Hydrogen Evolution from Pt/Ru-Coated p-Type WSe2 Photocathodes

被引:186
作者
McKone, James R.
Pieterick, Adam P.
Gray, Harry B. [1 ]
Lewis, Nathan S.
机构
[1] CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA
关键词
SURFACE RECOMBINATION VELOCITIES; INVERSION LAYER FORMATION; ELECTROCHEMICAL CHARACTERIZATION; ELECTRICAL-PROPERTIES; TUNGSTEN DISULFIDE; PHOTO-CATHODES; N-TYPE; SOLAR; EFFICIENT; PASSIVATION;
D O I
10.1021/ja308581g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Crystalline p-type WSe2 has been grown by a chemical vapor transport method. After deposition of noble metal catalysts, p-WSe2 photocathodes exhibited thermodynamically based photoelectrode energy-conversion efficiencies of >7% for the hydrogen evolution reaction under mildly acidic conditions, and were stable under cathodic conditions for at least 2 h in acidic as well as in alkaline electrolytes. The open circuit potentials of the photoelectrodes in contact with the H+/H-2 redox couple were very close to the bulk recombination/diffusion limit predicted from the Shockley diode equation. Only crystals with a prevalence of surface step edges exhibited a shift in flat-band potential as the pH was varied. Spectral response data indicated effective minority-carrier diffusion lengths of similar to 1 mu m, which limited the attainable photocurrent densities in the samples to similar to 15 mA cm(-2) under 100 mW cm(-2) of Air Mass 1.5G illumination.
引用
收藏
页码:223 / 231
页数:9
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