Defect chemistry of disordered solid-state electrolyte Li10GeP2S12. Issue 7 (3rd February 2020)

• Record Type: Journal Article
• Authors: Gorai, Prashun; Long, Hai; Jones, Eric; Santhanagopalan, Shriram; Stevanović, Vladan
• Is Part Of: Journal of materials chemistry. Volume 8:Issue 7(2020)
• Page Start: 3851
• Page End: 3858
• Publication Date: 2020-02-03
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c9ta10964a
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : Most solid-state electrolytes exhibit significant structural disorder, which requires careful consideration when modeling the defect energetics. Here, we model the native defect chemistry of a disordered solid electrolyte, Li10 GeP2 S12 . Abstract : Several classes of materials, including thiophosphates, garnets, argyrodites, and anti-perovskites, have been considered as electrolytes for all-solid-state batteries. Native point defects and dopants play a critical role in impeding or facilitating fast ion conduction in these solid electrolytes. Despite its significance, comprehensive studies of the native defect chemistry of well-known solid electrolytes is currently lacking, in part due their compositional and structural complexity. Most of these solid-state electrolytes exhibit significant structural disorder, which requires careful consideration when modeling the point defect energetics. In this work, we model the native defect chemistry of a disordered solid electrolyte, Li10 GeP2 S12 (LGPS), by uniquely combining ensemble statistics, accurate electronic structure, and modern first-principles defect calculations. We find that VLi, Lii, and PGe are the dominant defects. From these calculations, we determine the statistics of defect energetics; formation energies of the dominant defects vary over ∼140 meV. Combined with previously reported ab initio molecular dynamics simulations, we find that anti-sites PGe promote Li ion conductivity, suggesting LGPS growth under P-rich/Ge-poor conditions will enhance ion conductivity. To this end, we offer practical experimental guides to enhance ion conductivity.