期刊
JOURNAL OF PHYSICAL CHEMISTRY C
卷 115, 期 30, 页码 15048-15056出版社
AMER CHEMICAL SOC
DOI: 10.1021/jp201686g
关键词
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资金
- National Natural Science Foundation of China [21001036, 50902041]
- Natural Science Foundation of Heilongjiang Province [B200905]
- Foundation for University Key Teachers by the Heilongjiang Ministry of Education [1155G28]
- Innovation Foundation of Harbin City [2009RFQXG201]
- Universities of Heilongjiang [2011TD010]
Ti and Mg codoped Li3V2-2xTixMgx(PO4)(3) (x = 0, 0.05, 0.10, 0.20, and 0.25) samples were prepared by a sol-gel method. The effects of Ti and Mg codoping on the physical and electrochemical characteristics of Li3V2(PO4)(3) were investigated. Compared with the XRD pattern of the undoped sample, those of the Ti and Mg codoped samples have no extra reflections, which indicates that Ti and Mg enter the structure of Li3V2(PO4)(3). According to the results of charge-discharge measurements, the initial capacity of Li3V2-2xTixMgx(PO4)(3) at a low current density (0.2 C) decreases with increasing x. However, the discharge capacities at higher current densities (1 and 2 C) and the cycling stability are improved by a low amount of Ti and Mg codoping (x = 0.05), and moreover, EIS measurements indicate the lower charge transfer resistance of Li3V1.9Ti0.05Mg0.05(PO4)(3). The improved electrochemical performance of Li3V1.9Ti0.05Mg0.05(PO4)(3) can be attributed to its higher structural stability and smaller particle size. When xis higher than 0.05, the charge transfer resistance increases with increasing x, which leads to their poor electrochemical performance.
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