Dynamic Processes at the Electrode-Electrolyte Interface: Implications for Lithium Deposition Stability

IF 3.5 4区 化学 Q2 ELECTROCHEMISTRY ChemElectroChem Pub Date : 2024-10-23 DOI:10.1002/celc.202400222
Dr. Arghya Dutta
{"title":"Dynamic Processes at the Electrode-Electrolyte Interface: Implications for Lithium Deposition Stability","authors":"Dr. Arghya Dutta","doi":"10.1002/celc.202400222","DOIUrl":null,"url":null,"abstract":"<p>Lithium (Li) metal is a promising negative electrode material for high-energy-density rechargeable batteries, owing to its exceptional specific capacity, low electrochemical potential, and low density. However, challenges such as dendritic Li deposits, leading to internal short-circuits, and low Coulombic efficiency hinder the widespread adoption of lithium-metal batteries (LMBs). These issues stem from the morphological instability of Li deposition, influenced by dynamic processes at the electrolyte|Li interface. Understanding the interplay between electrolyte properties, interfacial kinetics, and Li deposition stability is crucial yet challenging due to their simultaneous occurrence and the complexity of the solid electrolyte interphase (SEI) layer. This review discusses three key dynamic processes influencing Li deposition: desolvation of Li<sup>+</sup> ions, transport through the SEI, and electrochemical reduction. The effects of electrolyte properties on these processes and their interplay with electroplating stability are discussed, highlighting contradictions in the literature and proposing explanations for the discrepancies. Despite numerous reviews on SEI structure and composition effects, this article emphasizes the kinetic aspects at interfaces, aiming to provide clarity and direction for future research in achieving stable Li deposition in LMBs.</p>","PeriodicalId":142,"journal":{"name":"ChemElectroChem","volume":"11 23","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2024-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/celc.202400222","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemElectroChem","FirstCategoryId":"92","ListUrlMain":"https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/celc.202400222","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0

Abstract

Lithium (Li) metal is a promising negative electrode material for high-energy-density rechargeable batteries, owing to its exceptional specific capacity, low electrochemical potential, and low density. However, challenges such as dendritic Li deposits, leading to internal short-circuits, and low Coulombic efficiency hinder the widespread adoption of lithium-metal batteries (LMBs). These issues stem from the morphological instability of Li deposition, influenced by dynamic processes at the electrolyte|Li interface. Understanding the interplay between electrolyte properties, interfacial kinetics, and Li deposition stability is crucial yet challenging due to their simultaneous occurrence and the complexity of the solid electrolyte interphase (SEI) layer. This review discusses three key dynamic processes influencing Li deposition: desolvation of Li+ ions, transport through the SEI, and electrochemical reduction. The effects of electrolyte properties on these processes and their interplay with electroplating stability are discussed, highlighting contradictions in the literature and proposing explanations for the discrepancies. Despite numerous reviews on SEI structure and composition effects, this article emphasizes the kinetic aspects at interfaces, aiming to provide clarity and direction for future research in achieving stable Li deposition in LMBs.

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
电极-电解质界面的动态过程:对锂沉积稳定性的影响
金属锂具有特殊的比容量、低电化学电位和低密度等优点,是一种很有前途的高能量密度可充电电池负极材料。然而,树枝状锂沉积导致内部短路和低库仑效率等挑战阻碍了锂金属电池(lmb)的广泛采用。这些问题源于锂沉积的形态不稳定性,受到电解质|Li界面动态过程的影响。了解电解质性质、界面动力学和锂沉积稳定性之间的相互作用至关重要,但由于它们同时发生和固体电解质界面相(SEI)层的复杂性,因此具有挑战性。本文综述了影响锂沉积的三个关键动力学过程:Li+离子的脱溶、SEI输运和电化学还原。讨论了电解质性质对这些过程的影响及其与电镀稳定性的相互作用,突出了文献中的矛盾,并提出了差异的解释。尽管对SEI结构和组成效应的研究有很多,但本文强调了界面动力学方面的研究,旨在为今后在LMBs中实现稳定的Li沉积提供清晰的思路和方向。
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
ChemElectroChem
ChemElectroChem ELECTROCHEMISTRY-
CiteScore
7.90
自引率
2.50%
发文量
515
审稿时长
1.2 months
期刊介绍: ChemElectroChem is aimed to become a top-ranking electrochemistry journal for primary research papers and critical secondary information from authors across the world. The journal covers the entire scope of pure and applied electrochemistry, the latter encompassing (among others) energy applications, electrochemistry at interfaces (including surfaces), photoelectrochemistry and bioelectrochemistry.
期刊最新文献
Front Cover: Electron Redistribution Drives Structural Ordering in Sulfate (SO4) Adlayers (ChemElectroChem 1/2026) Front Cover: Dynamics of the Galvanic Replacement Reaction of Silver by Gold: Phenomenological Models for Open Circuit Potential-Time Responsive Indicator (ChemElectroChem 22/2025) Hydrothermally Carbonized Corncob-Derived Hard Carbon Anodes for High-Performance Sodium-Ion Batteries Engineering Alloying and Conversion Interlayers for Anode-Less Solid-State Batteries Parametric Investigation of Electrochemical Synthesis of Ammonium Persulfate in Flow Reactor
×
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