In-situ transformation of Co(OH)2 into NH4CoPO4•H2O on Co foil: 3D self-supported electrocatalyst with asymmetric local atomic and electronic structure for enhanced oxygen evolution reaction

被引:6
作者
Che, Quande [1 ]
Xie, Xiaobin [2 ]
Ma, Qian [1 ]
Wang, Junpeng [1 ]
Zhu, Yuanna [1 ]
Shi, Ruixia [1 ]
Yang, Ping [1 ]
机构
[1] Jinan Univ, Sch Mat Sci & Engn, Jinan 250022, Shandong, Peoples R China
[2] Wuhan Univ Technol, Sch Mat Sci & Engn, Wuhan 430070, Hubei, Peoples R China
来源
JOURNAL OF ENERGY CHEMISTRY | 2020年 / 51卷
基金
中国国家自然科学基金;
关键词
Electrocatalysis; Oxygen evolution reaction; Transition-metal phosphate; NH4CoPO4 center dot H2O; BIFUNCTIONAL ELECTROCATALYST; HIGHLY EFFICIENT; WATER OXIDATION; PHOSPHATE; CATALYST; HYDROGEN; NANOFLAKES; HYBRID; CARBON; CO3O4;
D O I
10.1016/j.jechem.2020.03.072
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Development of high efficient and stable water oxidation catalysts is essential for the realization of industrial water-splitting systems. Herein, a novel approach involving an in-situ transformation of Co(OH)(2) nanosheets into NH4CoPO4 center dot H2O nanoplates on Co foil is reported. As a 3D self-supported oxygen revolution reaction (OER) electrocatalyst, the as-prepared NH4CoPO4 center dot H2O/Co exhibits remarkable catalytic activity and exceptional stability. Specifically, it can deliver a current density of 10 mA cm(-2) at a quite low overpotential of 254 mV with a small Tafel slope of 64.4 mV dec(-1) in alkaline electrolyte. Through experimental study and theoretical analysis, the excellent OER performance can be attributed to enriched exposed active sites, favorable electron/proton transfer and mass transport, and its unique asymmetric local atomic and electronic structure. Thus, this present research not only provides a practicable in-situ transformation strategy to design 3D self-supported electrocatalysts, but also enlightens a new way of developing transition-metal phosphates for efficient and stable water oxidation at atomic level. (c) 2020 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights reserved.
引用
收藏
页码:167 / 174
页数:8
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