Bi-functional electrocatalysis through synergetic coupling strategy of atomically dispersed Fe and Co active sites anchored on 3D nitrogen-doped carbon sheets for Zn-air battery

电催化剂 双功能 催化作用 化学 电池(电) 碳纤维 沸石咪唑盐骨架 电化学 析氧 咪唑酯 化学工程 纳米技术 无机化学 材料科学 电极 金属有机骨架 吸附 有机化学 物理化学 功率(物理) 物理 量子力学 复合材料 复合数 工程类
作者
Yan Luo,Jie Zhang,Jinwei Chen,Yihan Chen,Chenyang Zhang,Yingjian Luo,Gang Wang,Ruilin Wang
出处
期刊:Journal of Catalysis [Elsevier BV]
卷期号:397: 223-232 被引量:70
标识
DOI:10.1016/j.jcat.2021.03.030
摘要

Single atom catalysts (SACs) with unique structure gain much interest in the field of electrocatalysis and show a broad application prospect in long-life rechargeable Zn-air batteries. However, ingenious design and preparation of bi-metal SACs is still difficult to further enhance the bifunctional electrocatalytic activity. Herein, modified zeolitic imidazolate frameworks (SiO2@Fe-ZIF-8/67) was facilely designed to preparation atomically dispersed Fe and Co doping 3D nitrogen-doped carbon nanosheets ([email protected]). The Fe or Co single atoms are identified to be coordinated with N atoms and form FeN4, CoN4 or N3Fe-CoN3 anchored on 3D defect carbon, which act as reactive sites for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). Through synergetic coupling effect, [email protected] exhibits excellent electrochemical performance with ORR/OER potential gap of 0.80 V. Density functional theory (DFT) calculations further indicate the synergistic effect between Fe and Co in [email protected] towards the enhancing ORR activity. The as-prepared catalyst assembled Zn-air battery shows a maximum power density, and superb cycling stability, surpassing that based on commercial Pt/C + IrO2. Results from this study may provide a facile method for precious control of dual-metal single sites doped carbon with highly activity and durability for bifunctional electrocatalysis.
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