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Plastic film mulching (FM) became a general practice to enhance crop productivity and its net primary production (NPP), but it can increase greenhouse gas (GHG) emissions. The proper addition of organic amendments might effectively decrease the impact of FM on global warming. To evaluate the feasibility of biomass addition on decreasing this negative influence, cover crop biomass as a green manure was incorporated with different recycling levels (0-100% of aboveground biomass) under FM and no-mulching. The net global warming potential (GWP) which integrated with soil C stock change and GHG (N2O and CH4) fluxes with CO2-equivalent was evaluated during maize cultivation. Under the same biomass incorporation, FM significantly enhanced the grain productivity and NPP of maize by 22-61 and 18-58% over no-mulching, respectively. In contrast, FM also highly increased the respired C loss, which was 11-95% higher than NPP increase, over no-mulching. Irrespective with biomass recycling ratio and mulching system, negative NECB which indicates the decrease of soil C stock was observed, mainly due to big harvest removal. FM decreased more soil C stock by 57-158% over no-mulching, but its C stock was clearly increased with increasing biomass addition. FM significantly increased total N2O and CH4 fluxes by 4-61 and 140-600% over no-mulching, respectively. Soil C stock changes mainly decided net GWP scale, but N2O and CH4 fluxes negligibly influenced. As a result, FM highly increased net GWP over no-mulching, while this net GWP was clearly decreased with increasing biomass application. However, cover cropping, and its biomass recycling was not enough to compensate the negative impact of FM on global warming. Therefore, more biomass incorporation might be essential to compensate this negative effect of FM.

The current status and challenges associated with the production and utilization of cellulosic ethanol in Korea are reviewed in this paper. Cellulosic ethanol has emerged as a promising option for mitigating Korea's CO(2) emissions and enhancing its energy security. Korea's limited biomass resources is the most critical barrier to achieving its implementation targets for cellulosic ethanol. Efforts to identify new suitable biomass resources for cellulosic ethanol production are ongoing and intensive. Aquatic biomasses including macroalgae and plantation wastes collected in the Southeast Asia region have been found to have great potential as feedstocks for the production of cellulosic ethanol. R&D explorations into the development of technologies that can convert biomass materials to ethanol more efficiently also are underway. It is expected that cellulosic ethanol will be in supply from 2020 and that, by 2030, its use will have effectively reduced Korea's total gasoline consumption by 10%.

Abstract We report all-polymer solar cells with new electron-accepting (n-type) polymer nanoparticles, poly(2,7-bis(4-hexylthiophen-2-yl)-9H-fluoren-9-one-co-benzothiadiazole) (BHTF-co-BT), which were in-situ generated during polymerization reaction. The size of the BHTF-co-BT nanoparticles was ca. 5–15 nm with a particular single X-ray diffraction peak (d-spacing=1.3 nm), indicative of a highly ordered crystalline state, while their glass transition temperature was ~140 °C. Their band gap energy and ionization potential were 1.8 eV and 5.7 eV, respectively. The possibility of the BHTF-co-BT nanoparticles as an electron acceptor for both normal-type and inverted-type all-polymer (polymer:polymer) solar cells was examined by employing poly(3-hexylthiophene) (P3HT) as an electron donor. The normal-type P3HT:BHTF-co-BT solar cells exhibited promising open circuit voltage ( V oc =0.67–0.73 V) and fill factor (FF=51.3%), while a three-fold improved short circuit current density and higher V oc (0.77 V) were achieved for their inverted-type solar cells.

Abstractπ‐Conjugated polyelectrolytes (CPEs) have been studied as interlayers on top of a separate hole transport layer (HTL) to improve the wetting, interfacial defect passivation, and crystal growth of perovskites. However, very few CPE‐based HTLs have been reported without rational molecular design as ideal HTLs for perovskite solar cells (PeSCs). In this study, the authors synthesize a triphenylamine‐based anionic CPE (TPAFS‐TMA) as an HTL for p‐i‐n‐type PeSCs. TPAFS‐TMA has appropriate frontier molecular orbital (FMO) levels similar to those of the commonly used poly(bis(4‐phenyl)‐2,4,6‐trimethylphenylamine) (PTAA) HTL. The ionic and semiconducting TPAFS‐TMA shows high compatibility, high transmittance, appropriate FMO energy levels for hole extraction and electron blocking, as well as defect passivating properties, which are confirmed using various optical and electrical analyses. Thus, the PeSC with the TPAFS‐TMA HTL exhibits the best power conversion efficiency (PCE) of 20.86%, which is better than that of the PTAA‐based device (PCE of 19.97%). In addition, it exhibits negligible device‐to‐device variations in its photovoltaic performance, contrary to the device with PTAA. Finally, a large‐area PeSC (1 cm2) and mini‐module (3 cm2), showing PCEs of 19.46% and 18.41%, respectively, are successfully fabricated. The newly synthesized TPAFS‐TMA may suggest its great potential as an HTL for large‐area PeSCs.

