Evolution of Hydrogen Dynamics in Amorphous Ice with Density

被引:26
作者
Parmentier, A. [1 ,2 ]
Shephard, J. J. [3 ,4 ]
Romanelli, G. [1 ,2 ]
Senesi, R. [1 ,2 ,5 ]
Salzmann, C. G. [3 ]
Andreani, C. [1 ,2 ,5 ]
机构
[1] Univ Roma Tor Vergata, Dipartimento Fis, I-00133 Rome, Italy
[2] Univ Roma Tor Vergata, NAST Ctr, I-00133 Rome, Italy
[3] UCL, Dept Chem, London WC1H 0AJ, England
[4] Univ Durham, Dept Chem, Durham DH1 3LE, England
[5] CNR IPCF Sez Messina, I-98158 Messina, Italy
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2015年 / 6卷 / 11期
基金
英国工程与自然科学研究理事会;
关键词
GLASS-LIQUID TRANSITION; KINETIC-ENERGY; TEMPERATURE-DEPENDENCE; WATER; PRESSURE; POINT; STATE;
D O I
10.1021/acs.jpclett.5b00711
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
The single-particle dynamics of hydrogen atoms in several of the amorphous ices are reported using a combination of deep inelastic neutron scattering (DINS) and inelastic neutron scattering (INS). The mean kinetic energies of the hydrogen nuclei are found to increase with increasing density, indicating the weakening of hydrogen bonds as well as a trend toward steeper and more harmonic hydrogen vibrational potential energy surfaces. DINS shows much more pronounced changes in the O-H stretching component of the mean kinetic energy going from low- to high-density amorphous ices than indicated by INS and Raman spectroscopy. This highlights the power of the DINS technique to retrieve accurate ground-state kinetic energies beyond the harmonic approximation. In a novel approach, we use information from DINS and INS to determine the anharmonicity constants of the O-H stretching modes. Furthermore, our experimental kinetic energies will serve as important benchmark values for path-integral Monte Carlo simulations.
引用
收藏
页码:2038 / 2042
页数:5
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