Co/CoOx heterojunctions encapsulated N-doped carbon sheets via a dual-template-guided strategy as efficient electrocatalysts for rechargeable Zn-air battery

被引:49
作者
Zhong, Lin [1 ]
Zhou, Hu [1 ]
Li, Ruifeng [1 ]
Cheng, Hao [1 ]
Wang, Sheng [2 ]
Chen, Boyuan [1 ]
Zhuang, Yongyue [1 ]
Chen, Junfeng [1 ]
Yuan, Aihua [2 ]
机构
[1] Jiangsu Univ Sci & Technol, Sch Mat Sci & Engn, Zhenjiang 212003, Jiangsu, Peoples R China
[2] Jiangsu Univ Sci & Technol, Sch Environm & Chem Engn, Zhenjiang 212003, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrocatalyst; Zn-air batteries; Carbon sheet; Zeolitic imidazolate framework; OXYGEN REDUCTION; POROUS CARBON; CATALYSTS; GRAPHENE; NANOSHEETS;
D O I
10.1016/j.jcis.2021.04.084
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
Developing highly efficient oxygen electrocatalysts is of vital importance for rechargeable Zn-air batteries (ZABs). Herein, Co/CoOx nano-heterojunctions encapsulated into nitrogen-doped carbon sheets (NCS@Co/CoOx) are fabricated via a dual-template-guided approach by using zeolitic imidazolate frameworks (ZIFs) as templates. The synergistic integration of structural and compositional advantages endows such catalyst with superior catalytic properties to benchmark noble-metal catalysts. To be specific, the hierarchical micro/mesopores affords massive mass transport channels and maximizes the exposure of accessible active sites, whereas the NCS matrix accelerates electron transfer and prevents the self-aggregation of active species during the electrocatalytic reaction. Moreover, abundant and synergistic Co-based active sites (CoO, Co3O4, Co-N-x) greatly promote the catalytic activity. As the cathode of both liquid and flexible solid-state ZABs, excellent device properties are achieved, outperforming those assembled with commercial Pt/C+RuO2 catalyst. This work presents a feasible and cost-effective strategy for developing oxygen electrocatalysts derived from ZIFs templates. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:46 / 57
页数:12
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