V-doped Ni3N/Ni heterostructure with engineered interfaces as a bifunctional hydrogen electrocatalyst in alkaline solution: Simultaneously improving water dissociation and hydrogen adsorption

被引:45
|
作者
Zhang, Huan [1 ]
Wang, Juan [1 ]
Qin, Fengqi [1 ]
Liu, Huiling [1 ]
Wang, Cheng [1 ]
机构
[1] Tianjin Univ Technol, Sch Mat Sci & Engn, Inst New Energy Mat & Low Carbon Technol, Tianjin Key Lab Adv Funct Porous Mat, Tianjin 300384, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
interface engineering; doping; water dissociation; hydrogen adsorption; alkaline hydrogen electrocatalysis; OXYGEN EVOLUTION; NICKEL NITRIDE; OXIDATION REACTION; EFFICIENT; CARBON; NANOSHEETS; REDUCTION; NITROGEN; CORE; PERFORMANCE;
D O I
10.1007/s12274-021-3559-9
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Alkali-water electrolyzers and hydroxide exchange membrane fuel cells are emerging as promising technologies to realize hydrogen economy. Developing cost-effective electrode materials with high activities towards corresponding hydrogen evolution (HER) and oxidation (HOR) reactions plays a crucial role in commercial hydrogen production and utilization. Herein, we fabricated a V-doped Ni3N/Ni heterostructure (V-Ni3N/Ni) through a controlled nitridation treatment on a V-incorporated nickel hydroxide precursor. The resultant catalyst exhibits comparable catalytic activity and durability to commercial Pt/C in terms of both HER (a low overpotential of 44 mV at the current density of 10 mA.cm(-2)) and HOR (a high current density of 1.54 mA.cm(-2) at 0.1 V versus reversible hydrogen electrode) under alkaline conditions. The superior activity of V-Ni3N/Ni grown on different substrates further implies its intrinsic performance. Density functional theory (DFT) calculations reveal that the coupled metallic Ni and doped V can promote the water adsorption, accelerate the Volmer step of alkaline HER, as well as optimize the adsorption and desorption of hydrogen intermediate (H*) to reach a balanced Delta GH* value.
引用
收藏
页码:3489 / 3496
页数:8
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