材料科学
催化作用
石墨烯
阴极
化学工程
膜
蚀刻(微加工)
电池(电)
限制电流
基质(水族馆)
纳米技术
无机化学
电极
化学
电化学
物理化学
有机化学
图层(电子)
功率(物理)
工程类
地质学
物理
海洋学
量子力学
生物化学
作者
Jiachen Meng,Zhaofan Zhou,Yanqin Fu,Yulei Zhang
出处
期刊:Small
[Wiley]
日期:2025-06-22
卷期号:21 (33): e2503448-e2503448
被引量:3
标识
DOI:10.1002/smll.202503448
摘要
Abstract Despite the great potential of Fe single‐atom catalysts (SACs) to replace platinum‐based materials for oxygen reduction reaction (ORR), their synthesis is hindered by the strong tendency of atomic migration/aggregation and uncontrollable substrate etching during fabrication, impeding the direct synthesis of Fe SACs in the rational‐designed cathode for Zn‐air batteries. Herein, a self‐supporting hydrophobic edge‐rich graphene (ERG) membrane serves as a conductive carbon skeleton in the air cathode. Through a cascade limiting strategy involving α‐D‐glucose and melamine, atomically dispersed Fe–NC SACs are synthesized on the surfaces of ERG sheets without substrate damage. Systematic studies confirm that the chelation of Fe ions and their binding to N‐species at elevated temperatures are critical to achieving atomic dispersion. By optimizing the molar ratio of α‐D‐glucose/Fe(III) ions and utilizing the hydrophobic porous framework, the Zn‐air battery assembled with ERG@Glu&Fe‐40‐Mel membrane achieves a peak power density of 132 mW cm −2 and the enhanced stability compared to that employing commercial Pt/C catalyst.
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