricated through ultrasonic spray coating with Tergitol™ contents of 0, 1, 20 and 50 wt% in the CL and a constant PTFE amount of 50 wt%. The H2O contact angle decreases with increasing Tergitol™ content in the Fe-N-C CL, revealing an increased wettability. Furthermore, contact angles with conc. H3PO4 are determined at room temperature (RT) and 160 °C. With this approach the wetting behaviors of the CL at HT-PEMFC conditions are imitated. The contact angle of H3PO4 of the 0 wt% Tergitol™ GDE unveils a decrease of 39 % from RT to 160 °C, for the 1 wt% Tergitol™ GDE by only 4 % and by 15 % for the 20 wt% Tergitol™ GDE. No significant change is observed for the 50 wt% Tergitol™ GDE. Tergitol™ provides a sufficiently wetted surface at RT, whereas without Tergitol™ the Fe-N-C CL must be moistened at higher temperatures. Furthermore, the GDE performance is accessed by hot pressing a polybenzimidazole-based membrane onto the CL and subsequent electrochemically characterization in a half-cell setup under HT-PEMFC condition at 160 °C in conc. H3PO4 electrolyte. Figure 1 reveals the effect of Tergitol™ on the GDE performance. A surfactant content above 1 wt% leads to electrode flooding by the electrolyte and thus a performance decay, as the surfactant increased the CL wetting. The results are complemented by detection of the iron content of the GDEs by inductively coupled plasma mass spectrometry (ICP-MS) and scanning electron microscopy coupled to energy-dispersive X-ray spectroscopy (SEM/EDS) to compare CL morphologies and compositions along all GDEs. References: [1] J. Müller-Hülstede, T. Zierdt, H. Schmies, D. Schonvogel, Q. Meyer, C. Zhao, P. Wagner, and M. Wark, J. Power Sources, 537 231529 (2022). [2] T. Zierdt, J. Müller‐Hülstede, H. Schmies, D. Schonvogel, P. Wagner, and K. A. Friedrich, ChemElectroChem, 11 e202300583 (2024). [3] F. Mack, T. Morawietz, R. Hiesgen, D. Kramer, V. Gogel, and R. Zeis, Int J Hydrogen Energy, 41 (18), 7475-7483 (2016). [4] W. J. Lee, J. S. Lee, H. Y. Park, H. S. Park, S. Y. Lee, K. H. Song, and H. J. Kim, Int J Hydrogen Energy, 45 (57), 32825-32833 (2020). Figure 1
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more_vert DLR publication serv... arrow_drop_down ECS Meeting AbstractsArticle . 2024 . Peer-reviewedLicense: IOP Copyright PoliciesData sources: CrossrefECS TransactionsArticle . 2024 . Peer-reviewedLicense: IOP Copyright PoliciesData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1149/ma2024-02443040mtgabs&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type 2019 GermanyPublisher:Wiley Schonvogel, Dana; Nowotny, Manuel; Woriescheck, Tim; Multhaupt, Hendrik; Wagner, Peter; Dyck, Alexander; Agert, Carsten; Wark, Michael;Pt catalysts in proton exchange membrane fuel cells (PEMFC) typically use carbon blacks like Vulcan® based on fossil sources. Thus, an important research task is using sustainable supports in PEMFCs. Hydrothermal carbonization (HTC) converts biomasses into chars, which are possible substitutes for fossil-based carbons. In this study, a Pt catalyst derived from HTC of coconut shells is developed for catalysis of O2 reduction in acidic media. Thermal activation enlarges the specific surface area by factor of 7 to 546 m2 g-1, and generates electrical conductivity making the material suitable for catalysis. 1.8±0.5 nm Pt particles are well-distributed on the activated carbon. Cyclic and CO stripping voltammetry show an electrochemical surface area (ECSA) of 69±21 m2 gPt -1, being almost identical to that of the commercial catalyst using Vulcan® (69±6 m2 gPt-1). Although ECSAs are highly comparable, the activity for O2 reduction is lower compared to the commercial catalyst. HTC derived carbon has a lower degree of graphitization, less functional oxygen groups on its surface and a lower electrical conductivity than Vulcan®. This suggests different Pt–support interactions.
