Discovery of Electron–NeutralElectrides withPressure-Induced Superconductivity

Abstract Electrides have been largely restricted to electron-rich compositions, leaving the applications of electron–neutral electrides scarcely explored and poorly understood. Here we report the discovery of an electron–neutral ternary electride, LiAlGe, which undergoes an unusual pressure-driven evolution: a semiconducting, nonelectride F4̅3m-LiAlGe phase at ambient conditions transforms into metallic electride phases, F4̅3m- (6.4–13.7 GPa) and Cmmm-LiAlGe phase (13.7–40.0 GPa). First-principles calculations further predict superconductivity in both high-pressure phases. To extend this concept, we combined high-throughput computation with machine learning (ML) to identify ten additional electron–neutral electrides adopting the LiAlGe-type topology. ML analysis reveals that the cooperative interplay between distinct cation species and their atomic radii is a key descriptor governing electride formation in ternary neutral systems. We synthesized LiAlGe and experimentally verified its high-pressure behavior. Synchrotron X-ray measurements confirmed the predicted F4̅3m to Cmmm transition at 14.3 GPa, in excellent agreement with the calculated 13.7 GPa. Importantly, both high-pressure phases were found to be superconducting under appropriate pressures, validating the theoretical predictions and establishing electron–neutral electrides as a previously overlooked class of superconducting materials.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-08-18
DOI
https://doi.org/10.1021/jacs.6c13689
Primary Topic
Ammonia Synthesis and Nitrogen Reduction
Type
article
Field-Weighted Citation Impact
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article

Discovery of Electron–NeutralElectrides withPressure-Induced Superconductivity

Hideo Hosono, Cuiying Pei, Vladislav A. Blatov, Junjie Wang et al.
Journal of the American Chemical Society
Ammonia Synthesis and Nitrogen Reduction
article

Discovery of Electron–NeutralElectrides withPressure-Induced Superconductivity

Hideo Hosono, Cuiying Pei, Vladislav A. Blatov, Junjie Wang, Yanpeng Qi, Jiahao Yu
article en

Abstract

Abstract Electrides have been largely restricted to electron-rich compositions, leaving the applications of electron–neutral electrides scarcely explored and poorly understood. Here we report the discovery of an electron–neutral ternary electride, LiAlGe, which undergoes an unusual pressure-driven evolution: a semiconducting, nonelectride F4̅3m-LiAlGe phase at ambient conditions transforms into metallic electride phases, F4̅3m- (6.4–13.7 GPa) and Cmmm-LiAlGe phase (13.7–40.0 GPa). First-principles calculations further predict superconductivity in both high-pressure phases. To extend this concept, we combined high-throughput computation with machine learning (ML) to identify ten additional electron–neutral electrides adopting the LiAlGe-type topology. ML analysis reveals that the cooperative interplay between distinct cation species and their atomic radii is a key descriptor governing electride formation in ternary neutral systems. We synthesized LiAlGe and experimentally verified its high-pressure behavior. Synchrotron X-ray measurements confirmed the predicted F4̅3m to Cmmm transition at 14.3 GPa, in excellent agreement with the calculated 13.7 GPa. Importantly, both high-pressure phases were found to be superconducting under appropriate pressures, validating the theoretical predictions and establishing electron–neutral electrides as a previously overlooked class of superconducting materials.

Journal of the American Chemical Society
Tokyo Institute of Technology (JP), Northwestern Polytechnical University (CN), National Institute for Materials Science (JP), ShanghaiTech University (CN), Samara State Technical University (RU), Northwestern Polytechnic University (US)
Openalex Percentile: Top 27%
Ammonia Synthesis and Nitrogen Reduction
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Discovery of Electron–NeutralElectrides withPressure-Induced Superconductivity — Hideo Hosono, Cuiying Pei, et al. · Journal of the American Chemical Society (2026) | TGRS Research Map | TGRS