分解水
析氧
钒酸铋
材料科学
光激发
钒
钒酸盐
催化作用
铋
半导体
氧气
化学工程
光催化
无机化学
光电子学
化学
原子物理学
物理化学
电极
物理
电化学
冶金
激发态
有机化学
生物化学
工程类
作者
Tae Woo Kim,Kyoung-Shin Choi
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2014-02-14
卷期号:343 (6174): 990-994
被引量:3098
标识
DOI:10.1126/science.1246913
摘要
Bismuth vanadate (BiVO4) has a band structure that is well-suited for potential use as a photoanode in solar water splitting, but it suffers from poor electron-hole separation. Here, we demonstrate that a nanoporous morphology (specific surface area of 31.8 square meters per gram) effectively suppresses bulk carrier recombination without additional doping, manifesting an electron-hole separation yield of 0.90 at 1.23 volts (V) versus the reversible hydrogen electrode (RHE). We enhanced the propensity for surface-reaching holes to instigate water-splitting chemistry by serially applying two different oxygen evolution catalyst (OEC) layers, FeOOH and NiOOH, which reduces interface recombination at the BiVO4/OEC junction while creating a more favorable Helmholtz layer potential drop at the OEC/electrolyte junction. The resulting BiVO4/FeOOH/NiOOH photoanode achieves a photocurrent density of 2.73 milliamps per square centimenter at a potential as low as 0.6 V versus RHE.
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