Electrochemical Deposited Amorphous Bimetallic Nickle-Iron (Oxy)hydroxides Electrocatalysts for Highly Efficient Oxygen Evolution Reaction

被引:4
作者
Xu, Zhichao [2 ]
Wang, Jianmin [2 ]
Cai, Jiajia [2 ]
He, Yitao [2 ]
Hu, Jing [2 ]
Li, Haijin [1 ,2 ]
Li, Yongtao [1 ,3 ]
Zhou, Yong [4 ,5 ]
机构
[1] Anhui Univ Technol, Low Carbon Res Inst, Low Carbon New Mat Res Ctr, Maanshan 243002, Peoples R China
[2] Anhui Univ Technol, Sch Energy & Environm, Maanshan 243002, Peoples R China
[3] Anhui Univ Technol, Sch Mat Sci & Engn, Maanshan 243002, Peoples R China
[4] Nanjing Univ, Ecomat & Renewable Energy Res Ctr ERERC, Natl Lab Solid State Microstruct, Nanjing 210093, Peoples R China
[5] Nanjing Univ, Sch Phys, Nanjing 210093, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrocatalyst; Oxygen evolution reaction; NiFe (oxy)hydroxides; WATER OXIDATION; ELECTRODEPOSITION; NANOSHEETS; ARRAYS;
D O I
10.1007/s12678-022-00808-5
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
The low-cost and high-performance electrocatalysts, especially metal (oxy)hydroxides, for the oxygen evolution reaction (OER) have attracted considerable attention due to their promising OER activity. Amorphous electrocatalysts are often superior to their crystalline counterparts due to their more actives and structural flexibility. However, using traditional preparation techniques still presents a significant barrier. Herein, the amorphous NiFe (oxy)hydroxides on nickel foam (NF) with large surface area and small charge transfer resistance were fabricated by electrodeposition technique. The as-fabricated NiFe (oxy)hydroxides (Ni:Fe = 1:3) exhibited remarkable electrocatalytic activity and stability for OER with a low overpotential of 245 mV at a current density of 100 mA cm(-2), a small Tafel slope of 76.9 mV dec(-1), which was superior to that of noble metal electrocatalysts (RuO2) and most NiFe-based electrocatalysts. This work provides a facile and effective way to synthesis metal (oxy)hydroxide catalysts towards high-efficiency water splitting.
引用
收藏
页码:429 / 436
页数:8
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