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You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.eumore_vert DLR publication serv... arrow_drop_down add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=od______1640::5865aa1e25a425c226a06b7f53e80c85&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type 2019 GermanyPublisher:Wiley Schonvogel, Dana; Nowotny, Manuel; Woriescheck, Tim; Multhaupt, Hendrik; Wagner, Peter; Dyck, Alexander; Agert, Carsten; Wark, Michael;Pt catalysts in proton exchange membrane fuel cells (PEMFC) typically use carbon blacks like Vulcan® based on fossil sources. Thus, an important research task is using sustainable supports in PEMFCs. Hydrothermal carbonization (HTC) converts biomasses into chars, which are possible substitutes for fossil-based carbons. In this study, a Pt catalyst derived from HTC of coconut shells is developed for catalysis of O2 reduction in acidic media. Thermal activation enlarges the specific surface area by factor of 7 to 546 m2 g-1, and generates electrical conductivity making the material suitable for catalysis. 1.8±0.5 nm Pt particles are well-distributed on the activated carbon. Cyclic and CO stripping voltammetry show an electrochemical surface area (ECSA) of 69±21 m2 gPt -1, being almost identical to that of the commercial catalyst using Vulcan® (69±6 m2 gPt-1). Although ECSAs are highly comparable, the activity for O2 reduction is lower compared to the commercial catalyst. HTC derived carbon has a lower degree of graphitization, less functional oxygen groups on its surface and a lower electrical conductivity than Vulcan®. This suggests different Pt–support interactions.
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You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.eumore_vert DLR publication serv... arrow_drop_down add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Conference object , Other literature type 2022 GermanyBengen, Nina; Schonvogel, Dana; Müller-Hülstede, Julia; Schmies, Henrike; Wagner, Peter; Wark, Michael;add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=od______1640::39a620779985de7dec70a8ff312187ca&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu0 citations 0 popularity Average influence Average impulse Average Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Conference object , Other literature type 2022 GermanyBengen, Nina; Schonvogel, Dana; Müller-Hülstede, Julia; Schmies, Henrike; Wagner, Peter; Wark, Michael;add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=od______1640::39a620779985de7dec70a8ff312187ca&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu0 citations 0 popularity Average influence Average impulse Average Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=od______1640::39a620779985de7dec70a8ff312187ca&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Conference object , Other literature type 2022 GermanyPublisher:The Electrochemical Society Bengen, Nina; Schmies, Henrike; Müller-Hülstede, Julia; Schonvogel, Dana; Wagner, Peter; Wark, Michael;To improve the lifetime of polymer electrolyte membrane fuel cells (PEMFCs), optimization of the fuel cell components is necessary wherein one research focus is the stability of the platinum catalyst support. Due to the harsh conditions in PEMFCs, e.g. high potentials (≥ 0.85 VRHE) and low pH (≤ 2), the catalyst support, which commonly consists of a high surface area carbon, degrades.[1] This is mainly caused by carbon corrosion, which becomes significant at potentials above 1.1 VRHE.[2] Typically, commercially available and chemically derived raw oil based carbons are used as catalyst supports. The use of multi-walled carbon nanotubes (MWCNTs) as a more stable, graphitic catalyst support with high electrical conductivity is well known in literature.[3, 4] The production of MWCNTs is expensive, which makes upscaling difficult. However, a previous study of our group Schonvogel et al. showed low stability of biomass-based supports, which requires further optimization.[5] Therefore, an approach to increase the stability of the biomass-based carbon support is thermal graphitization to generate a stable and ordered carbon structure. This leads to an increased amount of sp2-hybridized carbon with increased crystallinity and increased graphitic degree. At this point, the use of activated biomasses as carbon support is a cheap and sustainable alternative to MWCNTs and commercially available carbon blacks, for example Vulcan XC-72®.[5, 6] In this work, novel composite supports using thermally treated activated sawdust and MWCNTs will be investigated as Pt-nanoparticle support towards their physical properties and electrochemical ORR activity and stability. Sawdust was steam activated at 750 °C for 1 h in nitrogen atmosphere to create a defined pore system. Afterwards, the activated sawdust (aSD) was mechanically mixed with 20 wt.