TY - JOUR
T1 - Ultrahigh-pressure polyamorphism in GeO2 glass with coordination number >6
AU - Kono, Yoshio
AU - Kenney-Benson, Curtis
AU - Ikuta, Daijo
AU - Shibazaki, Yuki
AU - Wang, Yanbin
AU - Shen, Guoyin
AU - Navrotsky, Alexandra
N1 - Funding Information:
ACKNOWLEDGMENTS. We acknowledge two anonymous reviewers for valuable comments. This study was performed at HPCAT (Sector 16), Advanced Photon Source, Argonne National Laboratory. This research is supported by Department of Energy (DOE)-National Nuclear Security Administration under Award DE-NA0001974 and DOE-Office of Basic Energy Sciences under Award DE-FG02-99ER45775. Advanced Photon Source is a US DOE Office of Science User Facility operated for the DOE Office of Science by Argonne National Laboratory under Contract DE-AC02-06CH11357. The PE cell program is partly supported by GeoSoilEnviroCARS, which is supported by the National Science Foundation-Earth Sciences (EAR-1128799) and Department of Energy-GeoSciences (DE-FG02-94ER14466). Y.W. acknowledges support from National Science Foundation EAR-1214376.
PY - 2016/3/29
Y1 - 2016/3/29
N2 - 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.
AB - 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.
KW - Glass
KW - High pressure
KW - Oxygen packing
KW - Polyamorphism
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U2 - 10.1073/pnas.1524304113
DO - 10.1073/pnas.1524304113
M3 - Article
AN - SCOPUS:84962128039
SN - 0027-8424
VL - 113
SP - 3436
EP - 3441
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 13
ER -