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

IF 16.1 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Xi-Long Wang, Yuan Li, Jia Liu, Shi-Jie Yang, Jiang-Kui Hu, Wei-Qi Mai, Rui Wen, Hong Yuan, Jia-Qi Huang
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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.
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
固态锂(Li)金属电池(sslmb)因其高能量密度和固有安全性被认为是最有前途的下一代电池技术之一。然而,副反应和锂枝晶生长等界面问题严重阻碍了sslmb的实际应用。在这篇论文中,我们提出了一个阳离子内建静电场来驱动阴离子衍生的双层固体电解质界面(SEI)的产生。三丁基甲基磷双(三氟甲磺酰基)亚胺(TMPB)阳离子在带负电荷的锂阳极表面的特异性吸附显著地阻止了易损聚乙烯氧化物(PEO)与锂金属之间的界面副反应。更重要的是,形成的阳离子内建静电场诱导Li盐阴离子定向捕获到Li金属表面,从而产生阴离子衍生的双层SEI,由机械柔性的富有机表层和富Li离子导电的无机底层组成。结果表明,在降低极化电压的情况下,Li||锂电池的寿命延长了1900小时以上。锂||LiFePO4全电池也表现出优异的循环稳定性,在0.5℃下200次循环中平均库仑效率保持在99.69%。这项工作为通过表面静电场调节减轻界面降解和促进均匀锂沉积提供了有价值的见解。
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来源期刊
CiteScore
26.60
自引率
6.60%
发文量
3549
审稿时长
1.5 months
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.
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