The potential of deoiled Azolla pinnata biomass (DAB) as electrode and substrate was evaluated for microbial fuel cell (MFC) operation. The anode electrode was fabricated using biochar obtained by subjecting DAB to pyrolysis at 600 °C, while the reducing sugars after hydrolysis of DAB by acid pretreatment was used as substrate. The post pyrolyzed biochar (P-DAB) was characterized for structural and elemental functionalities using SEM, XRD and Raman spectroscopy, whereas the reducing sugar obtained from hydrolyzed DAB (H-DAB) was analyzed for its composition. Experimental results indicated that at a given 3 g COD/L resulted in a voltage of 382 mV with 65.6% of COD reduction in closed circuit (CC) mode of operation. Cyclic voltammetric analysis depicted maximum oxidative and reductive peak currents of 3.42 mA and -4.0 mA. Noticeable peaks were also identified in CC (-0.2 V to +0.2 V and -0.19 V to -0.3 V) and OC (+0.2 V to +0.4 V and -0.1 V to -0.3 V) corresponding to complex IV cytochrome c couples (cytochrome Cox (Cyt Cox)/cytochrome Crd (Cyt Crd)), signifying the participation of electron carriers during electron transfer. The microbiome diversity showed dominance of Proteobacteria, a phylum known for exo-electrogenic bacterial species. The DAB-derived products account to environmental sustainability and support circular bioeconomy in a biorefinery mode.

The use of hyphenated LC-NMR and LC-MS techniques for the purpose of directly identifying the major constituents of Belamcanda chinensis was investigated. Reversed-phase isocratic chromatography was performed using an acetonitrile-water solvent system on a C18 column. The NMR spectrum yielded five main peaks, whose analysis revealed them to be 5, 6, 7, 3'-tetrahydroxy-4'-methoxyisoflavone (1), tectorigenin (2), iristectorigenin A (3), irigenin (4), and irisflorentine (5). The identification of these constituents was confirmed by performing LC-ESI-MS experiment. This study shows that hyphenated LC-NMR and LC-MS can be used for the rapid (70 min) identification of the isoflavonoids.

Due to their high surface areas and large pore volumes, porous carbons (PCs) are valuable materials for use as electrodes in energy storage and conversion devices. Biomass is an ideal precursor for the preparation of PCs in part because it is sustainable and eco-friendly. Herein, new methodology for converting agarose, a naturally occurring type of biomass that forms robust hydrogels, into PCs with tunable pore structures and high electrochemical performance is described. The synthetic process is straightforward and entails heating a gel that is composed of agarose and potassium oxalate (K 2 C 2 O 4 ). Since the salt transforms into gaseous byproducts at elevated temperatures, the decomposition process was harnessed to create activated, open pores as the hydrogel underwent carbonization. For example, a PC with a surface area of 1754.9 m 2 g –1 and a pore volume of 2.643 cm 3 g –1 was obtained by heating a mixture of agarose and K 2 C 2 O 4 in a 1:3 weight ratio at 700 °C. The material was subsequently used as the electrode material in a supercapacitor and found to display a specific capacitance of 166.0 F g –1 at 0.125 A g –1 . Varying the quantity of added K 2 C 2 O 4 resulted in predictable changes in porosity and thus offered a means to tune the textural properties and the electrochemical performance of the PCs. For example, changing the feed ratio of agarose to K 2 C 2 O 4 to 1:6 afforded a PC that exhibited a high persistent specific capacitance (64.1 F g –1 at 5 A g –1 after 10,000 cycles) and a high-power density (20 kW kg –1 at 10 A g –1 ).

AbstractThis paper presents an understanding of the fundamental carrier transport mechanism in hydrogenated amorphous silicon (a‐Si:H)‐based n/p junctions. These n/p junctions are, then, used as tunneling and recombination junctions (TRJ) in tandem solar cells, which were constructed by stacking the a‐Si:H‐based solar cell on the heterojunction with intrinsic thin layer (HIT) cell. First, the effect of activation energy (Ea) and Urbach parameter (Eu) of n‐type hydrogenated amorphous silicon (a‐Si:H(n)) on current transport in an a‐Si:H‐based n/p TRJ has been investigated. The photoluminescence spectra and temperature‐dependent current–voltage characteristics in dark condition indicates that the tunneling is the dominant carrier transport mechanism in our a‐Si:H‐based n/p‐type TRJ. The fabrication of a tandem cell structure consists of an a‐Si:H‐based top cell and an HIT‐type bottom cell with the a‐Si:H‐based n/p junction developed as a TRJ in between. The development of a‐Si:H‐based n/p junction as a TRJ leads to an improved a‐Si:H/HIT‐type tandem cell with a better open circuit voltage (Voc), fill factor (FF), and efficiency. The improvements in the cell performance was attributed to the wider band‐tail states in the a‐Si:H(n) layer that helps to an enhanced tunneling and recombination process in the TRJ. The best photovoltage parameters of the tandem cell were found to be Voc = 1430 mV, short circuit current density = 10.51 mA/cm2, FF = 0.65, and efficiency = 9.75%. Copyright © 2015 John Wiley & Sons, Ltd.