机构地区: 中国科学院广州能源研究所
出 处: 《无机化学学报》 2013年第5期1013-1018,共6页
摘 要: 以LiOH·H2O、Mn(CH3COO)2·4H2O和Ni(CH3COO)2·4H20为原料,分别用柠檬酸(CA)与乙二胺四乙酸(EDTA)为配位剂,采用溶胶凝胶法结合固相烧结法制备富锂固溶体正极材料Li[Li0.2Ni0.2Mn0.6dO2。通过X射线衍射(XRD)、扫描电子显微镜(SEM)、激光粒度仪对所得样品的结构、形貌、粒径分布进行了表征,并测试了材料的电化学性能。采用CA配位制备的材料的电化学性能优于用EDTA配位制备的材料的电化学性能,室温下以18mA·g-1的电流密度,在2.0—4.8V电压范围内充放电,用CA制备的材料首次充电比容量高达324mAh·g-1,首次库伦效率达82%;在180mA·g-1的电流下,其可逆比容量保持在120mAh·g-1。 Li-rich solid solution cathode material Li[Lio2Ni02Mn06]O2 was synthesized by a sol-gel method and subsequent solid-state sintering process, using LiOH'HzO, Mn(CH3COO)2.4H20 and H3COO)2.4H20 as raw materials, and citric acid (CA) and ethylene diamine tetraacetic acid (EDTA) as chelating agents, respectively. The as-synthesized materials were characterized by X-ray diffraction, scanning electron microscope and Laser Particle Size Analyzer, and the electrochemical properties of materials were investigated. The material using CA as chelating agent showed higher capacity and better rate performance than that using EDTA as chelating agent. The half-cell of Li/Li[Li0.2Ni0.2Mn0.6]O2 using CA as chelating agent delivered a charge specific capacity of 324 mAh'g-1 with an initial efficiency of 82% at a current density of 18 mA.g-1 between 2.0 and 4.8 V, and retained the reversible capacity of 120 mAh.g-1 even at a high current density of 180 mA.g-1.