Effect of Uniaxial Stack Pressure on the Performance of Nanocrystalline Electrolytes and Electrode Composites for All‐Solid‐State Fluoride‐Ion Batteries

Hong Chen, Tommi Aalto, V. Vanita, Oliver Clemens
{"title":"Effect of Uniaxial Stack Pressure on the Performance of Nanocrystalline Electrolytes and Electrode Composites for All‐Solid‐State Fluoride‐Ion Batteries","authors":"Hong Chen, Tommi Aalto, V. Vanita, Oliver Clemens","doi":"10.1002/sstr.202300570","DOIUrl":null,"url":null,"abstract":"If all‐solid‐state fluoride‐ion batteries want to compete with existing battery technologies, significant improvements in terms of cyclic stability are necessary to fully access the high specific capacities, which this battery concept can provide in theory. Herein, the development of a high‐pressure, high‐temperature battery operation stand for battery cycling under inert conditions inside a glovebox is reported. This stand is then used to investigate the effect of stack pressure on the cell performance of conversion‐based as well as intercalation‐based electrode materials for fluoride‐ion batteries. It is found that cyclic stability as well as energy efficiency is strongly increased compared to nonpressure conditions, which is assigned to sustained interparticle contact. Thus, the cell design must be considered carefully to be able to distinguish intrinsic material properties from percolation‐ and interphase‐related impacts on the cell behavior. Further, the effect of pressure on the ionic conductivity of common solid fluoride‐ion conductors is investigated.","PeriodicalId":21841,"journal":{"name":"Small Structures","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-05-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small Structures","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/sstr.202300570","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

If all‐solid‐state fluoride‐ion batteries want to compete with existing battery technologies, significant improvements in terms of cyclic stability are necessary to fully access the high specific capacities, which this battery concept can provide in theory. Herein, the development of a high‐pressure, high‐temperature battery operation stand for battery cycling under inert conditions inside a glovebox is reported. This stand is then used to investigate the effect of stack pressure on the cell performance of conversion‐based as well as intercalation‐based electrode materials for fluoride‐ion batteries. It is found that cyclic stability as well as energy efficiency is strongly increased compared to nonpressure conditions, which is assigned to sustained interparticle contact. Thus, the cell design must be considered carefully to be able to distinguish intrinsic material properties from percolation‐ and interphase‐related impacts on the cell behavior. Further, the effect of pressure on the ionic conductivity of common solid fluoride‐ion conductors is investigated.

Abstract Image

单轴叠加压力对全固态氟离子电池用纳米晶电解质和电极复合材料性能的影响
如果全固态氟离子电池想要与现有电池技术竞争,就必须在循环稳定性方面做出重大改进,以充分获得这种电池概念理论上可以提供的高比容量。本文报告了高压高温电池操作台的开发情况,该操作台用于在手套箱内的惰性条件下进行电池循环。然后,利用该操作台研究了堆栈压力对氟离子电池转换型和插层型电极材料的电池性能的影响。研究发现,与无压条件相比,循环稳定性和能量效率都有很大提高,这归因于粒子间的持续接触。因此,必须仔细考虑电池的设计,以便能够区分材料的固有特性与渗流和相间对电池行为的影响。此外,还研究了压力对常见固体氟离子导体离子电导率的影响。
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
CiteScore
17.30
自引率
0.00%
发文量
0
×
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