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The electronic structures of non-metal (N, S) doped cobalt phosphide catalysts and the catalytic mechanism for the hydrogen evolution reaction of ammonia borane: a theoretical study.
- Source :
-
New Journal of Chemistry . 1/28/2023, Vol. 47 Issue 4, p1724-1730. 7p. - Publication Year :
- 2023
-
Abstract
- In this paper, the structural characteristics and catalytic mechanism for hydrogen evolution of ammonia borane of non-metal (N, S) doped CoP catalysts were studied in detail by density functional theory (DFT) calculations. Specifically, we first investigated the structure of the cobalt phosphide catalyzed ammonia borane models. In addition, based on the most stable structures, the mechanism of the hydrogen evolution reaction of ammonia borane catalyzed by three catalysts was studied, and four feasible reaction paths for the hydrogen evolution reaction of ammonia borane catalyzed by three catalysts were discussed. By comparing the activation energies of the control steps of different reaction paths, the optimal reaction paths for the hydrogen evolution of ammonia borane catalyzed by three different catalysts were determined. The catalytic activities of the three catalysts for the hydrogen evolution of ammonia borane were compared. We found that the N-doped catalyst was beneficial to improve the catalytic activity of CoP for the catalytic hydrogen evolution of ammonia borane, while the catalytic activity of S-doped CoP for the catalytic hydrogen evolution of ammonia borane is relatively weak. These results reveal the relationship between the physical properties of CoP (and its non-metal-doped variants) and their catalytic activity. Finally, these findings can be used to explain the underlying mechanism reported in previous experimental studies from a microscopic perspective. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 11440546
- Volume :
- 47
- Issue :
- 4
- Database :
- Academic Search Index
- Journal :
- New Journal of Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 161444468
- Full Text :
- https://doi.org/10.1039/d2nj04535d