Beyond sixfold coordinated Si in SiO2 glass at ultrahigh pressures

被引:104
作者
Prescher, Clemens [1 ,2 ]
Prakapenka, Vitali B. [2 ]
Stefanski, Johannes [1 ]
Jahn, Sandro [1 ]
Skinner, Lawrie B. [3 ,4 ]
Wang, Yanbin [2 ]
机构
[1] Univ Cologne, Inst Geol & Mineral, D-50674 Cologne, Germany
[2] Univ Chicago, Ctr Adv Radiat Sources, Chicago, IL 60637 USA
[3] Argonne Natl Lab, Adv Photon Source, Xray Sci Div, Argonne, IL 60439 USA
[4] SUNY Stony Brook, Inst Mineral Phys, Stony Brook, NY 11794 USA
基金
美国国家科学基金会;
关键词
high pressure; polyamorphism; glass; oxygen packing; X-RAY-DIFFRACTION; MOLECULAR-DYNAMICS; SEISMIC EVIDENCE; VITREOUS SILICA; PREDICTION; LIQUID; ATOP; GEO2; MELT;
D O I
10.1073/pnas.1708882114
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We investigated the structure of SiO2 glass up to 172 GPa using high-energy X-ray diffraction. The combination of a multichannel collimator with diamond anvil cells enabled the measurement of structural changes in silica glass with total X-ray diffraction to previously unachievable pressures. We show that SiO2 first undergoes a change in Si-O coordination number from fourfold to sixfold between 15 and 50 GPa, in agreement with previous investigations. Above 50 GPa, the estimated coordination number continuously increases from 6 to 6.8 at 172 GPa. Si-O bond length shows first an increase due to the fourfold to sixfold coordination change and then a smaller linear decrease up to 172 GPa. We reconcile the changes in relation to the oxygen-packing fraction, showing that oxygen packing decreases at ultrahigh pressures to accommodate the higher than sixfold Si-O coordination. These results give experimental insight into the structural changes of silicate glasses as analogue materials for silicate melts at ultrahigh pressures.
引用
收藏
页码:10041 / 10046
页数:6
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