4.6 Article

Wide-angle X-ray diffraction and molecular dynamics study of medium-range order in ambient and hot water

期刊

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
卷 13, 期 44, 页码 19997-20007

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c1cp22804h

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资金

  1. National Science Foundation (US) [CHE-0809324]
  2. Basic Energy Sciences (BES) through the Stanford Synchrotron Radiation Lightsource (SSRL)
  3. Swedish Research Council

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We have developed wide-angle X-ray diffraction measurements with high energy-resolution and accuracy to study water structure at three different temperatures (7, 25 and 66 degrees C) under normal pressure. Using a spherically curved Ge crystal an energy resolution better than 15 eV has been achieved which eliminates influence from Compton scattering. The high quality of the data allows for a reliable Fourier transform of the experimental data resolving shell structure out to similar to 12 angstrom, i.e. 5 hydration shells. Large-scale molecular dynamics (MD) simulations using the TIP4P/2005 force-field reproduce excellently the experimental shell-structure in the range 4-12 angstrom although less agreement is seen for the first peak in the intermolecular pair-correlation function (PCF). The Shiratani-Sasai Local Structure Index [J. Chem. Phys. 104, 7671 (1996)] identifies a tetrahedral minority giving the intermediate-range oscillations in the O-O PCF and a disordered majority providing a more featureless background in this range. The current study supports the proposal that the structure of liquid water, even at high temperatures, can be described in terms of a two-state fluctuation model involving local structures related to the high-density and low-density forms of liquid water postulated in the liquid-liquid phase transition hypothesis.

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