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Heteroatom-Induced Accelerated Kinetics on Nickel Selenide for Highly Efficient Hydrazine-Assisted Water Splitting and Zn-Hydrazine Battery

Hydrazine-assisted water electrolysis is a promising energy conversion technology for highly efficient hydrogen production. Rational design of bifunctional electrocatalysts, which can simultaneously accelerate hydrogen evolution reaction (HER)/hydrazine oxidation reaction (HzOR) kinetics, is the key...

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Detalles Bibliográficos
Autores principales: Wang, Hao-Yu, Wang, Lei, Ren, Jin-Tao, Tian, Wen-Wen, Sun, Ming-Lei, Yuan, Zhong-Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10279626/
https://www.ncbi.nlm.nih.gov/pubmed/37337062
http://dx.doi.org/10.1007/s40820-023-01128-z
Descripción
Sumario:Hydrazine-assisted water electrolysis is a promising energy conversion technology for highly efficient hydrogen production. Rational design of bifunctional electrocatalysts, which can simultaneously accelerate hydrogen evolution reaction (HER)/hydrazine oxidation reaction (HzOR) kinetics, is the key step. Herein, we demonstrate the development of ultrathin P/Fe co-doped NiSe(2) nanosheets supported on modified Ni foam (P/Fe-NiSe(2)) synthesized through a facile electrodeposition process and subsequent heat treatment. Based on electrochemical measurements, characterizations, and density functional theory calculations, a favorable “2 + 2” reaction mechanism with a two-step HER process and a two-step HzOR step was fully proved and the specific effect of P doping on HzOR kinetics was investigated. P/Fe-NiSe(2) thus yields an impressive electrocatalytic performance, delivering a high current density of 100 mA cm(−2) with potentials of − 168 and 200 mV for HER and HzOR, respectively. Additionally, P/Fe-NiSe(2) can work efficiently for hydrazine-assisted water electrolysis and Zn-Hydrazine (Zn-Hz) battery, making it promising for practical application. [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40820-023-01128-z.