光催化
铋
催化作用
路易斯酸
空位缺陷
化学
基础(拓扑)
光化学
沮丧的刘易斯对
材料科学
产量(工程)
组合化学
纳米技术
有机化学
结晶学
冶金
数学
数学分析
作者
Qingli Wang,Zerui Miao,Yanfeng Zhang,Tingjiang Yan,Lingpeng Meng,Xuxu Wang
标识
DOI:10.1021/acscatal.1c05553
摘要
Photocatalytic reduction of CO2 into available organic compounds has received remarkable attention. However, photocatalytic CO2 reduction is limited to meet industrial application requirements because of the lack of effective photocatalysts. Surface frustrated Lewis pairs (FLP) are found in bismuth oxybromide (BiOBr), which are effective catalytic sites to activate and photocatalytically reduce CO2. Furthermore, the introduction of Ce4+ and oxygen vacancy can optimize both the electronic state and the FLP property of BiOBr. The combined experimental and theoretical characterizations reveal that Ce4+ and O2– can form the frustrated Lewis acid–base pairs, which can catch, excite, and reduce CO2 into CO at a high yield of 50.9 μL h–1, being 9.8 times as large as pristine BiOBr. This work illustrates a rational strategy for both construction of highly efficient photocatalysts and insights into the photocatalytic mechanism at the atomic level.
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