阳极
电化学
阴极
介电谱
材料科学
纳米颗粒
化学工程
容量损失
碳纤维
锂离子电池的纳米结构
离子
电极
纳米技术
分析化学(期刊)
无机化学
化学
复合材料
色谱法
有机化学
工程类
物理化学
复合数
作者
Bidhan Pandit,Bernard Fraisse,Lorenzo Stievano,Laure Monconduit,Moulay Tahar Sougrati
标识
DOI:10.1016/j.electacta.2022.139997
摘要
The cheap and non-toxic FePO4, which can be obtained from LiFePO4 recovered from spent Li-ion batteries, provides a reversible capacity of 103 mAh/g in coin cells, corresponding to 76% of theoretical capacity, with very good rate capability and stability. The study of the electrochemical mechanism during sodiation carried out by in situ X-ray diffraction (XRD) reveals a pure biphasic transition during Na+ (de)insertion. The chemical diffusion coefficient (DNa) determined from galvanostatic intermittent titration technique and electrochemical impedance spectroscopy varies in the range 10−16–10−10 cm2/s at room temperature depending on the degree of sodiation. As a proof of concept, a full cell fabricated using a carbon-coated FePO4@C cathode and a Na15Pb4 anode obtained by electrochemical sodiation of recyclable Pb, maintained 76% of the initial capacity over 100 cycles at constant C/10 rate. This outstanding electrochemical performance, based on the combination of the low-cost FePO4@C cathode with a recyclable lead-based anode, makes this new technology a promising real-world alternative for future commercial Na-ion systems.
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