催化作用
热解
氧还原
金属
Atom(片上系统)
燃料电池
材料科学
兴奋剂
氧原子
化学
化学工程
氧还原反应
纳米技术
无机化学
氧气
物理化学
有机化学
冶金
电化学
光电子学
计算机科学
电极
分子
嵌入式系统
工程类
作者
Ergui Luo,Chen Wang,Li Yang,Xian Wang,Liyuan Gong,Tuo Zhao,Jin Zhao,Junjie Ge,Changpeng Liu,Wei Xing
出处
期刊:Nano Research
[Springer Nature]
日期:2020-06-16
卷期号:13 (9): 2420-2426
被引量:48
标识
DOI:10.1007/s12274-020-2868-8
摘要
Fe/N/C material is the most competitive alternative to precious-metal catalysts for oxygen reduction. In view of the present consensus on active centers, further effort is directed at maximizing the density of single Fe atoms. Here, the imperfections in commonly used doping strategy of Fe for the synthesis of zeolitic imidazolateframework (ZIF)-derived Fe/N/C catalysts are revealed. More importantly, a strikingly improved catalyst is obtained by a ‘second pyrolysis’ method and delivers a half-wave potential of 0.825 V (vs. RHE) in acidic media. The strong confinement effect of carbonaceous host accounts for the formation of dense single-atom sites and thus the high activity. Our findings will potentially facilitate future improvement of M/N/C catalysts.
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