Journal
SURFACE SCIENCE
Volume 502, Issue -, Pages 474-484Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/S0039-6028(01)01995-1
Keywords
water; metallic surfaces; physical adsorption; ruthenium; scanning tunneling microscopy
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Four different hydration water molecules. a flat monomer, a tilted monomer, a tetramer cluster and an upright monomer, were observed on Ru(0 0 1). In Situ scanning tunneling microscopy (STM) images of M(1 1 1)-root3 x root7(HSO4- + H5O(2)(+)) (M - Pt, Ir, Au Ru(0 0 1)) in H2SO4 solution produced a zig-zag chain of hydration water molecules, revealing a large stabilization energy due to the formation of a hydrogen bonding network. Also 2 x 2-2CO + H2O structure was observed on both Ru(0 0 1) electrode and Ru(0 0 1) ultra-high vacuum surfaces by STM and low energy electron diffraction. These model double layers including over-layer water Molecules form it preferentially ordered structure in terms of hydrogen bonding at a negative electrode potential while also forming a disordered structure with a relatively random orientation in the over layer at a positive electrode potential. The preferential orientation of the large water dipole yields a strong electric field on the surface and lowers the frequencies of the adsorbed bisulfate S-O stretching or the CO stretching absorption band. (C) 2002 Elsevier Science B.V. All rights reserved.
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