Remarkably Stable Glassy GeS Densified at 8.3 GPa: Hidden Polyamorphism, Contrasting Optical Properties, Raman and DFT Studies, and Advanced Applications.

Glassy GeS, densified at 8.3 GPa, exhibits a strongly reduced bandgap, predominantly tetrahedral Ge environment, enhanced chemical disorder and partial 3-fold coordination of both germanium and sulfur, assuming two possible reaction paths under high pressure: (i) a simple dissociation 2Ge-S ⇄ Ge-Ge + S-S and (ii) a chemical disproportionation GeS ⇄ GeS + S. The observed electronic and structural changes remain intact for at least seven years under ambient conditions but are gradually evolving upon heating.

Pressure-Driven Chemical Disorder in Glassy AsS up to 14.7 GPa, Postdensification Effects, and Applications in Materials Design.

A small difference in energy between homopolar and heteropolar bonds and the glass-forming ability of pure chalcogens leads to unexpected trends in densification mechanisms of glassy chalcogenides compared to vitreous oxides. Using high-precision compressibility measurements and in situ high-energy X-ray diffraction up to 14.7 GPa, we show a new densification route in a canonical glass AsS.

Direct Volumetric Study of High-Pressure Driven Polyamorphism and Relaxation in the Glassy Germanium Chalcogenides.

High precision measurements were taken of the specific volume of glassy germanium chalcogenides GeSe2, GeS2, Ge17Se83, and Ge8Se92 under hydrostatic pressure to 8.5 GPa. For GeSe2 and GeS2 glasses in the pressure range to 3 GPa the behavior is an elastic one with bulk modulus softening at pressures above 2 GPa.

Nature of the structural transformations in B2O3 glass under high pressure.

We study high-pressure polyamorphism of B2O3 glass using x-ray diffraction up to 10 GPa in the 300-700 K temperature range, in situ volumetric measurements up to 9 GPa, and first-principles simulations. Under pressure, glass undergoes two-stage transformations including a gradual increase of the first B-O (O-B) coordination numbers above 5 GPa. The fraction of boron atoms in the fourfold-coordinated state at P<10 GPa is smaller than was assumed from inelastic x-ray scattering spectroscopy data, but is considerably larger than was previously suggested by the classical molecular dynamics simulations.

Pressure-induced structural transformation in radiation-amorphized zircon.

We study the response of a radiation-amorphized material to high pressure. We have used zircon ZrSiO4 amorphized by natural radiation over geologic times, and have measured its volume under high pressure, using the precise strain-gauge technique. On pressure increase, we observe apparent softening of the material, starting from 4 GPa.