Long-range Li+ dynamics in the lithium argyrodite Li7PSe6 as probed by rotating-frame spin-lattice relaxation NMR

被引:80
作者
Epp, V. [1 ]
Gun, O. [2 ]
Deiseroth, H. -J. [2 ]
Wilkening, M. [1 ]
机构
[1] Graz Univ Technol, Inst Chem & Technol Mat, Christian Doppler Lab Lithium Ion Batteries, A-8010 Graz, Austria
[2] Univ Siegen, D-57068 Siegen, Germany
关键词
NUCLEAR-MAGNETIC-RESONANCE; SOLID-STATE NMR; ION DYNAMICS; DIFFUSION PARAMETERS; LI-7; SPECTROSCOPY; CONDUCTIVITY; ELECTROLYTES; CONDUCTORS; CHALLENGES;
D O I
10.1039/c3cp44379e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Lithium-rich argyrodites belong to a relatively new group of fast ion conducting solids. They might serve as powerful electrolytes in all-solid-state lithium-ion batteries being, from a medium-term point of view, the key technology when safe energy storage systems have to be developed. Spin-lattice relaxation (SLR) nuclear magnetic resonance (NMR) measurements carried out in the rotating frame of reference turned out to be the method of choice to study Li dynamics in argyrodites. When plotted as a function of the inverse temperature, the SLR rates log(10)(R-1 rho) reveal an asymmetric diffusion-induced rate peak. The rate peak contains information on the Li jump rate, the activation energy of the hopping process as well as correlation effects. In particular, considering the high-temperature flank of the SLR NMR rate peak recorded in the rotating frame of reference, an activation energy of approximately 0.49 eV is found. This value represents long-range lithium jump diffusion in crystalline Li7PSe6. As an example, at 325 K the Li jump rate determined from SLR NMR is in the order of 1.4 x 10(5) s(-1). The pronounced asymmetry of the rate peak R-1 rho(1/T) points to correlated Li motion. It is comparable to that which is typically found for structurally disordered materials showing a broad range of correlation
引用
收藏
页码:7123 / 7132
页数:10
相关论文
共 75 条
[11]   Solid-state LiNMR with applications to the translational dynamics in ion conductors [J].
Boehmer, R. ;
Jeffrey, K. R. ;
Vogel, M. .
PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY, 2007, 50 (2-3) :87-174
[12]   Multiple-time correlation functions in spin-3/2 solid-state NMR spectroscopy [J].
Böhmer, R .
JOURNAL OF MAGNETIC RESONANCE, 2000, 147 (01) :78-88
[13]   Stimulated 7Li echo NMR spectroscopy of slow ionic motions in a solid electrolyte [J].
Böhmer, R ;
Jörg, T ;
Qi, F ;
Titze, A .
CHEMICAL PHYSICS LETTERS, 2000, 316 (5-6) :419-424
[14]   Mechanochemical synthesis of Li-argyrodite Li6PS5X (X = Cl, Br, I) as sulfur-based solid electrolytes for all solid state batteries application [J].
Boulineau, Sylvain ;
Courty, Matthieu ;
Tarascon, Jean-Marie ;
Viallet, Virginie .
SOLID STATE IONICS, 2012, 221 :1-5
[15]   NMR Multi-Time Correlation Functions of Ion Dynamics in Solids [J].
Brinkmann, Christian ;
Faske, Sandra ;
Koch, Barbara ;
Vogel, Michael .
ZEITSCHRIFT FUR PHYSIKALISCHE CHEMIE-INTERNATIONAL JOURNAL OF RESEARCH IN PHYSICAL CHEMISTRY & CHEMICAL PHYSICS, 2010, 224 (10-12) :1535-1553
[16]   NMR-STUDIES OF SUPERIONIC CONDUCTORS [J].
BRINKMANN, D .
PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY, 1992, 24 :527-552
[17]  
Bunde A., 2005, Diffusion in Condensed Matter, P813
[18]   Structure and dynamics of the fast lithium ion conductor "Li7La3Zr2O12" [J].
Buschmann, Henrik ;
Doelle, Janis ;
Berendts, Stefan ;
Kuhn, Alexander ;
Bottke, Patrick ;
Wilkening, Martin ;
Heitjans, Paul ;
Senyshyn, Anatoliy ;
Ehrenberg, Helmut ;
Lotnyk, Andriy ;
Duppel, Viola ;
Kienle, Lorenz ;
Janek, Juergen .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2011, 13 (43) :19378-19392
[19]   Li6PS5X:: A class of crystalline Li-rich solids with an unusually high Li+ mobility [J].
Deiseroth, Hans-Joerg ;
Kong, Shiao-Tong ;
Eckert, Hellmut ;
Vannahme, Julia ;
Reiner, Christof ;
Zaiss, Torsten ;
Schlosser, Marc .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (04) :755-758
[20]   Fast Li diffusion in crystalline LiBH4 due to reduced dimensionality: Frequency-dependent NMR spectroscopy [J].
Epp, V. ;
Wilkening, M. .
PHYSICAL REVIEW B, 2010, 82 (02)