Insights into the chemical and electrochemical behavior of halide and sulfide electrolytes in all-solid-state batteries†

IF 3.2 Q2 CHEMISTRY, PHYSICAL
Energy advances Pub Date : 2025-02-12 DOI:10.1039/D4YA00618F
Artur Tron, Alexander Beutl, Irshad Mohammad and Andrea Paolella
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引用次数: 0

Abstract

Conventional lithium-ion batteries (LIBs) have become widely used in small and large applications, but the use of toxic and flammable liquid electrolytes can lead to safety issues and reduced cell performance. New generation solid-state lithium batteries (SSBs) have the potential to replace LIBs due to their safety and potentially high energy density (>450 W h kg−1). The solid electrolyte (SE) is a crucial component in solid-state batteries. Among the available options, sulfide- and halide-based solid electrolytes stand out as promising candidates due to their high ionic conductivity and ease of processing. They are among the most prominent topics in solid electrolyte research for solid-state batteries. Despite their advantages like good compatibility with high-voltage cathodes and easy manufacturing, solid electrolytes still face issues of degradation of the Li metal/solid electrolyte interface. This is due to the formation of side reaction products at the interface, which inhibits lithium transport across it. The primary issue stems from the poor chemical and electrochemical stability of sulfide- and halide-based solid electrolytes when in contact with lithium metal. In this study, we have demonstrated that the composite electrolytes (Li3YCl4Br2:Li6PS5Cl) comprising halide and argyrodite can prevent the formation of unfavorable interactions between the solid electrolyte and the Li metal anode. The Li/Li-symmetric cells employing the Li3YCl4Br2:Li6PS5Cl electrolytes exhibited enhanced cycle life and high critical current density (CCD) from C/20 to C/2, compared to the symmetric cells utilizing only Li3YCl4Br2 or Li6PS5Cl electrolyte. Furthermore, the Li/Li3YCl4Br2/NCM half-cells demonstrated high initial coulombic efficiency and extended cycle life compared to half-cells utilizing traditional halide and argyrodite electrolytes. The approach described here offers a pathway to enhance halide-based solid-state batteries, providing a relatively simple and effective strategy.

Abstract Image

传统的锂离子电池(LIB)已广泛应用于小型和大型应用中,但使用有毒和易燃的液态电解质会导致安全问题和电池性能下降。新一代固态锂电池(SSB)因其安全性和潜在的高能量密度(450 W h kg-1),有可能取代液态锂离子电池。固态电解质(SE)是固态电池的重要组成部分。在可供选择的固态电解质中,硫化物和卤化物固态电解质因其离子电导率高和易于加工而成为前景广阔的候选材料。它们是固态电池固态电解质研究中最突出的课题之一。尽管固态电解质具有与高压阴极良好的兼容性和易于制造等优点,但仍面临着锂金属/固态电解质界面降解的问题。这是由于在界面上形成了副反应产物,从而抑制了锂在界面上的传输。主要问题源于硫化物和卤化物基固体电解质与锂金属接触时化学和电化学稳定性较差。在这项研究中,我们证明了由卤化物和文石组成的复合电解质(Li3YCl4Br2:Li6PS5Cl)可以防止固体电解质与锂金属阳极之间形成不利的相互作用。与仅使用 Li3YCl4Br2 或 Li6PS5Cl 电解质的对称电池相比,使用 Li3YCl4Br2:Li6PS5Cl 电解质的锂/锂对称电池显示出更长的循环寿命以及从 C/20 到 C/2 的高临界电流密度 (CCD)。此外,与使用传统卤化物和阿基锂电解质的半电池相比,锂/锂3YCl4Br2/NCM 半电池显示出较高的初始库仑效率和较长的循环寿命。本文所述的方法提供了一条增强卤化物固态电池的途径,提供了一种相对简单而有效的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
1.80
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0.00%
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