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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis surveys from Japan 3 (1999), S. 81-93 
    ISSN: 1572-8803
    Keywords: intermediates ; olefin metathesis ; NO reduction ; activation of catalyst ; active sites ; Pt–Rh catalyst ; alloy single crystal ; bimetallic single crystal ; quasi-compound ; reconstruction ; surface segregation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Why can solid surfaces promote a variety of chemical reactions? We supposed that active sites or active compounds are formed over the catalyst surface during catalysis or in pretreatment. Three topics are discussed from this viewpoint in this review. The first topic is an activation of inactive MoOx film to super-active olefin metathesis catalyst, where Mo=CHR sites are prepared on MoOx. A total mechanism for the productive and the cross metathesis of propene was firstly established on an activated catalyst by using deuterium labeled olefins. In the second topic, a new concept of quasi-compounds is discussed by using scanning tunneling microscopy (STM), and it is shown that the reaction of quasi-compounds yields (Cu)6 cluster and (–Cu–O–) strings on Ag(110). In the third topic, a self-activation of Pt–Rh alloy and Pt/Rh bimetallic surfaces during the reaction of NO + H2 is discussed by using single crystal surfaces. STM image showed that a Pt–Rh(100) surface is activated by reacting with oxygen where a specific array of Pt and Rh atoms is established. Formation of similar active sites on the other crystallographic surfaces is responsible for structure insensitive catalysis of Pt/Rh bimetallic surfaces.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 12 (1992), S. 1-6 
    ISSN: 1572-879X
    Keywords: Surface carbide ; surface nitride ; intermediates ; NO + H2 reaction ; methanation reaction ; catalysis on single crystal
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A key intermediate of the methanation reaction on nickel catalyst is a carbidic carbon. Accumulated carbidic intermediates on Ni(100) gives a p(2×2) p4g structure, whereas that on Ni(111) is too complex to be solved. A single domain carbide layer accidentally on Ni(111) allowed us to solve the structure explicitly. Comparison of the carbide layer on Ni(100) and that on Ni(111) showed that the carbon atoms are arranged by forming the same ordered structure. The carbide layers prepared on Ni(100), Ni(111) and Ni(110) have almost equal decomposition temperatures. Consequently, we can conclude that the same overlayer compound is formed on the three surfaces. Furthermore, the hydrogenation of the p4g carbide on Ni(100) occurs at almost equal rate to the turnover frequency of the catalytic methanation reaction. The structure insensitive methanation reaction on Ni(100), Ni(111) and Ni(110) is responsible for the same intermediate compound on these surfaces. The same strategy was applied to the reaction of NO with H2 on Pd(100), Rh(100) and Pt-Rh(100) surfaces, and ac(2×2)-N overlayer was isolated on each of these. The hydrogenation of the isolatedc(2×2)-N produced predominantly NH species, which indicates slow NH species hydrogenation.
    Type of Medium: Electronic Resource
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