催化作用
材料科学
双功能
过渡金属
电化学
碳纤维
化学工程
纳米颗粒
析氧
无机化学
纳米技术
物理化学
电极
化学
有机化学
复合材料
复合数
工程类
作者
Renxing Huang,Ying Lei,Dandan Zhang,Huaming Xie,Xingyong Liu,Hong‐Hui Wang
出处
期刊:NANO
[World Scientific]
日期:2020-06-01
卷期号:15 (06): 2050070-2050070
被引量:6
标识
DOI:10.1142/s1793292020500708
摘要
Carbon encapsulated transition metal catalysts receive extensive attention in electrochemical catalytic oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) due to the unique structure and highly adjustable electronic configuration. Herein, we synthesized 3D porous Active-N-rich graphene-like carbon layer-encapsulated Fe/Fe 3 C (Fe@NCG) via pyrolysis of a mixture of solvent-free assembled Fe-chitosan chelates and additional small molecule nitrogen source urea, wherein space-confinement effect of chelates suppressed agglomeration of [Formula: see text] ions and small molecule nitrogen source facilitated regulation of N configurations. The optimized catalyst Fe@NCG shows remarkable ORR/OER bifunctional catalytic activity with a half-wave potential of 0.86 V for ORR and a moderate potential difference of 0.85 V in alkaline medium. Comparative studies revealed that Active-N-rich carbon layer and inner well-dispersed Fe/Fe 3 C nanoparticles and the favorable interface structures between them were responsible for high catalytic activity. Excitingly, the assembled zinc-air battery with Fe@NCG catalysts exhibits a high open-circuit potential (1.45 V), extremely high peak power density (204.50[Formula: see text][Formula: see text] and energy density (814.70[Formula: see text]Wh[Formula: see text][Formula: see text]) as well as robust charge–discharge durability, surpassing those of noble metal catalyst. This proposed simple and universal strategy can also be extended to synthesize carbon encapsulated other transition metal electrocatalysts.
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