电化学
锂(药物)
磷酸铁锂
阴极
等离子体
磷酸盐
材料科学
磷酸铁
磷酸钒锂电池
无机化学
化学
化学工程
电极
物理化学
有机化学
物理
内分泌学
工程类
医学
量子力学
作者
Li Li,Yan Li,Chao Sun,Haijun Yang,Zhong Qiu,Jiayuan Xiang,Xinqi Liang,Anqi Tian,Liang Ma,Lili Sun,Long Wang,Chaojun Wang,Xiaokun Zhang,Yongqi Zhang,Yongqi Zhang,Fangfang Tu,Yuanyuan Jiang,Yuhong Zhang,Yuhong Zhang,Xinhui Xia
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2025-08-20
卷期号:39 (34): 16478-16484
标识
DOI:10.1021/acs.energyfuels.5c03985
摘要
Interface modulation on lithium iron phosphate (LiFePO4) cathodes is highly important for enhancing their high-rate capability and discharge capacities at high current densities. In order to further improve the ionic/electronic conductivity and reaction kinetics of LiFePO4 cathodes, in this work, we report a facile one-step low-temperature N2 plasma technology to modify the LiFePO4/C cathodes. During the plasma process, the LiFePO4/C (LFP/C) particles are rotated in the N2 plasma atmosphere, where numerous N-containing radicals can be induced into the outer carbon layer, leading to N-doped carbon (NC) and surface modification. The low-temperature N2 plasma will create more active sites and defects to reinforce capacity and reaction kinetics by providing creative transportation channels for lithium ions on the cathode/electrolyte interface, thus accelerating the electrochemical kinetics and reaction reversibility. Electrochemical impedance spectroscopy and simulated distribution of relaxation times further confirm the reduced interface resistance and enhanced electrochemical kinetics. Accordingly, the well-designed plasma treated LFP@C electrode shows a higher discharge capacity of 134.8 mAh g–1 at a high current density of 5 C, much better than the unmodified counterpart (109.8 mAh g–1). This facile plasma strategy effectively unlocks its viability for next-generation high-rate energy storage systems.
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