催化作用
硫黄
金属
电极
材料科学
锌
热解
聚吡咯
氢
氟
化学工程
氮气
纳米技术
化学
有机化学
电化学
物理化学
冶金
工程类
作者
Yazhou Zhou,Xiafang Tao,Guangbo Chen,Ruihu Lu,Ding Wang,Ming‐Xi Chen,Enquan Jin,Juan Yang,Haojun Liang,Yan Zhao,Xinliang Feng,Akimitsu Narita,Kläus Müllen
标识
DOI:10.1038/s41467-020-19599-8
摘要
Abstract Metal single-atom catalysts (M-SACs) have emerged as an attractive concept for promoting heterogeneous reactions, but the synthesis of high-loading M-SACs remains a challenge. Here, we report a multilayer stabilization strategy for constructing M-SACs in nitrogen-, sulfur- and fluorine-co-doped graphitized carbons (M = Fe, Co, Ru, Ir and Pt). Metal precursors are embedded into perfluorotetradecanoic acid multilayers and are further coated with polypyrrole prior to pyrolysis. Aggregation of the metals is thus efficiently inhibited to achieve M-SACs with a high metal loading (~16 wt%). Fe-SAC serves as an efficient oxygen reduction catalyst with half-wave potentials of 0.91 and 0.82 V (versus reversible hydrogen electrode) in alkaline and acid solutions, respectively. Moreover, as an air electrode in zinc–air batteries, Fe-SAC demonstrates a large peak power density of 247.7 mW cm −2 and superior long-term stability . Our versatile method paves an effective way to develop high-loading M-SACs for various applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI