Hierarchical CuS@ZnIn2S4 Hollow Double-Shelled p-n Heterojunction Octahedra Decorated with Fullerene C60 for Remarkable Selectivity and Activity of CO2 Photoreduction into CH4

被引:51
作者
Ding, Yi [1 ]
Chen, Yajie [1 ]
Guan, Zefeng [1 ]
Zhao, Yumeng [1 ]
Lin, Jing [1 ]
Jiao, Yuzhen [1 ]
Tian, Guohui [1 ]
机构
[1] Heilongjiang Univ, Key Lab Funct Inorgan Mat Chem, Minist Educ Peoples Republ China, Harbin 150080, Peoples R China
基金
中国国家自然科学基金; 黑龙江省自然科学基金;
关键词
CuS@ZnIn2S4; p-n heterojunction; hollow double-shelled octahedra; CO2; photoreduction; selectivity; VISIBLE-LIGHT; PHOTOCATALYSTS; REDUCTION; SCHEME; HETEROSTRUCTURE; NANOCOMPOSITES; NANOPARTICLES; FABRICATION; FRAMEWORK; SPHERES;
D O I
10.1021/acsami.1c20980
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In this work, a hollow double-shelled architecture, based on n-type ZnIn2S4 nanosheet-coated p-type CuS hollow octahedra (CuS@ZnIn2S4 HDSOs), is designed and fabricated as a p-n heterojunction photocatalyst for selective CO2 photoreduction into CH4. The resulting hybrids provide rich active sites and effective charge migration/separation to drive CO2 photoreduction, and meanwhile, CO detachment is delayed to increase the possibility of eight-electron reactions for CH4 production. As expected, the optimized CuS@ZnIn2S4 HDSOs manifest a CH4 yield of 28.0 mu mol g(-1) h(-1) and a boosted CH4 selectivity up to 94.5%. The decorated C-60 both possesses high electron affinity and improves catalyst stability and CO2 adsorption ability. Thus, the C-60-decorated CuS@ZnIn2S4 HDSOs exhibit the highest CH4 evolution rate of 43.6 mu mol g(-1) h(-1) and 96.5% selectivity. This work provides a rational strategy for designing and fabricating efficient heteroarchitectures for CO2 photoreduction.
引用
收藏
页码:7888 / 7899
页数:12
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