Lithium anode interlayer design for all-solid-state lithium-metal batteries

IF 60.1 1区 材料科学 Q1 ENERGY & FUELS
Zeyi Wang, Jiale Xia, Xiao Ji, Yijie Liu, Jiaxun Zhang, Xinzi He, Weiran Zhang, Hongli Wan, Chunsheng Wang
{"title":"Lithium anode interlayer design for all-solid-state lithium-metal batteries","authors":"Zeyi Wang, Jiale Xia, Xiao Ji, Yijie Liu, Jiaxun Zhang, Xinzi He, Weiran Zhang, Hongli Wan, Chunsheng Wang","doi":"10.1038/s41560-023-01426-1","DOIUrl":null,"url":null,"abstract":"All-solid-state lithium-metal batteries (ASSLBs) have attracted intense interest due to their high energy density and high safety. However, Li dendrite growth and high interface resistance remain challenging due to insufficient understanding of the mechanism. Here we develop two types of porous lithiophobic interlayer (Li7N2I–carbon nanotube and Li7N2I–Mg) to enable Li to plate at the Li/interlayer interface and reversibly penetrate into the porous interlayer. The experimental and simulation results reveal that a balance of lithiophobicity, electronic and ionic conductivities and interlayer’s porosity are the key enablers for stable Li plating/stripping at a high capacity. A fine-tuned Li7N2I–carbon nanotube interlayer enables Li/LNI/Li symmetric cell to achieve a high critical current density of 4.0 mA cm−2 at 4.0 mAh cm−2 at 25 °C; the Li7N2I–Mg interlayer enables a Li4SiO4@LiNi0.8Mn0.1Co0.1O2/Li6PS5Cl/20 µm-Li full cell to achieve an areal capacity of 2.2 mAh cm−2, maintaining 82.4% capacity retention after 350 cycles at 60 °C at a rate of 0.5 C. The interlayer design principle opens opportunities to develop safe and high energy ASSLBs. All-solid-state lithium-metal batteries are at the forefront of battery research and development. Here C. Wang and colleagues have developed an interlayer design strategy to address issues associated with lithium dendrite growth and interface resistance, resulting in substantial improvements in battery performance.","PeriodicalId":19073,"journal":{"name":"Nature Energy","volume":"9 3","pages":"251-262"},"PeriodicalIF":60.1000,"publicationDate":"2024-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Energy","FirstCategoryId":"88","ListUrlMain":"https://www.nature.com/articles/s41560-023-01426-1","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
引用次数: 0

Abstract

All-solid-state lithium-metal batteries (ASSLBs) have attracted intense interest due to their high energy density and high safety. However, Li dendrite growth and high interface resistance remain challenging due to insufficient understanding of the mechanism. Here we develop two types of porous lithiophobic interlayer (Li7N2I–carbon nanotube and Li7N2I–Mg) to enable Li to plate at the Li/interlayer interface and reversibly penetrate into the porous interlayer. The experimental and simulation results reveal that a balance of lithiophobicity, electronic and ionic conductivities and interlayer’s porosity are the key enablers for stable Li plating/stripping at a high capacity. A fine-tuned Li7N2I–carbon nanotube interlayer enables Li/LNI/Li symmetric cell to achieve a high critical current density of 4.0 mA cm−2 at 4.0 mAh cm−2 at 25 °C; the Li7N2I–Mg interlayer enables a Li4SiO4@LiNi0.8Mn0.1Co0.1O2/Li6PS5Cl/20 µm-Li full cell to achieve an areal capacity of 2.2 mAh cm−2, maintaining 82.4% capacity retention after 350 cycles at 60 °C at a rate of 0.5 C. The interlayer design principle opens opportunities to develop safe and high energy ASSLBs. All-solid-state lithium-metal batteries are at the forefront of battery research and development. Here C. Wang and colleagues have developed an interlayer design strategy to address issues associated with lithium dendrite growth and interface resistance, resulting in substantial improvements in battery performance.

Abstract Image

Abstract Image

全固态锂金属电池的锂阳极夹层设计
全固态锂金属电池(ASSLBs)因其高能量密度和高安全性而备受关注。然而,由于对其机理了解不足,锂枝晶的生长和高界面电阻仍然是一项挑战。在此,我们开发了两种多孔疏锂中间膜(Li7N2I-碳纳米管和 Li7N2I-Mg),使锂离子能够在锂/中间膜界面上板结,并可逆地渗透到多孔中间膜中。实验和模拟结果表明,疏锂性、电子和离子电导率以及层间孔隙率之间的平衡是实现稳定的高容量锂镀层/剥离的关键因素。经过微调的 Li7N2I 碳纳米管中间膜使锂/LNI/锂对称电池在 25 °C 下达到 4.0 mAh cm-2 的高临界电流密度;Li7N2I-Mg 中间膜使 Li4SiO4@LiNi0.8Mn0.1Co0.1O2/Li6PS5Cl/20 µm 锂全电池达到 2.2 mAh cm-2 的面积容量,在 60 °C 下以 0.5 C 的速率循环 350 次后保持 82.4% 的容量保持率。层间设计原理为开发安全、高能的 ASSLB 带来了机遇。
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
Nature Energy
Nature Energy Energy-Energy Engineering and Power Technology
CiteScore
75.10
自引率
1.10%
发文量
193
期刊介绍: Nature Energy is a monthly, online-only journal committed to showcasing the most impactful research on energy, covering everything from its generation and distribution to the societal implications of energy technologies and policies. With a focus on exploring all facets of the ongoing energy discourse, Nature Energy delves into topics such as energy generation, storage, distribution, management, and the societal impacts of energy technologies and policies. Emphasizing studies that push the boundaries of knowledge and contribute to the development of next-generation solutions, the journal serves as a platform for the exchange of ideas among stakeholders at the forefront of the energy sector. Maintaining the hallmark standards of the Nature brand, Nature Energy boasts a dedicated team of professional editors, a rigorous peer-review process, meticulous copy-editing and production, rapid publication times, and editorial independence. In addition to original research articles, Nature Energy also publishes a range of content types, including Comments, Perspectives, Reviews, News & Views, Features, and Correspondence, covering a diverse array of disciplines relevant to the field of energy.
×
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:604180095
Book学术官方微信