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- Yang, Yong, et al.
(författare)
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Evident Enhancement of Photoelectrochemical Hydrogen Production by Electroless Deposition of M-B (M = Ni, Co) Catalysts on Silicon Nanowire Arrays
- 2016
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Ingår i: ACS Applied Materials and Interfaces. - : American Chemical Society. - 1944-8244 .- 1944-8252. ; 8:44, s. 30143-30151
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Tidskriftsartikel (refereegranskat)abstract
- Modification of p-type Si surface by active and stable earth-abundant electrocatalysts is an effective strategy to improve the sluggish kinetics for the hydrogen evolution reaction (HER) at p-Si/electrolyte interface and to develop highly efficient and low-cost photocathodes for hydrogen production from water. To this end, Si nanowire (Si-NW) array has been loaded-with highly efficient electrocatalysts, M-B (M = Ni, Co), by facile and quick electroless plating to build M-B catalyst-modified Si nanowire-array-textured photocathodes for water reduction to H-2. Compared with the bare Si-NW array, composite Si-NWs/M-B arrays display evidently enhanced photoelectrochemical (PEC) performance. The onset potential (V-phon) of cathodic photocurrent is positively shifted by 530-540 mV to 0.44-0.45 V vs RHE, and the short-circuit current density (J(sc)) is up to 19.5 mA cm(-2) in neutral buffer solution under simulated 1 sun illumination. Impressively, the half-cell photopower conversion efficiencies (eta(hc)) of the optimized Si-NWs/Co-B (2.53%) and Si-NWs/Ni-B (2.45%) are comparable to that of Si-NWs/Pt (2.46%). In terms of the large J(sc), V-phon, and eta(hc) values, as well as the high Faradaic efficiency, Si-NW-s/M-B electrodes are among the top performing Si photocathodes which are modified with HER electrocatalysts but have no buried solid/solid junction.
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| 2. |
- Zhao, Yawei, et al.
(författare)
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Fine-tuning the coordination atoms of copper redox mediators : an effective strategy for boosting the photovoltage of dye-sensitized solar cells
- 2019
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Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry. - 2050-7488 .- 2050-7496. ; 7:20, s. 12808-12814
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Tidskriftsartikel (refereegranskat)abstract
- Natural systems have marvelously utilized copper complexes featuring sulfur-coordinating ligands, known as blue copper proteins, as efficient electron-transfer mediators in biological processes. Copper complexes with sulfur-coordinating ligands have been attempted as redox mediators in dye-sensitized solar cells (DSCs), the performance of which is not yet satisfactory and still remains less well explored. Herein, we report the application of new copper complexes bearing a tetradentate polythioether ligand, [(S-4)Cu](2+/+) (1(2+/+), S-4 = 1,4,8,11-tetrathiocyclotetradecane), as a redox mediator in DSCs in comparison with its N-4-tetradentate counterpart [(N-4)Cu](2+/+) (2(2+/+), N-4 = 1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecane). Impressively, the changes of coordination atoms from N to S positively shift the formal redox potential of the copper complexes by 600 mV, leading to a remarkably high photovoltage approaching 1.0 V. This is one of the highest photovoltage values reported thus far for DSCs based on copper redox mediators.
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