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   <subfield code="a">Surface and structural properties of pt/ceo2catalyst under preferential co oxidation in hydrogen (PROX)</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Detre Teschner, Attila Wootsch, Olga Pozdnyakova, Hermann Sauer, Axel Knop-Gericke, Robert Schlögl]</subfield>
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   <subfield code="a">Summary: Preferential oxidation of CO in the presence of excess hydrogen was studied on Pt/CeO2with 5% metal loading. Catalytic data were similar to those observed on 1% Pt/CeO2earlier [16]. The optimum temperature region is T£373 K; conversion and selectivity of CO oxidation strongly decreased at higher temperatures. High-pressure XPS indicated CO adsorbed on platinum particles and significant amount of water on the ceria surface. The top-most ceria surface re-oxidized as small amount of oxygen (3%) was introduced into the H2/CO feed. Despite this surface re-oxidation, high-resolution TEM after reaction indicated oxygen deficient ceria bulk structure, in which the defects formed a super-cell, with CeO1.695structure. The defective ceria is suggested to play an important role stabilizing the hydrogen bonded surface water, which (i) suppresses further hydrogen oxidation and (ii) reacts at the metal/support interface with linearly adsorbed CO in a low temperature water-gas-shift type reaction to produce CO2.&lt;/o:p&gt;</subfield>
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   <subfield code="a">preferential CO oxidation</subfield>
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