{"title":"Kinetically Dormant Ni-Rich Layered Cathode During High-Voltage Operation","authors":"Jiyu Cai, Xinwei Zhou, Luxi Li, Zhenzhen Yang, Xingkang Huang, Jiantao Li, Guanyi Wang, Qijia Zhu, Tianyi Li, Cheng-Jun Sun, Zengqing Zhuo, Ana Suzana, Jianming Bai, Ganesh Gudavalli, Niloofar Karami, Natasha A. Chernova, Shailesh Upreti, Brad Prevel, Wanli Yang, Yuzi Liu, Wenqian Xu, Yanbin Chen, Shunlin Song, Xuequan Zhang, Li Wang, Xiangming He, Feng Wang, Gui-Liang Xu, Zonghai Chen","doi":"10.1002/adma.202419253","DOIUrl":null,"url":null,"abstract":"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 LiNi<sub>0.83</sub>Mn<sub>0.1</sub>Co<sub>0.07</sub>O<sub>2</sub> 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.","PeriodicalId":114,"journal":{"name":"Advanced Materials","volume":"23 1","pages":""},"PeriodicalIF":27.4000,"publicationDate":"2025-03-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adma.202419253","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
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.
期刊介绍:
Advanced Materials, one of the world's most prestigious journals and the foundation of the Advanced portfolio, is the home of choice for best-in-class materials science for more than 30 years. Following this fast-growing and interdisciplinary field, we are considering and publishing the most important discoveries on any and all materials from materials scientists, chemists, physicists, engineers as well as health and life scientists and bringing you the latest results and trends in modern materials-related research every week.