激进的
光化学
甲苯
吸附
降级(电信)
化学
电子
分子
氧气
电子顺磁共振
活性氧
活动站点
活动层
X射线光电子能谱
化学物理
化学工程
有机化学
催化作用
图层(电子)
物理
计算机科学
工程类
电信
薄膜晶体管
核磁共振
量子力学
作者
Hong Wang,Qin Ren,Lei Xiao,Lvcun Chen,Ye He,Lin Yang,Yanjuan Sun,Fan Dong
标识
DOI:10.1016/j.jhazmat.2022.129329
摘要
Hydroxyl (⸱OH) and superoxide (⸱O2-) radicals are the main drivers for photocatalysis in toluene degradation, but their generation mechanisms are still ambiguous due to the lack of direct evidence. The spatially separated active sites for holes and electrons can help to clarify the dynamic process of radicals generation. By performing theoretical calculations, it is demonstrated that the spatially separated active sites for holes and electrons on the Bi2O2CO3 surface can be constructed by introducing oxygen vacancies in the [Bi2O2]2+ layer. H2O and O2 molecules can be better adsorbed and activated at hole and electron active sites, separately. Accordingly, the pristine and defective Bi2O2CO3 are prepared. The dynamic behavior of H2O and O2 molecules at the matching active sites is revealed, which indicates the efficient adsorption of reactants and the substantial production of radicals. Significantly, the specificity of the spatially separated holes and electrons active sites for ⸱OH and ⸱O2- radicals generation, respectively, is demonstrated by in situ EPR with the H2O vapor atmosphere. This work provides a design concept for unraveling reaction mechanisms to realize controllable radicals generation.
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