双功能
电催化剂
材料科学
催化作用
碳化
析氧
锌
氧化钴
碳纤维
钴
煅烧
化学工程
电池(电)
无机化学
纳米技术
化学
电化学
电极
冶金
有机化学
复合数
复合材料
扫描电子显微镜
功率(物理)
物理
物理化学
量子力学
工程类
作者
Meijie Chen,Shengbo Han,Ming Sun,Junshi Huang,Zeyu Li,Yingying Xu,Gao Cheng,Lin Yu
标识
DOI:10.1016/j.jallcom.2023.172511
摘要
Rechargeable zinc-air batteries need bifunctional electrocatalysts to improve the kinetics of both the oxygen reduction reaction (ORR) and the oxygen evolution reaction (OER). Herein, we prepare a CoO@NC catalyst employing the 'carbonization-solvothermal-calcination' method, which involves affixing CoO nanosheets to the nitrogen-doped carbon matrix derived from the loofah sponge. The synergy of NC and CoO components creates abundant active sites, and their hierarchical porous structure enables the swift movement of relevant species, thus allowing the CoO@NC catalyst to display remarkable bifunctional performance with a potential difference of 0.73 V. Additionally, the CoO@NC-driven zinc-air battery exhibits a remarkable peak power density of 112.4 mW cm-2 and works reliably for more than 200 hours, outperforming the commercial Pt/C-RuO2 catalysts. This research proposes a novel strategy for constructing noble-metal-free bifunctional electrocatalysts.
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