Heterogeneous Hollow Multi-Shelled Structures with Amorphous-Crystalline Outer-Shells for Sequentially Photoreduction of CO2

被引:42
|
作者
Wei, Yanze [1 ]
You, Feifei [1 ]
Zhao, Decai [1 ]
Wan, Jiawei [1 ,2 ]
Gu, Lin [3 ]
Wang, Dan [1 ,2 ]
机构
[1] Chinese Acad Sci, State Key Lab Biochem Engn, Inst Proc Engn, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Beijing Natl Lab Condensed Matter Phys, Inst Phys, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
Amorphous Phase; CO2; Photoreduction; Hollow Multi-Shell Structures; Nano-; Microreactor; Tandem Catalysis; METAL-ORGANIC FRAMEWORKS; PHOTOCATALYTIC REDUCTION; SELECTIVITY; EFFICIENT; LIGHT; GENERATION; SPECTRA; SURFACE; TIO2; CH4;
D O I
10.1002/anie.202212049
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Constructing delicate nano-/microreactors with tandem active sites in hierarchical architectures is a promising strategy for designing photocatalysts to realize the challenging but attractive CO2 reduction. Herein, hollow multi-shelled structure (HoMS) based microreactors with spatial ordered hetero-shells are fabricated, which achieve two-step CO2-to-CH4 photoreduction. The multiple inner CeO2 shells increase the number of active catalytic sites to ensure efficient first-step reaction for generating CO, along with enriching the local CO concentration. The second-step CO-to-CH4 reaction is consequently induced by amorphous TiO2 (A-TiO2) composites on the adjacent outer-most shell, thus realizing the CO2-to-CH4 conversion capability using one CeO2@CeO2/A-TiO2 HoMS. In-depth explorations in the microreactors provide compositional, structural, and interfacial guidance for engineering HoMS-based microreactors with temporally-spatially ordered shells toward efficient tandem catalysis.
引用
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页数:9
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