材料科学
纳米片
催化作用
碳纤维
化学工程
硫黄
二茂铁
化学气相沉积
氧气
无机化学
多孔性
电极
电化学
纳米技术
氧还原反应
沉积(地质)
可逆氢电极
氮气
电流密度
氧化还原
热解
活性炭
多孔介质
燃料电池
氧还原
析氧
功率密度
作者
Shichao Peng,Xilan Ma,Tiantian Luo,Zhaoyang Leng,Heng Cao,Zhao Lv,Tinglu Song,Xing Su,Quanqing Zhao,Huazhang Zhai,Liang Luo,Chuanbao Cao,Youqi Zhu,Meishuai Zou
出处
期刊:Small
[Wiley]
日期:2026-07-19
卷期号:22 (49): e74559-e74559
被引量:1
摘要
ABSTRACT Single‐atom Fe catalysts (Fe–SACs) are recognized as the effective alternative to platinum‐based counterparts for the oxygen reduction reaction (ORR). Maximizing availability efficiency of active sites is of great significance for Fe–SACs in practical application. Herein, an efficient chemical vapor deposition route is developed to generate Fe–SACs on porous carbon nanosheets for ORR. Metal‐organic framework (ZIF‐8) is converted into highly porous and N,S‐co‐doped carbon nanosheets as Fe–SACs support. Ferrocene is sublimated and deposited on carbon nanosheet support to generate isolated single‐atomic Fe sites. Spectral and microscopic investigations confirm that Fe elements in Fe–SACs are highly dispersed in carbon support and coordinated asymmetrically with nitrogen and sulfur atoms in Fe–N 3 S 1 configuration. The optimized Fe–SACs achieve outstanding alkaline ORR activity with a half‐wave potential of 0.91 V vs. RHE. After 10 000 cycles, the half‐wave potential only shows 16 mV decays. Furthermore, the rechargeable zinc–air batteries assembled with Fe–SACs as the air electrode can show a peak power density of 213 mW cm −2 and retain a stable voltage plateau over 10 000 charge–discharge cycles. This work affords an efficient strategy for preparing highly exposed Fe–SACs for energy‐related applications.
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