A Bismuth Vanadate-Cuprous Oxide Tandem Cell for Overall Solar Water Splitting

被引:215
作者
Bornoz, Pauline [1 ]
Abdi, Fatwa F. [2 ,3 ]
Tilley, S. David [4 ]
Dam, Bernard [3 ]
van de Krol, Roel [2 ]
Graetzel, Michael [4 ]
Sivula, Kevin [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Lab Mol Engn Optoelect Nanomat, Stn 6, CH-1015 Lausanne, Switzerland
[2] Helmholtz Zentrum Berlin Mat & Energie Gmbh, Inst Solar Fuels, D-14109 Berlin, Germany
[3] Delft Univ Technol, Dept Chem Engn, NL-2600 GA Delft, Netherlands
[4] Ecole Polytech Fed Lausanne, Lab Photon & Interfaces, CH-1015 Lausanne, Switzerland
基金
瑞士国家科学基金会;
关键词
OXYGEN-EVOLVING CATALYST; PHOTOELECTROCHEMICAL CELLS; HYDROGEN-PRODUCTION; OXIDATION; PHOTOCATALYSIS; PHOTOANODES; PHOTOLYSIS; FILMS;
D O I
10.1021/jp500441h
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Through examination of the optoelectronic and photoelectrochemical properties of BiVO4 and Cu2O photoelectrodes, we evaluate the feasibility of a BiVO4/Cu2O photoanode/photocathode tandem cell for overall unassisted solar water splitting. Using state-of-the-art photoelectrodes we identify current-matching conditions by altering the photoanode active layer thickness. By further employing water oxidation and reduction catalysts (Co-Pi and RuOx, respectively) together with an operating point analysis, we show that an unassisted solar photocurrent density on the order of 1 mA cm(-2) is possible in a tandem cell and moreover gain insight into routes for improvement. Finally, we demonstrate the unassisted 2-electrode operation of the tandem cell. Photocurrents corresponding to ca. 0.5% solar-to-hydrogen conversion efficiency were found to decay over the course of minutes because of the detachment of the Co-Pi catalyst. This aspect provides a fundamental challenge to the stable operation of the tandem cell with the currently employed catalysts.
引用
收藏
页码:16959 / 16966
页数:8
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