四方晶系
离子
原位
材料科学
相变
相(物质)
分析化学(期刊)
结晶学
凝聚态物理
化学
晶体结构
物理
色谱法
有机化学
作者
Vasiliki Faka,Martin Lange,Dominik Daisenberger,Thorben Böger,Xabier Martínez de Irujo-Labalde,M. Jewels Fallon,Gregor Kieslich,Wolfgang G. Zeier
标识
DOI:10.1021/acsmaterialslett.5c00593
摘要
The Na 3 Pn S 4 ( Pn = P, Sb) solid electrolytes are promising candidates for sodium solid-state batteries due to their potential high ionic conductivities. Structural modifications of these materials can induce a tetragonal-to-cubic phase transition, either by increasing temperature or by aliovalent substitutions. In this study, we introduce pressure as an alternative approach to observe the tetragonal-to-cubic phase transition in these materials. In situ synchrotron high-pressure powder X-ray diffraction shows a tetragonal-to-cubic phase transition at pressures of 2.9 GPa for Na 3 SbS 4 and 14.6 GPa for Na 3 PS 4 . Rietveld refinements and symmetry analysis provide insights into the displacive phase transition mechanism related to the motion of Na + and the rotation of the SbS 4 3– tetrahedra. Density functional theory calculations confirm that the cubic phase becomes thermodynamically favorable under high pressure compared to the tetragonal phase. These findings highlight the importance of high-pressure considerations in tailoring the properties of ionic conductors, an area that remains underexplored.
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