尖晶石
溶解
锰酸盐
锰
材料科学
镁
退火(玻璃)
无机化学
歧化
阴极
锂(药物)
化学工程
化学
冶金
催化作用
物理化学
电池(电)
功率(物理)
内分泌学
工程类
物理
医学
量子力学
生物化学
作者
Shaoyu Yang,Pu Yan,Wenda Bao,Haiyin Zhu,Xincan Cai,Lianqi Zhao,Yue Zhang,Weiyi Lin,Yingdong Deng,Yifan Wu,Jin Xie
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-09-20
卷期号:8 (10): 4278-4286
被引量:10
标识
DOI:10.1021/acsenergylett.3c01560
摘要
Surface degradation induced by the dissolution of manganese is a major failure mechanism that has hampered the large-scale adoption of spinel LiMn2O4 cathode material for decades. Although modifications based on restraining manganese disproportionation reactions have received much attention, many of these methods may sacrifice batteries' specific capacity and rate capability. Here, we present a strategy that surface-populated magnesium ion substitution at 8a tetrahedral sites in LiMn2O4 could significantly suppress spinel surface evolution and Mn dissolution during cycling. With a total trace amount of magnesium surface doping (0.3 wt %) introduced by ALD coating and annealing, the LiMn2O4 cathode shows a capacity retention of 98.6% after 250 cycles. This study reveals the role of atomic doping site selection and the significance of the electrode materials' surface stability at the charged state.
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