阳极
动能
阴极
密度泛函理论
离子
扩散
电流密度
材料科学
同质性(统计学)
兴奋剂
锂(药物)
电压
插层(化学)
化学物理
高压
化学
分析化学(期刊)
光电子学
物理
电极
热力学
物理化学
计算化学
无机化学
电气工程
有机化学
工程类
内分泌学
统计
医学
量子力学
色谱法
数学
作者
Yu Tang,Jun Zhao,He Zhu,Jincan Ren,Wei Wang,Yongjin Fang,Zhiyong Huang,Zijia Yin,Yalan Huang,Binghao Zhang,Tingting Yang,Tianyi Li,Leighanne C. Gallington,Si Lan,Yang Ren,Qi Liu
标识
DOI:10.1016/j.jechem.2022.11.044
摘要
High-voltage LiCoO2 (LCO) is an attractive cathode for ultra-high energy density lithium-ion batteries (LIBs) in the 3 C markets. However, the sluggish lithium-ion diffusion at high voltage significantly hampers its rate capability. Herein, combining experiments with density functional theory (DFT) calculations, we demonstrate that the kinetic limitations can be mitigated by a facial Mg2++Gd3+ co-doping method. The as-prepared LCO shows significantly enhanced Li-ion diffusion mobility at high voltage, making more homogenous Li-ion de/intercalation at a high-rate charge/discharge process. The homogeneity enables the structural stability of LCO at a high-rate current density, inhibiting stress accumulation and irreversible phase transition. When used in combination with a Li metal anode, the doped LCO shows an extreme fast charging (XFC) capability, with a superior high capacity of 193.1 mAh g−1 even at the current density of 20 C and high-rate capacity retention of 91.3% after 100 cycles at 5 C. This work provides a new insight to prepare XFC high-voltage LCO cathode materials.
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