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以硝酸铁、磷酸二氢铵、氢氧化锂为原料,以聚乙二醇PEG-4000为螯合剂和碳源,采用溶胶-凝胶法制备了LiFePO4/C。利用XRD、SEM、电化学性能测试等手段对LiFePO4/C的物相结构、形貌、电化学性能进行表征。结果表明:PEG-4000作为螯合剂和碳源,使得样品的粒径较小且分布均匀。650℃烧结18h所合成的样品具有最佳的电化学性能,0.1C首次充、放电容量分别为152.7、150.6 mAh/g;循环30次后容量为146 mAh/g,容量衰减率为3.05%。 相似文献
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Synthesis and characterization of triclinic structural LiVPO4F as possible 4.2 V cathode materials for lithium ion batteries 总被引:1,自引:1,他引:1
A potential 4.2 V cathode material LiVPO4F for lithium batteries was prepared by two-step reaction method based on a carbon-thermal reduction (CTR) process. Firstly, V2O5, NH4H2PO4 and acetylene black are reacted under an Ar atmosphere to yield VPO4. The transition-metal reduction is facilitated by the CTR based on C→CO transition. These CTR conditions favor stabilization of the vanadium as V^3+ as well as leaving residual carbon, which is useful in the subsequent electrode processing. Secondly, VPO4 reacts with ElF to yield LiVPO4F product. The property of the LiVPO4F was investigated by X-ray diffractometry (XRD), scanning electron microscopy (SEM) and electrochemical measurement. XRD studies show that LiVPO4F synthesized has triclinic structure(space group p I ), isostructural with the naturally occurring mineral tavorite, EiFePO4-OH. SEM image exhibits that the particle size is about 2μm together with homogenous distribution. Electrochemical test shows that the initial discharge capacity of LiVPO4F powder is 119 mA·h/g at the rate of 0.2C with an average discharge voltage of 4.2V (vs Ei/Li^+), and the capacity retains 89 mA·h/g after 30 cycles. 相似文献
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钟胜奎 《武汉理工大学学报(材料科学英文版)》2009,24(4):552-556
Y-doped LiVPO4F cathode materials were prepared by a carbothermal reduction(CTR) process. The properties of the Y-doped LiVPO4F samples were investigated by X-ray diffraction (XRD) and electrochemical measurements. XRD studies show that the Y-doped
LiVPO4F samples have the same triclinic structure as the undoped LiVPO4F. The Li extraction/insertion performances of Y-doped LiVPO4F samples were investigated through charge/discharge, cyclic voltammogram (CV), and electrochemical impedance spectra(EIS).
The optimal doping content of Y is x=0.04 in LiY
x
V1−x
PO4F system. The Y-doped LiVPO4F samples show a better cyclic ability. The electrode reaction reversibility is enhanced, and the charge transfer resistance
is decreased through the Y-doping. The improved electrochemical performances of the Y-doped LiVPO4F cathode materials are attributed to the addition of Y3+ ion by stabilizing the triclinic structure.
Funded by the Sponsor Teams for Innovation in the Construction of Talent Highlands in Guangxi Institutions of Higher Learning(GuiJiaoRen
[2007]71), Guangxi Natural Science Foundation(No.0832259), the Research Funds of the Guangxi Key Laboratory of Environmental
Engineering, Protection and Assessment Program to Sponsor Teams for Innovation in the Construction of Talent Highlands in
Guangxi Institutions of Higher Learning(GuiJiaoRen [2007]71) 相似文献
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采用固相球磨法制备了Li2FeP2O7/C正极材料,研究了烧结温度、碳包覆含量以及碳源对其结构、形貌以及电化学性能的影响。结果表明: 高温固相烧结合成样品的适宜温度为680 ℃,以柠檬酸为碳源、碳包覆量为5%时,合成的Li2FeP2O7/C晶型完整,晶粒较小且均匀,0.1C倍率下的放电比容量可达102.6 mAh/g,0.5C倍率下的初次放电比容量可达83.4 mAh/g,循环30次后放电比容量为80.7 mAh/g,展现了较好的循环性能以及倍率性能。 相似文献
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通过一步固相反应和两步固相反应分别合成LiVPO4F/C,采用XRD、SEM和电化学性能测试对LiVPO4F/C进行性能表征。XRD研究表明一步固相反应合成的LiVPO4F/C与两步固相反应合成的样品一样,均属于三斜晶系结构。SEM研究表明:一步固相反应合成的LiVPO4F/C颗粒比两步固相反应合成的样品颗粒小,一步固相反应合成的 LiVPO4F/C 样品电化学性能得到提高是由于草酸作为还原剂和碳源合成的样品颗粒变小。交流阻抗研究表明步固相反应合成的LiVPO4F/C样品电化学阻抗减小。 相似文献
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