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诊断和纠正固态聚合物电解质在增强固态锂硫电池中的失效。

Diagnosing and Correcting the Failure of the Solid-State Polymer Electrolyte for Enhancing Solid-State Lithium-Sulfur Batteries.

机构信息

State Key Lab of Fine Chemicals, Liaoning Key Lab for Energy Materials and Chemical Engineering, School of Chemical Engineering, Dalian University of Technology, Dalian, 116024, China.

State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023, China.

出版信息

Adv Mater. 2023 Jun;35(22):e2212039. doi: 10.1002/adma.202212039. Epub 2023 Apr 7.

Abstract

Solid-state polymer electrolytes (SPEs) attract great interest in developing high-performance yet reliable solid-state batteries. However, understanding of the failure mechanism of the SPE and SPE-based solid-state batteries remains in its infancy, posing a great barrier to practical solid-state batteries. Herein, the high accumulation and clogging of "dead" lithium polysulfides (LiPS) on the interface between the cathode and SPE with intrinsic diffusion limitation is identified as a critical failure cause of SPE-based solid-state Li-S batteries. It induces a poorly reversible chemical environment with retarded kinetics on the cathode-SPE interface and in bulk SPEs, starving the Li-S redox in solid-state cells. This observation is different from the case in liquid electrolytes with free solvent and charge carriers, where LiPS dissolve but remain alive for electrochemical/chemical redox without interfacial clogging. Electrocatalysis demonstrates the feasibility of tailoring the chemical environment in diffusion-restricted reaction media for reducing Li-S redox failure in the SPE. It enables Ah-level solid-state Li-S pouch cells with a high specific energy of 343 Wh kg on the cell level. This work may shed new light on the understanding of the failure mechanism of SPE for bottom-up improvement of solid-state Li-S batteries.

摘要

固态聚合物电解质(SPE)在开发高性能且可靠的固态电池方面引起了极大的兴趣。然而,对 SPE 和基于 SPE 的固态电池的失效机制的理解仍处于起步阶段,这对实际的固态电池构成了巨大的障碍。在此,我们发现,由于固有扩散限制,“死”的多硫化锂(LiPS)在阴极和 SPE 之间的界面上高度积累和堵塞,这是基于 SPE 的固态 Li-S 电池失效的一个关键原因。这导致在阴极-SPE 界面和整个 SPE 中形成了一个化学环境很差且动力学迟缓的区域,使得固态电池中的 Li-S 氧化还原反应受到抑制。这种观察结果与具有游离溶剂和电荷载流子的液态电解质不同,在液态电解质中,LiPS 溶解但保持电化学/化学氧化还原活性,而不会发生界面堵塞。电催化证明了在扩散受限的反应介质中调整化学环境的可行性,可用于减少 SPE 中 Li-S 氧化还原失效。该方法实现了具有 343 Wh kg 高比能量的 Ah 级固态 Li-S 软包电池,这为深入理解 SPE 的失效机制并对其进行改进以提升固态 Li-S 电池性能提供了新的思路。

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