% MWCNTs. The mixture was treated at high temperatures (1500, 1800 and 2100 °C, under Ar atmosphere) in a furnace. For comparison, MWCNTs only were thermally treated under the same conditions. Physical characterization of the supports was performed using low temperature nitrogen sorption for determination of surface properties and crystallinity powder x-ray diffractometry (PXRD) for analysis of the degree of graphitization. Next, these novel carbon materials were used as support for 40 wt.% platinum nanoparticles. The platinum content was determined using inductive coupled plasma with mass spectrometry (ICP-MS) and the platinum nanoparticle diameter was analyzed with transmission electron microcopy (TEM) resulting in mean diameters ≤ 2 nm. In order to evaluate the activity and stability of the synthesized platinum catalysts, electrochemical characterization was performed for most promising catalysts before and after an accelerated stress test (AST, 0.6 – 1.5 VRHE, 500 mV s-1, 5000 cycles). For electrochemical characterization a three-electrode setup with a rotating ring disc electrode (RRDE) was used. The electrochemical active surface area was obtained by hydrogen underpotential deposition (HUPD) and CO stripping method. In Figure 1 the ORR curves, mass activities (MA) determined at 0.9 VRHE and MA loss of Pt/gaSD_gMWCNTs_2100 and Pt/gMWCNTs_2100 before and after AST are shown. Our study reveals that the mixture of 20 wt.% MWCNTs with sustainable aSD and subsequent thermal treatment results in a catalyst with comparable MA and stability to Pt/MWCNTs_2100. Thus, the use of activated biomass as the main component in catalyst supports constitute a more sustainable and cheaper alternative to MWCNTs. Based on these results, thermal treatment at higher temperatures of ≥ 2500 °C and higher biomass content will be further investigated to increase the stability. [1] F. Ettingshausen, J. Kleemann, A. Marcu, G. Toth, H. Fuess, C. Roth, Fuel Cells 2011, 11, 238-245. [2] V. Bandlamudi, P. Bujlo, C. Sita, S. Pasupathi, Materials Today: Proceedings 2018, 5, 10602-10610. [3] V. N. Popov, Materials Science and Engineering: R: Reports 2004, 43, 61-102. [4] D. Schonvogel, J. Hülstede, P. Wagner, I. Kruusenberg, K. Tammeveski, A. Dyck, C. Agert, M. Wark, J. Electrochem. Soc. 2017, 164, F995-F1004. [5] D. Schonvogel, M. Nowotny, T. Woriescheck, H. Multhaupt, P. Wagner, A. Dyck, C. Agert, M. Wark, Energy Technology 2019, 7, 1900344. [6] M. Iwanow, T. Gartner, V. Sieber, B. Konig, Beilstein J Org Chem 2020, 16, 1188-1202. Figure 1
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You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.eu1 citations 1 popularity Average influence Average impulse Average Powered by BIP!
more_vert DLR publication serv... arrow_drop_down ECS Meeting AbstractsArticle . 2022 . Peer-reviewedLicense: IOP Copyright PoliciesData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1149/ma2022-02421556mtgabs&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Conference object , Other literature type 2022 GermanyPublisher:The Electrochemical Society Bengen, Nina; Schmies, Henrike; Müller-Hülstede, Julia; Schonvogel, Dana; Wagner, Peter; Wark, Michael;To improve the lifetime of polymer electrolyte membrane fuel cells (PEMFCs), optimization of the fuel cell components is necessary wherein one research focus is the stability of the platinum catalyst support. Due to the harsh conditions in PEMFCs, e.g. high potentials (≥ 0.85 VRHE) and low pH (≤ 2), the catalyst support, which commonly consists of a high surface area carbon, degrades.[1] This is mainly caused by carbon corrosion, which becomes significant at potentials above 1.1 VRHE.[2] Typically, commercially available and chemically derived raw oil based carbons are used as catalyst supports. The use of multi-walled carbon nanotubes (MWCNTs) as a more stable, graphitic catalyst support with high electrical conductivity is well known in literature.[3, 4] The production of MWCNTs is expensive, which makes upscaling difficult. However, a previous study of our group Schonvogel et al. showed low stability of biomass-based supports, which requires further optimization.[5] Therefore, an approach to increase the stability of the biomass-based carbon support is thermal graphitization to generate a stable and ordered carbon structure. This leads to an increased amount of sp2-hybridized carbon with increased crystallinity and increased graphitic degree. At this point, the use of activated biomasses as carbon support is a cheap and sustainable alternative to MWCNTs and commercially available carbon blacks, for example Vulcan XC-72®.