光电阴极
选择性
电解质
电催化剂
材料科学
光电化学
半导体
退火(玻璃)
电化学
氧化还原
可逆氢电极
纳米技术
碳纤维
光电化学电池
电极
化学
无机化学
光电子学
催化作用
电子
冶金
物理化学
工作电极
生物化学
物理
量子力学
复合材料
复合数
作者
Guosong Zeng,Guiji Liu,Gabriele Panzeri,Chanyeon Kim,Chengyu Song,Olivia Alley,Alexis T. Bell,Adam Z. Weber,Francesca M. Toma
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-12-09
卷期号:10 (1): 34-39
被引量:5
标识
DOI:10.1021/acsenergylett.4c02259
摘要
Light-driven reduction of CO2 into chemicals using a photoelectrochemical (PEC) approach is considered as a promising way to meet the carbon neutral target. The very top surface of the photoelectrode and semiconductor/electrolyte interface plays a pivotal role in defining the performance for PEC CO2 reduction. However, such impact remains poorly understood. Here, we report an electrodeposition-annealing route for tailoring surface composition of ZnTe photocathodes. Our work demonstrates that a Zn-rich surface on the ZnTe photocathode is essential to impact the CO2 reduction activity and selectivity. In particular, the Zn-rich surface not only facilitated the interfacial charge carrier transfer, but also acted as electrocatalyst for boosting carbon product selectivity and suppressing the hydrogen evolution reaction. This work provides a new avenue to optimize the photocathode, as well as improvement of the CO2RR performance.
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