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Guanine-derived core-shell FeCo alloy confined in graphene-like N-doped carbon as efficient bifunctional oxygen electrocatalysts for rechargeable Zn-air batteries
被引:5
作者:
Lin, Xin
[1
]
Cui, Longji
[1
]
Ding, Xueda
[1
]
Chen, Yiquan
[1
]
Wei, Qiaohua
[1
]
Huang, Baobing
[1
,2
]
Xie, Zailai
[1
]
机构:
[1] Fuzhou Univ, Fujian Prov Univ, Key Lab Adv Carbon Based Funct Mat, Fuzhou 350108, Fujian, Peoples R China
[2] Fuzhou Univ, Sch Adv Mfg, Jinjiang, injiang 362200, Fujian, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Guanine;
FeCo alloy;
Core-shell structure;
Bifunctional oxygen electrocatalysis;
Rechargeable Zn-air batteries;
NANOSHEETS;
BIOMASS;
D O I:
10.1016/j.jallcom.2024.174805
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:
Maximization the synergistic effect of each component in transition metal-carbon complexes is expected to improve the bifunctional oxygen electrocatalysis for rechargeable Zn-air batteries but is still challenging. Herein, nucleobase guanine is employed as a supramolecular precursor to generate the core (FeCo alloy)-shell (carbon) structure embedded in ultrathin graphene-like nitrogen-doped carbon nanosheets (FeCo@NCNSs) via a confinement pyrolysis strategy. Thanks to the generated core-shell structure and bimetallic synergistic effect, the as-prepared FeCo@NCNSs exhibits excellent electrochemical performance in both oxygen reduction reaction and oxygen evolution reaction. As a result, when served as the bifunctional air electrode for a practical Zn-air battery, FeCo@NCNSs exhibits a higher open-circuit voltage (1.553 V) and peak power density (197.30 mW cm-2), as well as the greatly improved long-term cyclic stability compared to the noble metal benchmarks. This work provides a promising approach to integrate various active sites for bifunctional oxygen electrocatalysis and inspires the exploration of simple but efficient electrocatalysts for energy storage and conversion.
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页数:9
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