Thin porous nanosheets of NiFe layered-double hydroxides toward a highly efficient electrocatalyst for water oxidation

被引:42
|
作者
Wu, Wei [1 ,2 ]
Liu, Jiang [1 ,2 ]
Chen, Gui [1 ,2 ]
Chen, Yu [1 ,3 ]
Xu, Chunli [1 ,2 ]
机构
[1] Shaanxi Normal Univ, Key Lab Appl Surface & Colloid Chem, Minist Educ, Xian 710119, Peoples R China
[2] Shaanxi Normal Univ, Sch Chem & Chem Engn, Changan West St 620, Xian 710119, Peoples R China
[3] Shaanxi Normal Univ, Sch Mat Sci & Engn, Xian 710062, Peoples R China
关键词
ZIF-67; LDH; Self-sacrificing template method; Co-precipitation method; OER; OXYGEN REDUCTION; HIGH-PERFORMANCE; ENERGY-STORAGE; COBALT; SHELL; ELECTRODE; GRAPHENE; FABRICATION; NANOCAGES; OXIDES;
D O I
10.1016/j.ijhydene.2019.11.108
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
NiFe layered double hydroxides (NiFe-LDH) are low cost and earth abundant electrocatalysts for oxygen evolution reaction (OER). Herein, the NiFe-LDH nanosheets induced by ZIF-67 (NiFe-LDH/ZIF-67) were prepared via a coupling method of a self-sacrificing template method and a co-precipitation method. Atomic force microscope and field emission transmission electron microscopy analysis indicate that NiFe-LDH/ZIF-67 consist of thin porous nanosheets. X-ray photoelectron spectra analysis show that NiFe-LDH/ZIF-67 contains more oxygen vacancies than pristine NiFe-LDH. The overpotential of NiFe-LDH/ZIF-67 is 222 mV at 10 mA cm(-2) for OER, lower than that of ZIF-67, pristine NiFe-LDH, and the commercial RuO2, indicating that its high electrocatalytic activity for OER. The high electrocatalytic activity of NiFe-LDH/ZIF-67 may be attributed to its thin porous nanosheet structure, which is derived from the structural influence of ZIF-67 and the coupling effect of a self-sacrificing template method and a co-precipitation method. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1948 / 1958
页数:11
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