反应性(心理学)
氧化物
材料科学
阴极
化学工程
复合材料
法律工程学
冶金
化学
工程类
物理化学
医学
替代医学
病理
作者
Xin Wang,Xin Zhou,Xiaohong Liu,Guilin Feng,Shuo Wang,Bin Zhang,Ping Zhang,Meihua Zuo,Wangyan Xing,Weifeng Fan,Heng Zhang,Genpin Lv,Wei Xiang
标识
DOI:10.1016/j.cej.2024.150795
摘要
Capacity fading of Ni-rich cathode is thought to originate from the formation of inactive rock-salt phase induced by surface reactivity and the isolation of active material caused by microcracks due to anisotropic volume contraction of grains. It is generally assumed that inhibiting the formation of microcracks within secondary particle by radially aligned microstructure is a vital aspect for suppressing capacity fading. However, the new researches about reduction of microcracks simply by certain electrolytes call a question on the origin of microcracks and the critical factor for the cycle life of cathodes. Herein, LiNi0.92Co0.04Mn0.04O2 cathodes with different surface characteristic and radially aligned microstructure were synthesized by doping with high valence elements using some hydroxide precursor. The effects of W6+ and/or Mo6+ induced surface phase and microstructure on electrochemical performance were investigated. Despite the inferior radially aligned, size-refined primary grains and higher degree of microcracks, W6+ doped cathode still possesses alleviated parasitic reactions, higher crystal structural stability and capacity retention than Mo6+ doped materials, because of the enhanced cathode-electrolyte interfacial stability. The results contend that the consequence of surface reactivity on determining cycle life of Ni-rich cathodes is more critical than that of microcracks, and efforts relating to constructing intact and uniform stable surface phase will exhibit greater potential to promote the performance of Ni-rich cathodes than microstructural refinement.
科研通智能强力驱动
Strongly Powered by AbleSci AI