Expediting solid electrolyte synthesis: Microwave-assisted wet synthesis of halogen-rich Li-argyrodite

IF 13.1 1区 化学 Q1 Energy
Suk-Ho Hwang , Seung-Deok Seo , Dohyun Kim , Jung Been Park , Sung-Chul Kim , Dong-Wan Kim
{"title":"Expediting solid electrolyte synthesis: Microwave-assisted wet synthesis of halogen-rich Li-argyrodite","authors":"Suk-Ho Hwang ,&nbsp;Seung-Deok Seo ,&nbsp;Dohyun Kim ,&nbsp;Jung Been Park ,&nbsp;Sung-Chul Kim ,&nbsp;Dong-Wan Kim","doi":"10.1016/j.jechem.2025.01.031","DOIUrl":null,"url":null,"abstract":"<div><div>Li-argyrodites are promising solid electrolytes (SEs) for solid-state Li-ion batteries (SSLBs), but their large-scale industrial application remains a challenge. Conventional synthesis methods for SEs suffer from long reaction times and high energy consumption. In this study, we present a wet process for the synthesis of halogen-rich argyrodite Li<sub>6−</sub><em><sub>a</sub></em>PS<sub>5−</sub><em><sub>a</sub></em>Cl<sub>1+</sub><em><sub>a</sub></em> precursors (LPSCl<sub>1+</sub><em><sub>a</sub></em>-P, <em>a</em> = 0–0.7) via an energy-saving microwave-assisted process. Utilizing vibrational heating, we accelerate the formation of Li-argyrodite precursor, even at excessive Cl-ion concentration, which significantly shortens the reaction time compared to traditional methods. After crystallization, we successfully synthesize the Li-argyrodite, Li<sub>5.5</sub>PS<sub>4.5</sub>Cl<sub>1.5</sub>, which exhibits the superior ionic conductivity (7.8 mS cm<sup>−1</sup>) and low activation energy (0.23 eV) along with extremely low electric conductivity. The Li<sub>5.5</sub>PS<sub>4.5</sub>Cl<sub>1.5</sub> exhibits superior Li compatibility owing to its high reversible striping/plating ability (over 5000 h) and high current density acceptability (1.3 mA cm<sup>−2</sup>). It also exhibits excellent cycle reversibility and rate capability with NCM622 cathode (148.3 mA h g<sup>−1</sup> at 1 C for 100 cycles with capacity retention of 85.6%). This finding suggests a potentially simpler and more scalable synthetic route to produce high-performance SEs.</div></div>","PeriodicalId":15728,"journal":{"name":"Journal of Energy Chemistry","volume":"104 ","pages":"Pages 527-539"},"PeriodicalIF":13.1000,"publicationDate":"2025-01-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Energy Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2095495625000725","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Energy","Score":null,"Total":0}
引用次数: 0

Abstract

Li-argyrodites are promising solid electrolytes (SEs) for solid-state Li-ion batteries (SSLBs), but their large-scale industrial application remains a challenge. Conventional synthesis methods for SEs suffer from long reaction times and high energy consumption. In this study, we present a wet process for the synthesis of halogen-rich argyrodite Li6−aPS5−aCl1+a precursors (LPSCl1+a-P, a = 0–0.7) via an energy-saving microwave-assisted process. Utilizing vibrational heating, we accelerate the formation of Li-argyrodite precursor, even at excessive Cl-ion concentration, which significantly shortens the reaction time compared to traditional methods. After crystallization, we successfully synthesize the Li-argyrodite, Li5.5PS4.5Cl1.5, which exhibits the superior ionic conductivity (7.8 mS cm−1) and low activation energy (0.23 eV) along with extremely low electric conductivity. The Li5.5PS4.5Cl1.5 exhibits superior Li compatibility owing to its high reversible striping/plating ability (over 5000 h) and high current density acceptability (1.3 mA cm−2). It also exhibits excellent cycle reversibility and rate capability with NCM622 cathode (148.3 mA h g−1 at 1 C for 100 cycles with capacity retention of 85.6%). This finding suggests a potentially simpler and more scalable synthetic route to produce high-performance SEs.

Abstract Image

求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Energy Chemistry
Journal of Energy Chemistry CHEMISTRY, APPLIED-CHEMISTRY, PHYSICAL
CiteScore
19.10
自引率
8.40%
发文量
3631
审稿时长
15 days
期刊介绍: The Journal of Energy Chemistry, the official publication of Science Press and the Dalian Institute of Chemical Physics, Chinese Academy of Sciences, serves as a platform for reporting creative research and innovative applications in energy chemistry. It mainly reports on creative researches and innovative applications of chemical conversions of fossil energy, carbon dioxide, electrochemical energy and hydrogen energy, as well as the conversions of biomass and solar energy related with chemical issues to promote academic exchanges in the field of energy chemistry and to accelerate the exploration, research and development of energy science and technologies. This journal focuses on original research papers covering various topics within energy chemistry worldwide, including: Optimized utilization of fossil energy Hydrogen energy Conversion and storage of electrochemical energy Capture, storage, and chemical conversion of carbon dioxide Materials and nanotechnologies for energy conversion and storage Chemistry in biomass conversion Chemistry in the utilization of solar 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:481959085
Book学术官方微信