Coadsorption, non-reactive displacement and cathodic desorption of ethene preadsorbed on Pd and Pt electrodes

被引:17
作者
Muller, U [1 ]
Dulberg, A [1 ]
Baltruschat, H [1 ]
机构
[1] Univ Bonn, Inst Phys & Theoret Chem, D-53117 Bonn, Germany
关键词
mass spectrometry; ethene; Cu-UPD; Pt-electrode; Pd-electrode;
D O I
10.1016/S0927-7757(97)00314-2
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
From both Pd and Pt electrodes, ethene is desorbed at low potentials under hydrogenation as shown by differential electrochemical mass spectrometry (DEMS). The deposition of Cu on the ethene-covered Pt surface leads to the desorption of only 10% of the adsorbate as ethene itself, contrary to the case of benzene, which can be almost completely displaced. The same amount of desorbing ethene is found when adbsorbing I(-) or CO onto the ethene-precovered surface. In the case of Pd, such a partial displacement is only observed when using I-as the displacing agent; CO and CU(2+) lead to coadsorption. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:155 / 164
页数:10
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