論文 Rigidity‐Driven Structural Isomers in the NaCl–Ga2S3 System: Implications for Energy Storage

Maria Bokova ORCID ; Mohammad Kassem ORCID ; Takeshi Usuki ; Andrey Tverjanovich ORCID ; Anton Sokolov ; Daniele Fontanari ; Alex C. Hannon ORCID ; Chris J. Benmore ORCID ; Igor Alekseev ; Shinji Kohara SAMURAI ORCID ; Pascal Roussel ORCID ; Maxim Khomenko ; Koji Ohara ORCID ; Yohei Onodera SAMURAI ORCID ; Arnaud Cuisset ORCID ; Eugene Bychkov ORCID

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引用
Maria Bokova, Mohammad Kassem, Takeshi Usuki, Andrey Tverjanovich, Anton Sokolov, Daniele Fontanari, Alex C. Hannon, Chris J. Benmore, Igor Alekseev, Shinji Kohara, Pascal Roussel, Maxim Khomenko, Koji Ohara, Yohei Onodera, Arnaud Cuisset, Eugene Bychkov. Rigidity‐Driven Structural Isomers in the NaCl–Ga2S3 System: Implications for Energy Storage. Small Science. 2024, (), 2400371. https://doi.org/10.48505/nims.4891

説明:

(abstract)

Alternative energy sources and energy storage, including all-solid-state batteries, require the search for innovative materials with promising functionalities. Systems with unusual chemical properties represent an insufficiently explored domain, concealing unexpected features. In particular, solids in eutectic systems typically undergo melting while preserving their chemical identity. Nevertheless, using diffraction and Raman spectroscopy over a wide temperature range, supported by first principles simulations, we unveil a rare phenomenon: phase-dependent chemical interactions between binary components in the NaCl-Ga2S3 system. In this unique occurrence, previously intact binary crystalline species transform upon melting into mixed liquid structural isomers, forming bonds with new partners. The chemical combinatorics, Na-Cl + Ga-S ⇄ Na-S + Ga-Cl, appears to be fully reversible for stable crystals and liquids. Despite this, rapidly frozen glasses out of thermodynamic equilibrium remain in a metastable isomeric state, offering remarkable properties, particularly a high room-temperature Na+ ion conductivity of 2.1 mS cm-1 with an activation energy of 0.249 eV, comparable to the best sodium halide superionic conductors and therefore encouraging for sodium solid-state batteries and energy applications. A rigidity paradigm is responsible for the observed phenomenon, as the extremely constrained Ga2S3 crystal lattice (with an average coordination 〈𝑟〉 = 3.2) does not survive viscous flow, breaking up at a short-range level. The removal of rigidity constraints and dense packing, approaching the optimally constrained disordered network with 〈𝑟〉 = 2.4, leads to a significant increase in empty space, as calculated using Dirichlet-Voronoi tessellation, which is the origin of high sodium diffusivity. Broadly, the rigidity-driven structural isomerism opens up an inspiring path to the discovery of atypical materials.

権利情報:

キーワード: all-solid-state batteries, neutron diffraction, X-ray diffraction

刊行年月日: 2024-10-01

出版者: Wiley

掲載誌:

  • Small Science (ISSN: 26884046) 2400371

研究助成金:

  • Campus France CPER ECRIN
  • Foundation for Promotion of Material Science and Technology of Japan 2017A1067
  • Foundation for Promotion of Material Science and Technology of Japan 2017B1771 and 2021B1197
  • U.S. Department of Energy DEAC02‐06CH11357

原稿種別: 著者最終稿 (Accepted manuscript)

MDR DOI: https://doi.org/10.48505/nims.4891

公開URL: https://doi.org/10.1002/smsc.202400371

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更新時刻: 2024-10-25 16:30:19 +0900

MDRでの公開時刻: 2024-10-25 16:30:20 +0900

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