Structural analysis of deeply charged Li(Ni0.95Co0.04Al0.01)O2 cathode  for Li-ion battery.

IF 7.5 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ChemSusChem Pub Date : 2024-11-27 DOI:10.1002/cssc.202401856
Byung Cheol Lee, Jeon Kim, Hee-Soo Kim, Geon-Tae Park, Yang-Kook Sun, Chong Seung Yoon
{"title":"Structural analysis of deeply charged Li(Ni0.95Co0.04Al0.01)O2 cathode  for Li-ion battery.","authors":"Byung Cheol Lee, Jeon Kim, Hee-Soo Kim, Geon-Tae Park, Yang-Kook Sun, Chong Seung Yoon","doi":"10.1002/cssc.202401856","DOIUrl":null,"url":null,"abstract":"<p><p>LiNi0.95Co0.04Al0.01O2 (NCA95) is charged up to 4.6 V to study its structural stability at a highly delithiated state using transmission electron microscopy (TEM). The TEM analysis shows that the localized depletion of Li ions near the surface triggers the transition from the H3 phase to the H4 phase with the H4 phase with the O1 stacking appearing as a series of stacking faults even at 4.4 V. The H3 → H4 transition appears to be irreversible and leads to the initial capacity loss. In addition, intraparticle cracks are observed when charged above 4.3 V. These intraparticle microcracks, unlike interparticle cracks that become sealed upon Li-uptake, likely remain during deintercalation, compromising the mechanical stability of the cathode and lead to fast deterioration of the cycling stability. The TEM analysis of the overcharged NCA95 cathode suggests a clear limit above which the cathode can be cycled without significant capacity loss. The introduction of doping elements that promote the migration of Ni2+ ions into the Li layer would hinder the H3 → H4 transition and help suppress the intraparticle cracks.</p>","PeriodicalId":149,"journal":{"name":"ChemSusChem","volume":" ","pages":"e202401856"},"PeriodicalIF":7.5000,"publicationDate":"2024-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemSusChem","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/cssc.202401856","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

LiNi0.95Co0.04Al0.01O2 (NCA95) is charged up to 4.6 V to study its structural stability at a highly delithiated state using transmission electron microscopy (TEM). The TEM analysis shows that the localized depletion of Li ions near the surface triggers the transition from the H3 phase to the H4 phase with the H4 phase with the O1 stacking appearing as a series of stacking faults even at 4.4 V. The H3 → H4 transition appears to be irreversible and leads to the initial capacity loss. In addition, intraparticle cracks are observed when charged above 4.3 V. These intraparticle microcracks, unlike interparticle cracks that become sealed upon Li-uptake, likely remain during deintercalation, compromising the mechanical stability of the cathode and lead to fast deterioration of the cycling stability. The TEM analysis of the overcharged NCA95 cathode suggests a clear limit above which the cathode can be cycled without significant capacity loss. The introduction of doping elements that promote the migration of Ni2+ ions into the Li layer would hinder the H3 → H4 transition and help suppress the intraparticle cracks.

用于锂离子电池的深充电 Li(Ni0.95Co0.04Al0.01)O2 正极的结构分析。
对 LiNi0.95Co0.04Al0.01O2 (NCA95) 充电至 4.6 V,利用透射电子显微镜 (TEM) 研究其在高度脱硫状态下的结构稳定性。透射电子显微镜分析表明,表面附近锂离子的局部耗尽引发了从 H3 相到 H4 相的转变,即使在 4.4 V 时,具有 O1 堆积的 H4 相也会以一系列堆积断层的形式出现。H3 → H4 转变似乎是不可逆的,并导致初始容量损失。与锂吸收后密封的粒子间裂缝不同,这些粒子内微裂缝很可能会在去交联过程中保留下来,从而损害阴极的机械稳定性,并导致循环稳定性快速下降。对过量充电的 NCA95 阴极进行的 TEM 分析表明,阴极在循环过程中不会出现明显的容量损失。引入促进 Ni2+ 离子迁移到锂层的掺杂元素将阻碍 H3 → H4 转变,并有助于抑制粒子内裂纹。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
ChemSusChem
ChemSusChem 化学-化学综合
CiteScore
15.80
自引率
4.80%
发文量
555
审稿时长
1.8 months
期刊介绍: ChemSusChem Impact Factor (2016): 7.226 Scope: Interdisciplinary journal Focuses on research at the interface of chemistry and sustainability Features the best research on sustainability and energy Areas Covered: Chemistry Materials Science Chemical Engineering Biotechnology
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信