Heterostructure of ultrafine FeOOH nanodots supported on CoAl-layered double hydroxide nanosheets as highly efficient electrocatalyst for water oxidation

被引:22
作者
Gang, Chuan [1 ]
Chen, Jiayi [1 ]
Chen, Qihao [1 ]
Chen, Yantao [1 ,2 ]
机构
[1] Tianjin Univ Technol, Sch Mat Sci & Engn, Tianjin Key Lab Photoelect Mat & Devices, Tianjin 300384, Peoples R China
[2] Nankai Univ, Coll Chem, Key Lab Adv Energy Mat Chem, Minist Educ, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
Heterostructure; Nanodot; Layered double hydroxides; Electrocatalyst; Water oxidation; OXYGEN EVOLUTION; BIFUNCTIONAL ELECTROCATALYST; GRAPHENE OXIDE; SIZE; NICKEL; PHOSPHIDES; CATALYSTS; HYDROGEN; SPHERES;
D O I
10.1016/j.jcis.2021.05.041
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
The supported and dispersed ultrafine active species for electrocatalytic water oxidation are quite promising for the high intrinsic activity. A novel heterostructure of ultrafine FeOOH nanodots with an average size of 2.3 nm supported on CoAl-LDH nanosheets, is constructed by a facile method under ambient conditions. The as-prepared FeOOH@CoAl-LDH shows a strong interfacial interaction upon the formation of heterostructure, and is demonstrated as a highly efficient and stable electrocatalyst that demands 272 mV to attain 50 mA cm(-2) and exhibits a Tafel slope of 40 mV dec(-1). Moreover, density functional theory calculations manifest the coupling of FeOOH with CoAl-LDH can effectively decrease the energy barrier during the water oxidation process by optimizing the adsorption free energy of intermediates in the reaction pathway. The successful development of FeOOH@CoAl-LDH can shed light on the design of novel electrocatalysts that can fully take advantages of small size, heterostructure and synergistic effect. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:594 / 601
页数:8
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