Linking the Photoinduced Surface Potential Difference to Interfacial Charge Transfer in Photoelectrocatalytic Water Oxidation

被引:43
作者
Chen, Ruotian [1 ]
Zhang, Deyun [1 ,2 ]
Wang, Ziyuan [1 ,3 ]
Li, Dongfeng [1 ,2 ]
Zhang, Lingcong [1 ]
Wang, Xiuli [1 ]
Fan, Fengtao [1 ]
Li, Can [1 ,2 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, iChEM,State Key Lab Catalysis, Dalian 116023, Liaoning, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Xiamen Univ, Coll Chem & Chem Engn, iChEM, Xiamen 361005, Peoples R China
基金
中国国家自然科学基金;
关键词
PHOTOELECTROLYSIS; CHEMISTRY; JUNCTIONS; KINETICS;
D O I
10.1021/jacs.2c12704
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Charge transfer at the semiconductor/solution interface is fundamental to photoelectrocatalytic water splitting. Although insights into charge transfer in the electrocatalytic process can be gained from the phenomenological Butler-Volmer theory, there is limited understanding of interfacial charge transfer in the photo-electrocatalytic process, which involves intricate effects of light, bias, and catalysis. Here, using operando surface potential measurements, we decouple the charge transfer and surface reaction processes and find that the surface reaction enhances the photovoltage via a reaction-related photoinduced charge transfer regime as demonstrated on a SrTiO3 photoanode. We show that the reaction-related charge transfer induces a change in the surface potential that is linearly correlated to the interfacial charge transfer rate of water oxidation. The linear behavior is independent of the applied bias and light intensity and reveals a general rule for interfacial transfer of photogenerated minority carriers. We anticipate the linear rule to be a phenomenological theory for describing interfacial charge transfer in photoelectrocatalysis.
引用
收藏
页码:4667 / 4674
页数:8
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