双功能
材料科学
过电位
锌
复合数
金属有机骨架
析氧
电催化剂
碳化
碳纤维
卟啉
无机化学
过渡金属
分解水
化学工程
催化作用
冶金
电极
吸附
复合材料
光化学
物理化学
有机化学
电化学
化学
工程类
扫描电子显微镜
光催化
作者
Min-Yi Yu,Yanfang Yao,Kun Fang,Lishui Chen,Liping Si,Haiyang Liu
标识
DOI:10.1021/acsami.3c18384
摘要
The main impediment to the development of zinc–air batteries is the sluggish kinetics of the oxygen reduction reaction (ORR) and the oxygen evolution reaction (OER). Transition metal N-doped carbon catalysts offer a promising alternative to noble metal catalysts, with metal–organic framework (MOF)-derived carbon material catalysts being particularly noteworthy. Here, we synthesized MxP-Z-C carbon catalysts by combining two-dimensional (2D) metal porphyrin-based MOFs (MxPMFs, x = Fe, Co, Ni, Mn) and three-dimensional zeolitic imidazole framework-8 (ZIF-8) through electrostatic interaction, followed by carbonization. ZIF-8 was inserted between the layers of MxPMFs to prevent its Π–Π stacking, allowing the active sites to become fully exposed. MxP-Z-C demonstrated an impressive catalytic activity for both the ORR and the OER reactions. Among them, FeP-Z-C showed the best catalytic activity. The half-wave potential for ORR was 0.92 V (vs the reversible hydrogen electrode (RHE)), while the overpotential for the OER was 290 mV. In addition, the zinc–air battery assembled by FeP-Z-C exhibited high power density (133.14 mW cm–2) and significant specific capacity (816 mAh gZn–1), indicating considerable potential as a bifunctional catalyst for electronic devices.
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