期刊
JOURNAL OF PHYSICAL CHEMISTRY C
卷 120, 期 20, 页码 10941-10950出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.6b02432
关键词
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资金
- Strong Research Environment Solar Fuels (Umea University)
- Artificial Leaf Project Umea (Knut & Alice Wallenberg foundation)
- Energimyndigheten
- Umea Core Facility for Electron Microscopy (UCEM)
- Vibrational Spectroscopy Platform
- X-ray laboratory at the Chemical Biological Centre (KBC) at Umea University
Oxygen evolution catalysts (OEC) are often employed on the surface of photoactive, semiconducting photoanodes to boost their kinetics and stability during photoelectrochemical water oxidation. However, the necessity of using optically transparent OEC to avoid parasitic light absorption by the OEC under front-side illumination is often neglected. Here, we show that furnishing the surface of a WO3 photoanode with suitable loading of FeOOH as a transparent OEC improved the photocurrent density by 300% at 1 V versus RHE and the initial photocurrent-to-O-2 Faradaic efficiency from similar to 70 to similar to 100%. The data from the photo-voltammetry, electrochemical impedance, and gas evolution measurements these improvements were a combined result of reduced hole-transfer resistance for water oxidation, minimized surface recombination of charge carriers, and improved stability against photocorrosion of WO3. We demonstrate the utility of transparent FeOOH-coated W(O)3 in a solar-powered, tandem water-splitting device by combining it with a double-junction Si solar cell and a Ni-Mo hydrogen evolution catalyst. This device performed at a solar-to-hydrogen conversion efficiency of 1.8% in near-neutral K2SO4 electrolyte.
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