Constructing Robust Interfacial Chemical Bond Enhanced Charge Transfer in S-Scheme 3D/2D Heterojunction for CO2 Photoreduction

被引:28
作者
Feng, Yilin [1 ,2 ]
Gong, Xiu [1 ,2 ]
Fan, Shuhan [1 ,2 ]
Jiang, Zhuojun [1 ,2 ]
Yang, Jingliang [1 ,2 ]
Qu, Yunpeng [1 ,2 ]
Chen, Yanli [1 ,2 ]
Peng, Qiong [1 ,2 ]
Ding, Junfei [1 ,2 ]
Shen, Hui [1 ,2 ]
Qi, Xiaosi [1 ,2 ]
Wang, Mingkui [3 ]
机构
[1] Guizhou Univ, Coll Phys, Guiyang 550025, Peoples R China
[2] Guizhou Univ, Guizhou Prov Key Lab Photoelect Technol & Applicat, Guiyang 550025, Peoples R China
[3] Huazhong Univ Sci & Technol, Sch Opt & Elect Informat, Wuhan Natl Lab Optoelect, Wuhan 430074, Hubei, Peoples R China
关键词
3D/2D-hollow structure; CO2; reduction; high selectivity; interfacial chemical bonds; S-scheme heterojunctions; HETEROSTRUCTURE; PHOTOCATALYST; REDUCTION;
D O I
10.1002/adfm.202403502
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A stable ZnTe@Cs3Sb2I9 catalyst with 3D/2D-hollow-composite structure is constructed for CO2 photocatalytic reduction via the in situ growth of Cs3Sb2I9 nanosheets on hollow ZnTe microspheres using lattice matching. The formed Tellurium-Antimony (Te & horbar;Sb) bonds improved the poor contact at the heterojunction interface, effectively promoted charge separation, and successfully suppressed photocorrosion. The unique core-shell structure not only strengthens light absorption but also improves CO2 adsorption capacity. Consequently, the S-scheme heterojunction with the synergistic effect of chemical bonds and 3D/2D-hollow-composite structure significantly enhances photocatalytic performance. The ZnTe@Cs3Sb2I9 photocatalyst offers a CO selectivity of 90.5%, which is higher than that of pure ZnTe (22.9%) and Cs3Sb2I9 (56.9%). This structure holds great promise for practical applications in CO2 photocatalytic reduction.
引用
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页数:10
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