材料科学
锰
尖晶石
溶解
锂(药物)
化学工程
插层(化学)
电池(电)
容量损失
无机化学
磷酸钒锂电池
氧化物
阳极
电化学
电解质
电极
阴极
化学
冶金
内分泌学
物理化学
功率(物理)
工程类
量子力学
物理
医学
作者
Haihui Chen,Tianyi Ma,Yingying Zeng,Xiuyan Guo,Xinping Qiu
标识
DOI:10.1007/s11595-017-1547-4
摘要
The capacity fade of spinel lithium manganese oxide in lithium-ion batteries is a bottleneck challenge for the large-scale application. The traditional opinion is that Mn(II) ions in the anode are reduced to the metallic manganese that helps for catalyzing electrolyte decomposition. This could poison and damage the solid electrolyte interface (SEI) film, leading to the the capacity fade in Li-ion batteries. We propose a new mechanism that Mn(II) deposites at the anode hinders and/or blocks the intercalation/de-intercalation of lithium ions,which leads to the capacity fade in Li-ion batteries. Based on the new mechanism assumption, a kind of new structure with core-shell characteristic is designed to inhabit manganese ion dissolution, thus improving electrochemical cycle performance of the cell. By the way, this mechanism hypothesis is also supported by the results of these experiments. The LiMn2-xTixO4 shell layer enhances cathode resistance to corrosion attack and effectively suppresses dissolution of Mn, then improves battery cycle performance with LiMn2O4 cathode, even at high rate and elevated temperature.
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