Revealing electron numbers-binding energy relationships in heterojunctions via in-situ irradiated XPS

被引:14
作者
Zhang, Yukun [1 ]
Zhang, Yongshang [2 ]
Hou, Ruohan [1 ]
Ai, Yinyin [1 ]
Cai, Meng [1 ]
Shi, Zuhao [3 ]
Zhang, Peng [1 ]
Shao, Guosheng [1 ]
机构
[1] Zhengzhou Univ, State Ctr Int Cooperat Designer Low Carbon & Envi, Sch Mat Sci & Technol, Zhengzhou, Henan, Peoples R China
[2] Zhengzhou Univ Light Ind, Sch Mat & Chem Engn, Zhengzhou 450001, Henan, Peoples R China
[3] Wuhan Univ Technol, State Key Lab Silicate Mat Architecture, Wuhan 430070, Peoples R China
来源
APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY | 2024年 / 356卷
基金
中国国家自然科学基金;
关键词
Heterojunction; Electron transfer; In-situ irradiated XPS; Photogenerated electrons;
D O I
10.1016/j.apcatb.2024.124223
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photogenerated charge transfer from photocatalysts to surface sites is a crucial step in guaranteeing photocatalytic efficiency, however, comprehending this process remains a challenge. While in-situ irradiated XPS (ISI-XPS) can function as a powerful method to investigate the electron transfer route and briefly determine the electron quantity under simulated photocatalytic conditions, the precise amount of transferred photogenerated electrons is still unknown. Based on an oxygen-doped ZnIn2S4 nanosheet on carbon nanofibers heterostructure catalysis, we discovered a potential means of calculating the precise quantity of photogenerated electrons through ISI-XPS. Additionally, we further propose a parameter to describe how many photogenerated electrons can participate in the photocatalytic reaction in conjunction with performance under monochromatic light and the corresponding electron count. Concurrently, the oxygen dopants serve as active sites to enhance the photocatalytic reaction process. This study presents a fresh outlook on the utilization of ISI-XPS and imparts a more profound understanding of the mechanism.
引用
收藏
页数:10
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