In-Situ Construction of Fe-Doped NiOOH on the 3D Ni(OH)2 Hierarchical Nanosheet Array for Efficient Electrocatalytic Oxygen Evolution Reaction

被引:0
|
作者
Li, Mengyang [1 ]
Wang, Mingran [1 ]
Wang, Qianwei [1 ]
Cao, Yang [1 ]
Gao, Jie [1 ]
Wang, Zhicheng [1 ]
Gao, Meiqi [1 ]
Duan, Guosheng [2 ]
Cao, Feng [1 ]
机构
[1] Northeastern Univ, Sch Mat Sci & Engn, Key Lab Anisotropy & Texture Mat MoE, Shenyang 110819, Peoples R China
[2] Shenyang Aerosp Univ, Sch Safety Engn, Shenyang 110136, Peoples R China
基金
中国国家自然科学基金;
关键词
OER activity; Fe-doped NiOOH; heterostructure; water-splitting; electrocatalysts; LAYERED DOUBLE HYDROXIDE; PRUSSIAN BLUE ANALOG; NICKEL FOAM; NI; BETA-NI(OH)(2); NANOPARTICLES; PERFORMANCE; IMPURITIES; CATALYSTS; FILM;
D O I
10.3390/ma17184670
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
Accessible and superior electrocatalysts to overcome the sluggish oxygen evolution reaction (OER) are pivotal for sustainable and low-cost hydrogen production through electrocatalytic water splitting. The iron and nickel oxohydroxide complexes are regarded as the most promising OER electrocatalyst attributed to their inexpensive costs, easy preparation, and robust stability. In particular, the Fe-doped NiOOH is widely deemed to be superior constituents for OER in an alkaline environment. However, the facile construction of robust Fe-doped NiOOH electrocatalysts is still a great challenge. Herein, we report the facile construction of Fe-doped NiOOH on Ni(OH)(2) hierarchical nanosheet arrays grown on nickel foam (FeNi@NiA) as efficient OER electrocatalysts through a facile in-situ electrochemical activation of FeNi-based Prussian blue analogues (PBA) derived from Ni(OH)(2). The resultant FeNi@NiA heterostructure shows high intrinsic activity for OER due to the modulation of the overall electronic energy state and the electrical conductivity. Importantly, the electrochemical measurement revealed that FeNi@NiA exhibits a low overpotential of 240 mV at 10 mA/cm(2) with a small Tafel slope of 62 mV dec(-1) in 1.0 M KOH, outperforming the commercial RuO2 electrocatalysts for OER.
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页数:13
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