Thermodynamic Studies of PEG (Mw 20,000) Adsorption onto a Polycrystalline Gold Electrode

被引:14
作者
Mendez, Alia [1 ]
Moron, L. E. [1 ]
Ortiz-Frade, L. [1 ]
Meas, Y. [1 ]
Ortega-Borges, R. [1 ]
Trejo, G. [1 ]
机构
[1] Ctr Invest & Desarrollo Tecnol Electroquim, Pedro Escobedo 76703, Queretaro, Mexico
关键词
QUARTZ-CRYSTAL MICROBALANCE; COPPER ELECTROPLATING BATH; ELECTRICAL DOUBLE-LAYER; POLYETHYLENE-GLYCOL; ORGANIC ADDITIVES; ZINC ELECTRODEPOSITION; POLYMER ADSORPTION; PHASE-TRANSITIONS; CL-IONS; ACID;
D O I
10.1149/1.3551501
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Cyclic voltammetry, differential capacity, and chronocoulometry were employed in a quantitative study of polyethylene glycol (Mw 20000) (PEG(20000)) adsorption onto a polycrystalline Au substrate. The surface tension, film pressure, relative Gibbs surface excess, and the Gibbs energy of adsorption were determined as a function of the electrode potential. The results indicated that, in the potential interval studied (-0.9 to 0.35 V vs saturated calomel electrode), PEG(20000) adsorbed onto the polycrystalline Au surface via its oxygen atoms as a flat submonolayer of rodlike molecules. The adsorbed mass increased considerably with the increasing PEG(20000) concentration and more positive potential. In addition, the surface tension decreased as the quantity of PEG(20000) adsorbed on the surface rose with the increasing PEG(20000) concentration, an effect characteristic of surface active agents. The maximum surface concentration was found to be 4.59 x 10(-10) moloxygen cm(-2) for the highest PEG(20000) concentration studied (100 mu M). The Gibbs energy of adsorption (Delta G(ads)) was determined using the Henry adsorption isotherm. On the basis of the Delta G(ads) values obtained, it was concluded that the PEG(20000) molecules were weakly chemisorbed on the polycrystalline Au surface. (C) 2011 The Electrochemical Society. [DOI: 10.1149/1.3551501] All rights reserved.
引用
收藏
页码:F45 / F51
页数:7
相关论文
共 59 条
[1]   Role of polyethylene glycol in electrodeposition of zinc-chromium alloys [J].
Akiyama, T ;
Kobayashi, S ;
Ki, J ;
Ohgai, T ;
Fukushima, H .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 2000, 30 (07) :817-822
[2]   An EQCM study of polyethyleneglycol 8000 adsorption and its coadsorption with Cl- ions on Pt in perchloric acid solutions [J].
Bahena, E ;
Méndez, R ;
Meas, Y ;
Ortega, R ;
Salgado, L ;
Trejo, G .
ELECTROCHIMICA ACTA, 2004, 49 (06) :989-997
[3]   Influence of additives on Cu electrodeposition mechanisms in acid solution: direct current study supported by non-electrochemical measurements [J].
Bonou, L ;
Eyraud, M ;
Denoyel, R ;
Massiani, Y .
ELECTROCHIMICA ACTA, 2002, 47 (26) :4139-4148
[4]  
BUESSHERMAN C, 1992, ADSORPTION MOL METAL, P77
[5]   SOME OBSERVATIONS ON INNER LAYER AT MERCURY-ELECTROLYTE INTERFACE [J].
COOPER, IL ;
HARRISON, JA .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1975, 66 (02) :85-98
[6]   Influence of surface roughness on the quartz crystal microbalance response in a solution - New configuration for QCM studies [J].
Daikhin, L ;
Urbakh, M .
FARADAY DISCUSSIONS, 1997, 107 :27-38
[7]  
Damaskin B.B., 1971, Adsorption of Organic Compounds on Electrodes
[8]  
DINI JW, 1993, MAT SCI COATINGS SUB, pCH7
[9]  
Fleer G.J., 1998, Polymers at Interfaces
[10]   SOME MECHANISMS OF ACTION OF ADDITIVES IN ELECTRODEPOSITION PROCESSES [J].
FRANKLIN, TC .
SURFACE & COATINGS TECHNOLOGY, 1987, 30 (04) :415-428