Co-Fe-B Nanochain Electrocatalysts for Oxygen Evolution at High Current Density

被引:19
|
作者
Patil, Komal [1 ]
Babar, Pravin [2 ]
Li, Xue [3 ]
Karade, Vijay [1 ]
Kim, Sugil [1 ]
Jang, Su Young [1 ]
Bhoite, Pravin [4 ]
Kim, Jin Hyeok [1 ]
机构
[1] Chonnam Natl Univ, Optoelect Convergence Res Ctr, Dept Mat Sci & Engn, Gwangju 61186, South Korea
[2] King Abdullah Univ Sci & Technol KAUST, KAUST Catalysis Ctr KCC, Phys Sci & Engn PSE, Thuwal 23955, Saudi Arabia
[3] Chosun Univ, Dept Mat Sci & Engn, Gwangju 61452, South Korea
[4] Dept Chem, Wai 412803, Maharashtra, India
基金
新加坡国家研究基金会;
关键词
transition metal boride; oxygen evolution reaction (OER); nanochains; water oxidation; electrocatalyst; high current density; REDUCED GRAPHENE OXIDE; HYDROGEN EVOLUTION; NANOSHEET ARRAYS; CARBON NANOTUBES; EFFICIENT WATER; COBALT-BORIDE; NICKEL FOAM; REDUCTION; HYDROXIDE; CATALYSTS;
D O I
10.1021/acsanm.2c00312
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Constructing earth-abundant, robust, and cheap-tomake electrode materials for the oxygen evolution reaction (OER) is crucial for the practical application of hydrogen energy. In this work, we prepare amorphous cobalt iron boride (Co-Fe-B) nanochains on a nickel foam (labeled as Co-Fe-B/NF) via one-pot sodium borohydride reduction of Co2+ and Fe2+ at room temperature and use them to boost the performance of OER. The as-prepared Co-Fe-B nanochains exhibit promising catalytic activity with low overpotentials of 270 and 280 mV at higher current densities of 50 and 100 mA cm(-2), respectively, and a much lower Tafel slope of 36 mV dec(-1) for OER. In addition, the Co-Fe-B shows excellent stability for more than 50 h at a high current density of 100 mA cm(-2). The satisfactory electrocatalytic performance is mainly due to the synergy between the metal ions (Co and Fe) and plentiful catalytically active sites of the one-dimensional chain-like structure, which improves the atom utilization efficiency.
引用
收藏
页码:6260 / 6267
页数:8
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