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Platinum films, ultrathin, structure

Work with ultrathin and thick fringe-free platinum films has shown that not only does the product distribution change with catalyst structure, but the specific rate of raction (per unit platinum area) changes also (30). The data in Fig. 12 for the reaction of 2-methylpentane and n-hexane show a decrease in the specific rate with increasing particle size. [Pg.43]

The investigation on the electrochemical epitaxial growth of palladium on gold and platinum singlemonolayer coverage of palladium on Pt(lll) electrode by the immersion technique for the first time [74]. Llorca and coworkers investigated the irreversibly adsorbed palladium on Pt(hiJ) in acidic solution [75] and reported that electrocatalytic activity for the oxidation of formic acid on the Pt(lOO) electrodes vras improved drastically by the palladium-adlayer modification, while that on the Pt(lll) electrode was not greatly affected by the Pd-modification [76]. However, it is difficult to prepare an ultrathin film of palladium with various thickness by the immersion technique, and STM observation of the atomic structure of these surfaces is not available yet. [Pg.479]


See other pages where Platinum films, ultrathin, structure is mentioned: [Pg.6]    [Pg.6]    [Pg.35]    [Pg.43]    [Pg.85]    [Pg.8]    [Pg.66]    [Pg.70]    [Pg.215]    [Pg.475]    [Pg.12]    [Pg.171]    [Pg.460]    [Pg.229]    [Pg.318]    [Pg.382]   
See also in sourсe #XX -- [ Pg.6 , Pg.7 , Pg.8 ]




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Films structuring

Ultrathin

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