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Updated: Mar 24, 2026

High Pressure Single Crystal Diffraction at PX^2
Published on: January 16, 2017
Ultrahigh-pressure polyamorphism in GeO2 glass with coordination number >6
Yoshio Kono1, Curtis Kenney-Benson2, Daijo Ikuta2
1High Pressure Collaborative Access Team, Geophysical Laboratory, Carnegie Institution of Washington, Argonne, IL 60439; ykono@ciw.edu.
Abstract:
Knowledge of pressure-induced structural changes in glasses is important in various scientific fields as well as in engineering and industry. However, polyamorphism in glasses under high pressure remains poorly understood because of experimental challenges. Here we report new experimental findings of ultrahigh-pressure polyamorphism in GeO2 glass, investigated using a newly developed double-stage large-volume cell. The Ge-O coordination number (CN) is found to remain constant at ∼6 between 22.6 and 37.9 GPa. At higher pressures, CN begins to increase rapidly and reaches 7.4 at 91.7 GPa. This transformation begins when the oxygen-packing fraction in GeO2 glass is close to the maximal dense-packing state (the Kepler conjecture = ∼0.74), which provides new insights into structural changes in network-forming glasses and liquids with CN higher than 6 at ultrahigh-pressure conditions.
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