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Kinetically Dormant Ni‐Rich Layered Cathode During High‐Voltage Operation

材料科学 阴极 电压 化学工程 高压 光电子学 纳米技术 电气工程 工程类
作者
Jiyu Cai,Xinwei Zhou,Luxi Li,Zhenzhen Yang,Xingkang Huang,Jiantao Li,Guanyi Wang,Qijia Zhu,Tianyi Li,Cheng‐Jun Sun,Zengqing Zhuo,Ana F. Suzana,Jianming Bai,Ganesh Sainadh Gudavalli,Niloofar Karami,Natasha A. Chernova,S. Upreti,Brad Prevel,W. L. Yang,Yuzi Liu
出处
期刊:Advanced Materials [Wiley]
卷期号:37 (14): e2419253-e2419253 被引量:23
标识
DOI:10.1002/adma.202419253
摘要

The degradation of Ni-rich cathodes during long-term operation at high voltage has garnered significant attention from both academia and industry. Despite many post-mortem qualitative structural analyses, precise quantification of their individual and coupling contributions to the overall capacity degradation remains challenging. Here, by leveraging multiscale synchrotron X-ray probes, electron microscopy, and post-galvanostatic intermittent titration technique, the thermodynamically irreversible and kinetically reversible capacity loss is successfully deconvoluted in a polycrystalline LiNi0.83Mn0.1Co0.07O2 cathode during long-term charge/discharge cycling in full cell configuration. Contradicting the dramatic capacity loss, the layered structure remains highly alive even after 1000 cycles at 4.6 V while undergoing a three-order of magnitude reduction in the mass transfer kinetics, leading to almost fully recoverable capacity under kinetic-free conditions. Such kinetic dormant behavior after cycling is not simply ascribed to poor chemical diffusion by reconstructed cathode surface but highly synchronizes with the lattice strain evolution stemming from the structural heterogeneity between deeply delithiated layered and degraded rock-salt phases at high voltage. These findings deepen the degradation mechanism of high-voltage cathodes to achieve long-cycling and fast-charging performance.
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