Anodic hydrazine oxidation assisted hydrogen evolution over bimetallic RhIr mesoporous nanospheres

被引:29
|
作者
Zhang, Mei [1 ]
Wang, Ziqiang [1 ]
Duan, Zhongyao [1 ]
Wang, Shengqi [1 ]
Xu, You [1 ]
Li, Xiaonian [1 ]
Wang, Liang [1 ]
Wang, Hongjing [1 ]
机构
[1] Zhejiang Univ Technol, Coll Chem Engn, State Key Lab Breeding Base Green Chem Synth Tech, Hangzhou 310014, Peoples R China
基金
中国国家自然科学基金;
关键词
OXYGEN REDUCTION; HIGH-PERFORMANCE; EFFICIENT; ELECTROCATALYSTS; NANOSPONGES; NANOWIRES; CATALYSTS; SITES;
D O I
10.1039/d1ta05564j
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
Replacing the sluggish anodic oxygen evolution reaction with the thermodynamically favorable hydrazine oxidation reaction (HzOR) is a powerful energy-saving approach for hydrogen production, and the efficiency of this process mainly relies on the design of a highly active catalyst. Herein, we propose a facile micelle-assisted reduction method for the development of uniform RhIr mesoporous nanospheres (RhIr MNs). Benefiting from the 3D mesoporous morphology and favorable electron structure, the RhIr MNs show superior electrocatalytic activity compared to the Rh MNs for both the hydrogen evolution reaction (HER) and HzOR in alkaline media. When the RhIr MNs are used as a bifunctional catalyst for the two-electrode overall hydrazine splitting, it only requires a low voltage of 0.13 V to afford 10 mA cm(-2), much lower than that of the overall water splitting system. This proposed approach is universal for the rational design of efficient bifunctional Rh-based nanomaterials for hydrazine-assisted water splitting.
引用
收藏
页码:18323 / 18328
页数:6
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