首页> 外文期刊>Journal of Electroanalytical Chemistry: An International Journal Devoted to All Aspects of Electrode Kinetics, Interfacial Structure, Properties of Electrolytes, Colloid and Biological Electrochemistry >CO ADSORPTION AND OXIDATION ON PT(111) ELECTRODES MODIFIED BY IRREVERSIBLY ADSORBED ARSENIC IN SULPHURIC ACID MEDIUM - COMPARISON WITH BISMUTH-MODIFIED ELECTRODES
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CO ADSORPTION AND OXIDATION ON PT(111) ELECTRODES MODIFIED BY IRREVERSIBLY ADSORBED ARSENIC IN SULPHURIC ACID MEDIUM - COMPARISON WITH BISMUTH-MODIFIED ELECTRODES

机译:硫酸中不可逆吸附砷修饰的PT(111)电极上的Co吸附和氧化-铋修饰电极的比较

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CO adsorption and stripping on Pt(111) electrodes modified by irreversibly adsorbed bismuth and arsenic were studied in sulphuric acid medium. Coadsorbed bismuth and CO form a mixed adlayer, whereas arsenic tends to desorb in the presence of CO. Both adatoms modify the CO stripping process, resulting in the catalysis of CO oxidation, in which arsenic is more effective than bismuth. Fourier transform IR (FTIR) studies demonstrate that bismuth stabilizes the adsorbed CO, while arsenic shows the opposite effect. In both cases, linear CO is the only species present on the electrode surface at high adatom coverage. The catalysis mechanism is an adatom-mediated oxygen transfer for both cases, with an additional electronic effect when arsenic is on the surface. Using the CO stripping charge after adequate correction, the values of the CO coverage for the different adatom coverages were calculated. The results of the CO coverage agree well with the behaviour shown in the FTIR experiments. [References: 31]
机译:研究了在硫酸介质中CO的吸附和汽提在不可逆地吸附铋和砷修饰的Pt(111)电极上的行为。共吸附的铋和CO形成混合的附加层,而砷在存在CO的情况下趋于解吸。两个原子均改变了CO的汽提过程,导致了CO氧化的催化作用,其中砷比铋更有效。傅里叶变换红外光谱(FTIR)研究表明,铋可以稳定吸附的一氧化碳,而砷则具有相反的作用。在这两种情况下,线性CO都是在高原子覆盖率的情况下出现在电极表面的唯一物质。在两种情况下,催化机理都是由吸附剂介导的氧转移,当砷在表面上时具有额外的电子效应。使用适当校正后的CO汽提电荷,计算出不同吸附原子覆盖率的CO覆盖率值。 CO覆盖的结果与FTIR实验中显示的行为非常吻合。 [参考:31]

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