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Platinum coverage theory

Presently, the oxidation of methanol on pure platinum has more academic interest than practical application once DMFC universally employs platinum based materials having two or more metals as an anodic catalyst In absence of methanoUc inteimediate readsorption, the maximum reactiOTi rate for CO oxidation is 100-fold smaller than maximum reaction rate for CO adsorption from methanol dehydrogenation steps [11]. Indeed, the mechanism of methanol oxidation on platinum is expected to be equal to that on its alloys despite different kinetics which would result in a selection of pathway. In terms of complex activation theory, alloyed Pt is intend to lower the Ea barrier for CO adsorption, thus driving methanol oxidation to completion. As previously established [3], there are several factors that affect the calculated activation energy for the MOR at a given potential, such as coverage of methanoUc intermediates and anion adsorption from the electrolyte as well as pH and oxide formation processes. [Pg.37]


See other pages where Platinum coverage theory is mentioned: [Pg.130]    [Pg.58]    [Pg.85]    [Pg.682]    [Pg.881]    [Pg.197]    [Pg.779]    [Pg.106]    [Pg.132]    [Pg.348]    [Pg.441]    [Pg.339]    [Pg.175]   
See also in sourсe #XX -- [ Pg.120 ]




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Platinum coverage

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