A Superaerophobic Bimetallic Selenides Heterostructure for Efficient Industrial-Level Oxygen Evolution at Ultra-High Current Densities

被引:40
作者
Jiaxin Yuan [1 ]
Xiaodi Cheng [1 ]
Hanqing Wang [1 ]
Chaojun Lei [1 ]
Sameer Pardiwala [1 ]
Bin Yang [1 ]
Zhongjian Li [1 ]
Qinghua Zhang [2 ]
Lecheng Lei [1 ]
Shaobin Wang [3 ]
Yang Hou [1 ,4 ,5 ]
机构
[1] Key Laboratory of Biomass Chemical Engineering of Ministry of Education, College of Chemical and Biological Engineering, Zhejiang University
[2] Zhejiang Provincial Key Laboratory of Advanced Chemical Engineering Manufacture Technology,College of Chemical and Biological Engineering, Zhejiang University
[3] School of Chemical Engineering and Advanced Materials, The University of Adelaide
[4] Institute of Zhejiang University-Quzhou
[5] Ningbo Research Institute, Zhejiang University
关键词
D O I
暂无
中图分类号
TQ426 [催化剂(触媒)]; TQ116.14 [氧气、液氧的生产与储运];
学科分类号
081705 [工业催化]; 082003 [油气储运工程];
摘要
Cost-e ective and stable electrocatalysts with ultra-high current densities for electrochemical oxygen evolution reaction(OER) are critical to the energy crisis and environmental pollution. Herein, we report a superaerophobic three dimensional(3D) heterostructured nanowrinkles of bimetallic selenides consisting of crystalline NiSe2 and NiFe2Se4 grown on NiFe alloy(NiSe2/NiFe2Se4@NiFe) prepared by a thermal selenization procedure. In this unique 3D heterostructure, numerous nanowrinkles of NiSe2/NiFe2Se4 hybrid with a thickness of ~ 100 nm are grown on NiFe alloy in a uniform manner. Profiting by the large active surface area and high electronic conductivity, the superaerophobic NiSe2/NiFe2Se4@NiFe heterostructure exhibits excellent electrocatalytic activity and durability towards OER in alkaline media, outputting the low potentials of 1.53 and 1.54 V to achieve ultra-high current densities of 500 and 1000 mA cm-2, respectively, which is among the most active Ni/Fe-based selenides, and even superior to the benchmark Ir/C catalyst. The in-situ derived FeOOH and NiOOH species from NiSe2/NiFe2Se4@NiFe are deemed to be e cient active sites for OER.
引用
收藏
页码:217 / 228
页数:12
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