Synthesis, Structural Analysis, and Degradation Behavior of Potassium Tin Chloride as Chloride‐Ion Batteries Conversion Electrode Material

Author:

Panja Soutam1ORCID,Miao Yidong1ORCID,Döhn Johannes2,Choi Jaehoon1,Fleischmann Simon1ORCID,Guddehalli Chandrappa Shivaraju1ORCID,Diemant Thomas1,Groß Axel12ORCID,Karkera Guruprakash1ORCID,Fichtner Maximilian13ORCID

Affiliation:

1. Helmholtz Institute Ulm for Electrochemical Energy Storage (HIU) 89081 Ulm Germany

2. Institute of Theoretical Chemistry Ulm University 89081 Ulm Germany

3. Institute of Nanotechnology Karlsruhe Institute of Technology (KIT) 76021 Karlsruhe Germany

Abstract

AbstractChloride–ion batteries (CIBs) offer a compelling alternative to conventional battery systems, particularly in applications demanding cost‐effectiveness and resource sustainability. However, the development of tailored electrode materials remains a critical bottleneck for CIB advancement. In this study, an untapped class of perovskite‐based material, potassium hexachlorostannate (K2SnCl6, denoted as KSC) is synthesized via a facile mechanochemical route for the first time. The prepared KSC is subjected to various characterization techniques to confirm its crystal structure and morphology. Herein, KSC exhibits intriguing electrochemical performance in a non‐aqueous CIB configuration, utilizing a lithium metal counter electrode. Furthermore, ex situ X‐ray diffraction (XRD) and X‐ray photoelectron spectroscopy (XPS) analysis, reveal a conversion reaction mechanism involving chloride ion shuttling and provide insights into structural evolution during cycling. Moreover, the density functional theory (DFT) studies support additional degradation products that can potentially limit the performance of these materials as potential battery electrodes in CIBs.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

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