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用于开发具有锂金属电极的固态电池的氧化物|硫化物异质离子界面稳定性评估:以LLZO|LiPSCl和LLZO|LiPS为例

Evaluation of Oxide|Sulfide Heteroionic Interface Stability for Developing Solid-State Batteries with a Lithium-Metal Electrode: The Case of LLZO|LiPSCl and LLZO|LiPS.

作者信息

Merola Leonardo, Singh Vipin K, Palmer Max, Eckhardt Janis K, Benz Sebastian L, Fuchs Till, Nazar Linda F, Sakamoto Jeff, Richter Felix H, Janek Jürgen

机构信息

Institute of Physical Chemistry and Center for Materials Research (ZfM), Justus-Liebig-University Giessen, Heinrich-Buff-Ring 17, Giessen D-35392, Germany.

Department of Chemistry and Waterloo Institute of Nanotechnology, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.

出版信息

ACS Appl Mater Interfaces. 2024 Oct 9;16(40):54847-54863. doi: 10.1021/acsami.4c11597. Epub 2024 Sep 24.

Abstract

Developing solid-state batteries (SSB) with a lithium metal electrode (LME) using only one type of solid electrolyte (SE) is a significant challenge since no SE fits all the requirements imposed by both electrodes. A possible solution is using multilayer SSBs with an LME where the drawbacks of each SE are overcome by using layers of different SEs. However, research on inorganic SE|SE heteroionic interfaces is still quite preliminary, especially regarding oxide|sulfide heteroionic interfaces. This work reports the electrochemical investigation of the heteroionic interface between LiAlLaZrO (Al-LLZO) and two representative materials for sulfide-based SEs: argyrodite-based LiPSCl (LPSCl) and glass-like LiPS (LPS711). Through in-depth temperature- and pressure-dependent impedance analyses of multilayer symmetric cells at equilibrium (i.e., no current load), the electrical properties of the heteroionic interfaces are assessed. The pressure-dependent kinetic of the Al-LLZO|LPSCl pair is interpreted with the concept of geometric constriction resistance and show that its resistance is lower than for the Al-LLZO|LPS711 pair. Furthermore, the effect of Al-LLZO surface treatment on the electrical properties of the Al-LLZO|LPSCl heteroionic interface is evaluated. Such investigation shows that the value of the interface activation energy decreases when the Al-LLZO surface is heat treated, revealing a significant influence of the carbonate/hydroxide passivation layer on the heteroionic interface. Additionally, by cycling the symmetric cell for 900 h at 1.0 mAh·cm, it is revealed that the Al-LLZO|LPSCl interface has a lower impedance increase than the Al-LLZO|LPS711 interface, especially if the Al-LLZO is heat treated. With this work, we highlight that the oxide|argyrodite combination can be a promising candidate for multilayer SSBs with an LME. However, we show that an optimized LLZO surface treatment and chemical analysis of the interface are recommended for future research.

摘要

仅使用一种类型的固体电解质(SE)来开发带有锂金属电极(LME)的固态电池(SSB)是一项重大挑战,因为没有一种SE能满足两个电极所提出的所有要求。一种可能的解决方案是使用带有LME的多层SSB,其中通过使用不同SE的层来克服每种SE的缺点。然而,关于无机SE|SE异质离子界面的研究仍然相当初步,特别是关于氧化物|硫化物异质离子界面。这项工作报道了LiAlLaZrO(Al-LLZO)与两种代表性的硫化物基SE材料:银硫锗矿型LiPSCl(LPSCl)和玻璃状LiPS(LPS711)之间异质离子界面的电化学研究。通过对多层对称电池在平衡状态(即无电流负载)下进行深入的温度和压力依赖性阻抗分析,评估了异质离子界面的电学性质。用几何收缩电阻的概念解释了Al-LLZO|LPSCl对的压力依赖性动力学,并表明其电阻低于Al-LLZO|LPS711对。此外,评估了Al-LLZO表面处理对Al-LLZO|LPSCl异质离子界面电学性质的影响。此类研究表明,当Al-LLZO表面进行热处理时,界面活化能的值会降低,这揭示了碳酸盐/氢氧化物钝化层对异质离子界面有重大影响。此外,通过在1.0 mAh·cm下对对称电池进行900小时的循环,发现Al-LLZO|LPSCl界面的阻抗增加低于Al-LLZO|LPS711界面,特别是在Al-LLZO经过热处理的情况下。通过这项工作,我们强调氧化物|银硫锗矿组合对于带有LME的多层SSB可能是一个有前景的候选材料。然而,我们表明,未来的研究建议对LLZO表面进行优化处理并对界面进行化学分析。

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