光催化
降级(电信)
化学
离域电子
异质结
石墨烯
载流子
氧化物
电子转移
化学工程
光化学
电子顺磁共振
激进的
光电子学
材料科学
催化作用
有机化学
电信
计算机科学
工程类
物理
核磁共振
作者
Zhi Zhu,Xiaohan Xing,Qi Qi,Wenjing Shen,Hong‐Yue Wu,Dongyi Li,Binrong Li,Jialin Liang,Xu Tang,Jun Zhao,Hongping Li,Pengwei Huo
出处
期刊:Chinese Journal of Structural Chemistry
日期:2023-11-07
卷期号:42 (12): 100194-100194
被引量:50
标识
DOI:10.1016/j.cjsc.2023.100194
摘要
A specific type S-scheme photocatalyst CeO2@N-GO/g-C3N4 was successfully synthesized, resulting in a 2-mercaptobenzothiazole (MBT) degradation rate of 100%, which is more than twice that of g-C3N4 and CeO2. The improved degradation performance can be attributed to the introduction of N-graphene oxide (N-GO), which facilitates the electron transfer. Additionally, the unique Ce4+ → Ce3+ conversion property enhances the charge carrier utilization, and thereby the photocatalytic activity. Furthermore, theoretical calculations suggest the formation of an interfacial internal electric field (IEF) formed between CeO2 (the (200) and (311) planes) and g-C3N4 (the (002) plane) to enhance the delocalization of the charge carriers. Moreover, various photoelectrochemical analyses are employed for the in-depth mechanism on MBT degradation and IEF-induced S-scheme over CeO2@N-GO/g-C3N4, where the differential charge proves the electron transfer path from CeO2 to g-C3N4 that significantly prolong its lifetime. The radical capture and electron spin resonance (ESR) results proved the existence of the active species of •OH, •O2−, and h+ in the S-scheme photocatalytic system.
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