Palladium oxide as a novel oxygen evolution catalyst on BiVO4 photoanode for photoelectrochemical water splitting

被引:58
|
作者
Kim, Jin Hyun [1 ,2 ]
Jang, Ji Wook [3 ]
Kang, Hyun Joon [1 ,2 ]
Magesh, Ganesan [3 ]
Kim, Jae Young [3 ]
Kim, Ju Hun [1 ,2 ]
Lee, Jinwoo [1 ,2 ]
Lee, Jae Sung [3 ]
机构
[1] Pohang Univ Sci & Technol POSTECH, Sch Environm Sci & Engn, Pohang 790784, South Korea
[2] Pohang Univ Sci & Technol POSTECH, Dept Chem Engn, Pohang 790784, South Korea
[3] Ulsan Natl Inst Sci & Technol, Sch Energy & Chem Engn, Ulsan 689798, South Korea
基金
新加坡国家研究基金会;
关键词
BiVO4; Photocatalyst; Electrocatalyst; Palladium oxide; Surface charge separation; VISIBLE-LIGHT; OXIDATION; EFFICIENT; PERFORMANCE; DECOMPOSITION; COMPOSITE; ELECTRODE;
D O I
10.1016/j.jcat.2014.06.015
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
Various oxygen evolution electrocatalysts including cobalt phosphate, FeOOH, Ag+, and metal oxides MOx (M = Co, Mn, Ni, Cu, Rh, Jr, Ru, Pd) were loaded on BiVO4 photoanode for photoelectrochemical water splitting under simulated solar light. In all cases, the electocatalysts increased photocurrent generation and brought cathodic shifts of current onset potential. The screening test led to discovery of a novel PdOx-loaded BiVO4 electrode that showed the best performance in terms of fivefold increase in photocurrent, the largest onset potential shift, and dramatically improved stability, relative to bare BiVO4. To assess the role of the electrocatalyst in a quantitative way, photooxidation of sulfite ion was investigated as a sacrificial agent to obtain charge separation yields in the bulk and on the surface of BiVO4. The analysis clearly demonstrated that electrocatalysts reduced surface charge recombination with no effect on bulk recombination. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:126 / 134
页数:9
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