Room temperature COad desorption/exchange kinetics on pt electrodes -: A combined in situ IR and mass spectrometry study

被引:36
作者
Heinen, Martin [1 ]
Chen, Yan-Xia [1 ,2 ]
Jusys, Zenonas [1 ]
Behm, Rolf Jurgen [1 ]
机构
[1] Univ Ulm, Inst Catalysis & Surface Chem, D-89069 Ulm, Germany
[2] Univ Sci & Technol China, Natl Lab Phys Sci Microscale, Dept Phys Chem, Hefei 230026, Peoples R China
关键词
infrared spectroscopy; isotope exchange; kinetics; mass spectrometry; spectroelectrochemistry;
D O I
10.1002/cphc.200700425
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
The room temperature desorption and exchange of CO in a saturated CO adlayer on a Pt electrode, at potentials for below the onset of oxidation, was investigated by isotope labeling experiments, using a novel spectroelectrochemical setup, which allows the simultaneous detection of adsorbed species by in situ IR spectroscopy and of volatile (side) products and reactants by online mass spectrometry under controlled electrolyte flow conditions. Time-resolved IR spectra show a rapid, statistical exchange of pre-adsorbed (COad)-C-13 by (COad)-C-12 in (CO)-C-12 containing electrolyte; mass spectrometric data reveal first-order exchange kinetics, with the rate increasing with CO partial pressure. The increasing COad desorption rate in equilibrium with a CO containing electrolyte is explained by a combination of an increasing COad coverage upon increasing the CO pressure, and a decrease of the CO adsorption energy with coverage, due to repulsive COad-COad interactions.
引用
收藏
页码:2484 / 2489
页数:6
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