作者: Th Löffler , E Drbalkova , P Janderka , P Königshoven , H Baltruschat
DOI: 10.1016/S0022-0728(03)00263-8
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摘要: Abstract The adsorption of naphthalene, tetraline and biphenyl at Pt(111), roughened Pt(111) polycrystalline Pt electrodes was studied using differential electrochemical mass spectrometry (DEMS). From the amount CO 2 evolved during oxidation adsorbate layers, coverages were estimated to be around 0.2 nmol cm −2 for all three molecules. However, in case naphthalene tetraline, charges per molecule are somewhat (20–30%) larger than expected theoretically, indicating that does not lead only , but also other, nonvolatile products. Adsorbed can largely desorbed potentials hydrogen region below as itself from completely hydrogenated product bicyclohexyl a Pt(111). Interestingly usual electrode is much less active towards hydrogenation, leading cyclohexylbenzene main desorption product. Less half formed or under same conditions, again surface being least, most complete hydrogenation.