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水热法制备树叶状LiFePO4/C复合正极材料
引用本文:云强,周园,海春喜,申月,李翔,张丽娟,李松,丁秀萍.水热法制备树叶状LiFePO4/C复合正极材料[J].无机化学学报,2015,31(5):880-887.
作者姓名:云强  周园  海春喜  申月  李翔  张丽娟  李松  丁秀萍
作者单位:中国科学院青海盐湖研究所盐湖资源化学重点实验室, 西宁 810008;中国科学院大学, 北京 100049;中国科学院青海盐湖研究所盐湖资源化学重点实验室, 西宁 810008;中国科学院青海盐湖研究所盐湖资源化学重点实验室, 西宁 810008;中国科学院青海盐湖研究所盐湖资源化学重点实验室, 西宁 810008;中国科学院青海盐湖研究所盐湖资源化学重点实验室, 西宁 810008;中国科学院大学, 北京 100049;中国科学院青海盐湖研究所盐湖资源化学重点实验室, 西宁 810008;中国科学院大学, 北京 100049;中国科学院青海盐湖研究所盐湖资源化学重点实验室, 西宁 810008;中国科学院大学, 北京 100049;中国科学院青海盐湖研究所盐湖资源化学重点实验室, 西宁 810008
基金项目:国家高技术研究发展计划(863)(No.2013AA110100);国家重点基础研究发展计划(973)(No.2014CB660806);中国科学院“西部之光”人才培养计划(No.Y412041007);2014年西宁市科技项目(No.2014-6-24)资助。
摘    要:采用柠檬酸辅助水热法合成了高分散性树叶状LiFePO4/C复合正极材料。利用X射线衍射、傅里叶红外光谱、扫描电镜、高分辨率透射电镜和选区电子衍射分析了材料的形貌结构。结果表明,柠檬酸对树叶状LiFePO4/C复合材料的形成具有促进作用。该材料的最大暴露晶面为(010)晶面,且分散性较好。与颗粒状LiFePO4/C材料相比,该材料呈现出更高的放电比容量和更好的倍率性能,在0.1C和5C倍率下,放电比容量分别为158和126mAh·g-1,其原因是由于锂离子沿010]方向的扩散距离缩短,从而使锂离子扩散系数显著增大。

关 键 词:材料科学  水热合成  电化学  LiFePO4/C  树叶状  柠檬酸
收稿时间:2015/1/27 0:00:00
修稿时间:2015/2/25 0:00:00

Hydrothermal Synthesis of Leaf-like LiFePO4/C Cathode Composites
YUN Qiang,ZHOU Yuan,HAI Chun-Xi,SHEN Yue,LI Xiang,ZHANG Li-Juan,LI Song and DING Xiu-Ping.Hydrothermal Synthesis of Leaf-like LiFePO4/C Cathode Composites[J].Chinese Journal of Inorganic Chemistry,2015,31(5):880-887.
Authors:YUN Qiang  ZHOU Yuan  HAI Chun-Xi  SHEN Yue  LI Xiang  ZHANG Li-Juan  LI Song and DING Xiu-Ping
Institution:Key Laboratory of Salt Lake Resources Chemistry of Qinghai Province, Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining 810008, China;University of Chinese Academy of Sciences, Beijing 100049, China;Key Laboratory of Salt Lake Resources Chemistry of Qinghai Province, Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining 810008, China;Key Laboratory of Salt Lake Resources Chemistry of Qinghai Province, Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining 810008, China;Key Laboratory of Salt Lake Resources Chemistry of Qinghai Province, Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining 810008, China;Key Laboratory of Salt Lake Resources Chemistry of Qinghai Province, Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining 810008, China;University of Chinese Academy of Sciences, Beijing 100049, China;Key Laboratory of Salt Lake Resources Chemistry of Qinghai Province, Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining 810008, China;University of Chinese Academy of Sciences, Beijing 100049, China;Key Laboratory of Salt Lake Resources Chemistry of Qinghai Province, Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining 810008, China;University of Chinese Academy of Sciences, Beijing 100049, China;Key Laboratory of Salt Lake Resources Chemistry of Qinghai Province, Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining 810008, China
Abstract:Highly-dispersed LiFePO4/C composite with micro-leaf structure was synthesized by a facile citric acid-assisted hydrothermal method in this study. Crystal structure and morphology of samples were investigated by XRD, FTIR, SEM, HR-TEM and selected area electron diffraction (SAED). The characterization results indicate that citric acid accelerates the formation of leaf-like LiFePO4/C composite. The as-prepared leaf-like LiFePO4/C composite with an enlarged (010) plane has high dispersibility. By comparing the electrochemical properties of the LiFePO4/C particles in our study, the LiFePO4/C micro-leaves exhibit larger discharge capacity and better rate performance, which deliver a discharge capacity of 158 mAh·g-1 at 0.1C and 126 mAh·g-1 at 5C. The enhanced performance perhaps is attributed to the reduced Li-ion diffusion paths along the 010] direction and larger Li-ion diffusion coefficient.
Keywords:materials science  hydrothermal synthesis  electrochemistry  LiFePO4/C  micro-leaf  citric acid
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