异质结
光催化
过氧化氢
X射线光电子能谱
材料科学
制氢
降级(电信)
可见光谱
三元运算
化学工程
电子顺磁共振
光化学
复合数
氧化还原
化学
氢
催化作用
光电子学
复合材料
有机化学
电信
工程类
冶金
物理
程序设计语言
核磁共振
计算机科学
作者
Zhe Li,Dongcai Shen,Xin Hu,Xiaolong Yang,Yiming Li,Mutai Bao
出处
期刊:Chemosphere
[Elsevier BV]
日期:2023-09-22
卷期号:343: 140234-140234
被引量:20
标识
DOI:10.1016/j.chemosphere.2023.140234
摘要
Effective and durable photocatalysts are essential for the decomposition of persistent contaminants and the generation of hydrogen peroxide. In this study, we successfully constructed an S-type heterojunction by in situ growing Bi2O3 nanocrystals and NH2-MIL-101(Fe) onto surface-modified g-C3N4. The process of charge transfer in the S-type heterojunction was confirmed using ISI-XPS, DFT calculations, capture experiments, and EPR signals. The combined influence of the heterojunction and MOF demonstrated remarkable photocatalytic performance in the breakdown of tetracycline (TC) and the generation of hydrogen peroxide (H2O2). In the enhanced setup (10%-NH2-MIL-101(Fe)@MCN/Bi2O3), full degradation of TC was accomplished within 50 min under visible light exposure. Additionally, a notable H2O2 yield of 655.63 μmol/g was attained, all achieved without the necessity of sacrificial agents or supplementary oxygen. Based on the outcomes of the dual functionality, the exceptional performance of the ternary composite material can be ascribed to the collaborative influence of the heterojunction and MOF. This collaborative effect expands the light absorption range in the visible region, suppresses the recombination of electron-hole pairs, and enhances the photocatalytic redox ability. The system demonstrates significant potential in the efficient in situ production of H2O2 and removal of recalcitrant organic pollutants in pure water.
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