Freezing Temperatures, Ice Nanotubes Structures, and Proton Ordering of TIP4P/ICE Water inside Single Wall Carbon Nanotubes

被引:28
作者
Pugliese, P. [1 ]
Conde, M. M. [1 ]
Rovere, M. [1 ]
Gallo, P. [1 ]
机构
[1] Univ Roma, Dipartimento Matemat & Fis, Via Vasca Navale 84, I-00146 Rome, Italy
关键词
CONFINED WATER; PHASE-TRANSITION; GRAPHENE; DESALINATION; PROTEINS; METHANE; MODELS; GROWTH; POINT; FLOW;
D O I
10.1021/acs.jpcb.7b06306
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 very recent experimental paper importantly and unexpectedly showed that water in carbon nanotubes is already in the solid ordered phase at the temperature where bulk water boils. The water models used so far in literature for molecular dynamics simulations in carbon nanotubes show freezing temperatures lower than the experiments. We present here results from molecular dynamics simulations of water inside single walled carbon nanotubes using an extremely realistic model for both liquid and icy water, the TIP4P/ICE. The water behavior inside nanotubes of different diameters has been studied upon cooling along the isobars at ambient pressure starting from temperatures where water is in a liquid state. We studied the liquid/solid transition, and we observed freezing temperatures higher than in bulk water and that depend on the diameter of the nanotube. The maximum freezing temperature found is 390 K, which is in remarkable agreement with the recent experimental measurements. We have also analyzed the ice structure called "ice nanotube" that water forms inside the single walled carbon nanotubes when it freezes. The ice forms observed are in agreement with previous results obtained with different water models. A novel finding, a partial proton ordering, is evidenced in our ice nanotubes at finite temperature.
引用
收藏
页码:10371 / 10381
页数:11
相关论文
共 45 条
  • [1] A potential model for the study of ices and amorphous water:: TIP4P/Ice -: art. no. 234511
    Abascal, JLF
    Sanz, E
    Fernández, RG
    Vega, C
    [J]. JOURNAL OF CHEMICAL PHYSICS, 2005, 122 (23)
  • [2] Gromacs: High performance molecular simulations through multi-level parallelism from laptops to supercomputers
    Abraham, Mark James
    Murtola, Teemu
    Schulz, Roland
    Páll, Szilárd
    Smith, Jeremy C.
    Hess, Berk
    Lindah, Erik
    [J]. SoftwareX, 2015, 1-2 : 19 - 25
  • [3] Agrawal KV, 2017, NAT NANOTECHNOL, V12, P267, DOI [10.1038/NNANO.2016.254, 10.1038/nnano.2016.254]
  • [4] Evolution of methane during gas hydrate dissociation
    Bagherzadeh, S. Alireza
    Alavi, Saman
    Ripmeester, John A.
    Englezos, Peter
    [J]. FLUID PHASE EQUILIBRIA, 2013, 358 : 114 - 120
  • [5] Reaction coordinates and rates from transition paths
    Best, RB
    Hummer, G
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (19) : 6732 - 6737
  • [6] Flow and structure of fluids in functionalized nanopores
    Bordin, Jose Rafael
    Barbosa, Marcia C.
    [J]. PHYSICA A-STATISTICAL MECHANICS AND ITS APPLICATIONS, 2017, 467 : 137 - 147
  • [7] Unusual hydrogen bonding in water-filled carbon nanotubes
    Byl, Oleg
    Liu, Jin-Chen
    Wang, Yang
    Yim, Wai-Leung
    Johnson, J. Karl
    Yates, John T., Jr.
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (37) : 12090 - 12097
  • [8] Heat transfer enhancement in water when used as PCM in thermal energy storage
    Cabeza, LF
    Mehling, H
    Hiebler, S
    Ziegler, F
    [J]. APPLIED THERMAL ENGINEERING, 2002, 22 (10) : 1141 - 1151
  • [9] Water Desalination across Nanoporous Graphene
    Cohen-Tanugi, David
    Grossman, Jeffrey C.
    [J]. NANO LETTERS, 2012, 12 (07) : 3602 - 3608
  • [10] Determining the three-phase coexistence line in methane hydrates using computer simulations
    Conde, M. M.
    Vega, C.
    [J]. JOURNAL OF CHEMICAL PHYSICS, 2010, 133 (06)