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        <identifier>oai:www.ideals.illinois.edu:2142/84155</identifier>
        <datestamp>2023-07-11</datestamp>
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          <dc:contributor>Gewirth, Andrew A.</dc:contributor>
          <dc:creator>Xiao, Li</dc:creator>
          <dc:date>2015-09-25T22:13:14Z</dc:date>
          <dc:date>2015-09-25T22:13:14Z</dc:date>
          <dc:date>10000-01-01</dc:date>
          <dc:date>2004</dc:date>
          <dc:date>2004</dc:date>
          <dc:description>Finally, thiocyanate (SCN) adsorption on Au electrode is examined. Both the calculations and the spectroscopy show that three different geometries are adopted by SCN in the potential region studied (0.0 V &amp;le; E &amp;le; 1.2 V vs. NHE). At low potential both N-bound and S-bound forms are found, at intermediate potentials around Epzc the S-bound form dominates, and at high potentials SCN associates with the surface via a bridging geometry. The different Stark slopes observed for the C-N stretch in the end-on and bridging forms are attributed to the lowest unoccupied molecular orbital (LUMO).</dc:description>
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  Previous issue date: 2004</dc:description>
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Lift date: Forever
Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs</dc:description>
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          <dc:description>259 p.</dc:description>
          <dc:description>Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 2004.</dc:description>
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          <dc:title>Dioxygen Electroreduction on Electrode Surfaces</dc:title>
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            <department>Chemistry</department>
            <discipline>Chemistry</discipline>
            <grantor>University of Illinois at Urbana-Champaign</grantor>
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