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碳包覆LiFe0.5Co0.5PO4固溶体正极材料的制备及其电化学性能
引用本文:钟艳君,吴振国,田海,郭孝东,钟本和,王辛龙.碳包覆LiFe0.5Co0.5PO4固溶体正极材料的制备及其电化学性能[J].无机化学学报,2018,34(8):1581-1589.
作者姓名:钟艳君  吴振国  田海  郭孝东  钟本和  王辛龙
作者单位:四川大学化学工程学院, 成都 610065,四川大学化学工程学院, 成都 610065,四川大学化学工程学院, 成都 610065,四川大学化学工程学院, 成都 610065,四川大学化学工程学院, 成都 610065,四川大学化学工程学院, 成都 610065
基金项目:四川大学专职博士后研发基金(No.2017SCU12018)和国家重点研发计划(No.2017YFB0307504)资助项目。
摘    要:分别以四水磷酸铁(FePO4·4H2O)和二水草酸亚铁(FeC2O4·2H2O)为铁源,采用简单便捷的流变相法制备了碳包覆LiFe0.5Co0.5PO4固溶体材料(LiFe0.5Co0.5PO4/C,简称为LFCP/C)。采用X射线衍射(XRD)、扫描电镜(SEM)、透射电镜(TEM)、恒流充放电等测试手段对复合材料的物相、形貌结构和电化学性能进行了表征和测试。结果表明,2种铁源得到的材料均为橄榄石晶型结构且结晶度良好,二者在颗粒尺寸分布、碳包覆效果和电化学性能方面具有显著的差别。用作锂离子电池正极材料时,以FeC2O4·2H2O为原料得到的LFCP/C具有更优异的电性能:在2.5~5.0 V电压范围内,0.1C倍率下(1C=150 mA·g-1),放电比容量为137.5 mAh·g-1,在10C仍具有57.6 mAh·g-1的放电比容量;0.5C循环100次后容量仍保持78.1%。该样品更佳的电化学性能主要得益于其更小的平均颗粒尺寸,更高的比表面积和理想的碳包覆效果。

关 键 词:锂离子电池  LiFe0.5Co0.5PO4/C  流变相法  铁源  电化学性能
收稿时间:2018/4/23 0:00:00
修稿时间:2018/5/31 0:00:00

Synthesis and Electrochemical Performances of Carbon Coated LiFe0.5Co0.5PO4 Solid Solution as Cathode Materials
ZHONG Yan-Jun,WU Zhen-Guo,TIAN Hai,GUO Xiao-Dong,ZHONG Ben-He and WANG Xin-Long.Synthesis and Electrochemical Performances of Carbon Coated LiFe0.5Co0.5PO4 Solid Solution as Cathode Materials[J].Chinese Journal of Inorganic Chemistry,2018,34(8):1581-1589.
Authors:ZHONG Yan-Jun  WU Zhen-Guo  TIAN Hai  GUO Xiao-Dong  ZHONG Ben-He and WANG Xin-Long
Institution:School of Chemical Engineering, Sichuan University, Chengdu 610065, China,School of Chemical Engineering, Sichuan University, Chengdu 610065, China,School of Chemical Engineering, Sichuan University, Chengdu 610065, China,School of Chemical Engineering, Sichuan University, Chengdu 610065, China,School of Chemical Engineering, Sichuan University, Chengdu 610065, China and School of Chemical Engineering, Sichuan University, Chengdu 610065, China
Abstract:Cabon coated LiFe0.5Co0.5PO4 solid solution (LiFe0.5Co0.5PO4/C, LFCP/C) were synthesized via a facile rheological phase method using iron phosphate tetrahydrate (FePO4·4H2O) and iron oxalate dihydrate (FeC2O4·2H2O) as iron source, respectively. The phase composition, particle morphology and electrochemical performance for the as-prepared materials were characterized by methods including X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM) and galvanostatic charge-discharge measurements. Results demonstrate that both LFCP/C samples possess olivine structure with high crystallinity, while there are significant difference in particle size distribution, carbon coating effect and electrochemical properties. As cathode for lithium ion batteries (LIBs), the LFCP/C obtained by FeC2O4·2H2O as reactant exhibits better electrochemical performance than that by FePO4·4H2O, delivering a specific discharge capacity of 137.5 mAh·g-1 at 0.1C (1C=150 mA·g-1) rate in the voltage range of 2.5~5.0 V, and even at 10C rate, a specific capacity of 57.6 mAh·g-1 is still maintained. Meanwhile, it shows excellent cyclability with a capacity retention rate of 78.1% after 100 cycles at 0.5C. The better electrochemical performance of LFCP/C obtained by FeC2O4·2H2O can be mainly ascribed to its smaller average particle size, higher BET specific surface area, and more appealing carbon coating effect.
Keywords:lithium ion battery  LiFe0  5Co0  5PO4/C  rheological phase method  iron source  electrochemical performance
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