3D V-Ni3S2@CoFe-LDH core-shell electrocatalysts for efficient water oxidation

被引:44
|
作者
Tong, Rui [1 ]
Xu, Miao [1 ]
Huang, Haiming [1 ]
Wu, Chengrui [1 ]
Luo, Xiao [1 ]
Cao, Minglei [1 ]
Li, Xingxing [1 ]
Hu, Xiaosai [2 ]
Wang, Shuangpeng [3 ,4 ]
Pan, Hui [3 ,4 ]
机构
[1] Hubei Univ Automot Technol, Sch Math Phys & Optoelect Engn, Shiyan 442002, Peoples R China
[2] Yancheng Inst Technol, Coll Text & Clothing, Yancheng, Jiansu Province, Peoples R China
[3] Univ Macau, Inst Appl Phys & Mat Engn, Joint Key Lab, Minist Educ, Macau, Peoples R China
[4] Univ Macau, Fac Sci & Technol, Dept Phys & Chem, Macau, Peoples R China
关键词
OER; VeNi(3)S(2)@CoFe-LDH; Core-shell; Overpotential; Tafel slope; LDH NANOSHEETS; METAL PHOSPHIDE; EVOLUTION; HYDROGEN; STRATEGIES; REDUCTION; NANORODS; CATALYST; SYSTEMS; ARRAYS;
D O I
10.1016/j.ijhydene.2021.09.190
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
Studying cheap and efficient electrocatalysts is of great significance to promote the sluggish kinetics of oxygen evolution reaction (OER). Here, we adopted a simple two-step method to successfully prepare the 3D V-Ni3S2@CoFe-LDH core-shell electrocatalyst. The V-Ni3S2@CoFe-LDH/NF shows excellent OER performance with low overpotential (190 mV at 10 mA/cm(2) and 240 mV at 50 mA/cm(2)), small Tafel slope (26.8 mV/dec) and good longterm durability. Excitingly, to reach the same current density, V-Ni3S2@CoFe-LDH/NF electrode even needs much smaller overpotential than RuO2. Furthermore, the outstanding OER activity of V-Ni3S2@CoFe-LDH/NF is ascribed to the following reasons: (1) V-Ni3S2 nanorod cores improve the conductivity and ensure the fast charge transfer; (2) CoFe-LDH nanosheets interconnected with each other provide more exposed active sites; (3) the unique 3D core-shell structures are favorable for electrolyte diffusion and gas releasing. Our work indicates that building 3D core-shell heterostructure will be a useful way to design good electrocatalysts. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:39636 / 39644
页数:9
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