Construction of interfacial engineering on CoP nanowire arrays with CoFe-LDH nanosheets for enhanced oxygen evolution reaction

被引:29
作者
Feng, Hao [1 ]
Sun, Xun [1 ]
Guan, Xin [1 ]
Zheng, Dengchao [1 ]
Tian, Wenli [1 ]
Li, Chengyi [1 ]
Li, Chuiyu [1 ]
Yan, Minglei [2 ,3 ]
Yao, Yadong [1 ]
机构
[1] Sichuan Univ, Coll Mat Sci & Engn, Chengdu 610064, Sichuan, Peoples R China
[2] Nanjing Univ, Sch Chem & Chem Engn, Key Lab Mesoscop Chem MOE, Nanjing 210023, Jiangsu, Peoples R China
[3] Nanjing Univ, Sch Chem & Chem Engn, Jiangsu Prov Lab Nanotechnol, Nanjing 210023, Jiangsu, Peoples R China
关键词
CoP nanowires; CoFe-LDH nanosheets; Core-shell heterostructure; Oxygen evolution reaction; BIFUNCTIONAL ELECTROCATALYSTS; EFFICIENT; CATALYSTS; DESIGN;
D O I
10.1016/j.flatc.2021.100225
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
Transition metal phosphides have recently emerged as promising alternatives for oxygen evolution reaction (OER). Herein, the OER performance of CoP nanowires was significantly enhanced by coupling with the cobaltiron layered double hydroxide (CoFe-LDH) nanosheets. The three-dimensional (3D) CoP@CoFe-LDH nanoarays heterostructure was fabricated by the sequential steps of hydrothermal process, phosphorization and electrodeposition. The as-prepared CoP@CoFe-LDH possesses well core?shell structure with a synergistic heterointerface between CoP and CoFe-LDH, in which the CoP core improves the conductivity and the CoFe-LDH shell affords abundant active sites. Furthermore, the 3D hierarchical architecture facilitates the electrolyte ions access and O2 gas liberation. Consequently, the optimized CoP@CoFe-LDH exhibits excellent OER performance with low overpotential (240 mV @ 40 mA cm-2), small Tafel slope (69.2 mV dec-1), superior intrinsic activity and high stability in 1 M KOH. This study demonstrates an efficient route to design the advanced OER catalysts by constructing the 3D core?shell heterostructure.
引用
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页数:6
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