Xi-Long Wang, Yuan Li, Jia Liu, Shi-Jie Yang, Jiang-Kui Hu, Wei-Qi Mai, Rui Wen, Hong Yuan, Jia-Qi Huang
{"title":"一种坚固的双层固体电解质界面,由阳离子特异性吸附诱导的内置静电场实现,用于长循环固态锂金属电池","authors":"Xi-Long Wang, Yuan Li, Jia Liu, Shi-Jie Yang, Jiang-Kui Hu, Wei-Qi Mai, Rui Wen, Hong Yuan, Jia-Qi Huang","doi":"10.1002/anie.202421101","DOIUrl":null,"url":null,"abstract":"Solid‐state lithium (Li) metal batteries (SSLMBs) are considered as one of the most promising next‐generation battery technologies due to their high energy density and intrinsic safety. However, interfacial issues such as side reactions and Li dendrite growth severely hinder the practical application of SSLMBs. In this contribution, we proposed a cationic built‐in electrostatic field to drive the generation of an anion‐derived dual‐layered solid electrolyte interphase (SEI). The specific adsorption of tributylmethyl‐phosphonium bis(trifluoromethanesulfonyl)imide (TMPB) cations onto negatively charged Li anode surface significantly prevents interfacial side reactions between vulnerable polyethylene oxide (PEO) and Li metal. More importantly, the formed cationic built‐in electrostatic field induces the targeted trapping of Li‐salt anions onto the Li metal surface, leading to the generation of an anion‐derived dual‐layered SEI, composed of a mechanically flexible organic‐rich surface layer and a Li‐ion conductive inorganic‐rich bottom layer. As a result, the Li||Li cell demonstrated an extended lifespan of over 1900 hours with the reduced polarization voltage. The Li||LiFePO4 full cell also exhibited excellent cycling stability, maintaining an average Coulombic efficiency of 99.69% over 200 cycles at 0.5 C. This work provides valuable insights into mitigating interfacial degradation and promoting uniform Li deposition through surface electrostatic field regulation.","PeriodicalId":125,"journal":{"name":"Angewandte Chemie International Edition","volume":"8 1","pages":""},"PeriodicalIF":16.1000,"publicationDate":"2025-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Robust Dual‐Layered Solid Electrolyte Interphase Enabled by Cation Specific Adsorption‐Induced Built‐In Electrostatic Field for Long‐Cycling Solid‐State Lithium Metal Batteries\",\"authors\":\"Xi-Long Wang, Yuan Li, Jia Liu, Shi-Jie Yang, Jiang-Kui Hu, Wei-Qi Mai, Rui Wen, Hong Yuan, Jia-Qi Huang\",\"doi\":\"10.1002/anie.202421101\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Solid‐state lithium (Li) metal batteries (SSLMBs) are considered as one of the most promising next‐generation battery technologies due to their high energy density and intrinsic safety. However, interfacial issues such as side reactions and Li dendrite growth severely hinder the practical application of SSLMBs. In this contribution, we proposed a cationic built‐in electrostatic field to drive the generation of an anion‐derived dual‐layered solid electrolyte interphase (SEI). The specific adsorption of tributylmethyl‐phosphonium bis(trifluoromethanesulfonyl)imide (TMPB) cations onto negatively charged Li anode surface significantly prevents interfacial side reactions between vulnerable polyethylene oxide (PEO) and Li metal. More importantly, the formed cationic built‐in electrostatic field induces the targeted trapping of Li‐salt anions onto the Li metal surface, leading to the generation of an anion‐derived dual‐layered SEI, composed of a mechanically flexible organic‐rich surface layer and a Li‐ion conductive inorganic‐rich bottom layer. As a result, the Li||Li cell demonstrated an extended lifespan of over 1900 hours with the reduced polarization voltage. The Li||LiFePO4 full cell also exhibited excellent cycling stability, maintaining an average Coulombic efficiency of 99.69% over 200 cycles at 0.5 C. This work provides valuable insights into mitigating interfacial degradation and promoting uniform Li deposition through surface electrostatic field regulation.\",\"PeriodicalId\":125,\"journal\":{\"name\":\"Angewandte Chemie International Edition\",\"volume\":\"8 1\",\"pages\":\"\"},\"PeriodicalIF\":16.1000,\"publicationDate\":\"2025-01-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Angewandte Chemie International Edition\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1002/anie.202421101\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Angewandte Chemie International Edition","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/anie.202421101","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
A Robust Dual‐Layered Solid Electrolyte Interphase Enabled by Cation Specific Adsorption‐Induced Built‐In Electrostatic Field for Long‐Cycling Solid‐State Lithium Metal Batteries
Solid‐state lithium (Li) metal batteries (SSLMBs) are considered as one of the most promising next‐generation battery technologies due to their high energy density and intrinsic safety. However, interfacial issues such as side reactions and Li dendrite growth severely hinder the practical application of SSLMBs. In this contribution, we proposed a cationic built‐in electrostatic field to drive the generation of an anion‐derived dual‐layered solid electrolyte interphase (SEI). The specific adsorption of tributylmethyl‐phosphonium bis(trifluoromethanesulfonyl)imide (TMPB) cations onto negatively charged Li anode surface significantly prevents interfacial side reactions between vulnerable polyethylene oxide (PEO) and Li metal. More importantly, the formed cationic built‐in electrostatic field induces the targeted trapping of Li‐salt anions onto the Li metal surface, leading to the generation of an anion‐derived dual‐layered SEI, composed of a mechanically flexible organic‐rich surface layer and a Li‐ion conductive inorganic‐rich bottom layer. As a result, the Li||Li cell demonstrated an extended lifespan of over 1900 hours with the reduced polarization voltage. The Li||LiFePO4 full cell also exhibited excellent cycling stability, maintaining an average Coulombic efficiency of 99.69% over 200 cycles at 0.5 C. This work provides valuable insights into mitigating interfacial degradation and promoting uniform Li deposition through surface electrostatic field regulation.
期刊介绍:
Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.