钝化
锂(药物)
材料科学
离子
兴奋剂
扩散
扩散阻挡层
光电子学
化学
纳米技术
图层(电子)
物理
医学
有机化学
内分泌学
热力学
作者
Guorong Chen,Meng Zhu,Yafei Huang,Mi Lu,Alena A. Nevar,Natalia Dudko,Liyi Shi,Lei Huang,Н. В. Тарасенко,Dengsong Zhang
出处
期刊:Social Science Research Network
[Social Science Electronic Publishing]
日期:2023-01-01
摘要
High-voltage lithium cobalt oxide (LCO) has been widely used in 5G smart electronics. However, maintaining the stability of high-voltage LCO structures under fast charging and discharging conditions is still a challenge that hinders its application in fast-charging lithium-ion batteries. Here, we propose a new idea of fully supported lattice network and self-passivating surface to construct a fast-charging cathode and realize high performance fast-charging lithium-ion battery. A fully supported lattice network can be achieved by one-step solid-phase sintering of Sn and S co-doping LCO, reducing the energy barrier of lithium(Li)ion transport and allowing rapid Li ion solid-state diffusion. The self-passivating surface is formed on the surface of LCO-Sn0.6 by de-solvation with solvent molecules, which significantly increases the adsorption energy of EC and LiPF6 on LCo-Sn0.6, and greatly reduces the absorption ability of EC and LiPF6 on LCo-Sn0.6 to form effective CEI membranes. The superior performance with high capacity (114 mA h g-1) under extremely fast charging conditions (20 C, 1 C=274 mA g-1) is achieved on Sn and S co-doped LCO cathode, that is, it can reach more than 60% SOC after only 2 minutes of fast charging. In situ Raman spectroscopy and in situ XRD further confirm the reversible transformation of Sn and S co-doped LCO microstructure during charge and discharge processes. These results provide a platform for the design of novel fast-charging cathode materials with fully supported lattice network and self-passivating surface, while stabilizing lattice structure and significantly enhancing ionic solid-state diffusion dynamics.
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