With a Little Help from 31P NMR: From Localized Hopping to Long-Range Li+ Transport in Argyrodite-Type Li6PS5I

Activity: Talk or presentationTalk at workshop, seminar or courseScience to science

Description

Li6PS5I acts as a perfect model substance to study length-scale dependent diffusion parameters in an ordered matrix. It provides Li-rich cages which offer rapid, but localized Li+ translational jump processes. As jumps between these cages are assumed to be much less frequent, long-range ion transport is sluggish resulting in ionic conductivities in the order of 10−6 S cm−1 at room temperature [1]. In contrast, the site disordered analogues Li6PS5X (X= Br, Cl) are known as fast ion conductors as structural disorder facilities intercage dynamics [1]. As yet, the two extremely distinct jump processes in Li6PS5I have not been visualized separately.
Here, we used a combination of 31P and 7Li NMR relaxation measurements to probe this bimodal dynamic behavior, that is, ultrafast intracage Li+ hopping and the much slower Li+ intercage exchange process. While the first is to be characterized by an activation energy of ca. 0.2 eV as directly measured by 7Li NMR [1,2], the latter is best observed indirectly by 31P NMR pointing to an activation energy of 0.44 eV. This value perfectly agrees with that probed by direct current conductivity spectroscopy being sensitive to long-range ion transport for which the intercage jumps are the rate limiting step.
Moreover, also quantitative agreement in terms of diffusion coefficients is observed. The solid-state diffusion coefficient Dσ obtained from conductivity spectroscopy agrees very well with that from 31P NMR (DNMR ≈ 4.6  10−15 cm2 s−1). DNMR was directly extracted from the pronounced diffusion-controlled 31P NMR spin-lock spin-lattice relaxation peak appearing at 366 K. The influence of rotational jump processes of the PS43- polyanions on Li+ dynamics (and vice versa) is discussed as well [2,3]. In conclusion, cation and anion site disorder in the Li6PS5X family is the key property to understand the extraordinarily high ionic conductivities seen for the samples with X = Br, Cl [4].
[1] I. Hanghofer, M. Brinek, S. L. Eisbacher, B. Bitschnau, M. Volck, V. Hennige, I. Hanzu, D. Rettenwander, H. M. R. Wilkening, Phys. Chem. Chem. Phys. 21 (2019) 8489.
[2] I. Hanghofer, B. Gadermaier, and H. M. R. Wilkening, Chem. Mater. 31 (2019) 4591.
[3] M. Brinek, C. Hiebl, K. Hogrefe, I. Hanghofer, and H. M. R. Wilkening, J. Phys. Chem. C 124 (2020) 22934.
[4] M. Gombotz, K. Hogrefe, R. Zettl, B. Gadermaier, and H. M. R. Wilkening, Phil. Trans. A, 2021, in press.
Period14 Sep 2021
Event title1st Energy Landscapes and Structure of Ion Conducting Solids Workshop and Bunsen-Kolloquium
Event typeWorkshop
LocationMarburg, Germany
Degree of RecognitionInternational