光化学
单线态氧
光催化
氧气
活性氧
辐照
材料科学
离解(化学)
选择性
表面光电压
电子转移
化学
化学工程
催化作用
光谱学
物理化学
工程类
物理
有机化学
核物理学
量子力学
生物化学
作者
Yanbiao Shi,Zhiping Yang,Lujia Shi,Hao Li,Xupeng Liu,Xu Zhang,Jundi Cheng,Chuan Liang,Shiyu Cao,Furong Guo,Xiao Liu,Zhihui Ai,Lizhi Zhang
标识
DOI:10.1021/acs.est.2c03769
摘要
The photocatalytic O2 activation for pollutant removal highly depends on the controlled generation of desired reactive oxygen species (ROS). Herein, we demonstrate that the robust excitonic effect of BiOBr nanosheets, which is prototypical for singlet oxygen (1O2) production to partially oxidize NO into a more toxic intermediate NO2, can be weakened by surface boronizing via inducing a staggered band alignment from the surface to the bulk and simultaneously generating more surface oxygen vacancy (VO). The staggered band alignment destabilizes excitons and facilitates their dissociation into charge carriers, while surface VO traps electrons and efficiently activates O2 into a superoxide radical (•O2-) via a one-electron-transfer pathway. Different from 1O2, •O2- enables the complete oxidation of NO into nitrate with high selectivity that is more desirable for safe indoor NO remediation under visible light irradiation. This study provides a facile excitonic effect manipulating method for layered two-dimensional photocatalysts and sheds light on the importance of managing ROS production for efficient pollutant removal.
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