Novel broken symmetry phase from N2O at high pressures and high temperatures -: art. no. 135504

被引:55
作者
Somayazulu, M
Madduri, A
Goncharov, AF
Tschauner, O
McMillan, PF
Mao, HK
Hemley, RJ
机构
[1] Carnegie Inst Sci, Geophys Lab, Washington, DC 20015 USA
[2] Carnegie Inst Sci, Ctr High Pressure Res, Washington, DC 20015 USA
[3] Thomas Jefferson High Sch Sci & Technol, Alexandria, VA 22312 USA
[4] Royal Inst Great Britain, London, England
[5] UCL, London, England
关键词
D O I
10.1103/PhysRevLett.87.135504
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Simple molecular solids become unstable at high pressures, typically transforming to dense framework and/or metallic structures. We report formation of an unusual ionic solid NO+ NO3- (nitrosonium nitrate) from N2O at pressures above 20 GPa and temperatures above 1000 K. Synchrotron x-ray diffraction indicates that the compound crystallizes with a structure related to the aragonite form of CaCO3 and NaNO3. Raman and infrared spectroscopic data indicate that the structure is noncentrosymmetric and exhibits a strong pressure dependent charge transfer and orientational order.
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