{"title":"Beyond Polymerization: In Situ Coupled Fluorination Enables More Stable Interfaces for Solid-State Lithium Batteries","authors":"Xunjie Yin, Yong Guo, Sijia Chi, Yiran Jia, Fangbing Li, Jiangshan Qi, Xuerui Yi, Shichao Wu, Quan-Hong Yang","doi":"10.1021/jacs.4c15079","DOIUrl":null,"url":null,"abstract":"In situ polymerization strategies hold great promise for enhancing the physical interfacial stability in solid-state batteries, yet (electro)chemical degradation of polymerized interfaces, especially at high voltages, remains a critical challenge. Herein, we find interphase engineering is crucial for the polymerization process and polymer stability and pioneer an in situ polymerization-fluorination (Poly-FR) strategy to create durable interfaces with excellent physical and (electro)chemical stabilities, achieved by designing a bifunctional initiator for both polymerization and on-surface lithium donor reactions. The integrated in situ fluorination converts Li<sub>2</sub>CO<sub>3</sub> impurities on LiNi<sub>0.8</sub>Co<sub>0.1</sub>Mn<sub>0.1</sub>O<sub>2</sub> (NCM811) surfaces into LiF-rich interphases, effectively inhibiting the aggressive (de)lithiation intermediates and protecting the interface from underlying chemical degradation, thereby surpassing the stability limitations of polymerization alone. Furthermore, the Poly-FR mediated symmetric Li|Li cells achieve an impressive cycling stability of up to 12,000 h. Solid-state cells with NCM811 cathodes and Li metal anodes realize an ultrastable cycling performance of 400 cycles with 83.4% retention at a high voltage of 4.5 V. This work points toward advanced in situ polymerization and beyond.","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":"58 1","pages":""},"PeriodicalIF":14.4000,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/jacs.4c15079","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
In situ polymerization strategies hold great promise for enhancing the physical interfacial stability in solid-state batteries, yet (electro)chemical degradation of polymerized interfaces, especially at high voltages, remains a critical challenge. Herein, we find interphase engineering is crucial for the polymerization process and polymer stability and pioneer an in situ polymerization-fluorination (Poly-FR) strategy to create durable interfaces with excellent physical and (electro)chemical stabilities, achieved by designing a bifunctional initiator for both polymerization and on-surface lithium donor reactions. The integrated in situ fluorination converts Li2CO3 impurities on LiNi0.8Co0.1Mn0.1O2 (NCM811) surfaces into LiF-rich interphases, effectively inhibiting the aggressive (de)lithiation intermediates and protecting the interface from underlying chemical degradation, thereby surpassing the stability limitations of polymerization alone. Furthermore, the Poly-FR mediated symmetric Li|Li cells achieve an impressive cycling stability of up to 12,000 h. Solid-state cells with NCM811 cathodes and Li metal anodes realize an ultrastable cycling performance of 400 cycles with 83.4% retention at a high voltage of 4.5 V. This work points toward advanced in situ polymerization and beyond.
期刊介绍:
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