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        <identifier>oai:www.ideals.illinois.edu:2142/25219</identifier>
        <datestamp>2023-07-10</datestamp>
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        <setSpec>col_2142_5131</setSpec>
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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>Chiang, Tai-Chang</dc:contributor>
          <dc:creator>Shapiro, Alan Paul</dc:creator>
          <dc:date>2011-06-02T16:14:35Z</dc:date>
          <dc:date>2011-06-02T16:14:35Z</dc:date>
          <dc:date>10000-01-01</dc:date>
          <dc:date>1987</dc:date>
          <dc:description>Angle-resolved photoemission spectroscopy was used to study Ag(lll) I
monolayers on six different substrates: Ni(OOl), Ni(lll), Cu(OOl),
Cu(lll), Au(lll), and Si(lll)-(7x7). The properties of surface states
were also examined for several related systems: Cu(lll) covered by
various thicknesses of Ag, and a bare Cu(332) stepped surface. Monolayer
overlayers that are incommensurate with the substrate [Ag on Ni(OOl),
Ni(lll), and Cu(lll)] or commensurate with the substrate only over a large
unit cell [Ag on Cu(OOl)] show electronic structures essentially
independent of the substrate orientation and material, except for an
overall shift in binding energy. The overlayer electronic structure is
somewhat different for the Ag/Au(lll) system, where there is a nearly
perfect overlayer-substrate lattice match as well as substantial overlap
in energy bands of like characters. In the Ag/Si system, partially
disordered overlayer growth and a strongly corrugated substrate surface
structure cause the overlayer features in the spectra to broaden
substantially. For thicker Ag overlayers on Cu(lll), the growth mode of
the Ag was determined to be layer by layer despite the large mismatch
between the two lattices. The Cu(lll} surface state was observed to
evolve monotonically for increasing Ag overlayer thickness to eventually
become the Ag(lll) surface state. The measured rate of shift of the
surface state binding energy can be explained qualitatively in terms of
the degree of localization of the surface-state wave functions. For the
stepped Cu(332) surface, a feature believed to be an L-gap surface state
is observed just below the Fermi edge in the photoemission spectra. The
properties this surface state are compared with known properties of the
Cu(lll) L-gap surface state.</dc:description>
          <dc:description>Submitted by Carolyn Mead (cmead2@illinois.edu) on 2011-06-02T16:14:35Z
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  Previous issue date: 1987</dc:description>
          <dc:description>Restriction data tranferred 2014-07-01T11:13:15-05:00
Original Data
Group with Access UIUC Users [automated]
Release Date: none
Reason: Thesis</dc:description>
          <dc:description>Item marked as restricted to the 'UIUC Users [automated]' Group (id=2) by Carolyn Mead (cmead2@illinois.edu) on 2011-06-02T16:14:36Z
Item is restricted indefinitely.</dc:description>
          <dc:description>Thesis</dc:description>
          <dc:description>U of I Only</dc:description>
          <dc:identifier>1057755</dc:identifier>
          <dc:identifier>http://hdl.handle.net/2142/25219</dc:identifier>
          <dc:language>en</dc:language>
          <dc:rights>1987 Alan Paul Shapiro</dc:rights>
          <dc:subject>photoemission studies</dc:subject>
          <dc:subject>thin metallic overlayer systems</dc:subject>
          <dc:subject>electronic structure</dc:subject>
          <dc:title>Photoemission studies of thin metallic overlayer sytems</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>
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