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用于高性能锂金属电池的乳酸锂改性聚烯烃隔膜

Lithium Lactate Modified Polyolefin Separators for High-Performance Lithium Metal Batteries.

作者信息

Wang Lulu, Yan Lingxiao, Wang Hongyan, Li Chenying, Xue Song

机构信息

Tianjin Key Laboratory of Organic Solar Cells and Photochemical Conversion, School of Chemistry & Chemical Engineering, Tianjin University of Technology, Tianjin, 300384, China.

出版信息

Langmuir. 2025 Aug 12;41(31):20555-20566. doi: 10.1021/acs.langmuir.5c01838. Epub 2025 Jul 30.

Abstract

As the fast-paced evolution of high energy density rechargeable batteries continues, the lower lithium ion (Li) mobility of polyolefin separators has become a major bottleneck in the adoption of lithium metal electrodes. With undesired Li-anion solvated structures in the electrolyte, previous separator modification strategies are generally confronted with the dilemma of concurrently enhancing the Li transference number and reducing the anion transference number, as well as overall conductivity. Here, a strategy are reported to prepare high-performance separators with polyolefin separators coated by lactic acid lithium with the assistance of dopamine hydrochloride and triethanolamine, which can achieve a stable LMB operation at 1 C for 600 cycles with a capacity retention of 92%, substantially outperforming pristine PP separator. The ultrathin polar modification layer on the surface of the PP separator renders optimal electrolyte wettability and notable electrolyte uptake. The electrostatically repellent nature of the negatively charged -COO moieties on the ion permeable layers can effectively increase the Li transference number without sacrificing the overall ion conductivity. The ionic conductivity of the DL2-PP separator reaches 1.2 mS cm, and the lithium-ion mobility is 0.68, enabling a rapid, selective and uniform Li flux through the separator. DFT calculations are utilized to analyze the underlying mechanism. Such features can facilitate uniform nucleation/deposition of Li and mitigate Li dendrite growth, leading to enhanced battery durability and safety.

摘要

随着高能量密度可充电电池的快速发展,聚烯烃隔膜中锂离子迁移率较低已成为采用锂金属电极的主要瓶颈。由于电解质中存在不理想的锂阴离子溶剂化结构,以往的隔膜改性策略通常面临着同时提高锂迁移数和降低阴离子迁移数以及整体电导率的困境。在此,报道了一种策略,即在盐酸多巴胺和三乙醇胺的辅助下,用乳酸锂涂覆聚烯烃隔膜来制备高性能隔膜,该隔膜可在1 C下稳定运行600次循环,容量保持率为92%,大大优于原始聚丙烯隔膜。聚丙烯隔膜表面的超薄极性改性层具有最佳的电解质润湿性和显著的电解质吸收率。离子渗透层上带负电荷的-COO基团的静电排斥性质可以有效地提高锂迁移数,而不牺牲整体离子电导率。DL2-PP隔膜的离子电导率达到1.2 mS cm,锂离子迁移率为0.68,使得锂离子能够快速、选择性和均匀地通过隔膜。利用密度泛函理论计算来分析其潜在机制。这些特性有助于锂的均匀成核/沉积,并减轻锂枝晶的生长,从而提高电池的耐久性和安全性。

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