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    <title>Structure-reactivity relationships in CeO2-supported Cu catalysts</title>
    <subTitle>influence of formation, structure and stability of active sites on catalytic performance in preferential CO oxidation (PROX)</subTitle>
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  <abstract type="Summary">The preferential oxidation (PROX) of CO is an effective and practical strategy to reduce trace amounts of CO to a very low level (&lt; 5 ppm) from the H2-rich stream used as fuel for proton exchange membrane fuel cells. Cu catalysts have been proven to be cheap alternatives to the costly noble metal-based catalysts due to their high activity, selectivity, and stability. However, most of the previous investigations used a higher Cu loading, normally more than 5 wt% preventing any reliable conclusions about the nature of the active sites (Cu single sites, dimmers, clusters and/or nanoparticles).&lt;eng&gt;</abstract>
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  <note type="statement of responsibility">vorgelegt von Hayder Jawad Abed</note>
  <note>GutachterInnen: Ralf Ludwig (Universität Rostock, Institut für Chemie) ; Angelika Brückner (Leibniz-Institut für Katalyse e. V.)</note>
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      <title>Structure-reactivity relationships in CeO2-supported Cu catalysts</title>
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