{"title":"通过声空化调控石榴石型固态电解质中Li2CO3的绿色策略","authors":"Pavitra Srivastava, Behrouz Bazri, Dheeraj Kumar Maurya, Yuan-Ting Hung, Da-Hua Wei* and Ru-Shi Liu*, ","doi":"10.1021/acsenergylett.5c0036810.1021/acsenergylett.5c00368","DOIUrl":null,"url":null,"abstract":"<p >Garnet-type Li<sub>6.75</sub>La<sub>3</sub>Zr<sub>1.75</sub>Ta<sub>0.25</sub>O<sub>12</sub> (LLZTO) holds significant potential as a solid-state electrolyte (SSE) comprising promising features such as high Li<sup>+</sup> conductivity, wide electrochemical stability window, and compatibility with Li-metal. However, air exposure forms a thick Li<sub>2</sub>CO<sub>3</sub> passivation layer (∼50 nm), which hinders storage, handling, and interfacial performance, especially for LLZTO nanoparticles (NPs) with a high surface area. This study introduces a scalable, green sonication-assisted method to control the Li<sub>2</sub>CO<sub>3</sub> layer thickness (<10 nm), which enhances air stability without compromising ionic conduction. <i>In-situ</i> ambient-pressure X-ray photoelectron spectroscopy (AP-XPS) further reveals the carbonate formation mechanism under atmospheric conditions. Electrochemical tests in ceramic-in-polymer (CIP) and polymer-in-ceramic (PIC) composite polymer electrolytes (CPEs) confirm that regulated Li<sub>2</sub>CO<sub>3</sub> does not degrade the performance of passivated-LLZTO. The chemical-free, green approach suggested in this work maintains electrochemical properties, which enables scalable use of LLZTO-based SSEs for next-generation Li-metal batteries.</p>","PeriodicalId":16,"journal":{"name":"ACS Energy Letters ","volume":"10 4","pages":"1725–1732 1725–1732"},"PeriodicalIF":18.2000,"publicationDate":"2025-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/epdf/10.1021/acsenergylett.5c00368","citationCount":"0","resultStr":"{\"title\":\"Green Strategy for Li2CO3 Regulation in Garnet-Type Solid-State Electrolytes via Acoustic Cavitation\",\"authors\":\"Pavitra Srivastava, Behrouz Bazri, Dheeraj Kumar Maurya, Yuan-Ting Hung, Da-Hua Wei* and Ru-Shi Liu*, \",\"doi\":\"10.1021/acsenergylett.5c0036810.1021/acsenergylett.5c00368\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Garnet-type Li<sub>6.75</sub>La<sub>3</sub>Zr<sub>1.75</sub>Ta<sub>0.25</sub>O<sub>12</sub> (LLZTO) holds significant potential as a solid-state electrolyte (SSE) comprising promising features such as high Li<sup>+</sup> conductivity, wide electrochemical stability window, and compatibility with Li-metal. However, air exposure forms a thick Li<sub>2</sub>CO<sub>3</sub> passivation layer (∼50 nm), which hinders storage, handling, and interfacial performance, especially for LLZTO nanoparticles (NPs) with a high surface area. This study introduces a scalable, green sonication-assisted method to control the Li<sub>2</sub>CO<sub>3</sub> layer thickness (<10 nm), which enhances air stability without compromising ionic conduction. <i>In-situ</i> ambient-pressure X-ray photoelectron spectroscopy (AP-XPS) further reveals the carbonate formation mechanism under atmospheric conditions. Electrochemical tests in ceramic-in-polymer (CIP) and polymer-in-ceramic (PIC) composite polymer electrolytes (CPEs) confirm that regulated Li<sub>2</sub>CO<sub>3</sub> does not degrade the performance of passivated-LLZTO. The chemical-free, green approach suggested in this work maintains electrochemical properties, which enables scalable use of LLZTO-based SSEs for next-generation Li-metal batteries.</p>\",\"PeriodicalId\":16,\"journal\":{\"name\":\"ACS Energy Letters \",\"volume\":\"10 4\",\"pages\":\"1725–1732 1725–1732\"},\"PeriodicalIF\":18.2000,\"publicationDate\":\"2025-03-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.acs.org/doi/epdf/10.1021/acsenergylett.5c00368\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Energy Letters \",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acsenergylett.5c00368\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Energy Letters ","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsenergylett.5c00368","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Green Strategy for Li2CO3 Regulation in Garnet-Type Solid-State Electrolytes via Acoustic Cavitation
Garnet-type Li6.75La3Zr1.75Ta0.25O12 (LLZTO) holds significant potential as a solid-state electrolyte (SSE) comprising promising features such as high Li+ conductivity, wide electrochemical stability window, and compatibility with Li-metal. However, air exposure forms a thick Li2CO3 passivation layer (∼50 nm), which hinders storage, handling, and interfacial performance, especially for LLZTO nanoparticles (NPs) with a high surface area. This study introduces a scalable, green sonication-assisted method to control the Li2CO3 layer thickness (<10 nm), which enhances air stability without compromising ionic conduction. In-situ ambient-pressure X-ray photoelectron spectroscopy (AP-XPS) further reveals the carbonate formation mechanism under atmospheric conditions. Electrochemical tests in ceramic-in-polymer (CIP) and polymer-in-ceramic (PIC) composite polymer electrolytes (CPEs) confirm that regulated Li2CO3 does not degrade the performance of passivated-LLZTO. The chemical-free, green approach suggested in this work maintains electrochemical properties, which enables scalable use of LLZTO-based SSEs for next-generation Li-metal batteries.
ACS Energy Letters Energy-Renewable Energy, Sustainability and the Environment
CiteScore
31.20
自引率
5.00%
发文量
469
审稿时长
1 months
期刊介绍:
ACS Energy Letters is a monthly journal that publishes papers reporting new scientific advances in energy research. The journal focuses on topics that are of interest to scientists working in the fundamental and applied sciences. Rapid publication is a central criterion for acceptance, and the journal is known for its quick publication times, with an average of 4-6 weeks from submission to web publication in As Soon As Publishable format.
ACS Energy Letters is ranked as the number one journal in the Web of Science Electrochemistry category. It also ranks within the top 10 journals for Physical Chemistry, Energy & Fuels, and Nanoscience & Nanotechnology.
The journal offers several types of articles, including Letters, Energy Express, Perspectives, Reviews, Editorials, Viewpoints and Energy Focus. Additionally, authors have the option to submit videos that summarize or support the information presented in a Perspective or Review article, which can be highlighted on the journal's website. ACS Energy Letters is abstracted and indexed in Chemical Abstracts Service/SciFinder, EBSCO-summon, PubMed, Web of Science, Scopus and Portico.