光电阴极
材料科学
光电流
氧化物
分解水
太阳能燃料
光电化学
光催化
半导体
光电子学
化学工程
兴奋剂
氧化铟锡
光电解
电解质
电极
铟
阳极
氧化锡
金属
无机化学
析氧
锡
阳极氧化
氢
光电化学电池
纳米技术
氢燃料
制氢
钒酸铋
电化学
太阳能
双金属片
可逆氢电极
作者
Sanghyun Bae,Thomas Moehl,David Yong,Peng Zeng,S. David Tilley
出处
期刊:Joule
[Elsevier BV]
日期:2025-10-25
卷期号:9 (11): 102172-102172
被引量:1
标识
DOI:10.1016/j.joule.2025.102172
摘要
Summary
The development of efficient, stable, and earth-abundant photoanodes for solar water oxidation is critical to advancing photoelectrochemical and photocatalytic systems for large-scale renewable fuel production. Here, we demonstrate that p-type Cu2O, typically studied as a photocathode material, can be used as a high-performance photoanode through judicious engineering of charge carrier-selective contacts on thermally oxidized Cu2O sheets. The introduction of Ga2O3, TiO2, and indium tin oxide (ITO) layers as an electron-selective back contact, combined with Al2O3, Au, and Ni front layers, significantly enhanced charge separation and electron transfer. The champion Cu2O photoanode exhibited a photocurrent density of 8.65 mA cm−2 at 1.23 V vs. the reversible hydrogen electrode in alkaline media, which is the highest reported for metal oxide photoanodes. These findings highlight the pivotal role of charge carrier-selective interface engineering in broadening the scope of available semiconductor materials for photo(electro)catalytic oxidation reactions, irrespective of the doping type of the light-absorbing material.
科研通智能强力驱动
Strongly Powered by AbleSci AI