[5, 6] In this work, novel composite supports using thermally treated activated sawdust and MWCNTs will be investigated as Pt-nanoparticle support towards their physical properties and electrochemical ORR activity and stability. Sawdust was steam activated at 750 °C for 1 h in nitrogen atmosphere to create a defined pore system. Afterwards, the activated sawdust (aSD) was mechanically mixed with 20 wt.% MWCNTs. The mixture was treated at high temperatures (1500, 1800 and 2100 °C, under Ar atmosphere) in a furnace. For comparison, MWCNTs only were thermally treated under the same conditions. Physical characterization of the supports was performed using low temperature nitrogen sorption for determination of surface properties and crystallinity powder x-ray diffractometry (PXRD) for analysis of the degree of graphitization. Next, these novel carbon materials were used as support for 40 wt.% platinum nanoparticles. The platinum content was determined using inductive coupled plasma with mass spectrometry (ICP-MS) and the platinum nanoparticle diameter was analyzed with transmission electron microcopy (TEM) resulting in mean diameters ≤ 2 nm. In order to evaluate the activity and stability of the synthesized platinum catalysts, electrochemical characterization was performed for most promising catalysts before and after an accelerated stress test (AST, 0.6 – 1.5 VRHE, 500 mV s-1, 5000 cycles). For electrochemical characterization a three-electrode setup with a rotating ring disc electrode (RRDE) was used. The electrochemical active surface area was obtained by hydrogen underpotential deposition (HUPD) and CO stripping method. In Figure 1 the ORR curves, mass activities (MA) determined at 0.9 VRHE and MA loss of Pt/gaSD_gMWCNTs_2100 and Pt/gMWCNTs_2100 before and after AST are shown. Our study reveals that the mixture of 20 wt.% MWCNTs with sustainable aSD and subsequent thermal treatment results in a catalyst with comparable MA and stability to Pt/MWCNTs_2100. Thus, the use of activated biomass as the main component in catalyst supports constitute a more sustainable and cheaper alternative to MWCNTs. Based on these results, thermal treatment at higher temperatures of ≥ 2500 °C and higher biomass content will be further investigated to increase the stability. [1] F. Ettingshausen, J. Kleemann, A. Marcu, G. Toth, H. Fuess, C. Roth, Fuel Cells 2011, 11, 238-245. [2] V. Bandlamudi, P. Bujlo, C. Sita, S. Pasupathi, Materials Today: Proceedings 2018, 5, 10602-10610. [3] V. N. Popov, Materials Science and Engineering: R: Reports 2004, 43, 61-102. [4] D. Schonvogel, J. Hülstede, P. Wagner, I. Kruusenberg, K. Tammeveski, A. Dyck, C. Agert, M. Wark, J. Electrochem. Soc. 2017, 164, F995-F1004. [5] D. Schonvogel, M. Nowotny, T. Woriescheck, H. Multhaupt, P. Wagner, A. Dyck, C. Agert, M. Wark, Energy Technology 2019, 7, 1900344. [6] M. Iwanow, T. Gartner, V. Sieber, B. Konig, Beilstein J Org Chem 2020, 16, 1188-1202. Figure 1
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For further information contact us at helpdesk@openaire.eu1 citations 1 popularity Average influence Average impulse Average Powered by BIP!
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For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article 2024 GermanyPublisher:Royal Society of Chemistry (RSC) Funded by:DFGDFGWartner, Garlef; Müller-Hülstede, Julia; Trzesniowski, Hanna; Wark, Michael; Wagner, Peter; Seidel, Robert;doi: 10.1039/d4se00342j
Novel biomass based Fe–N–C catalysts exhibit a higher density of FeNx type sites with different redox characteristics compared to carbon black based Fe–N–Cs. These different characteristics are influenced by heteroatom doping and undercoordination.
add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.euAccess RoutesGreen hybrid 0 citations 0 popularity Average influence Average impulse Average Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article 2024 GermanyPublisher:Royal Society of Chemistry (RSC) Funded by:DFGDFGWartner, Garlef; Müller-Hülstede, Julia; Trzesniowski, Hanna; Wark, Michael; Wagner, Peter; Seidel, Robert;doi: 10.1039/d4se00342j
Novel biomass based Fe–N–C catalysts exhibit a higher density of FeNx type sites with different redox characteristics compared to carbon black based Fe–N–Cs. These different characteristics are influenced by heteroatom doping and undercoordination.
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For further information contact us at helpdesk@openaire.euAccess RoutesGreen hybrid 0 citations 0 popularity Average influence Average impulse Average Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1039/d4se00342j&type=result"></script>'); --> </script>
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