ジャーナル論文 Li Jump Diffusion and Long-Range Transport in Garnet Single Crystals: Spanning the kHz–GHz Range
Jana Königsreiter (author) (この著者で検索)
;
Jonas Spychala (author) (この著者で検索)
ORCID ;
Gergö Horvath (author) (この著者で検索)
;
Kunimitsu Kataoka (author) (この著者で検索)
ORCID ;
Florian Stainer (author) (この著者で検索)
ORCID ; ORCID SAMURAI ;
H. Martin R. Wilkening (author) (この著者で検索)
ORCID
コレクション

引用
Jana Königsreiter, Jonas Spychala, Gergö Horvath, Kunimitsu Kataoka, Florian Stainer, Junji Akimoto, H. Martin R. Wilkening. Li Jump Diffusion and Long-Range Transport in Garnet Single Crystals: Spanning the kHz–GHz Range. Chemistry of Materials. 2026, 38 (14), 7254-7266. https://doi.org/10.1021/acs.chemmater.6c00979

説明:

(abstract)

Understanding and controlling Li-ion transport in garnet-type oxides is central to advancing solid electrolytes for all-solid-state energy storage systems. Garnet electrolytes have long been recognized for their high ionic conductivity, and the availability of large single crystals now enables a direct, frequency-resolved view of Li-ion dynamics over a broad time window. In such structurally and chemically homogeneous systems, responses from electrical and nuclear magnetic resonance measurements are expected to align, yielding a consistent picture of frequency-dependent Li-ion hopping processes. Here, we investigate single-crystalline Li6.5La3Zr1.5Ta0.5O12 and probe ion dynamics from the kHz to GHz range using a combination of 7Li nuclear spin relaxation (NSR) and electrical conductivity spectroscopy. Long-range transport (5 × 10–4 S cm–1 at 293 K) is consistently described by activation energies in the range of 0.41 to 0.47 eV, whereas localized ion dynamics, observed, e.g., by laboratory-frame NSR, are associated with much lower barriers of approximately 0.22 eV. In comparison with single-crystalline Li6La3ZrTaO12, which exhibits reduced ionic mobility, we propose that changes in ionic mobility are compensated by a higher effective charge-carrier concentration Nc in systems with lower Li contents. For Li6.5La3Zr1.5Ta0.5O12, the Li+ mobility is higher by approximately 1 order of magnitude; however, the resulting conductivity only slightly exceeds that of Li6La3ZrTaO12, presumably due to a lower density of mobile charge carriers. This finding highlights that Nc is a key parameter to consider in these systems that indeed sensitively governs the practical ionic conductivity.

権利情報:

キーワード: lithium, dynamics, diffusion, NMR, solid electrolytes, garnet, single crystals

刊行年月日: 2026-07-28

出版者: American Chemical Society (ACS)

掲載誌:

  • Chemistry of Materials (ISSN: 08974756) vol. 38 issue. 14 p. 7254-7266

研究助成金:

  • Austrian Science Fund 10.55776/ESP1533525
  • German Research Council (DFG) WI3600 4-1

原稿種別: 出版者版 (Version of record)

MDR DOI:

公開URL: https://doi.org/10.1021/acs.chemmater.6c00979

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更新時刻: 2026-07-29 09:34:13 +0900

MDRでの公開時刻: 2026-07-29 12:29:21 +0900

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