Co/Co3O4 Heterojunctions Encased in Porous N-Doped Carbon Nanocapsules for High-Performance Cathode of Rechargeable Zinc-Air Batteries

被引:0
|
作者
Xu, Hui-Min [1 ]
Zhu, Hong-Rui [1 ]
Zhang, Zhi-Jie [1 ]
Huang, Chen-Jin [1 ]
Shuai, Ting-Yu [1 ]
Zhan, Qi-Ni [1 ]
Li, Gao-Ren [1 ]
机构
[1] Sichuan Univ, Coll Mat Sci & Engn, Chengdu 610065, Peoples R China
基金
中国国家自然科学基金;
关键词
OXYGEN REDUCTION REACTION; CATALYSTS; NANOPARTICLES; OXIDATION; EFFICIENT; SITES;
D O I
10.1021/acs.inorgchem.3c03660
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A long-term goal of rechargeable zinc-air batteries (ZABs) has always been to design bifunctional electrocatalysts that are robust, effective, and affordable for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). It has become a feasible method to construct metal/metal oxide interfaces to achieve superior electrocatalytic performance for ORR and OER by enhanced charge transfer. In this study, Co/Co3O4 heterojunctions were successfully prepared and encased in porous N-doped mesoporous carbon (Co/Co3O4@NC) via a simple condensation-carbonization-etching method. The extensive specific surface area of Co/Co3O4@NC facilitates effective interaction between the electrolyte and the catalyst, thereby enabling sufficient exposure of active sites for the ORR and the OER, consequently enhancing the rate of transport of active species. The well-designed Co/Co3O4@NC delivers superior ORR catalytic activity with a half-wave potential of 0.82 V (vs RHE) and a low overpotential of 347 mV at 10 mA cm(-2) for OER in alkaline solution. The power density of Co/Co3O4@NC-based alkaline aqueous ZAB (156.5 mW cm(-2)) is superior to the commercial Pt/C + IrO2-based alkaline aqueous ZAB, and the cycling stability of ZAB is up to 220 h. In addition, Co/Co3O4@NC-based ZAB shows a high power density (50.1 mW cm(-2)). The construction of metal/metal oxide heterojunction encased in N-doped mesoporous carbon provides a novel route for the design of bifunctional electrocatalysts for high-performance ZABs.
引用
收藏
页码:3702 / 3711
页数:10
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