High performance LiFePO4/CN cathode material promoted by polyaniline as carbon-nitrogen precursor

被引:37
|
作者
Avci, Ercan [1 ]
Mazman, Muhsin [1 ]
Uzun, Davut [1 ]
Bicer, Emre [1 ]
Sener, Tansel [1 ]
机构
[1] TUBITAK, Marmara Res Ctr, Energy Inst, TR-41470 Gebze, Kocaeli, Turkey
关键词
Polyaniline chloride; LiFePO4; Polymer pyrolysis; Carbon-nitrogen coating; Crosslinking; Solid state synthesis; LITHIUM-ION BATTERIES; LIFEPO4/POLYANILINE COMPOSITE CATHODE; POSITIVE-ELECTRODE MATERIALS; ELECTROCHEMICAL PROPERTIES; PHOSPHO-OLIVINES; PYROLYSIS; NANOCOMPOSITE; STORAGE; ACIDS;
D O I
10.1016/j.jpowsour.2013.04.030
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A facile and efficient solid state synthesis of carbon and nitrogen coated lithium iron phosphate (LiFePO4/CN) cathode material is achieved via polymer-pyrolysis method using polyaniline-chloride (PANI-CI). The current investigation is comparatively analyzed with the results of the composite of LiFePO4/C (LFP/C) synthesized using sucrose as carbon precursor. The optimized LiFePO4/CN (LFP/CN) composite is synthesized at 700 degrees C using 10 wt.% PANI-CI. The composite exhibits remarkable improvement in capacity, cyclability and rate capability compared to those of LFP/C. The specific discharge capacities as high as 164 mAh g(-1) (theoretical capacity: 170 mAh g(-1)) at 0.1 C and 100 mAh g(-1) at 10 C rates were achieved with LFP/CN. In addition, the composite exhibits a long-term cycling stability with the capacity loss of only 10% after 1000 cycles. PANI-CI shifts the size distribution of the composite to nanometer scale (approximately 150 nm), however the addition of sucrose does not have such an effect. LFP/CN contains 1.6 wt.% nitrogen and 15.8 wt.% carbon. LFP particles are mostly coated with a few nanometers thick C-N layer forming a core-shell structure. The possible crosslinking mechanism of PANI-Cl upon pyrolysis on size reduction and formation of uniform carbon/nitrogen coating on LFP are also discussed. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:328 / 337
页数:10
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