The structural and morphological changes of the Lithium superionic conductor Li GeP S , prepared via a widely used ball milling-heating method over a comprehensive heat treatment range (50 - 700 °C), are investigated. Based on the phase composition, the formation process can be distinctly separated into four zones: Educt, Intermediary, Formation, and Decomposition zone. It is found that instead of Li GeS -Li PS binary crystallization process, diversified intermediate phases, including GeS in different space groups, multiphasic lithium phosphosulfides (Li P S ), and cubic Li Ge PS phase, are involved additionally during the formation and decomposition of Li GeP S . Furthermore, the phase composition at temperatures around the transition temperatures of different formation zones shows a significant deviation. At 600 °C, Li GeP S is fully crystalline, while the sample decomposed to complex phases at 650 °C with 30 wt.% impurities, including 20 wt.% amorphous phases. These findings over such a wide temperature range are first reported and may help provide previously lacking insights into the formation and crystallinity control of Li GeP S .
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http://dx.doi.org/10.1002/smll.202300850 | DOI Listing |
Adv Sci (Weinh)
December 2024
Department of Chemistry and Biochemistry, Florida State University, Tallahassee, FL, 32306, USA.
Localized atomistic disorder in halide-based solid electrolytes (SEs) can be leveraged to boost Li mobility. In this study, Li transport in structurally modified LiHoCl, via Br introduction and Li deficiency, is explored. The optimized Li Ho Cl Br achieves an ionic conductivity of 3.
View Article and Find Full Text PDFNat Nanotechnol
November 2024
Department of Mechanical and Materials Engineering, Western University, London, Ontario, Canada.
The advancement of all-solid-state lithium metal batteries requires breakthroughs in solid-state electrolytes (SSEs) for the suppression of lithium dendrite growth at high current densities and high capacities (>3 mAh cm) and innovation of SSEs in terms of crystal structure, ionic conductivity and rigidness. Here we report a superionic conducting, highly lithium-compatible and air-stable vacancy-rich β-LiN SSE. This vacancy-rich β-LiN SSE shows a high ionic conductivity of 2.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
Department of Electrical and Electronic Information Engineering, Toyohashi University of Technology, 1-1 Hibarigaoka, Tenpaku-cho, Aichi 441-8580, Japan.
The lithium thiophosphate group of solid electrolytes (SEs) is considered one of the best lithium-ion conductors that could be compatible with liquid electrolytes. However, the interface stability of lithium thiophosphate SEs against the lithium anode and oxide cathode could be a challenge due to severe degradation over charge-discharge cycles. In this study, we aim to analyze and introduce the addition of halides into lithium thiophosphate SEs with a molar ratio of 3LiPS to 1LiM (M = Cl, Br, I) in order not only to improve ion conductivity but also to increase the interface stability of the SEs.
View Article and Find Full Text PDFSmall
November 2024
CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing, 100190, P. R. China.
Silicon is a promising anode material candidate but encounters volume change and capacity decay issues. Although diverse demonstrations in structural and interfacial engineering, the performance toward industrial applications remains to be improved. Herein, a controlled interfacial tailoring strategy is proposed for micro-nano hierarchically structured silicon.
View Article and Find Full Text PDFChemSusChem
November 2024
State Key Laboratory of Advanced Electromagnetic Technology, School of Electrical and Electronic Engineering, Huazhong University of Science and Technology, Wuhan, 430074, China.
Chlorine-rich lithium argyrodite is considered as a promising superionic conductor electrolyte, but its practical application is limited due to poor air stability and instability toward lithium metal. In this work, BiF is proposed as a multi-functional dopant for electrolyte modification, and the effects on the ionic conductivity, air stability, critical current density, and electrolyte/Li metal interfacial stability are studied. The results show that the doped electrolyte LiPBiSClF (LPBiSClF) still maintains a relatively high ionic conductivity of 5.
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