4.5 Article Proceedings Paper

Water at surfaces and interfaces: From molecules to ice and bulk liquid

Journal

PROGRESS IN SURFACE SCIENCE
Volume 93, Issue 4, Pages 87-107

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.progsurf.2018.09.004

Keywords

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Funding

  1. Office of Basic Energy Sciences (BES), Division of Materials Sciences and Engineering, of the U.S. Department of Energy (DOE) [DE-AC02-05CH11231, FWP KC31SM]
  2. German Science Foundation (DFG) through the Cluster of Excellence Engineering of Advanced Materials [EXC 315]
  3. European Research Council [637831]
  4. MINECO, Spain [MAT2016-77852-C2-1-R, SEV-2015-0496]
  5. European Research Council (ERC) [637831] Funding Source: European Research Council (ERC)

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The structure and growth of water films on surfaces is reviewed, starting from single molecules to two-dimensional wetting layers, and liquid interfaces. This progression follows the increase in temperature and vapor pressure from a few degrees Kelvin in ultra-high vacuum, where Scanning Tunneling and Atomic Force Microscopies (STM and AFM) provide crystallographic information at the molecular level, to ambient conditions where surface sensitive spectroscopic techniques provide electronic structure information. We show how single molecules bind to metal and non-metal surfaces, their diffusion and aggregation. We examine how water molecules can be manipulated by the STM tip via excitation of vibrational and electronic modes, which trigger molecular diffusion and dissociation. We review also the adsorption and structure of water on non-metal substrates including mica, alkali halides, and others under ambient humid conditions. We finally discuss recent progress in the exploration of the molecular level structure of solid-liquid interfaces, which impact our fundamental understanding of corrosion and electrochemical processes.

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