用于锂离子电池的高 C 率高性能电纺 LiFePO4/碳纳米纤维自立式阴极

D. Conti, Claudia Urru, Giovanna Bruni, Pietro Galinetto, B. Albini, V. Berbenni, D. Capsoni
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引用次数: 0

摘要

本研究通过电纺丝法合成了用于 LIB 的 LiFePO4/CNF 自立阴极。与传统的胶带浇铸阴极(70-85 wt%)相比,使用了较低的活性材料量(12.3 和 34.5 wt%)。表征技术(XRPD、SEM、TEM、EDS、拉曼光谱和热重分析)证实,无粘结剂电极中保持了磷酸铁锂的橄榄石型结构,活性材料均匀地分散在碳纳米纤维中。电化学研究表明,与为进行比较而临时制备的 LiFePO4 带铸阴极(活性材料含量为 80 wt%)相比,独立电极具有更高的 Li+ 扩散系数(1.36 × 10-11 cm2/s)和更好的可逆性。与带铸阴极相比,34.5 wt% 的磷酸铁锂自立式阴极显示出较低的容量衰减、良好的可逆性和稳定性,在 C 速率高于 5C 时容量值更高,在 1C 循环 1000 次并进一步循环至 20C 时寿命更长。值得注意的是,只需 34.5 wt% 的活性材料就能获得更好的电化学性能。这些结果证明了 CNF 基质在承载 LiFePO4、促进电解质渗透和与活性材料接触以及提高电子导电性方面的重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High C-Rate Performant Electrospun LiFePO4/Carbon Nanofiber Self-Standing Cathodes for Lithium-Ion Batteries
In the present study, LiFePO4/CNF self-standing cathodes for LIBs are synthesized by electrospinning. A lower active material amount (12.3 and 34.5 wt%) is used, compared to the conventional tape-casted cathodes (70–85 wt%). The characterization techniques (XRPD, SEM, TEM, EDS, Raman spectroscopy, and thermogravimetry) confirm that the olivine-type structure of LiFePO4 is maintained in the binder-free electrodes, and the active material is homogeneously dispersed into and within the carbon nanofibers. The electrochemical investigation demonstrates that higher Li+ diffusion coefficients (1.36 × 10−11 cm2/s) and improved reversibility are reached for free-standing electrodes, compared to the LiFePO4 tape-casted cathode (80 wt% of active material) appositely prepared for comparison. The 34.5 wt% LiFePO4 self-standing cathode displays a lower capacity fading, good reversibility and stability, enhanced capacity values at C-rates higher than 5C, and a good lifespan when cycled 1000 cycles at 1C and further cycled up to 20C, compared to the tape-casted counterpart. Notably, the improved electrochemical performances are obtained by only the 34.5 wt% of active material. The results evidence the relevant role of the CNF matrix suitable to host LiFePO4, to promote electrolyte permeation and contact with the active material, and to increase the electronic conductivity.
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CiteScore
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