共 60 条
Structural engineering and carbon enrichment in V2CTx MXene: An approach for enhanced supercapacitive charge storage
被引:32
作者:

Yadav, Ashish
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机构:
Univ Delhi, Dept Chem, Delhi 110007, India Univ Delhi, Dept Chem, Delhi 110007, India

Singal, Shobhita
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h-index: 0
机构:
Univ Delhi, Dept Chem, Delhi 110007, India Univ Delhi, Dept Chem, Delhi 110007, India

Soni, Prakshi
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h-index: 0
机构:
Univ Delhi, Dept Chem, Delhi 110007, India Univ Delhi, Dept Chem, Delhi 110007, India

Singh, Gurmeet
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h-index: 0
机构:
Univ Delhi, Dept Chem, Delhi 110007, India Univ Delhi, Dept Chem, Delhi 110007, India

Sharma, Raj Kishore
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机构:
Univ Delhi, Dept Chem, Delhi 110007, India Univ Delhi, Dept Chem, Delhi 110007, India
机构:
[1] Univ Delhi, Dept Chem, Delhi 110007, India
关键词:
MXenes;
Metal organic framework;
Porous carbon;
Supercapacitor;
POROUS CARBON;
CARBIDE MXENE;
PERFORMANCE;
VANADIUM;
NANOPARTICLES;
ELECTRODE;
ANODE;
D O I:
10.1016/j.jallcom.2022.167859
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:
We report a highly electroactive vanadium carbide MXene in a carbon matrix (V2CTx @C), synthesized with the assistance of metal organic frameworks (MOFs). The morphological changes in the stacked nanosheets of V2CTx MXene resulted in the formation of exfoliated carbon enriched V2CTx nanodiscs which exhibited 3 times increased specific surface area, augmented electronic conductivity, and enhanced electrode/elec-trolyte interfacial contact area. This altogether led to a high specific capacitance (551 F g-1 at 2 A g-1), remarkable rate performance (317 F g-1 at 10 A g-1), and outstanding cycling stability (88.1% retention after 5000 GCD cycles) of the V2CTx @C electrode. The V2CTx @C || V2CTx @C symmetric cell operates up to 1.2 V, displaying ultrahigh energy/power density (48.6 Wh kg-1 and 552 W kg-1). This work provides a new strategy for structural engineering in MXene based electrode materials for next generation energy storage devices. (c) 2022 Elsevier B.V. All rights reserved.
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