Unexpected compound reformation in the dense selenium-hydrogen system

The H 2 Se molecule and the van der Waals compound (H 2 Se) 2 H 2 are both unstable upon room temperature compression, dissociating into their constituent elements above 22 GPa. Through a series of high pressure-high temperature diamond anvil cell experiments, we report the unexpected formation of a...

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Published inCommunications materials Vol. 6; no. 1; pp. 193 - 7
Main Authors Hu, Huixin, Kuzovnikov, Mikhail A., Shuttleworth, Hannah A., Marqueño, Tomas, Yan, Jinwei, Osmond, Israel, Gorelli, Federico A., Gregoryanz, Eugene, Dalladay-Simpson, Philip, Ackland, Graeme J., Peña-Alvarez, Miriam, Howie, Ross T.
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Published London Nature Publishing Group UK 01.12.2025
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Abstract The H 2 Se molecule and the van der Waals compound (H 2 Se) 2 H 2 are both unstable upon room temperature compression, dissociating into their constituent elements above 22 GPa. Through a series of high pressure-high temperature diamond anvil cell experiments, we report the unexpected formation of a novel compound, SeH 2 (H 2 ) 2 at pressures above 94 GPa. X-ray diffraction reveals the metallic sublattice to adopt a tetragonal ( I 4 1 / a m d ) structure with density functional theory calculations finding a small distortion due to the orientation of H 2 molecules. The structure comprises of a network of zig-zag H-Se chains with quasi-molecular H 2 molecular units hosted in the prismatic Se interstices. Electrical resistance measurements demonstrate that SeH 2 (H 2 ) 2 is non-metallic up to pressures of 148 GPa. Investigations into the Te-H system up to pressures of 165 GPa and 2000 K yielded no compound formation. The combined results suggest that the high pressure phase behavior of each chalcogen hydride is unique and more complex than previously thought. High-pressure studies of chalcogen hydrides reveal complex phase behaviors, challenging existing assumptions about their stability and composition. Here, the authors discover a novel compound, SeH 2 (H 2 ) 2 , at pressures above 94 GPa, characterized by a unique tetragonal structure, highlighting the intricate nature of high-pressure chemistry and its implications for material science.
AbstractList The H 2 Se molecule and the van der Waals compound (H 2 Se) 2 H 2 are both unstable upon room temperature compression, dissociating into their constituent elements above 22 GPa. Through a series of high pressure-high temperature diamond anvil cell experiments, we report the unexpected formation of a novel compound, SeH 2 (H 2 ) 2 at pressures above 94 GPa. X-ray diffraction reveals the metallic sublattice to adopt a tetragonal ( I 4 1 / a m d ) structure with density functional theory calculations finding a small distortion due to the orientation of H 2 molecules. The structure comprises of a network of zig-zag H-Se chains with quasi-molecular H 2 molecular units hosted in the prismatic Se interstices. Electrical resistance measurements demonstrate that SeH 2 (H 2 ) 2 is non-metallic up to pressures of 148 GPa. Investigations into the Te-H system up to pressures of 165 GPa and 2000 K yielded no compound formation. The combined results suggest that the high pressure phase behavior of each chalcogen hydride is unique and more complex than previously thought. High-pressure studies of chalcogen hydrides reveal complex phase behaviors, challenging existing assumptions about their stability and composition. Here, the authors discover a novel compound, SeH 2 (H 2 ) 2 , at pressures above 94 GPa, characterized by a unique tetragonal structure, highlighting the intricate nature of high-pressure chemistry and its implications for material science.
Abstract The H2Se molecule and the van der Waals compound (H2Se)2H2 are both unstable upon room temperature compression, dissociating into their constituent elements above 22 GPa. Through a series of high pressure-high temperature diamond anvil cell experiments, we report the unexpected formation of a novel compound, SeH2(H2)2 at pressures above 94 GPa. X-ray diffraction reveals the metallic sublattice to adopt a tetragonal (I41/a m d) structure with density functional theory calculations finding a small distortion due to the orientation of H2 molecules. The structure comprises of a network of zig-zag H-Se chains with quasi-molecular H2 molecular units hosted in the prismatic Se interstices. Electrical resistance measurements demonstrate that SeH2(H2)2 is non-metallic up to pressures of 148 GPa. Investigations into the Te-H system up to pressures of 165 GPa and 2000 K yielded no compound formation. The combined results suggest that the high pressure phase behavior of each chalcogen hydride is unique and more complex than previously thought.
