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液体或无机固体电解质的锂硫电池的电极-电解质界面。

Electrode-Electrolyte Interfaces in Lithium-Sulfur Batteries with Liquid or Inorganic Solid Electrolytes.

机构信息

Materials Science and Engineering Program & Texas Materials Institute, The University of Texas at Austin , Austin, Texas 78712, United States.

出版信息

Acc Chem Res. 2017 Nov 21;50(11):2653-2660. doi: 10.1021/acs.accounts.7b00460. Epub 2017 Nov 7.

Abstract

Electrode-electrolyte interfacial properties play a vital role in the cycling performance of lithium-sulfur (Li-S) batteries. The issues at an electrode-electrolyte interface include electrochemical and chemical reactions occurring at the interface, formation mechanism of interfacial layers, compositional/structural characteristics of the interfacial layers, ionic transport across the interface, and thermodynamic and kinetic behaviors at the interface. Understanding the above critical issues is paramount for the development of strategies to enhance the overall performance of Li-S batteries. Liquid electrolytes commonly used in Li-S batteries bear resemblance to those employed in traditional lithium-ion batteries, which are generally composed of a lithium salt dissolved in a solvent matrix. However, due to a series of unique features associated with sulfur or polysulfides, ether-based solvents are generally employed in Li-S batteries rather than simply adopting the carbonate-type solvents that are generally used in the traditional Li-ion batteries. In addition, the electrolytes of Li-S batteries usually comprise an important additive, LiNO. The unique electrolyte components of Li-S batteries do not allow us to directly take the interfacial theories of the traditional Li-ion batteries and apply them to Li-S batteries. On the other hand, during charging/discharging a Li-S battery, the dissolved polysulfide species migrate through the battery separator and react with the Li anode, which magnifies the complexity of the interfacial problems of Li-S batteries. However, current Li-S battery development paths have primarily been energized by advances in sulfur cathodes. Insight into the electrode-electrolyte interfacial behaviors has relatively been overshadowed. In this Account, we first examine the state-of-the-art contributions in understanding the solid-electrolyte interphase (SEI) formed on the Li-metal anode and sulfur cathode in conventional liquid-electrolyte Li-S batteries and how the resulting chemical and physical properties of the SEI affect the overall battery performance. A few strategies recently proposed for improving the stability of SEI are briefly summarized. Solid Li-ion conductive electrolytes have been attempted for the development of Li-S batteries to eliminate the polysulfide shuttle issues. One approach is based on a concept of "all-solid-state Li-S battery," in which all the cell components are in the solid state. Another approach is based on a "hybrid-electrolyte Li-S battery" concept, in which the solid electrolyte plays roles both as a Li-ion conductor for the electrochemical reaction and as a separator to prevent polysulfide shuttle. However, these endeavors with the solid electrolyte are not able to provide an overall satisfactory cell performance. In addition to the low ionic conductivity of solid-state electrolytes, a critical issue lies in the poor interfacial properties between the electrode and the solid electrolyte. This Account provides a survey of the relevant research progress in understanding and manipulating the interfaces of electrode and solid electrolytes in both the "all-solid-state Li-S batteries" and the "hybrid-electrolyte Li-S batteries". A recently proposed "semi-solid-state Li-S battery" concept is also briefly discussed. Finally, future research and development directions in all the above areas are suggested.

摘要

电极-电解质界面性质在锂硫(Li-S)电池的循环性能中起着至关重要的作用。电极-电解质界面存在的问题包括界面处发生的电化学和化学反应、界面层的形成机制、界面层的组成/结构特征、离子在界面处的传输以及界面处的热力学和动力学行为。了解上述关键问题对于开发提高 Li-S 电池整体性能的策略至关重要。Li-S 电池中常用的液体电解质与传统锂离子电池中使用的电解质相似,通常由溶解在溶剂基质中的锂盐组成。然而,由于硫或多硫化物具有一系列独特的特性,醚基溶剂通常用于 Li-S 电池,而不是简单地采用传统 Li-ion 电池中通常使用的碳酸盐型溶剂。此外,Li-S 电池的电解质通常包含一种重要的添加剂 LiNO。Li-S 电池的独特电解质成分不允许我们直接将传统锂离子电池的界面理论应用于 Li-S 电池。另一方面,在对 Li-S 电池进行充电/放电时,溶解的多硫化物通过电池隔膜迁移并与 Li 阳极反应,这增加了 Li-S 电池界面问题的复杂性。然而,目前 Li-S 电池的发展路径主要受到硫阴极的进展推动。对电极-电解质界面行为的了解相对被忽视。在本专题介绍中,我们首先考察了在传统液体电解质 Li-S 电池中理解锂金属阳极和硫阴极上形成的固体电解质界面(SEI)的最新研究进展,以及 SEI 的化学和物理性质如何影响整体电池性能。简要总结了最近提出的一些改善 SEI 稳定性的策略。为了消除多硫化物穿梭问题,已经尝试使用固体锂离子导电电解质来开发 Li-S 电池。一种方法基于“全固态 Li-S 电池”的概念,其中所有电池组件都处于固态。另一种方法基于“混合电解质 Li-S 电池”的概念,其中固体电解质既是电化学反应的锂离子导体,又是防止多硫化物穿梭的隔膜。然而,这些使用固体电解质的尝试并不能提供整体令人满意的电池性能。除了固态电解质的低离子电导率外,一个关键问题在于电极与固体电解质之间的界面性能不佳。本专题介绍提供了对理解和控制“全固态 Li-S 电池”和“混合电解质 Li-S 电池”中电极和固体电解质界面的相关研究进展的综述。还简要讨论了最近提出的“半固态 Li-S 电池”概念。最后,提出了在所有上述领域的未来研究和发展方向。

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