Abstract
As a promising candidate for solid-state electrolytes in Li-ion batteries, the garnet-type Li-ion conductor series Li5+xLa3Nb2−xZrxO12 (LLNZO) (0 ≤ x ≤ 2) exhibits high ionic conductivity at room temperature. However, no previous single-crystal growth or characterization has been reported for LLNZO compositions 0 ≤ x ≤ 1. To obtain a complete understanding of the trend in the structure-property relationship in this class of materials, we used the floating zone (FZ) method to grow a single crystal of Li5.5La3Nb1.5Zr0.5O12 that was 4 mm in diameter and 10 mm in length. Using Laue neutron single-crystal diffraction, two distinct Li sites were observed: tetrahedral 24d and octahedral 96h sites. The maximum entropy method (MEM) based on neutron single-crystal diffraction data was used to map Li nuclear density and estimate that the bottleneck of Li transport exists between neighboring tetrahedral and octahedral sites, and that Li is delocalized between split octahedral sites. Room-temperature Li-ion conductivity in Li5.5La3Nb1.5Zr0.5O12 measured with electrochemical impedance spectroscopy (EIS) was 1.37 × 10−4 S cm−1. The Li migration activation energy was estimated to be 0.50 eV from EIS and 0.47 eV from dielectric relaxation measurements. The Li-ion jump attempt rate was estimated to be 1.47 × 1012 Hz while the time scale of successful migration is 10−7 to 10−6 s.
Original language | English |
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Pages (from-to) | 21754-21766 |
Number of pages | 13 |
Journal | Journal of Materials Chemistry A |
Volume | 11 |
Issue number | 40 |
DOIs | |
State | Published - Sep 25 2023 |
Externally published | Yes |
Funding
This work made use of the bulk crystal growth facility of the NSF's Platform for the Accelerated Realization, Analysis, and Discovery of Interface Materials (PARADIM), which is supported by the National Science Foundation under Cooperative Agreement No. DMR-2039380. C. R. and H. J. acknowledge funding provided by NSF Career Grant 2145832 and The University of Utah. Acknowledgement is made to the donors of the American Chemical Society Petroleum Research Fund for partial support of this research. A portion of this work was performed at the National High Magnetic Field Laboratory, which is supported by National Science Foundation Cooperative Agreement No. DMR-2128556, the State of Florida, and the U.S. Department of Energy. Research conducted at the Center for High-Energy X-ray Science (CHEXS) is supported by the National Science Foundation (BIO, ENG and MPS Directorates) under award DMR-1829070.
Funders | Funder number |
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National Science Foundation | DMR-2039380, 2145832 |
U.S. Department of Energy | DMR-1829070 |
American Chemical Society Petroleum Research Fund | DMR-2128556 |
University of Utah | |
State of Florida |