Co-Doping Engineered High Performance Ni-Rich Layered Cathode

IF 11.8 2区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Small Pub Date : 2025-04-03 DOI:10.1002/smll.202502152
Kaili Li, Weixin Chen, Mingqiu Duan, Zhiling Liu, Dilxat Muhtar, Xiangjie Yang, Kai Ning, Fangyan Xie, Xia Lu
{"title":"Co-Doping Engineered High Performance Ni-Rich Layered Cathode","authors":"Kaili Li,&nbsp;Weixin Chen,&nbsp;Mingqiu Duan,&nbsp;Zhiling Liu,&nbsp;Dilxat Muhtar,&nbsp;Xiangjie Yang,&nbsp;Kai Ning,&nbsp;Fangyan Xie,&nbsp;Xia Lu","doi":"10.1002/smll.202502152","DOIUrl":null,"url":null,"abstract":"<p>Although layered oxides of LiNi<sub>x</sub>Co<sub>y</sub>Mn<sub>z</sub>O<sub>2</sub> (NCM, x + y + z = 1) are promising high energy density cathode materials, they still face significant challenges such as the cracks caused by anisotropic strain and poor structural and thermal stability upon building high-performance rechargeable lithium-ion batteries (LIBs) for scale-up industrialization. Under this circumstance, the La and Mg elements are theoretically and experimentally introduced into the layered NCM cathode to modify the primary particles synergistically by the lattice orientation regulation and surface perovskite-phase coating. The synthesized La/Mg co-doped NCM cathode delivers a discharge-specific capacity of 203 mAh g<sup>−1</sup> at 0.1 C and 126.2 mAh g<sup>−1</sup> at 10 C (1C = 200 mA g<sup>−1</sup>), which results from the radial grain orientation by incorporating trace amount of dopants, as well as the enhancements on both ionic and electronic conductivities. Further analysis discloses the formation of the La-based perovskite protective layer on the surface, which plays a key role in stabilizing the lattice oxygen ions upon cycling and increasing both structural and thermal stabilities of the cathode. This one-step co-doping strategy provides a rewarding avenue toward developing practical NCM cathodes and high-performance, durable rechargeable Li batteries.</p>","PeriodicalId":228,"journal":{"name":"Small","volume":"21 21","pages":""},"PeriodicalIF":11.8000,"publicationDate":"2025-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/smll.202502152","RegionNum":2,"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

Although layered oxides of LiNixCoyMnzO2 (NCM, x + y + z = 1) are promising high energy density cathode materials, they still face significant challenges such as the cracks caused by anisotropic strain and poor structural and thermal stability upon building high-performance rechargeable lithium-ion batteries (LIBs) for scale-up industrialization. Under this circumstance, the La and Mg elements are theoretically and experimentally introduced into the layered NCM cathode to modify the primary particles synergistically by the lattice orientation regulation and surface perovskite-phase coating. The synthesized La/Mg co-doped NCM cathode delivers a discharge-specific capacity of 203 mAh g−1 at 0.1 C and 126.2 mAh g−1 at 10 C (1C = 200 mA g−1), which results from the radial grain orientation by incorporating trace amount of dopants, as well as the enhancements on both ionic and electronic conductivities. Further analysis discloses the formation of the La-based perovskite protective layer on the surface, which plays a key role in stabilizing the lattice oxygen ions upon cycling and increasing both structural and thermal stabilities of the cathode. This one-step co-doping strategy provides a rewarding avenue toward developing practical NCM cathodes and high-performance, durable rechargeable Li batteries.

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
共掺杂工程高性能富镍层状阴极
虽然LiNixCoyMnzO2的层状氧化物(NCM, x + y + z = 1)是很有前途的高能量密度正极材料,但在构建高性能可充电锂离子电池(LIBs)进行大规模工业化时,仍面临着各向异性应变引起的裂缝和较差的结构和热稳定性等重大挑战。在这种情况下,从理论上和实验上将La和Mg元素引入层状NCM阴极中,通过晶格取向调节和表面钙钛矿相涂层协同修饰初生颗粒。合成的La/Mg共掺杂NCM阴极在0.1℃和10℃(1C = 200 mA g - 1)下的放电比容量分别为203 mAh g - 1和126.2 mAh g - 1,这是由于微量掺杂剂的径向晶粒取向以及离子和电子电导率的增强。进一步分析表明,表面形成了la基钙钛矿保护层,这对稳定循环时晶格氧离子和提高阴极的结构和热稳定性起着关键作用。这种一步共掺杂策略为开发实用的NCM阴极和高性能、耐用的可充电锂电池提供了一条有益的途径。
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 去求助
来源期刊
Small
Small 工程技术-材料科学:综合
CiteScore
17.70
自引率
3.80%
发文量
1830
审稿时长
2.1 months
期刊介绍: Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments. With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology. Small's readership includes biochemists, biologists, biomedical scientists, chemists, engineers, information technologists, materials scientists, physicists, and theoreticians alike.
期刊最新文献
Kinetically Controlled Phase Separation Governing Hole Transport in Conjugated Polymer/Insulating Polymer Blend Films. Manganese Oxide Catalysts for Lithium-Oxygen Batteries: Structures, Mechanisms, and Reaction Pathway Engineering. Manipulating Thermal Transport of 2D MOFs by Hierarchical Structural Design. Gradient Mo Engineering in [100]-Oriented CuWO4 Films for Boosted Photoelectrochemical Water Splitting. Engineering Asymmetric Cu0/Cu+ Interfaces for Record-Efficiency Ammonia Electrosynthesis From Dilute Nitrate in Neutral Media.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1