TY - JOUR
T1 - Water at surfaces and interfaces
T2 - From molecules to ice and bulk liquid
AU - Shimizu, Tomoko K.
AU - Maier, Sabine
AU - Verdaguer, Albert
AU - Velasco-Velez, Juan Jesus
AU - Salmeron, Miquel
N1 - Funding Information:
This work was supported by the Office of Basic Energy Sciences (BES), Division of Materials Sciences and Engineering, of the U.S. Department of Energy (DOE) under Contract No. DE-AC02-05CH11231, through the Structure and Dynamics of Materials Interfaces program (FWP KC31SM). S.M. acknowledges funding from the by the German Science Foundation (DFG) through the Cluster of Excellence EXC 315 “Engineering of Advanced Materials” and as the European Research Council (ERC-2014-StG SURFLINK No. 637831 ). A.V. acknowledges funding from projects MAT2016-77852-C2-1-R and SEV-2015-0496 , MINECO , Spain.
Publisher Copyright:
© 2018
PY - 2018/12
Y1 - 2018/12
N2 - 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.
AB - 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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U2 - 10.1016/j.progsurf.2018.09.004
DO - 10.1016/j.progsurf.2018.09.004
M3 - Review article
AN - SCOPUS:85055908188
SN - 0079-6816
VL - 93
SP - 87
EP - 107
JO - Progress in Surface Science
JF - Progress in Surface Science
IS - 4
ER -