Paper
4 April 2007 Mixed-ion linear actuation of PPy and PEDOT in propylene carbonate-triflate electrolytes
Rudolf Kiefer, Paul A. Kilmartin, Graham A. Bowmaker, Ralph P. Cooney, Jadranka Travas-Sejdic
Author Affiliations +
Abstract
Investigations of the actuation properties of free standing PPy and PEDOT films in a propylene carbonate-triflate electrolyte (PC/TBACF3SO3) under isotonic (constant load) conditions are presented in this work. The PPy film showed mixed ion movement during charging and discharging in cyclic voltammetric and chronoamperometric experiments. At a potential of -1.0 V the maximum strain was in the range of 1-2 % whereas at the anodic potential of +1.0 V strains in the range of 3-4 % were observed. Cyclic voltammetry experiments at higher scan rates to 10 mV/s led to a decrease in the anodic strain and an increase in the cathodic strain before it declined at higher scan rates. The free-standing PEDOT films showed mainly cathodic actuation at the potential -1.0 V and the size of actuation was again dependent upon the scan rate. Cation movement is discussed in terms of the immobilisation of CF3SO3- anions during polymerisation. Extended potential step experiments showed good actuation and low creep in the potential range between 0.0 and +1.0 V. The surface morphology (SEM) showed an open porous structure for PEDOT in contrast to the smooth morphology of PPy.
© (2007) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Rudolf Kiefer, Paul A. Kilmartin, Graham A. Bowmaker, Ralph P. Cooney, and Jadranka Travas-Sejdic "Mixed-ion linear actuation of PPy and PEDOT in propylene carbonate-triflate electrolytes", Proc. SPIE 6524, Electroactive Polymer Actuators and Devices (EAPAD) 2007, 65240U (4 April 2007); https://doi.org/10.1117/12.715089
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Cited by 7 scholarly publications.
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KEYWORDS
Polymers

Polymer thin films

Polymerization

Electrodes

Ions

Scanning electron microscopy

Actuators

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