Density minimum of confined water at low temperatures: a combined study by small-angle scattering of X-rays and neutrons

被引:61
作者
Erko, M. [1 ]
Wallacher, D. [2 ]
Hoell, A. [3 ]
Hauss, T. [2 ]
Zizak, I. [3 ]
Paris, O. [1 ]
机构
[1] Univ Leoben, Inst Phys, A-8700 Leoben, Austria
[2] Helmholtz Ctr Berlin Mat & Energy, D-14109 Berlin, Germany
[3] Helmholtz Ctr Berlin Mat & Energy, D-12489 Berlin, Germany
关键词
SUPERCOOLED WATER; DYNAMIC CROSSOVER; PORE-SIZE; PROTEIN HYDRATION; SILICA; BEHAVIOR; DIFFRACTION; RELAXATION;
D O I
10.1039/c2cp24075k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A simple explanation is given for the low-temperature density minimum of water confined within cylindrical pores of ordered nanoporous materials of different pore size. The experimental evidence is based on combined data from in-situ small-angle scattering of X-rays (SAXS) and neutrons (SANS), corroborated by additional wide-angle X-ray scattering (WAXS). The combined scattering data cannot be described by a homogeneous density distribution of water within the pores, as was originally suggested from SANS data alone. A two-step density model reveals a wall layer covering approximately two layers of water molecules with higher density than the residual core water in the central part of the pores. The temperature-induced changes of the scattering signal from both X-rays and neutrons are consistent with a minimum of the average water density. We show that the temperature at which this minimum occurs depends monotonically on the pore size. Therefore we attribute this minimum to a liquid-solid transition of water influenced by confinement. For water confined in the smallest pores of only 2 nm in diameter, the density minimum is explained in terms of a structural transition of the surface water layer closest to the hydrophilic pore walls.
引用
收藏
页码:3852 / 3858
页数:7
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