The H2Se molecule and the van der Waals compound (H2Se)2H2 are both unstable upon room temperature compression, dissociating into their constituent elements above 22 GPa. Through a series of high pressure-high temperature diamond anvil cell experiments, we report the unexpected formation of a novel compound, SeH2(H2)2 at pressures above 94 GPa. X-ray diffraction reveals the metallic sublattice to adopt a tetragonal (I41/amd) structure with density functional theory calculations finding a small distortion due to the orientation of H2 molecules. The structure comprises of a network of zig-zag H-Se chains with quasi-molecular H2 molecular units hosted in the prismatic Se interstices. Electrical resistance measurements demonstrate that SeH2(H2)2 is non-metallic up to pressures of 148 GPa. Investigations into the Te-H system up to pressures of 165 GPa and 2000 K yielded no compound formation. The combined results suggest that the high pressure phase behavior of each chalcogen hydride is unique and more complex than previously thought.High-pressure studies of chalcogen hydrides reveal complex phase behaviors, challenging existing assumptions about their stability and composition. Here, the authors discover a novel compound, SeH2(H2)2, at pressures above 94 GPa, characterized by a unique tetragonal structure, highlighting the intricate nature of high-pressure chemistry and its implications for material science.
The H 2 Se molecule and the van der Waals compound (H 2 Se) 2 H 2 are both unstable upon room temperature compression, dissociating into their constituent elements above 22 GPa. Through a series of high pressure-high temperature diamond anvil cell experiments, we report the unexpected formation of a novel compound, SeH 2 (H 2 ) 2 at pressures above 94 GPa. X-ray diffraction reveals the metallic sublattice to adopt a tetragonal ( I 4 1 / a m d ) structure with density functional theory calculations finding a small distortion due to the orientation of H 2 molecules. The structure comprises of a network of zig-zag H-Se chains with quasi-molecular H 2 molecular units hosted in the prismatic Se interstices. Electrical resistance measurements demonstrate that SeH 2 (H 2 ) 2 is non-metallic up to pressures of 148 GPa. Investigations into the Te-H system up to pressures of 165 GPa and 2000 K yielded no compound formation. The combined results suggest that the high pressure phase behavior of each chalcogen hydride is unique and more complex than previously thought.
ArticleNumber 193
Author Kuzovnikov, Mikhail A.
Shuttleworth, Hannah A.
Marqueño, Tomas
Dalladay-Simpson, Philip
Ackland, Graeme J.
Peña-Alvarez, Miriam
Hu, Huixin
Osmond, Israel
Gregoryanz, Eugene
Howie, Ross T.
Yan, Jinwei
Gorelli, Federico A.
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Snippet The H 2 Se molecule and the van der Waals compound (H 2 Se) 2 H 2 are both unstable upon room temperature compression, dissociating into their constituent...
The H 2 Se molecule and the van der Waals compound (H 2 Se) 2 H 2 are both unstable upon room temperature compression, dissociating into their constituent...
The H2Se molecule and the van der Waals compound (H2Se)2H2 are both unstable upon room temperature compression, dissociating into their constituent elements...
Abstract The H2Se molecule and the van der Waals compound (H2Se)2H2 are both unstable upon room temperature compression, dissociating into their constituent...
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SubjectTerms 639/301/119/1002
639/638/440/94
639/766/119/2795
Chemistry and Materials Science
Decomposition
Density functional theory
Diamond anvil cells
High pressure
High temperature
Hydrides
Hydrogen
Interstices
Lasers
Materials Science
Molecular chains
Phase transitions
Room temperature
Selenium
Spectrum analysis
Superconductivity
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Title Unexpected compound reformation in the dense selenium-hydrogen system
URI https://link.springer.com/article/10.1038/s43246-025-00899-9
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https://pubmed.ncbi.nlm.nih.gov/PMC12370533
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Volume 6
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