How to quantify and avoid finite size effects in computational studies of crystal nucleation: The case of heterogeneous ice nucleation

被引:18
作者
Hussain, Sarwar [1 ]
Haji-Akbari, Amir [1 ]
机构
[1] Yale Univ, Dept Chem & Environm Engn, New Haven, CT 06520 USA
基金
美国国家科学基金会;
关键词
MOLECULAR-DYNAMICS SIMULATIONS; HOMOGENEOUS NUCLEATION; WATER; KINETICS; MODEL; CRYSTALLIZATION; THERMODYNAMICS; INTERFACES; LIQUIDS; ORDER;
D O I
10.1063/5.0026355
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
Computational studies of crystal nucleation can be impacted by finite size effects, primarily due to unphysical interactions between crystalline nuclei and their periodic images. It is, however, not always feasible to systematically investigate the sensitivity of nucleation kinetics and mechanism to system size due to large computational costs of nucleation studies. Here, we use jumpy forward flux sampling to accurately compute the rates of heterogeneous ice nucleation in the vicinity of square-shaped model structureless ice nucleating particles (INPs) of different sizes and identify three distinct regimes for the dependence of rate on the INP dimension, L. For small INPs, the rate is a strong function of L due to the artificial spanning of critical nuclei across the periodic boundary. Intermediate-sized INPs, however, give rise to the emergence of non-spanning "proximal" nuclei that are close enough to their periodic images to fully structure the intermediary liquid. While such proximity can facilitate nucleation, its effect is offset by the higher density of the intermediary liquid, leading to artificially small nucleation rates overall. The critical nuclei formed at large INPs are neither spanning nor proximal. Yet, the rate is a weak function of L, with its logarithm scaling linearly with 1/L. The key heuristic emerging from these observations is that finite size effects will be minimal if critical nuclei are neither spanning nor proximal and if the intermediary liquid has a region that is structurally indistinguishable from the supercooled liquid under the same conditions.
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页数:13
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共 73 条
  • [1] Molecular dynamics simulations of the liquid-vapor interface of a molten salt. II. Finite size effects and comparison to experiment
    Aguado, A
    Scott, W
    Madden, PA
    [J]. JOURNAL OF CHEMICAL PHYSICS, 2001, 115 (18) : 8612 - 8619
  • [2] Forward flux sampling-type schemes for simulating rare events: Efficiency analysis
    Allen, Rosalind J.
    Frenkel, Daan
    ten Wolde, Pieter Rein
    [J]. JOURNAL OF CHEMICAL PHYSICS, 2006, 124 (19)
  • [3] Effect of material flexibility on the thermodynamics and kinetics of hydrophobically induced evaporation of water
    Altabet, Y. Elia
    Haji-Akbari, Amir
    Debenedetti, Pablo G.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2017, 114 (13) : E2548 - E2555
  • [4] Heterogeneous Ice Nucleation Controlled by the Coupling of Surface Crystallinity and Surface Hydrophilicity
    Bi, Yuanfei
    Cabriolu, Raffaela
    Li, Tianshu
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2016, 120 (03) : 1507 - 1514
  • [5] FINITE SIZE EFFECTS ON PHASE-TRANSITIONS
    BINDER, K
    [J]. FERROELECTRICS, 1987, 73 (1-2) : 43 - 67
  • [6] Calculation of the surface tension from Monte Carlo simulations: Does the model impact on the finite-size effects?
    Biscay, F.
    Ghoufi, A.
    Goujon, F.
    Lachet, V.
    Malfreyt, P.
    [J]. JOURNAL OF CHEMICAL PHYSICS, 2009, 130 (18)
  • [7] CRYSTALLIZATION OF FCC (111) AND (100) CRYSTAL-MELT INTERFACES - A COMPARISON BY MOLECULAR-DYNAMICS FOR THE LENNARD-JONES SYSTEM
    BURKE, E
    BROUGHTON, JQ
    GILMER, GH
    [J]. JOURNAL OF CHEMICAL PHYSICS, 1988, 89 (02) : 1030 - 1041
  • [8] Molecular Dynamics Simulations of the Influence of Drop Size and Surface Potential on the Contact Angle of Ionic-Liquid Droplets
    Burt, Ryan
    Birkett, Greg
    Salanne, Mathieu
    Zhao, X. S.
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2016, 120 (28) : 15244 - 15250
  • [9] Molecular simulations of heterogeneous ice nucleation. II. Peeling back the layers
    Cox, Stephen J.
    Kathmann, Shawn M.
    Slater, Ben
    Michaelides, Angelos
    [J]. JOURNAL OF CHEMICAL PHYSICS, 2015, 142 (18)
  • [10] Molecular simulations of heterogeneous ice nucleation. I. Controlling ice nucleation through surface hydrophilicity
    Cox, Stephen J.
    Kathmann, Shawn M.
    Slater, Ben
    Michaelides, Angelos
    [J]. JOURNAL OF CHEMICAL PHYSICS, 2015, 142 (18)