Yufang He, Li Wang, Aiping Wang, Bo Zhang, Hiep Pham, Jonghyun Park, Xiangming He
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引用次数: 0
摘要
多尺度模拟是构建数字电池以改进电池设计和应用的重要基础。实验证明,富锂固体电解质相(SEI)对锂金属电池的电化学性能至关重要。然而,富含锂F的SEI对各种电解质配方都很敏感,其基本机制仍不清楚。本文综述了不同电解质配方中富锂F SEI的结构和形成机理。在此基础上,进一步讨论了由电解质衍生物种在锂金属阳极(LMA)上的初始吸附决定的富锂辉石 SEI 的可能成膜机制。该研究提出,由于锂金属阳极的润湿性较差,单个锂氟化物物种遵循 Volmer-Weber 成膜模式。而添加剂衍生物种与锂粉的协同吸附促进了弗兰克-范德默尔韦薄膜生长模式,从而在 LMA 表面形成均匀的锂粉沉积。这一观点为了解高锂辉石含量、锂辉石润湿性和均匀富锂辉石 SEI 的高性能之间的关系提供了新的视角。它揭示了添加剂辅助协同吸附对均匀富锂离子电致发光生长的重要性,有助于合理设计电解质配方和高性能 LMA,并为多尺度模拟 SEI 提供了启示。
Insight into uniform filming of LiF-rich interphase via synergistic adsorption for high-performance lithium metal anode
Multi-scale simulation is an important basis for constructing digital batteries to improve battery design and application. LiF-rich solid electrolyte interphase (SEI) is experimentally proven to be crucial for the electrochemical performance of lithium metal batteries. However, the LiF-rich SEI is sensitive to various electrolyte formulas and the fundamental mechanism is still unclear. Herein, the structure and formation mechanism of LiF-rich SEI in different electrolyte formulas have been reviewed. On this basis, it further discussed the possible filming mechanism of LiF-rich SEI determined by the initial adsorption of the electrolyte-derived species on the lithium metal anode (LMA). It proposed that individual LiF species follow the Volmer–Weber mode of film growth due to its poor wettability on LMA. Whereas, the synergistic adsorption of additive-derived species with LiF promotes the Frank-Vander Merwe mode of film growth, resulting in uniform LiF deposition on the LMA surface. This perspective provides new insight into the correlation between high LiF content, wettability of LiF, and highperformance of uniform LiF-rich SEI. It disclosed the importance of additive assistant synergistic adsorption on the uniform growth of LiF-rich SEI, contributing to the reasonable design of electrolyte formulas and high-performance LMA, and enlightening the way for multi-scale simulation of SEI.