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Construction of hierarchical In2O3/In2S3-ZnCdS ternary microsphere heterostructures for efficient photocatalytic nitrogen fixation.

Authors :
Huang, Liangliang
Peng, Tao
Wang, Rui
He, Beibei
Jin, Jun
Wang, Huanwen
Gong, Yansheng
Source :
Dalton Transactions: An International Journal of Inorganic Chemistry. 8/7/2024, Vol. 53 Issue 29, p12291-12300. 10p.
Publication Year :
2024

Abstract

Photocatalytic ammonia production holds immense promise as an environmentally sustainable approach to nitrogen fixation. In this study, In2O3/In2S3-ZnCdS ternary heterostructures were successfully constructed through an innovative in situ anion exchange process, coupled with a low-temperature hydrothermal method for ZnCdS (ZCS) incorporation. The resulting In2O3/In2S3-ZCS photocatalyst was proved to be highly efficient in converting N2 to NH3 under mild conditions, eliminating the need for sacrificial agents or precious metal catalysts. Notably, the NH4+ yield of In2O3/In2S3-0.5ZCS reached a significant level of 71.2 μmol g−1 h−1, which was 10.47 times higher than that of In2O3 (6.8 μmol g−1 h−1) and 3.22 times higher than that of In2O3/In2S3 (22.1 μmol g−1 h−1). This outstanding performance can be attributed to the ternary heterojunction configuration, which significantly extends the lifetime of photogenerated carriers and enhances the spatial separation of electrons and holes. The synergistic interplay between CdZnS, In2S3, and In2O3 in the heterojunction facilitates electron transport, thereby boosting the rate of the photocatalytic nitrogen fixation reaction. Our study not only validates the efficacy of ternary heterojunctions in photocatalytic nitrogen fixation but also offers valuable insights for the design and construction of such catalysts for future applications. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14779226
Volume :
53
Issue :
29
Database :
Academic Search Index
Journal :
Dalton Transactions: An International Journal of Inorganic Chemistry
Publication Type :
Academic Journal
Accession number :
178562998
Full Text :
https://doi.org/10.1039/d4dt01605j