Sha Peng, Jia Chen, Yu Li, Ying Tao, Lei Zhang, Jiyan Liu, Zhihong Liu, Xueqing Liu
{"title":"固态电池中快速传导和均匀锂沉积的垂直排列离子通道","authors":"Sha Peng, Jia Chen, Yu Li, Ying Tao, Lei Zhang, Jiyan Liu, Zhihong Liu, Xueqing Liu","doi":"10.1002/cey2.70152","DOIUrl":null,"url":null,"abstract":"<p>The random distribution of one-dimensional nanofillers in composite polymer electrolytes (CPEs) typically results in tortuous ion transport pathways, severely limiting ionic conductivity and Li⁺ flux uniformity. Herein, an innovative electric field-assisted strategy is proposed to construct vertically aligned ion channels in CPEs using lithiated halloysite nanotubes (HNTs–SO₃Li) embedded within a polyurethane acrylate/polyethylene glycol diacrylate (PUA/PEGDA) matrix. Under an alternating electric field, the nanotubes orient perpendicularly, forming continuous, low-tortuosity pathways that significantly enhance room-temperature ionic conductivity. The aligned structure not only shortens Li⁺ transport distances but also homogenizes ion flux at the electrode interface, effectively suppressing lithium dendrite growth. Electrochemical characterization reveals exceptional stability. Three-dimensional structural reconstruction and ion transport simulations further demonstrate that the ordered channels promote uniform Li⁺ distribution and faster ion kinetics compared to disordered systems. This study provides a scalable and efficient approach to designing high-performance CPEs for next-generation solid-state batteries, addressing critical challenges in ionic conductivity, interfacial stability, and dendrite suppression.</p>","PeriodicalId":33706,"journal":{"name":"Carbon Energy","volume":"8 3","pages":""},"PeriodicalIF":24.2000,"publicationDate":"2026-03-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cey2.70152","citationCount":"0","resultStr":"{\"title\":\"Vertically Aligned Ion Pathways for Fast Conduction and Uniform Lithium Deposition in Solid-State Batteries\",\"authors\":\"Sha Peng, Jia Chen, Yu Li, Ying Tao, Lei Zhang, Jiyan Liu, Zhihong Liu, Xueqing Liu\",\"doi\":\"10.1002/cey2.70152\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The random distribution of one-dimensional nanofillers in composite polymer electrolytes (CPEs) typically results in tortuous ion transport pathways, severely limiting ionic conductivity and Li⁺ flux uniformity. Herein, an innovative electric field-assisted strategy is proposed to construct vertically aligned ion channels in CPEs using lithiated halloysite nanotubes (HNTs–SO₃Li) embedded within a polyurethane acrylate/polyethylene glycol diacrylate (PUA/PEGDA) matrix. Under an alternating electric field, the nanotubes orient perpendicularly, forming continuous, low-tortuosity pathways that significantly enhance room-temperature ionic conductivity. The aligned structure not only shortens Li⁺ transport distances but also homogenizes ion flux at the electrode interface, effectively suppressing lithium dendrite growth. Electrochemical characterization reveals exceptional stability. Three-dimensional structural reconstruction and ion transport simulations further demonstrate that the ordered channels promote uniform Li⁺ distribution and faster ion kinetics compared to disordered systems. This study provides a scalable and efficient approach to designing high-performance CPEs for next-generation solid-state batteries, addressing critical challenges in ionic conductivity, interfacial stability, and dendrite suppression.</p>\",\"PeriodicalId\":33706,\"journal\":{\"name\":\"Carbon Energy\",\"volume\":\"8 3\",\"pages\":\"\"},\"PeriodicalIF\":24.2000,\"publicationDate\":\"2026-03-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cey2.70152\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Carbon Energy\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/cey2.70152\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/12/21 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Carbon Energy","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cey2.70152","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/12/21 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Vertically Aligned Ion Pathways for Fast Conduction and Uniform Lithium Deposition in Solid-State Batteries
The random distribution of one-dimensional nanofillers in composite polymer electrolytes (CPEs) typically results in tortuous ion transport pathways, severely limiting ionic conductivity and Li⁺ flux uniformity. Herein, an innovative electric field-assisted strategy is proposed to construct vertically aligned ion channels in CPEs using lithiated halloysite nanotubes (HNTs–SO₃Li) embedded within a polyurethane acrylate/polyethylene glycol diacrylate (PUA/PEGDA) matrix. Under an alternating electric field, the nanotubes orient perpendicularly, forming continuous, low-tortuosity pathways that significantly enhance room-temperature ionic conductivity. The aligned structure not only shortens Li⁺ transport distances but also homogenizes ion flux at the electrode interface, effectively suppressing lithium dendrite growth. Electrochemical characterization reveals exceptional stability. Three-dimensional structural reconstruction and ion transport simulations further demonstrate that the ordered channels promote uniform Li⁺ distribution and faster ion kinetics compared to disordered systems. This study provides a scalable and efficient approach to designing high-performance CPEs for next-generation solid-state batteries, addressing critical challenges in ionic conductivity, interfacial stability, and dendrite suppression.
期刊介绍:
Carbon Energy is an international journal that focuses on cutting-edge energy technology involving carbon utilization and carbon emission control. It provides a platform for researchers to communicate their findings and critical opinions and aims to bring together the communities of advanced material and energy. The journal covers a broad range of energy technologies, including energy storage, photocatalysis, electrocatalysis, photoelectrocatalysis, and thermocatalysis. It covers all forms of energy, from conventional electric and thermal energy to those that catalyze chemical and biological transformations. Additionally, Carbon Energy promotes new technologies for controlling carbon emissions and the green production of carbon materials. The journal welcomes innovative interdisciplinary research with wide impact. It is indexed in various databases, including Advanced Technologies & Aerospace Collection/Database, Biological Science Collection/Database, CAS, DOAJ, Environmental Science Collection/Database, Web of Science and Technology Collection.