Impact of the Alkali Cation on the Oscillatory Electro-Oxidation of Ethylene Glycol on Platinum

被引:27
|
作者
Sitta, Elton [1 ,2 ]
Nagao, Raphael [3 ]
Kiss, Istvan Z. [3 ]
Varela, Hamilton [1 ]
机构
[1] Univ Sao Paulo, Inst Chem Sao Carlos, BR-13560970 Sao Paulo, Brazil
[2] Univ Fed Sao Carlos, Dept Chem, BR-13565905 Sao Paulo, Brazil
[3] St Louis Univ, Dept Chem, St Louis, MO 63103 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2015年 / 119卷 / 03期
基金
美国国家科学基金会; 巴西圣保罗研究基金会;
关键词
FORMIC-ACID OXIDATION; ELECTROCHEMICAL OSCILLATORS; NONCOVALENT INTERACTIONS; POTENTIAL OSCILLATIONS; MECHANISTIC ASPECTS; ANION ADSORPTION; METAL CATION; INSTABILITIES; PT(100); CO;
D O I
10.1021/jp5105505
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
We report the effect of alkali cation (Li+, Na+, and K+) on the oscillatory electro-oxidation of ethylene glycol in alkaline media. As experimentally verified, the nature of the alkali cation strongly impacts the waveform and frequency of the potential oscillations. The oscillation frequencies decrease in the order KOH > NaOH > LiOH, which also corresponds to the ascending order of the surface blockage due to the noncovalent interactions. On the other hand, the estimated rate constant of poison formation, k(p), under oscillatory regime is higher in the presence of KOH rather than NaOH, both acting as the supporting electrolytes. In order to shed light on the relationships between the kinetic and dynamical features, we performed numerical simulations based on a generic model which includes the time evolution of cation coverage. Overall, we were able to reproduce the major features observed experimentally; k(p) was assigned to the electrochemical steps of C-C bond breaking instead of direct noncovalent interactions between the hydrated alkali cation and surface oxides. Finally, the results are rationalized in terms of the cation influence on the feedback loops and of the underlying surface chemistry.
引用
收藏
页码:1464 / 1472
页数:9
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