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

Author:

Feng Yilin1,Gong Xiu1ORCID,Fan Shuhan1,Jiang Zhuojun1,Yang Jingliang1,Qu Yunpeng1,Chen Yanli1,Peng Qiong1,Ding Junfei1,Shen Hui1,Qi Xiaosi1ORCID,Wang Mingkui2

Affiliation:

1. College of Physics & Guizhou Province Key Laboratory for Photoelectric Technology and Application Guizhou University Guiyang 550025 China

2. Wuhan National Laboratory for Optoelectronics School of Optical and Electronic Information Huazhong University of Science and Technology Wuhan Hubei 430074 China

Abstract

AbstractA 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─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.

Funder

Natural Science Foundation of Guizhou Province

National Natural Science Foundation of China

Publisher

Wiley

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