Highly accessible atomically dispersed FeNx sites coupled with Fe3C@C core-shell nanoparticles boost the oxygen catalysis for ultra-stable rechargeable Zn-air batteries

被引:43
|
作者
Srinivas, Katam [1 ,2 ]
Chen, Zhuo [3 ]
Ma, Fei [1 ,2 ]
Chen, Anran [4 ]
Zhang, Ziheng [1 ,2 ]
Wu, Yu [1 ,2 ]
Zhu, Ming-qiang [3 ]
Chen, Yuanfu [1 ,2 ]
机构
[1] Univ Elect Sci & Technol China, Sch Elect Sci & Engn, Chengdu 610054, Peoples R China
[2] Univ Elect Sci & Technol China, State Key Lab Elect Thin Films & Integrated Devic, Chengdu 610054, Peoples R China
[3] Northwest A&F Univ, Coll Mech & Elect Engn, Yangling 712100, Shaanxi, Peoples R China
[4] Yunnan Univ, Sch Mat & Energy, Kunming 650091, Yunnan, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
MNx sites; Core-shell nanoparticle; Synergistic interactions; Oxygen reduction reaction; Zn-air battery; POROUS CARBON; ACTIVE-SITES; REDUCTION; ELECTROCATALYSTS; NANOSHEETS;
D O I
10.1016/j.apcatb.2023.122887
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
It is significant but challenging to develop a cost-effective, high-efficiency, and stable bifunctional electrocatalyst of oxygen reduction and evolution reactions (ORR and OER) for rechargeable Zn-air batteries. Herein, we present a novel bifunctional catalyst constructed by highly accessible atomically dispersed MNx sites coupled with core-shell nanoparticles (M-Phen-800; M = Fe, Co, and Ni) from easily accessible M-Phenanthroline (M-Phen) com-plexes. Due to the synergistically induced symmetric charge distribution around FeNx sites by Fe3C@C core-shell nanoparticles, Fe-Phen-800 exhibits exceptional onset (E-onset = 0.994 V) and half-wave (E-1/2 = 0.878 V) potentials for ORR and a very low overpotential of 285 mV @ 10 mA cm(-2) (E-j=10) for OER, indicating excellent bifunctional activity (Delta E = E-j=10 - E-1/2 = 0.637 V) over the state-of-the-art Pt/C-RuO2 (0.702 V) combination. Moreover, the Fe-Phen-800-based Zn-air battery demonstrates a remarkable energy density of 1022 Wh kg(-1) and greater cycling stability (>800 cycles) than the commercial Pt/C-RuO2 battery.
引用
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页数:13
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