Dynamics of Hydroxyl Anions Promotes Lithium Ion Conduction in Antiperovskite Li2OHCl

Li2OHCl is an exemplar of the antiperovskite family of ionic conductors, for which high ionic conductivities have been reported, but in which the atomic-level mechanism of ion migration is unclear. The stable phase is both crystallographically defective and disordered, having ∼1/3 of the Li sites va...

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Published inChemistry of materials Vol. 32; no. 19; pp. 8481 - 8491
Main Authors Wang, Fei, Evans, Hayden A, Kim, Kwangnam, Yin, Liang, Li, Yiliang, Tsai, Ping-Chun, Liu, Jue, Lapidus, Saul H, Brown, Craig M, Siegel, Donald J, Chiang, Yet-Ming
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 13.10.2020
American Chemical Society (ACS)
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Summary:Li2OHCl is an exemplar of the antiperovskite family of ionic conductors, for which high ionic conductivities have been reported, but in which the atomic-level mechanism of ion migration is unclear. The stable phase is both crystallographically defective and disordered, having ∼1/3 of the Li sites vacant, while the presence of the OH– anion introduces the possibility of rotational disorder that may be coupled to cation migration. Here, complementary experimental and computational methods are applied to understand the relationship between the crystal chemistry and ionic conductivity in Li2OHCl, which undergoes an orthorhombic to cubic phase transition near 311 K (≈38 °C) and coincides with the more than a factor of 10 change in ionic conductivity (from 1.2 × 10–5mS/cm at 37 °C to 1.4 × 10–3 mS/cm at 39 °C). X-ray and neutron experiments conducted over the temperature range 20–200 °C, including diffraction, quasi-elastic neutron scattering (QENS), the maximum entropy method (MEM) analysis, and ab initio molecular dynamics (AIMD) simulations, together show conclusively that the high lithium ion conductivity of cubic Li2OHCl is correlated to “paddlewheel” rotation of the dynamic OH– anion. The present results suggest that in antiperovskites and derivative structures a high cation vacancy concentration combined with the presence of disordered molecular anions can lead to high cation mobility.
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AC02-06CH11357; DMR-1419807
USDOE Office of Science (SC), Basic Energy Sciences (BES)
National Science Foundation (NSF)
F.W., H.A.E., and K.K. contributed equally to this work.
Author Contributions
ISSN:0897-4756
1520-5002
DOI:10.1021/acs.chemmater.0c02602