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Structural Evolution and Electrochemical Performance of Li2MnSiO4/C Nanocomposite as Cathode Material for Li-Ion Batteries

机译:Li2MnSiO4 / C纳米复合材料作为锂离子电池正极材料的结构演变和电化学性能

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High capacity Li2MnSiO4/C nanocomposite with good rate performance was prepared via a facile sol-gel method using ascorbic acid as carbon source. It had a uniform distribution on particle size of approximately 20 nm and a thin outlayer of carbon. The galvanostatic charge-discharge measurement showed that the Li2MnSiO4/C electrode could deliver an initial discharge capacity of 257.1 mA h g−1(corresponding to 1.56 Li+) at a current density of 10 mA g−1at 30°C, while the Li2MnSiO4electrode possessed a low capacity of 25.6 mA h g−1. Structural amorphization resulting from excessive extraction of Li+during the first charge was the main reason for the drastic capacity fading. Controlling extraction of Li+could inhibit the amorphization of Li2MnSiO4/C during the delithiation, contributing to a reversible structural change and good cycling performance.
机译:以抗坏血酸为碳源,通过简便的溶胶-凝胶法制备了高速率性能的高容量Li2MnSiO4 / C纳米复合材料。它在约20 nm的粒径上分布均匀,并有一层薄的碳层。恒电流充放电测量表明,Li2MnSiO4 / C电极在30°C时电流密度为10 mA g-1时,初始放电容量为257.1 mA h g-1(相当于1.56 Li +)。 25.6 mA h g-1的低容量。第一次充电过程中过量提取Li +导致的结构非晶化是容量急剧下降的主要原因。控制Li +的萃取可以抑制Li2MnSiO4 / C在脱锂过程中的非晶化,从而有助于可逆的结构变化和良好的循环性能。

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