Ultrafine CoFe Alloy Nanoparticles Confined in Highly Ordered Mesoporous Carbon Films as Catalysts for the Oxygen Evolution Reaction

被引:0
作者
Zhou, Yi [1 ]
Guo, Yanna [1 ]
Yamauchi, Yusuke [2 ,3 ,4 ]
Sugahara, Yoshiyuki [1 ,5 ]
机构
[1] Waseda Univ, Sch Adv Sci & Engn, Shinjuku, Tokyo 1698555, Japan
[2] Nagoya Univ, Sch Engn, Dept Mat Sci & Engn, Nagoya 4648601, Japan
[3] Univ Queensland, Sch Chem Engn, Brisbane, Qld 4072, Australia
[4] Univ Queensland, AIBN, Brisbane, Qld 4072, Australia
[5] Waseda Univ, Kagami Mem Res Inst Mat Sci & Technol, Shinjuku, Tokyo 1690051, Japan
基金
日本学术振兴会;
关键词
highly ordered mesoporouscarbon films; ultrafine bimetallicnanoparticles; dip-coating; oxygen evolution reaction; QUANTITATIVE SAXS ANALYSIS; THIN-FILMS; BIFUNCTIONAL ELECTROCATALYSTS; RATIONAL DESIGN; POROUS CARBON; REDUCTION; HYBRID; HYDROGEN; SURFACE; XPS;
D O I
10.1021/acsanm.4c04249
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Thin carbon films with two different kinds of mesoporous structures (three-dimensional (3D) cubic and two-dimensional (2D) hexagonal) loaded with CoFe alloy nanoparticles have been successfully synthesized by a dip-coating method with high-temperature calcination under a N2 atmosphere. Ultrafine bimetallic CoFe nanoparticles are introduced into these two types of mesoporous carbon films as electrochemically active sites. Comparable experiments indicate that the 3D cubic mesoporous carbon film with embedded ultrafine CoFe nanoparticles exhibites a larger electrochemical surface area and lower charge transfer impedance compared with the 2D hexagonal mesoporous carbon film as a supporting material. This material shows a superior electrochemical catalytic performance for the oxygen evolution reaction (OER) with a lower overpotential (eta 10) of 366 mV (j = 10 mA cm-2), outperforming a 2D hexagonal mesoporous carbon film (386 mV) at the same current density.
引用
收藏
页码:25360 / 25368
页数:9
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