Boosting Ion Transport and Stability in Halide Solid Electrolytes via S and F Codoping
Artikel i vetenskaplig tidskrift, 2025
Structural and compositional modification of solid-state electrolytes (SSEs) is a common approach to improve ionic conductivity and interfacial stability, yet the mechanisms remain unclear. Here, we studied Li2ZrCl6 (LZC) codoped with sulfur (S) and fluorine (F). X-ray and neutron diffraction with bond valence site energy (BVSE) simulations reveal that codopant-induced lattice distortion facilitates ion transport. The S/F codoped sample achieves a room-temperature ionic conductivity of 0.51 mS cm-1, twice that of pristine LZC (0.26 mS cm-1). Advanced characterizations further show that S and F participate in forming the solid electrolyte interphase (SEI), enhancing the electrode interfacial stability. As a result, solid-state batteries with the codoped SSE deliver capacity retentions of 97.1% at 0.1 C and 82.8% at 0.5 C. This study demonstrates the synergistic effects of structural modulation on ionic conduction and SEI formation, providing insights for designing high-performance SSEs.
Solid electrolytes
Ionic conductivity
Halogens
Inorganic compounds
Batteries
Författare
Priya Ganesan
Karlsruher Institut für Technologie (KIT)
Helmholtz Institute Ulm
Ramon Zimmermanns
Helmholtz Institute Ulm
Karlsruher Institut für Technologie (KIT)
Guillaume Navallon
Helmholtz Institute Ulm
Karlsruher Institut für Technologie (KIT)
Yang Hu
Karlsruher Institut für Technologie (KIT)
Helmholtz Institute Ulm
Thomas Diemant
Karlsruher Institut für Technologie (KIT)
Helmholtz Institute Ulm
Gabriel J. Cuello
Institut Laue-Langevin
Ines Puente Orench
Institut Laue-Langevin
Blanka Detlefs
European Synchrotron Radiation Facility (ESRF)
Ritambhara Gond
Chalmers, Elektroteknik, Elkraftteknik
Alberto Varzi
Helmholtz Institute Ulm
Karlsruher Institut für Technologie (KIT)
Jianneng Liang
Karlsruher Institut für Technologie (KIT)
Helmholtz Institute Ulm
Maximilian Fichtner
Helmholtz Institute Ulm
Karlsruher Institut für Technologie (KIT)
ACS Energy Letters
23808195 (eISSN)
Vol. 10 11Ämneskategorier (SSIF 2025)
Materialkemi
Oorganisk kemi
DOI
10.1021/acsenergylett.5c02729