Oscillatory electro-oxidation of ethanol on platinum studied by in situ ATR-SEIRAS

被引:7
作者
Silva, Marcio F. [1 ]
Delmonde, Marcelo V. F. [2 ,4 ]
Batista, Bruno C. [1 ]
Boscheto, Emerson [3 ]
Varela, Hamilton [2 ]
Camara, Giuseppe A. [1 ]
机构
[1] Univ Fed Mato Grosso do Sul, Inst Quim, CP 549, BR-79070900 Campo Grande, MS, Brazil
[2] Univ Sao Paulo, Inst Quim Sao Carlos, CP 780, BR-13560970 Sao Carlos, SP, Brazil
[3] Univ Fed Sul & Sudeste Para, BR-68507590 Maraba, PA, Brazil
[4] Inst Fed Parana, BR-85555000 Palmas, PR, Brazil
基金
巴西圣保罗研究基金会;
关键词
Ethanol electro-oxidation; Potential oscillations; ATR-SEIRAS; Electrocatalysis; ENHANCED INFRARED-ABSORPTION; FORMIC-ACID OXIDATION; ELECTROCHEMICAL OXIDATION; FORMALDEHYDE OXIDATION; POTENTIAL OSCILLATIONS; METHANOL OXIDATION; SURFACE-STRUCTURE; ETHYLENE-GLYCOL; ELECTRODE; ADSORPTION;
D O I
10.1016/j.electacta.2018.10.019
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
We report the study of the oscillatory electro-oxidation of ethanol on platinum surfaces under galvanostatic conditions. In order to correlate the features of potential oscillations with the surface chemistry of different adsorbates, we use in situ surface-enhanced infrared absorption spectroscopy in the attenuated total reflectance mode (ATR-SEIRAS). Results show that the maintenance of the oscillatory state does not seem to be particularly correlated with the CO surface coverage, conversely to what is observed for methanol. Indeed, our data suggest that oscillations continue as long as the coverage of molecular fragments from ethanol (regardless its nature) remain within a range that allows the coexistence of surface oxides (responsible for the activation of the surface throughout oxidation steps). Our results throw some light in the oscillatory kinetics of ethanol by establishing an unequivocal correlation between the features of the galvanostatic oscillations and the dynamics of the adsorbed species. (c) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:166 / 173
页数:8
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