4.6 Article

Non-hexagonal ice at hexagonal surfaces: the role of lattice mismatch

Journal

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 14, Issue 22, Pages 7944-7949

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2cp23438f

Keywords

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Funding

  1. Office of Science of the U.S. Department of Energy [DE-AC02-05CH11231]
  2. EPSRC [EP/F067496]
  3. Office of Science and Technology through EPSRC
  4. U.S. Department of Energy's (DOE) Office of Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences
  5. ERC
  6. EPSRC [EP/J010480/1, EP/F067496/1] Funding Source: UKRI
  7. Engineering and Physical Sciences Research Council [EP/J010480/1, EP/F067496/1] Funding Source: researchfish

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It has long been known that ice nucleation usually proceeds heterogeneously on the surface of a foreign body. However, little is known at the microscopic level about which properties of a material determine its effectiveness at nucleating ice. This work focuses on the long standing, conceptually simple, view on the role of a good crystallographic match between bulk ice and the underlying substrate. We use grand canonical Monte Carlo to generate the first overlayer of water at the surface and find that the traditional view of heterogeneous nucleation does not adequately account for the array of structures that water may form at the surface. We find that, in order to describe the structures formed, a good match between the substrate and the nearest neighbour oxygen-oxygen distance is a better descriptor than a good match to the bulk ice lattice constant.

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