Hierarchical Highly Wrinkled Trimetallic NiFeCu Phosphide Nanosheets on Nanodendrite Ni3S2/Ni Foam as an Efficient Electrocatalyst for the Oxygen Evolution Reaction

被引:52
|
作者
Khodabakhshi, Meysam [1 ]
Chen, Shumin [1 ]
Ye, Tian [1 ]
Wu, Hao [1 ]
Yang, Li [1 ]
Zhang, Wenfeng [1 ]
Chang, Haixin [1 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Mat Sci & Engn, Quantum Nano Matter & Device Lab, State Key Lab Mat Proc & Die & Mould Technol, Wuhan 430074, Peoples R China
关键词
trimetallic NiFeCu phosphide; highly wrinkled nanosheet; Ni3S2; nanodendrite; water splitting; oxygen evolution reaction; DOUBLE HYDROXIDE NANOSHEETS; METAL-ORGANIC FRAMEWORKS; BIFUNCTIONAL ELECTROCATALYSTS; WATER OXIDATION; P ALLOY; ELECTROCHEMICAL EVOLUTION; NANOWIRE ARRAY; ALKALINE; CU; PERFORMANCE;
D O I
10.1021/acsami.0c11732
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The sluggish oxygen evolution reaction (OER) and costly noble-metal oxide catalysts hinder the vast usage of environmentally friendly water splitting for hydrogen production. Elemental doping by partial replacing of parent metal elements with elements of higher electronegativity is considered to be one of the most efficient strategies to promote the electrocatalytic OER performance. In this work, we synthesize an efficient hierarchical highly wrinkled NiFeCu phosphide nanosheet on nanodendrite Ni3S2/NiF substrates through partial replacement of Cu instead of Ni and Fe in NiFeP@Ni3S2/NiF by using a facile electrodeposition method. The NiFeCuPpNi(3)S(2)/NiF electrocatalyst needs only 230, 282, and 351 mV to reach 10, 50, and 100 mA x cm(-2), respectively. Notably, this electrocatalyst shows one of the lowest OER overpotentials at 10 mA/cm(-2) for metal phosphides and endured the OER at 20 mA x cm(-2) for 18 h with negligible voltage elevation. The X-ray photoelectron spectroscopy (XPS), double-layer capacitance (C-dl) plots, and electrochemical impedance spectroscopy show that the partial Cu doping in NiFeP@Ni3S2/NiF not only can change the electron density around Ni and Fe but also can increase the electrochemically active surface area and conductivity of electrocatalysts.
引用
收藏
页码:36268 / 36276
页数:9
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