异质结
半导体
光电子学
材料科学
光电阴极
电子转移
纳米技术
离子
光伏
电子
光伏系统
化学
物理
电气工程
光化学
工程类
有机化学
量子力学
作者
Hongzheng Dong,Xiangyu Pan,Yuancai Gong,Mengfan Xue,Pin Wang,SocMan Ho‐Kimura,Yingfang Yao,Hao Xin,Wenjun Luo,Zhigang Zou
标识
DOI:10.1038/s41467-023-43916-6
摘要
In the past decades, a band alignment theory has become a basis for designing different high-performance semiconductor devices, such as photocatalysis, photoelectrocatalysis, photoelectrostorage and third-generation photovoltaics. Recently, a faradaic junction model (coupled electron and ion transfer) has been proposed to explain charge transfer phenomena in these semiconductor heterojunctions. However, the classic band alignment theory cannot explain coupled electron and ion transfer processes because it only regulates electron transfer. Therefore, it is very significant to explore a suitable design concept for regulating coupled electron and ion transfer in order to improve the performance of semiconductor heterojunctions. Herein, we propose a potential window alignment theory for regulating ion transfer and remarkably improving the photoelectrocatalytic performance of a MoS2/Cd-Cu2ZnSnS4 heterojunction photocathode. Moreover, we find that a faradaic potential window, rather than the band position of the intermediate layer, is a criterion for identifying interface charge transfer direction. This finding can offer different perspectives for designing high-performance semiconductor heterojunctions with suitable potential windows for solar energy conversion and storage.
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