Highly efficient nitrogen fixation over S-scheme heterojunction photocatalysts with enhanced active hydrogen supply

Author:

Bao Tong1,Xi Yamin1,Zhang Chaoqi1,Du Peiyang1,Xiang Yitong1,Li Jiaxin1,Yuan Ling1,Yu Chengzhong12,Liu Chao1

Affiliation:

1. School of Chemistry and Molecular Engineering, East China Normal University , Shanghai 200241 , China

2. Australian Institute for Bioengineering and Nanotechnology, The University of Queensland , Brisbane 4072 , Australia

Abstract

ABSTRACT Photocatalytic N2 fixation is a promising strategy for ammonia (NH3) synthesis; however, it suffers from relatively low ammonia yield due to the difficulty in the design of photocatalysts with both high charge transfer efficiency and desirable N2 adsorption/activation capability. Herein, an S-scheme CoSx/ZnS heterojunction with dual active sites is designed as an efficient N2 fixation photocatalyst. The CoSx/ZnS heterojunction exhibits a unique pocket-like nanostructure with small ZnS nanocrystals adhered on a single-hole CoSx hollow dodecahedron. Within the heterojunction, the electronic interaction between ZnS and CoSx creates electron-deficient Zn sites with enhanced N2 chemisorption and electron-sufficient Co sites with active hydrogen supply for N2 hydrogenation, cooperatively reducing the energy barrier for N2 activation. In combination with the promoted photogenerated electron-hole separation of the S-scheme heterojunction and facilitated mass transfer by the pocket-like nanostructure, an excellent N2 fixation performance with a high NH3 yield of 1175.37 μmol g−1 h−1 is achieved. This study provides new insights into the design of heterojunction photocatalysts for N2 fixation.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Oxford University Press (OUP)

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