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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Kočí, Jan | Prague |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Gładysiak, Andrzej
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article
Compressed Arsenolite As4O6 and Its Helium Clathrate As4O6·2He
Abstract
The crystal structure of arsenolite, the cubic polymorph of molecular arsenic(III) oxide, has been determined by single-crystal X-ray diffraction up to 30 GPa. The bulk of the crystal is monotonically compressed with no detectable anomalies to 60% of the initial volume at 30 GPa. The experimental As4O6 crystal compression exceeds that obtained by various theoretical models within the density functional theory framework. The As4O6 molecules are deformed toward a more tetrahedral shape. A surprising property of arsenolite immersed in helium has been revealed above 3 GPa; the As4O6·2He clathrate is formed in the surface layer increasingly deeper with pressure. Interestingly, this is the first example of helium clathrate formed in situ with a solid molecular oxide and proof that helium may permeate even nonporous single crystals in high-pressure diffraction studies. This indicates it is an important and general phenomenon that needs to be taken into account when conducting high-pressure diffraction studies in helium.