Zijun Fang, Junjie Fang, Guorong Hu, Yanbing Cao, Huan Li, Quanjun Fu, Ke Bai, Zhongdong Peng, Ke Du
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引用次数: 0
Abstract
A simple and scalable synthesis route for LiFe0.67Mn0.33PO4/C cathode material using spray drying combined with high-temperature solid phase technology was developed. With Li3PO4 as the lithium source and cost-effective Mn3O4 replacing part of the iron, this process is compatible with the industrial production line of LiFePO4. X-ray diffraction (XRD) confirmed that the synthesized material exhibited a single-phase olivine structure with a space group of Pnma. Scanning electron microscopy (SEM) revealed a spherical morphology. The synthesized material exhibits excellent rate and cycling performance under the low-grain micro-strain and conductive carbon network structure. Electrochemical testing demonstrated initial discharge capacities of 164, 163, 160, 157, 150, and 128 mAh g−1 at rates of 0.1, 0.2, 0.5, 1, 2, and 5 C, respectively. Moreover, 96.16% of the capacity is retained after 200 cycles at 1C. This approach offers a viable pathway for the preparation of LiFe1-xMnxPO4/C positive electrode materials with high energy density and high rate performance.
研究了喷雾干燥结合高温固相技术制备LiFe0.67Mn0.33PO4/C正极材料的工艺路线。该工艺以Li3PO4为锂源,以性价比高的Mn3O4代替部分铁,与LiFePO4的工业生产线兼容。x射线衍射(XRD)证实,合成材料为具有Pnma空间基团的单相橄榄石结构。扫描电镜(SEM)显示其呈球形。合成的材料在低晶粒微应变和导电碳网结构下表现出优异的速率和循环性能。电化学测试表明,在0.1、0.2、0.5、1、2和5℃的倍率下,电池的初始放电容量分别为164、163、160、157、150和128 mAh g - 1。此外,在1C下进行200次循环后,仍能保留96.16%的容量。该方法为制备具有高能量密度和高倍率性能的LiFe1-xMnxPO4/C正极材料提供了一条可行的途径。
期刊介绍:
Ionics is publishing original results in the fields of science and technology of ionic motion. This includes theoretical, experimental and practical work on electrolytes, electrode, ionic/electronic interfaces, ionic transport aspects of corrosion, galvanic cells, e.g. for thermodynamic and kinetic studies, batteries, fuel cells, sensors and electrochromics. Fast solid ionic conductors are presently providing new opportunities in view of several advantages, in addition to conventional liquid electrolytes.