Cation exchange behavior during the redox switching of poly (3,4-ethylenedioxythiophene) films

被引:12
作者
Gruia, Violeta-Tincuta [1 ]
Ispas, Adriana [1 ]
Efimov, Igor [2 ]
Bund, Andreas [1 ]
机构
[1] Tech Univ Ilmenau, Electrochem & Electroplating Grp, Gustav Kirchhoff Str 6, D-98693 Ilmenau, Germany
[2] Univ Leicester, Dept Chem, Mat Ctr, Leicester LE1 7RH, Leics, England
关键词
PEDOT; Cation exchange; EQCM; Electropolymerization; SDS; QUARTZ-CRYSTAL MICROBALANCE; SODIUM TOSYLATE SOLUTIONS; CHARGE-TRANSFER REACTIONS; CONDUCTING POLYMERS; PEDOT LAYERS; DODECYL-SULFATE; ELECTROCHEMICAL PROPERTIES; POLYPYRROLE FILMS; PART; ION;
D O I
10.1007/s10008-020-04809-6
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Poly (3,4-ethylenedioxythiophene), PEDOT, films were synthesized at room temperature by potentiodynamic and potentiostatic step deposition in aqueous solutions containing EDOT monomer and LiClO4. In some solutions, the effect of small amounts of sodium dodecylsulfate, SDS, on the polymerization rate of EDOT and on the stiffness of the obtained PEDOT film was studied. The obtained PEDOT films were transferred in aqueous solutions containing cations with different molar mass, such as H+, Li+, Na+, K+, and Cs+. The apparent molar masses of the exchanged species during potentiodynamic experiments were determined by in situ microgravimetry. These measurements underlined the importance of the electrolyte chosen for electropolymerization process. It is known that SDS anions can be trapped inside the polymer layer during electropolymerization, providing them with a cation exchange behavior. However, even if the PEDOT films were deposited from an electrolyte without SDS, they still acted as cation exchangers.
引用
收藏
页码:3231 / 3244
页数:14
相关论文
共 68 条
[1]   Electrochemical materials science: tailoring intrinsically conducting polymers. The example: substituted thiophenes [J].
Alhalasah, W ;
Holze, R .
JOURNAL OF SOLID STATE ELECTROCHEMISTRY, 2005, 9 (12) :836-844
[2]   EQCM studies of polypyrrole films. Part 2. Exposure to aqueous sodium tosylate solutions under thermodynamically non-permselective conditions [J].
Bruckenstein, S ;
Brzezinska, K ;
Hillman, AR .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2000, 2 (06) :1221-1229
[3]   EQCM studies of polypyrrole films. 1. Exposure to aqueous sodium tosylate solutions under thermodynamically permselective conditions [J].
Bruckenstein, S ;
Brzezinska, K ;
Hillman, AR .
ELECTROCHIMICA ACTA, 2000, 45 (22-23) :3801-3811
[4]   Application of PEDOT layers for the electrogravimetric detection of sulphate and phosphate in aqueous media [J].
Bund, A. ;
Peipmann, R. .
ELECTROCHIMICA ACTA, 2008, 53 (11) :3772-3778
[5]   Investigations on metal depositions and dissolutions with an improved EQCMB based on quartz crystal impedance measurements [J].
Bund, A ;
Schwitzgebel, G .
ELECTROCHIMICA ACTA, 2000, 45 (22-23) :3703-3710
[6]   Effect of the solvent and the anion on the doping/dedoping behavior of poly(3,4-ethylenedioxythiophene) films studied with the electrochemical quartz microbalance [J].
Bund, A ;
Neudeck, S .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (46) :17845-17850
[7]   Characterization of the viscoelasticity and the surface roughness of electrochemically prepared conducting polymer films by impedance measurements at quartz crystals [J].
Bund, A ;
Schneider, M .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2002, 149 (09) :E331-E339
[8]   MEASUREMENT OF INTERFACIAL PROCESSES AT ELECTRODE SURFACES WITH THE ELECTROCHEMICAL QUARTZ CRYSTAL MICROBALANCE [J].
BUTTRY, DA ;
WARD, MD .
CHEMICAL REVIEWS, 1992, 92 (06) :1355-1379
[9]   Conducting polymer coatings in electrochemical technology - Part 1 - Synthesis and fundamental aspects [J].
Campbell, S. A. ;
Breakspear, Y. Li S. ;
Walsh, F. C. ;
Smith, J. R. .
TRANSACTIONS OF THE INSTITUTE OF METAL FINISHING, 2007, 85 (05) :237-244
[10]   Morphology and conductivity of PEDOT layers produced by different electrochemical routes [J].
Castagnola, Valentina ;
Bayon, Chloe ;
Descamps, Emeline ;
Bergaud, Christian .
SYNTHETIC METALS, 2014, 189 :7-16