Synergic effects of FeOOH and CoNi2Se4 bilayer nanosheets as highly efficient electrocatalysts for the oxygen evolution reaction

被引:6
作者
Park, Jong-Young [1 ]
Rajesh, John Anthuvan [1 ]
Kang, Soon-Hyung [2 ]
Ahn, Kwang-Soon [1 ]
机构
[1] Yeungnam Univ, Sch Chem Engn, Gyongsan 712749, South Korea
[2] Chonnam Natl Univ, Dept Chem Educ, Gwangju 500757, South Korea
基金
新加坡国家研究基金会;
关键词
Transition metals; Selenides; Oxyhydroxides; Oxygen evolution reaction; Synergic effects; BIFUNCTIONAL ELECTROCATALYSTS; AMORPHOUS FEOOH; NICKEL FOAM; NI FOAM; SELENIDE; NANOSTRUCTURES; CATALYSTS; OER;
D O I
10.1016/j.jallcom.2023.169979
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 substantial growth of nonprecious and inexpensive electrocatalysts for the oxygen evolution reaction (OER) is vital for commercial usage. In this work, cobalt nickel selenide (CoNi2Se4, called CNSe) thin film nanosheet heterojunctions with iron oxyhydroxide (FeOOH) thin film nanosheets were grown directly on a nickel foam substrate (Ni-foam) using an electrodeposition method. The electrocatalytic activity of CNSe/ FeOOH bilayer nanosheets was evaluated for OER studies using its CNSe and FeOOH counterparts. The CNSe/ FeOOH bilayer thin film exhibited a low overpotential of 222 mV to deliver a benchmark current density of 10 mA cm-2, which was lower than that of the CNSe (327 mV) and FeOOH (276 mV) electrocatalysts. The bilayer electrocatalyst delivered remarkable long-term electrochemical stability for more than 120 h at a constant current density of 10 mA cm-2. The excellent activity was attributed to the synergic effects of CNSe/FeOOH with high electrochemical active sites and feasible charge transfer ability. This study provides new insights for designing a different class of materials using a simple electrochemical deposition route for high-performance OER kinetics.(c) 2023 Elsevier B.V. All rights reserved.
引用
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页数:10
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