Kono Yoshio, Kenney-Benson Curtis, Ikuta Daijo, Shibazaki Yuki, Wang Yanbin, Shen Guoyin
High Pressure Collaborative Access Team, Geophysical Laboratory, Carnegie Institution of Washington, Argonne, IL 60439;
Frontier Research Institute for Interdisciplinary Sciences, Tohoku University, Aoba-ku, Sendai 980-8578, Japan;
Proc Natl Acad Sci U S A. 2016 Mar 29;113(13):3436-41. doi: 10.1073/pnas.1524304113. Epub 2016 Mar 14.
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.
了解玻璃中压力诱导的结构变化在各个科学领域以及工程和工业中都很重要。然而,由于实验挑战,高压下玻璃中的多晶型现象仍知之甚少。在这里,我们报告了使用新开发的双级大体积单元对GeO2玻璃中的超高压多晶型现象进行研究的新实验结果。发现Ge-O配位数(CN)在22.6至37.9 GPa之间保持在约6不变。在更高的压力下,CN开始迅速增加,并在91.7 GPa时达到7.4。当GeO2玻璃中的氧堆积分数接近最大密堆积状态(开普勒猜想=约0.74)时,这种转变开始,这为超高压条件下具有高于6的CN的网络形成玻璃和液体的结构变化提供了新的见解。