38 research outputs found
From random walk to single-file diffusion
We report an experimental study of diffusion in a quasi-one-dimensional (q1D)
colloid suspension which behaves like a Tonks gas. The mean squared
displacement as a function of time is described well with an ansatz
encompassing a time regime that is both shorter and longer than the mean time
between collisions. This ansatz asserts that the inverse mean squared
displacement is the sum of the inverse mean squared displacement for short time
normal diffusion (random walk) and the inverse mean squared displacement for
asymptotic single-file diffusion (SFD). The dependence of the single-file 1D
mobility on the concentration of the colloids agrees quantitatively with that
derived for a hard rod model, which confirms for the first time the validity of
the hard rod SFD theory. We also show that a recent SFD theory by Kollmann
leads to the hard rod SFD theory for a Tonks gas.Comment: 4 pages, 4 figure
Surface Crystallization in a Liquid AuSi Alloy
X-ray measurements reveal a crystalline monolayer at the surface of the
eutectic liquid Au_{82}Si_{18}, at temperatures above the alloy's melting
point. Surface-induced atomic layering, the hallmark of liquid metals, is also
found below the crystalline monolayer. The layering depth, however, is
threefold greater than that of all liquid metals studied to date. The
crystallinity of the surface monolayer is notable, considering that AuSi does
not form stable bulk crystalline phases at any concentration and temperature
and that no crystalline surface phase has been detected thus far in any pure
liquid metal or nondilute alloy. These results are discussed in relation to
recently suggested models of amorphous alloys.Comment: 12 pages, 3 figures, published in Science (2006
Monovalent Ion Condensation at the Electrified Liquid/Liquid Interface
X-ray reflectivity studies demonstrate the condensation of a monovalent ion
at the electrified interface between electrolyte solutions of water and
1,2-dichloroethane. Predictions of the ion distributions by standard
Poisson-Boltzmann (Gouy-Chapman) theory are inconsistent with these data at
higher applied interfacial electric potentials. Calculations from a
Poisson-Boltzmann equation that incorporates a non-monotonic ion-specific
potential of mean force are in good agreement with the data.Comment: 4 pages, 4 figure
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Atomic-Scale Surface Demixing in a Eutectic Liquid BiSn Alloy
Resonant x-ray reflectivity of the surface of the liquid phase of the Bi43Sn57 eutectic alloy reveals atomic-scale demixing extending over three near-surface atomic layers. Because of the absence of an underlying atomic lattice which typically defines adsorption in crystalline alloys, studies of adsorption in liquid alloys provide unique insight on interatomic interactions at the surface. The observed composition modulation could be accounted for quantitatively by the Defay-Prigogine and Strohl-King multilayer extensions of the single-layer Gibbs model, revealing a near-surface domination of the attractive Bi-Sn interaction over the entropy.Engineering and Applied Science
Anomalous layering at the liquid Sn surface
X-ray reflectivity measurements on the free surface of liquid Sn are
presented. They exhibit the high-angle peak, indicative of surface-induced
layering, also found for other pure liquid metals (Hg, Ga and In). However, a
low-angle peak, not hitherto observed for any pure liquid metal, is also found,
indicating the presence of a high-density surface layer. Fluorescence and
resonant reflectivity measurements rule out the assignment of this layer to
surface-segregation of impurities. The reflectivity is modelled well by a 10%
contraction of the spacing between the first and second atomic surface layers,
relative to that of subsequent layers. Possible reasons for this are discussed.Comment: 8 pages, 9 figures; to be submitted to Phys. Rev. B; updated
references, expanded discussio
Atomic-scale surface demixing in a eutectic liquid BiSn alloy
Resonant x-ray reflectivity of the surface of the liquid phase of the
BiSn eutectic alloy reveals atomic-scale demixing extending over
three near-surface atomic layers. Due to the absence of underlying atomic
lattice which typically defines adsorption in crystalline alloys, studies of
adsorption in liquid alloys provide unique insight on interatomic interactions
at the surface. The observed composition modulation could be accounted for
quantitatively by the Defay-Prigogine and Strohl-King multilayer extensions of
the single-layer Gibbs model, revealing a near-surface domination of the
attractive Bi-Sn interaction over the entropy.Comment: 4 pages (two-column), 3 figures, 1 table; Added a figure, updated
references, discussion; accepted at Phys. Rev. Let
Surface oxidation of liquid Sn
We report the results of an x-ray scattering study that reveals oxidation
kinetics and formation of a previously unreported crystalline phase of SnO at
the liquid-vapour interface of Sn. Our experiments reveal that the pure liquid
Sn surface does not react with molecular oxygen below an activation pressure of
\~5.0*10-6 Torr. Above that pressure a rough solid Sn oxide grows over the
liquid metal surface. Once the activation pressure has been exceeded the
oxidation proceeds at pressures below the oxidation pressure threshold. The
observed diffraction pattern associated with the surface oxidation does not
match any of the known Sn oxide phases. The data have an explicit signature of
the face-centred cubic structure, however it requires lattice parameters that
are about 9% smaller than those reported for cubic structures of high-pressure
phases of Sn oxides.
Keywords: X-ray scattering, diffraction, and reflection; Oxidation; Surface
chemical reaction; Surface structure, morphology, roughness, and topography;
Tin; Tin oxides; Liquid surfaces; Polycrystalline thin filmsComment: 18 pages, 6 figures, 1 table; Submitted to Surface Scienc