Vanadium-Doped Heterointerfaced Ni3N-MoOx Nanosheets with Optimized H and H2O Adsorption for Effective Alkaline Hydrogen Electrocatalysis

被引:4
作者
Ren, Jin-Tao [1 ]
Yang, Dandan [1 ]
Chen, Lei [1 ]
Yuan, Zhong-Yong [1 ]
机构
[1] Nankai Univ, Sch Mat Sci & Engn, Tianjin 300350, Peoples R China
基金
中国国家自然科学基金;
关键词
electronic interaction; hydrogen evolution; hydrogen oxidation; interface engineering; nickel nitrides; NICKEL NITRIDE; EVOLUTION; OXIDATION;
D O I
10.1002/smll.202406335
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nickel (Ni)-based materials represent a compelling avenue as platinum alternatives in the realm of alkaline hydrogen electrocatalysis. However, conventional nickel nitrides (Ni3N) have long been hindered by sluggish hydrogen evolution kinetics in alkaline environments, owing to inadequate adsorption strengths of both hydrogen and water molecules. Herein, a novel approach is presented involving the design of vanadium (V)-doped Ni3N/MoOx heterogeneous nanosheets (V-Ni3N@MoOx), engineered to achieve optimized adsorption strengths for hydrogen evolution and oxidation reactions (HER/HOR). Theoretical insights underscore the superior catalytic performance of this composite, attributed to a synergistic interplay between unique V doping and the heterointerfaced structure. This synergistic effect not only fine-tunes the electronic structure, establishing an optimal d band center to mitigate proton over-bonding, but also ameliorates the energy barrier through enhanced H2O dissociation capability. Consequently, V-Ni3N@MoOx manifests remarkable catalytic activities, evincing an overpotential of 56 mV at 10 mA cm-2 for HER and an exchange current density of 1.91 mA cm-2 for HOR in alkaline media. Notably, the stability assessment reveals the enduring performance of V-Ni3N@MoOx for HER/HOR, exhibiting no activity decay over extended operational durations. This study underscores the efficacy of heterogeneous interface modulation as a transformative strategy in designing Ni-based materials for alkaline hydrogen electrocatalysis.
引用
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页数:9
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