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Electron Transfer‐Induced Metal Spin‐Crossover at NiCo2S4/ReS2 2D–2D Interfaces for Promoting pH‐universal Hydrogen Evolution Reaction.

Authors :
Pei, Chengang
Kim, Min‐Cheol
Li, Yuankai
Xia, Chengkai
Kim, Jaekyum
So, Won
Yu, Xu
Park, Ho Seok
Kim, Jung Kyu
Source :
Advanced Functional Materials. 1/20/2023, Vol. 33 Issue 4, p1-11. 11p.
Publication Year :
2023

Abstract

The development of an efficient pH‐universal hydrogen evolution reaction (HER) electrocatalyst is essential for practical hydrogen production. Here, an efficient and stable pH‐universal HER electrocatalyst composed of the strongly coupled 2D NiCo2S4 and 2D ReS2 nanosheets (NiCo2S4/ReS2) is demonstrated. The NiCo2S4/ReS2 2D–2D nanocomposite is directly grown on the surface of the carbon cloth substrate, which exhibits excellent HER performance with overpotentials of 85 and 126 mV at a current density of 10 mA cm−2 and Tafel slopes of 78.3 and 67.8 mV dec−1 under both alkaline and acidic conditions, respectively. Theoretical and experimental characterizations reveal that the chemical coupling between NiCo2S4 and ReS2 layers induces electron transfer from Ni and Co to interfacial Re‐neighbored S atoms, enabling beneficial H atom adsorption and desorption for both acidic and alkaline HER. Simultaneously, an electron transfer‐induced spin‐crossover generates high‐spin interfacial Ni and Co atoms that promote water dissociation kinetics at the NiCo2S4/ReS2 interface, which is the origin of the superior alkaline HER activity. NiCo2S4/ReS2 also shows decent catalytic activity and long‐term durability for oxygen evolution reaction, and finally bifunctionality for overall water splitting. This study suggests a rational strategy to enhance water dissociation kinetics by inducing spin‐crossover via electron transfer. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1616301X
Volume :
33
Issue :
4
Database :
Academic Search Index
Journal :
Advanced Functional Materials
Publication Type :
Academic Journal
Accession number :
161472691
Full Text :
https://doi.org/10.1002/adfm.202210072