Quasielastic and inelastic neutron scattering investigation of fragile-to-strong crossover in deeply supercooled water confined in nanoporous silica matrices

被引:91
|
作者
Liu, Li
Chen, Sow-Hsin
Faraone, Antonio
Yen, Chun-Wan
Mou, Chung-Yuan
Kolesnikov, Alexander I.
Mamontov, Eugene
Leao, Juscelino
机构
[1] MIT, Dept Nucl Sci & Engn, Cambridge, MA 02139 USA
[2] NIST, Ctr Neutron Res, Gaithersburg, MD 20899 USA
[3] Univ Maryland, Dept Mat Sci & Engn, College Pk, MD 20742 USA
[4] Natl Taiwan Univ, Dept Chem, Taipei 10764, Taiwan
[5] Argonne Natl Lab, Intense Pulsed Neutron Source Div, Argonne, IL 60439 USA
关键词
D O I
10.1088/0953-8984/18/36/S03
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
We investigated, using quasi-elastic and inelastic neutron scattering, the slow single-particle dynamics of water confined in laboratory synthesized nanoporous silica matrices, MCM-41-S, with pore diameters ranging from 10 to 18 angstrom. Inside the pores of these matrices, the freezing process of water is strongly inhibited down to 160 K. We analysed the quasi-elastic part of the neutron scattering spectra with a relaxing-cage model and determined the temperature and pressure dependence of the Q-dependent translational relaxation time and its stretch exponent beta for the time dependence of the self- intermediate scattering function. The calculated Q-independent average translational relaxation time shows a fragile-to-strong (FS) dynamic crossover for pressures lower than 1600 bar. Above this pressure, it is no longer possible to discern the characteristic feature of the FS crossover. Identification of this end point with the predicted second low-temperature critical point of water is discussed. A subsequent inelastic neutron scattering investigation of the librational band of water indicates that this FS dynamic crossover is associated with a structural change of the hydrogen-bond cage surrounding a typical water molecule from a denser liquid-like configuration to a less-dense ice-like open structure.
引用
收藏
页码:S2261 / S2284
页数:24
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