材料科学
锆
阴极
兴奋剂
过渡金属
电化学
容量损失
化学工程
锂(药物)
储能
电池(电)
Crystal(编程语言)
电极
纳米技术
光电子学
化学
冶金
物理化学
催化作用
量子力学
程序设计语言
功率(物理)
内分泌学
工程类
物理
医学
生物化学
计算机科学
作者
Zhi Zhang,Bo Hong,Maoyi Yi,Xinming Fan,Zhian Zhang,Xiaobing Huang,Yanqing Lai
标识
DOI:10.1016/j.cej.2022.136825
摘要
Single-crystal Ni-rich layered cathode (SC-NCM) is economically appealing for high-energy–density lithium-ion battery but its life span in practical application, especially under high-voltage operation, is significantly hindered by its poor structural instability, irreversible phase transitions, and sluggish electrochemical reaction kinetic. Herein, in-situ zirconium and titanium co-doped single-crystal LiNi0.6Co0.1Mn0.3O2 (Z/[email protected]) material is rationally designed as the structurally and electrochemically stable cathodes for high-energy density batteries. Both the experimental analyses and theoretical calculations reveal that the synergistic effect of Zr/Ti co-doping at transition metal (TM) sites of SC-NCM materials. can not only effectively enhance the Li+ diffusion mobility but also release the internal stress concentration as well as reducing the cationic disordering. As a result, the material-level specific energy of 715 Wh kg−1 is achieved for the single-crystal LiNi0.598Co0.08Mn0.3Zr0.002Ti0.002O2 (Z/[email protected]) cathode at 2.75–4.6 V with a satisfying capacity retention of 88.5 % after 150 cycles. Impressively, the pouch-type full cell of Zr/[email protected]||graphite with a practical area capacity of 4.96 mAh cm−2 delivers an superior capacity retention of 80.6 % after 4000 cycles, which could be expected to extend the battery life-span to more than a decade for electric vehicles. It suggests that engineering the dual-doping in SC-NCM cathodes may provide an effective path toward the low-cost, excellent long-term cycling stability, and high energy density of lithium-ion batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI