Journal
ENERGY & FUELS
Volume 35, Issue 9, Pages 8358-8364Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.energyfuels.1c00438
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Funding
- National Natural Science Foundation of China [51872192, 51672182, 52025028, 51772197]
- Natural Science Foundation of Jiangsu Province [BK20180002]
- Natural Science Foundation of the Jiangsu Higher Education Institutions of China [19KJA170001]
- Natural Science Foundation of the Priority Academic Program Development (PAPD) of Jiangsu Higher Education Institutions
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The ordered structure of V2O5 nanopores formed by electrochemical anodization exhibits favorable electrochemical performance for sodium storage, with high reversible capacity and cycling stability.
Vanadium oxide has a high theoretical capability for sodium storage, but this capability has often been plagued by sluggish electrochemical reaction kinetics upon sodiation/desodiation. To alleviate this problem, we report on an ordered structure of V2O5 nanopores by electrochemical anodization. The nanopores are amorphous in structure, 30-40 nm in diameter, and similar to 2.4 mu m in depth, exhibiting favorable electrochemical performance for sodium. In the potential range between 1.5 and 3.8 V, the nanoporous architecture of V2O5 displays a reversible capacity of 177 mAh g(-1) with initial coulombic efficiency of 74% and retains a capacity of 69 mAh g(-1) over 50 cycles at a higher rate of 100 mA g(-1). The open framework of nanopores and the isotropic properties of the amorphous structure are believed to be responsible for the appealing electrochemical performance of anodized V2O5.
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