异质结
电子转移
光催化
吉布斯自由能
肖特基势垒
电子
带隙
制氢
材料科学
氢
化学
光电子学
物理
光化学
热力学
催化作用
二极管
有机化学
量子力学
生物化学
作者
Yilei Li,Qing Zhao,Yang Zhang,Yunchao Li,Louzhen Fan,Fa-tang Li,Xiaohong Li
标识
DOI:10.1016/j.apcatb.2021.120763
摘要
Photocatalysis has been facing challenging problems especially the inefficient photocarriers transfer at the interfaces. Here, based on Ksp difference, we prepare the sequential heterojunction of CoS/CdS/CuS via sequential cation exchange strategy, and propose the concept of "electron-welcome zone", where the point-to-point contact can be formed at the interface, thus providing continuous electron transport channels. HAADF-STEM EDS line test indicates the formation of designed structures, and the p/n junction is confirmed by band structure and Mott-Schottky analysis. Theoretical calculation indicates that CoS reduces the Gibbs free energy of the reaction. TRPL spectra show that the existence of "electron welcome zone" greatly improves the lifetime of electrons. This sequential structure enable the optimal H2 production rate to reach 123.2 mmol g−1 h−1 with AQE of 45.6%, which is among the highest values of CdS-based photocatalysts. This work opens new way to efficient photogenerated carrier transfer channel for solar-energy conversion.
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