催化作用
化学
氧气
还原(数学)
氧还原
氧还原反应
化学工程
核化学
有机化学
电化学
物理化学
数学
电极
工程类
几何学
作者
Fang Li,Xiaobo Ding,Qing-Cheng Cao,Yuan-Hang Qin,Li Yang,Cun-Wen Wang
标识
DOI:10.1016/j.ijhydene.2021.11.015
摘要
In recent years, Co, N co-doped carbon (Co–N–C) materials as oxygen reduction reaction (ORR) catalysts have attracted great attention because of their good ORR stability as well as decent activity. Co-doped zeolitic imidazolate framework-8 (Co@ZIF-8) as the precursor for synthesizing Co–N–C has attracted great interest recently. Co@ZIF-8 synthesis method may affect the properties of the as-synthesized Co@ZIF-8 precursors, which will surely affect the properties and ORR performance of Co@ZIF-8-derived Co–N–C catalysts. Herein, three methods, viz. room-temperature stirring method, reflux method, and hydrothermal method, were used to synthesize Co@ZIF-8 precursors. Physical characterization shows that the synthesis method has a great influence on the textural properties, composition, and graphitization degree of the as-synthesized Co–N–C catalysts. Electrochemical characterization shows that Co–N–C-R synthesized with reflux method exhibits an onset potential (E onset ) of 0.905 V, a half-wave potential (E 1/2 ) of 0.792 V and a limiting current density (J L ) of 5.85 mA cm −2 in acidic media, which are higher than those of Co–N–C–S (E onset = 0.870 V, E 1/2 = 0.770 V, J L = 4.71 mA cm −2 ) and Co–N–C–H (E onset = 0.892 V, E 1/2 = 0.785 V, J L = 4.68 mA cm −2 ) synthesized with room-temperature stirring method and hydrothermal method, respectively. The better ORR activity observed on Co–N–C-R can be attributed to its larger graphitization degree and larger mesopore volume. Catalytic stability test shows that Co–N–C-R has negligible activity loss after 5000 potential cycles. This work demonstrates that reflux method is a more suitable method for synthesizing Co–N–C catalysts for ORR. • Three methods are used to synthesize Co-doped ZIF-8 (Co@ZIF-8) precursors. • Co@ZIF-8-R synthesized with reflux method is more suitable for Co–N–C synthesis. • Co@ZIF-8-R-derived Co–N–C-R exhibits an E 1/2 of 0.792 V in acidic media. • Co–N–C-R shows negligible activity loss after 5000 potential cycles.
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