کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5439298 | 1398194 | 2016 | 9 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Preparation of porous-structured LiFePO4/C composite by vacuum sintering for lithium-ion battery
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
مهندسی مواد
سرامیک و کامپوزیت
پیش نمایش صفحه اول مقاله

چکیده انگلیسی
The LiFePO4/C (LFP/C) composite as a cathode material for lithium-ion battery was synthesized by solid-state reaction under vacuum sintering condition (20-5 Pa). The effects of vacuum sintering temperature and time on the phase composition, morphological structure, and electrochemical performance of LFP/C composite were investigated by X-ray diffraction, scanning electron microscopy, galvanostatic charge-discharge cycling test, and electrochemical impedance spectroscopy. The synthetic LFP/C composite possessed uniform particle-size distribution with porous architecture upon sintering at 650 °C for 12 h and thus exhibited the highest discharge capacity and best cycle performance. The complete decomposition of citric acid at a suitable temperature under vacuum condition resulted in the formation of porous structure. Compared with atmospheric argon sintering, vacuum sintering method led to the formation of porous architecture, the porous sample showed excellent cycle performance with less than 2% capacity loss after 80 cycles at 0.2 C, and reached the discharge specific capacity of 87.6 mAh gâ1 at 10 C rate, these are better than that of atmospheric argon sintering. The LFP/C composite prepared under vacuum sintering also reduced the optimum sintering temperature by nearly 100 °C compared with that prepared under atmospheric argon sintering.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Ceramics International - Volume 42, Issue 16, December 2016, Pages 18303-18311
Journal: Ceramics International - Volume 42, Issue 16, December 2016, Pages 18303-18311
نویسندگان
Yaochun Yao, Pengwei Qu, Xiangkun Gan, Xiaopeng Huang, Quanfeng Zhao, Feng Liang,