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        <identifier>oai:www.ideals.illinois.edu:2142/31302</identifier>
        <datestamp>2023-07-10</datestamp>
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        <thesis xmlns="http://www.ndltd.org/standards/metadata/etdms/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.ndltd.org/standards/metadata/etdms/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdms11.xsd http://purl.org/dc/elements/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdmsdc.xsd">
          <dc:contributor>Robinson, Ian K.</dc:contributor>
          <dc:creator>Walko, Donald Alan</dc:creator>
          <dc:date>2012-05-30T22:12:33Z</dc:date>
          <dc:date>2012-05-30T22:12:33Z</dc:date>
          <dc:date>10000-01-01</dc:date>
          <dc:date>2000</dc:date>
          <dc:description>X-ray diffraction has, within the past two decades, developed into a powerful analytical
tool for determining the atomic structure of crystalline surfaces. The dual advantages of
high intensity and high resolution have made this technique thrive at synchrotron radiation
sources. The experiments in this thesis extend surface x-ray diffraction to metal surfaces
with particularly low symmetry: the multilayer surface structure of a-Ga(OlO), complicated
by the low symmetry of the bulk, and Cu(115), a regularly stepped surface which spontaneously
facets when exposed to oxygen. The equations describing surface x-ray diffraction
are derived, with attention paid to assumptions made during the derivation and limitations
of the technique. In particular, the theory of scattering from a rough surface is generalized
to permit various models of roughness. The surface diffraction chamber in which these experiments
were performed is briefly described, along with the load lock which allows samples
to be inserted without opening the entire vacuum chamber to atmosphere.
We have determined the surface structure of a-Ga(OlO) near its melting point using xray
diffraction. Due to the low symmetry of the a-Ga bulk structure, two distinct bulk
truncations of the (010) surface are possible. Of these two ways, we find the true surface is
formed by cutting through dimer bonds (i.e., between metallic bilayers). The contraction of
the metallic bonds and expansion of the covalent bonds at the surface imply that the surface
is more metallic than the bulk. Our results suggest that a-Ga is fundamentally composed
not of Ga2 dimers, but of corrugated metallic bilayers which can be modeled as deltahedral
clusters.
Cu(OOl) vicinal surfaces facet when exposed to 0. We have studied this process on
Cu(115), which transforms from a clean surface to 104 and 113 facets, using surface 
ray diffraction. Unlike a-Ga(010), the low symmetry of these surfaces is due to their high
Miller indices, i. e., the stepped nature of the surfaces. The Cu(115) surface exhibits a complex
interlayer relaxation accounted for by basic elasticity theory; the vertical displacements
of the three surface atoms correlate to those of the subsurface atoms directly below. The
O/Cu(104) facets do not, as previously proposed, involve any missing Cu rows, but the top
three rows are expanded away from the bulk; the Cu-0 chains which stabilize this surface
are similar to those present on other 0 on Cu reconstructions. A complete structure determination
was not possible for the 0 /Cu(113) facets, due to significant disorder, but an
unambiguous (3x 1) reconstruction was observed.
Besides being instrumental in determining the static structure of surfaces and facets,
surface x-ray diffraction allows us to noninvasively observe, in situ, the evolution of the
faceting surface. We find that the faceting is driven by the formation of O/Cu(104) facets:
0 exposure induces spinodal decomposition of the (115) surface into (104) and (014) facets,
which form spontaneously, and also disordered, stepped facets, whose orientation gradually
changes from (115) to (113) as the (104) facets grow. We identify three temperature regimes
which have qualitatively different faceting processes, shedding light on the temperature dependence
of the equilibrium crystal shape for part of the 0-covered Cu system. During the
faceting process, the time evolution follows a slow dynamic scaling behavior, consistent with
either a logarithmic or power-law dependence.
Throughout this thesis, comparisons are made with results obtained by other surfacesensitive
techniques. The complimentarity of these techniques is worth emphasizing; despite
the power of surface x-ray diffraction in solving crystal structures, its ability to interpret and
explain the properties of these surfaces is greatly enhanced by microscopy, spectroscopy, and
other diffraction techniques, as well as theoretical and numerical studies.</dc:description>
          <dc:description>Submitted by William Weathers (weathrs2@illinois.edu) on 2012-05-30T22:12:33Z
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  Previous issue date: 2000</dc:description>
          <dc:description>Item marked as restricted to the 'UIUC Users [automated]' Group (id=2) by William Weathers (weathrs2@illinois.edu) on 2012-05-30T22:12:33Z
Item is restricted indefinitely.</dc:description>
          <dc:description>Restriction data tranferred 2014-07-01T11:33:27-05:00
Original Data
Group with Access UIUC Users [automated]
Release Date: none
Reason: Thesis</dc:description>
          <dc:description>Thesis</dc:description>
          <dc:description>U of I Only</dc:description>
          <dc:identifier>http://hdl.handle.net/2142/31302</dc:identifier>
          <dc:identifier>4285164</dc:identifier>
          <dc:language>en</dc:language>
          <dc:rights>©2000 Walko</dc:rights>
          <dc:subject>X-ray diffraction</dc:subject>
          <dc:subject>crystalline surfaces</dc:subject>
          <dc:subject>Gallium (010)</dc:subject>
          <dc:subject>Copper(115)</dc:subject>
          <dc:title>Structure and faceting of low-symmetry metal surfaces</dc:title>
          <dc:type>Dissertation / Thesis</dc:type>
          <dc:type>text</dc:type>
          <degree>
            <department>Physics</department>
            <discipline>Physics</discipline>
            <disciplineCode>University of Illinois at Urbana-Champaign</disciplineCode>
            <level>Dissertation</level>
            <name>Ph.D.</name>
          </degree>
        </thesis>
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