Boosting Ionic Conductivity and Air Stability in Bromide-Rich Thioarsenate Argyrodite Solid Electrolytes

Journal Article (2025)
Author(s)

Ruihua Zhou (Wuhan University of Technology)

Ajay Gautam (TU Delft - RST/Storage of Electrochemical Energy)

Emmanuelle Suard (Institut Laue Langevin)

Shenghao Li (Wuhan University of Technology)

Swapna Ganapathy (TU Delft - RST/Storage of Electrochemical Energy)

Kai Chen (Qingtao Energy Development Inc.)

Xin Zhang (Wuhan University of Technology)

Ce Wen Nan (Tsinghua University)

Shuo Wang (Wuhan University of Technology)

Marnix Wagemaker (TU Delft - RST/Storage of Electrochemical Energy)

DOI related publication
https://doi.org/10.1002/adfm.202420971 Final published version
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Publication Year
2025
Language
English
Bibliographical Note
Green Open Access added to TU Delft Institutional Repository 'You share, we take care!' - Taverne project https://www.openaccess.nl/en/you-share-we-take-care Otherwise as indicated in the copyright section: the publisher is the copyright holder of this work and the author uses the Dutch legislation to make this work public.
Journal title
Advanced Functional Materials
Issue number
20
Volume number
35
Article number
2420971
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Abstract

Lithium argyrodite thiophosphate superionic conductors are being explored as promising solid electrolytes for all-solid-state batteries, primarily due to their high ionic conductivity and ease of processing. Yet, these electrolytes present challenges such as chemical instability in humid conditions and incompatibility with cathode materials. Although some lithium argyrodites show improved air stability, their ionic conductivity deteriorates below the practically required value. Herein, based on hard soft acid base theory, a new family of lithium argyrodite, as solid solution Li6−xAsS5−xBr1+x (for 0.0 ≤ x ≤ 0.6), has been proposed to address these issues. Through a combination of neutron diffraction, NMR spectroscopy, and electrochemical impedance spectroscopy, it has been determined that the partial substitution of S2− by Br− weakens interactions within the Li+ “cage”, facilitating long lithium-ion movement throughout the structure. An additional T4 Li+ site is identified, offering a lower energy barrier for inter-cage jumps. Consequently, the Li5.5AsS4.5Br1.5 member of the composition series exhibits a higher Li-ion diffusivity resulting in a remarkable ionic conductivity of 15.4 mS cm−1. Compared with lithium thiophosphates, the Li5.5AsS4.5Br1.5 also shows excellent air stability. This research opens a new avenue for developing air-stable sulfide solid electrolytes with high ionic conductivity necessitated for practical application in solid-state batteries.

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