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description Publicationkeyboard_double_arrow_right Article , Journal 2018 ItalyPublisher:Wiley Alessio Dessì; Matteo Monai; Matteo Bessi; Tiziano Montini; Massimo Calamante; Alessandro Mordini; Gianna Reginato; Cosimo Trono; Paolo Fornasiero; Lorenzo Zani;AbstractDonor–acceptor dyes are a well‐established class of photosensitizers, used to enhance visible‐light harvesting in solar cells and in direct photocatalytic reactions, such as H2 production by photoreforming of sacrificial electron donors (SEDs). Amines—typically triethanolamine (TEOA)—are commonly employed as SEDs in such reactions. Dye‐sensitized photoreforming of more sustainable, biomass‐derived alcohols, on the other hand, was only recently reported by using methanol as the electron donor. In this work, several rationally designed donor–acceptor dyes were used as sensitizers in H2 photocatalytic production, comparing the efficiency of TEOA and EtOH as SEDs. In particular, the effect of hydrophobic chains in the spacer and/or the donor unit of the dyes was systematically studied. The H2 production rates were higher when TEOA was used as SED, whereas the activity trends depended on the SED used. The best performance was obtained with TEOA by using a sensitizer with just one bulky hydrophobic moiety, propylenedioxythiophene, placed on the spacer unit. In the case of EtOH, the best‐performing sensitizers were the ones featuring a thiazolo[5,4‐d]thiazole internal unit, needed for enhancing light harvesting, and carrying alkyl chains on both the donor part and the spacer unit. The results are discussed in terms of reaction mechanism, interaction with the SED, and structural/electrochemical properties of the sensitizers.
CNR ExploRA arrow_drop_down ChemSusChemArticle . 2018 . Peer-reviewedLicense: Wiley Online Library User AgreementData sources: CrossrefUniversità degli Studi di Siena: USiena airArticle . 2018Data sources: Bielefeld Academic Search Engine (BASE)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=10.1002/cssc.201701707&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess Routesbronze 37 citations 37 popularity Top 10% influence Top 10% impulse Top 10% Powered by BIP!
more_vert CNR ExploRA arrow_drop_down ChemSusChemArticle . 2018 . Peer-reviewedLicense: Wiley Online Library User AgreementData sources: CrossrefUniversità degli Studi di Siena: USiena airArticle . 2018Data sources: Bielefeld Academic Search Engine (BASE)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=10.1002/cssc.201701707&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu
description Publicationkeyboard_double_arrow_right Article , Journal 2018 ItalyPublisher:Wiley Alessio Dessì; Matteo Monai; Matteo Bessi; Tiziano Montini; Massimo Calamante; Alessandro Mordini; Gianna Reginato; Cosimo Trono; Paolo Fornasiero; Lorenzo Zani;AbstractDonor–acceptor dyes are a well‐established class of photosensitizers, used to enhance visible‐light harvesting in solar cells and in direct photocatalytic reactions, such as H2 production by photoreforming of sacrificial electron donors (SEDs). Amines—typically triethanolamine (TEOA)—are commonly employed as SEDs in such reactions. Dye‐sensitized photoreforming of more sustainable, biomass‐derived alcohols, on the other hand, was only recently reported by using methanol as the electron donor. In this work, several rationally designed donor–acceptor dyes were used as sensitizers in H2 photocatalytic production, comparing the efficiency of TEOA and EtOH as SEDs. In particular, the effect of hydrophobic chains in the spacer and/or the donor unit of the dyes was systematically studied. The H2 production rates were higher when TEOA was used as SED, whereas the activity trends depended on the SED used. The best performance was obtained with TEOA by using a sensitizer with just one bulky hydrophobic moiety, propylenedioxythiophene, placed on the spacer unit. In the case of EtOH, the best‐performing sensitizers were the ones featuring a thiazolo[5,4‐d]thiazole internal unit, needed for enhancing light harvesting, and carrying alkyl chains on both the donor part and the spacer unit. The results are discussed in terms of reaction mechanism, interaction with the SED, and structural/electrochemical properties of the sensitizers.
CNR ExploRA arrow_drop_down ChemSusChemArticle . 2018 . Peer-reviewedLicense: Wiley Online Library User AgreementData sources: CrossrefUniversità degli Studi di Siena: USiena airArticle . 2018Data sources: Bielefeld Academic Search Engine (BASE)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=10.1002/cssc.201701707&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess Routesbronze 37 citations 37 popularity Top 10% influence Top 10% impulse Top 10% Powered by BIP!
more_vert CNR ExploRA arrow_drop_down ChemSusChemArticle . 2018 . Peer-reviewedLicense: Wiley Online Library User AgreementData sources: CrossrefUniversità degli Studi di Siena: USiena airArticle . 2018Data sources: Bielefeld Academic Search Engine (BASE)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=10.1002/cssc.201701707&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu