离子
离子电导率
快离子导体
介电谱
固态核磁共振
魔角纺纱
电导率
电解质
无定形固体
电化学
结晶学
材料科学
中子衍射
离子键合
核磁共振波谱
化学
化学物理
分析化学(期刊)
物理化学
核磁共振
晶体结构
物理
电极
有机化学
作者
Pengbo Wang,Sawankumar V. Patel,Jason E. Roberts,Brian E. Francisco,Yan‐Yan Hu
出处
期刊:ACS materials letters
[American Chemical Society]
日期:2024-04-18
卷期号:6 (5): 2059-2064
被引量:1
标识
DOI:10.1021/acsmaterialslett.4c00488
摘要
Thiophosphates show promise as solid electrolytes for all-solid-state batteries (ASSBs), particularly Li3PS4-based materials, due to their cost-effectiveness and stability. To enhance conductivity for high-power applications, we developed affordable Li3PS4-LiCl (LPSCls) solid electrolytes with an ionic conductivity of ∼1.1 mS/cm (Li3PS4:LiCl = 2:1, 200 °C). Our study examines the long- and short-range structural order and ion dynamics of LPSCls, using neutron diffraction, magic-angle-spinning nuclear magnetic resonance (MAS NMR), and electrochemical impedance spectroscopy (EIS). 31P NMR reveals a unique disordered anion structure comprising a blend of Cl-modified β, γ, and amorphous PS43– units. Additionally, NMR relaxometry highlights enhanced Li+ mobility enabled by this diverse anion sublattice, allowing Li+ ions to migrate efficiently among different anions with similar affinity. Our findings unveil novel anion species within LPSCls, offering insights for optimizing ionic conductivity in solid electrolytes for ASSBs.
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