Morphology controlled lithium storage in Li3VO4 anodes

Li3VO4 (LVO) anode materials with controllable morphologies ranging from spherical-assemblies, single-crystal nanorods, and flower shapes to bulk-shapes were fabricated via a solvothermal approach using different alcohols (i.e., ethanol, methanol, propanol, and butanol). XRD, SEM, BET, Raman and FTI...

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Bibliographic Details
Main Authors: Yang, Guang, Zhang, Bowei, Feng, Jianyong, Lu, Yu, Wang, Zhiqiang, Aravindan, Vanchiappan, Aravind, Muthiah, Liu, Jilei, Srinivasan, Madhavi, Shen, Zexiang, Huang, Yizhong
Other Authors: School of Materials Science & Engineering
Format: Article
Language:English
Published: 2018
Subjects:
Online Access:https://hdl.handle.net/10356/88060
http://hdl.handle.net/10220/44608
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Institution: Nanyang Technological University
Language: English
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Summary:Li3VO4 (LVO) anode materials with controllable morphologies ranging from spherical-assemblies, single-crystal nanorods, and flower shapes to bulk-shapes were fabricated via a solvothermal approach using different alcohols (i.e., ethanol, methanol, propanol, and butanol). XRD, SEM, BET, Raman and FTIR and galvanostatic charge/discharge measurements were carried out to correlate their structure/morphology with their electrochemical characteristics. The experimental results reveal that both structure and morphology play important roles in the Li+ ion storage of LVO, which degrades in the sequential order from nanorods, to spheres, to flowers and finally to bulk. The LVO nanorods are hierarchical and have a small particle size, high specific surface area, and high crystallinity; thus, they exhibit the largest Li+ ion diffusion coefficient and best electrochemical performance among the four electrodes. Moreover, coating carbon on the single-crystal LVO nanorods further enhances their Li+ ion storage ability. Consequently, the carbon-coated LVO nanorods deliver a high reversible capacity of 440 mA h g−1 at 0.1 A g−1 with good cycling stability and demonstrate great practical application. In addition, the results promote a better fundamental understanding of the Li+ ion storage behavior in LVO and provide insight into the optimal design of LVO and other vanadium-based electrode materials.