Modulating interfacial electronic structure of CoNi LDH nanosheets with Ti3C2Tx MXene for enhancing water oxidation catalysis

被引:124
|
作者
Hu, Liuyong [1 ]
Li, Minyi [2 ]
Wei, Xiaoqian [2 ]
Wang, Hengjia [2 ]
Wu, Yu [2 ]
Wen, Jing [1 ]
Gu, Wenling [2 ]
Zhu, Chengzhou [2 ]
机构
[1] Wuhan Inst Technol, Sch Mat Sci & Engn, Wuhan 430205, Peoples R China
[2] Cent China Normal Univ, Coll Chem, Int Joint Res Ctr Intelligent Biosensing Technol, Key Lab Pesticide & Chem Biol,Minist Educ, Wuhan 430079, Peoples R China
关键词
Interfacial electronic engineering; Oxygen evolution reaction; Nonprecious metal catalysts; MXene; Layered double hydroxide; LAYERED DOUBLE HYDROXIDE; ELECTROCATALYTIC OXYGEN EVOLUTION; ENERGY-CONVERSION; NI; EXFOLIATION; GRAPHENE; HYDROGEN; HYBRID; ARRAYS;
D O I
10.1016/j.cej.2020.125605
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Developing efficient nonprecious metal electrocatalysts is urgently needed to promote the sluggish kinetics of oxygen evolution reaction (OER). Transition metals-based layered double hydroxides (LDH) have been considered as highly active OER catalysts, while low conductivity and limited active site exposures hinder their further applications. Herein, CoNi LDH/Ti3C2Tx MXene is facilely constructed by using Ti3C2Tx coated nickel foam as support to load CoNi LDH through electrodeposition. Surprisingly, a significant enhancement in OER activity of pristine CoNi LDH is achieved due to the metallic conductivity and hydrophilic and electronegative surface of Ti3C2Tx. Importantly, CoNi LDH/Ti3C2Tx displays prominent OER performance and stability in alkaline medium, which exhibits a low overpotential of 257.4 mV to reach current density of 100 mA/cm(2) and a small Tafel slope of 68 mV/dec. The experimental and calculated results demonstrate electron transfer from CoNi LDH to Ti3C2Tx plays a significant role in boosting OER activity by lowering the binding strength of intermediates.
引用
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页数:6
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