Lithium ion conductivity in Li2S–P2S5 glasses – building units and local structure evolution during the crystallization of superionic conductors Li3PS4, Li7P3S11 and Li4P2S7. Issue 34 (16th August 2017)

• Record Type: Journal Article
• Authors: Dietrich, Christian; Weber, Dominik A.; Sedlmaier, Stefan J.; Indris, Sylvio; Culver, Sean P.; Walter, Dirk; Janek, Jürgen; Zeier, Wolfgang G.
• Is Part Of: Journal of materials chemistry. Volume 5:Issue 34(2017)
• Page Start: 18111
• Page End: 18119
• Publication Date: 2017-08-16
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c7ta06067j
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : The local structure phase diagram of (Li2 S) x (P2 S5 )100− x thiophosphates derived from pair distribution function crystallization experiments. Abstract : Motivated by the high lithium ion conductivities of lithium thiophosphate glasses, a detailed study is performed on the local chemical nature of the thiophosphate building units within these materials. Using Raman and 31 P MAS NMR (Magic Angle Spinning – Nuclear Magnetic Resonance) spectroscopy, the continuous change from dominant P2 S7 4− (di-tetrahedral) anions to PS4 3− (mono-tetrahedral) anions with increasing Li2 S fraction in the (Li2 S) x (P2 S5 )(100− x ) glasses is observed. In addition, synchrotron pair distribution function analysis (PDF) of synchrotron X-ray total scattering data is employed to monitor in situ crystallization and phase evolution in this class of materials. Depending on the composition, different crystalline phases evolve, which possess different decomposition temperatures into less conducting phases. The results highlight the critical influence of the local anionic building units on the cation mobility and thermal stability, with PS4 3− tetrahedra forming the most thermally robust glass ceramics with the highest ionic conductivity.