材料科学
兴奋剂
电解质
掺杂剂
电化学
氧化钴
阴极
价(化学)
锂钴氧化物
离子
锂(药物)
氧化物
分析化学(期刊)
锂离子电池
电极
光电子学
电池(电)
物理化学
热力学
冶金
功率(物理)
化学
物理
量子力学
色谱法
医学
内分泌学
作者
Lianqi Zhao,Pu Yan,Tianying Liu,Xingzhi Wang,Zeyu Wang,Cong Wu,Wenda Bao,Haiyin Zhu,Yue Zhang,Jin Xie
标识
DOI:10.1021/acsami.3c05667
摘要
High-voltage lithium cobalt oxide (LiCoO2) has the highest volumetric energy density among commercial cathode materials in lithium-ion batteries due to its high working voltage and compacted density. However, under high voltage (4.6 V), the capacity of LiCoO2 fades rapidly due to parasitic reactions of high-valent cobalt with the electrolyte and the loss of lattice oxygen at the interface. In this study, we report a temperature-driven anisotropic doping phenomenon of Mg2+ that results in surface-populated Mg2+ doping to the side of the (003) plane of LiCoO2. Mg2+ dopants enter the Li+ sites, lower the valence state of Co ions with less hybridization between the O 2p and Co 3d orbitals, promote the formation of surface Li+/Co2+ anti-sites, and suppress lattice oxygen loss on the surface. As a result, the modified LiCoO2 demonstrates excellent cycling performance under 4.6 V, reaching an energy density of 911.2 Wh/kg at 0.1C and retaining 92.7% (184.3 mAh g-1) of its capacity after 100 cycles at 1C. Our results highlight a promising avenue for enhancing the electrochemical performance of LiCoO2 by anisotropic surface doping with Mg2+.
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