Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Electroactive polymer

Figure 17.49 Cyclic voltammery of Co(DTB)32 + at a transparent PEDOT modified FTO. Scan speed 100 mV/s, potential referred to SCE. The smaller peak centered at about —650 mV is determined by the intrinsic polymer electroactivity. PEDOT was grown by multiple scan deposition (three scans), cycling the potential between —0.7 and +1.5 V versus SCE with a scan speed of 20mV/s. From Bignozzi et al., unpublished results. Figure 17.49 Cyclic voltammery of Co(DTB)32 + at a transparent PEDOT modified FTO. Scan speed 100 mV/s, potential referred to SCE. The smaller peak centered at about —650 mV is determined by the intrinsic polymer electroactivity. PEDOT was grown by multiple scan deposition (three scans), cycling the potential between —0.7 and +1.5 V versus SCE with a scan speed of 20mV/s. From Bignozzi et al., unpublished results.
As with the majority of ISEs, all of the aforementioned receptors are immobilised within close proximity to the transducer element. However, conducting polymers (electroactive conjugated polymers) are now emerging rapidly as one of the most promising classes of transducer for use within chemical sensors. Here, the receptor can be doped within the polymer matrix, i.e. within the transducer element itself. This will facilitate the production of reliable, cost-effective, miniaturised anion-selective sensors, as it will be possible to move away from plasticiser-based membranes, but allow for ion recognition sites in conjunction with all-solid-state ion-to-electron transducers. [Pg.108]

Lyons, M.E.G. 1994. Electrocatalysis using electroactive polymers, electroactive composites and microheterogeneous systems. Analyst 119, 805-826. [Pg.292]

In this chapter, attention is focused on a number of polymers that are either themselves characterized by special properties or are modified for special uses. These include high-temperature and fire-resistant polymers, electroactive polymers, polymer electrolytes, liquid crystal polymers (LCPs), polymers in photoresist applications, ionic polymers, and polymers as reagent carriers and catalyst supports. [Pg.543]

The general procedure consists in applying an electrochemical signal to the working electrode dipped in the solution containing the electrolyte and the monomer for an appropriate time. Then, the electrode is washed and rinsed, and the electrolysis medium is replaced by a monomer-free electrolyte solution in order to check the polymer electroactivity. [Pg.250]

Akle BJ, Leo DJ (2008) Single-walled earbon nanotubes ionic polymer electroactive hybrid transducers. J Intell Mater Syst Struct 19 905-915 Akle BJ, Bennett MD, Leo DJ (2006) High-strain ionomeric-ionic hquid electroactive actuators. [Pg.168]

Deshpande SD, Kim J, Yun SR (2005b) Studies on conducting polymer electroactive paper actuators effect of humidity and electrode thickness. Smart Mater Struct 14 876-880. doi 10.1088/0964-1726/14/4/048... [Pg.251]

Table 20.8 contains a compilation of literature entries on the voltammetry of conducting polymer films. The scope of these studies is similar to that of the transient experiments discussed in Section V.A in terms of the types of electrodes and media employed. Both cyclic and hydrodynamic voltammetry have been used as shown in Table 20.8. Other aspects under discussion include the mathematic modeling of cyclic voltammo-grams [277,278], the occurrence and origin of prewaves in the cyclic voltammograms [319], the use of very fast scan rates [220], structural relaxation effects and their manifestation in voltammetry [304,317,320], the inactivation of polymer electroactivity when driven to extreme potentials, and the so-called polythiophene paradox [225,226,306,321]. Unusual media and cryogenic temperatures have also been employed for the volta-mmetric observation of doping phenomena [322-325]. Dual-electrode voltammetry (Section II.1) has been performed on derivatized polypyrrole [290] in an attempt to deconvolute the electronic and ionic contributions to the overall conductivity of the sample as a function of electrode potential. Finally, voltammetry has been carried out in the solid state , i.e., in the absence of electrolyte solutions [215,323]. Table 20.8 contains a compilation of literature entries on the voltammetry of conducting polymer films. The scope of these studies is similar to that of the transient experiments discussed in Section V.A in terms of the types of electrodes and media employed. Both cyclic and hydrodynamic voltammetry have been used as shown in Table 20.8. Other aspects under discussion include the mathematic modeling of cyclic voltammo-grams [277,278], the occurrence and origin of prewaves in the cyclic voltammograms [319], the use of very fast scan rates [220], structural relaxation effects and their manifestation in voltammetry [304,317,320], the inactivation of polymer electroactivity when driven to extreme potentials, and the so-called polythiophene paradox [225,226,306,321]. Unusual media and cryogenic temperatures have also been employed for the volta-mmetric observation of doping phenomena [322-325]. Dual-electrode voltammetry (Section II.1) has been performed on derivatized polypyrrole [290] in an attempt to deconvolute the electronic and ionic contributions to the overall conductivity of the sample as a function of electrode potential. Finally, voltammetry has been carried out in the solid state , i.e., in the absence of electrolyte solutions [215,323].
The size-exclusion and ion-exchange properties of zeoHtes have been exploited to cause electroactive species to align at a zeoHte—water interface (233—235). The zeoHte thus acts as a template for the self-organization of electron transfer (ET) chains that may find function as biomimetic photosynthetic systems, current rectifiers, and photodiodes. An example is the three subunit ET chain comprising Fe(CN)g anion (which is charge-excluded from the anionic zeoHte pore stmcture), Os(bipyridine)3 (which is an interfacial cation due to size exclusion of the bipyridine ligand), and an intrazeoHte cation (trimethylamino)methylferrocene (F J ). A cationic polymer bound to the (CN) anion holds the self-assembled stmcture at an... [Pg.209]

Conducting Polymer Blends, Composites, and Colloids. Incorporation of conducting polymers into multicomponent systems allows the preparation of materials that are electroactive and also possess specific properties contributed by the other components. Dispersion of a conducting polymer into an insulating matrix can be accompHshed as either a miscible or phase-separated blend, a heterogeneous composite, or a coUoidaHy dispersed latex. When the conductor is present in sufftcientiy high composition, electron transport is possible. [Pg.39]

Efficiency of the Polymerization Charge in Producing Electroactive Polymers... [Pg.324]

The final conclusion from the different kinetic studies that simultaneously followed productivity, consumed current, storage capacity of the obtained films, and the current efficiency in generating electroactive polymer in the final film is that any electropolymerization of conducting polymers occurs together a partial degradation of the electroactive polymer. The final film is a mixed material. From the kinetic studies we know the variables that increase or deplete the degradation reaction in relation to the polymerization reaction. [Pg.329]

The polymer-solvent interaction parameter, which is a key constant defining the physical chemistry of every polymer in a solvent, can be obtained from electrochemical experiments. Definition and inclusion of this interaction was a milestone in the development of polymer science at the beginning of the 1950s. We hope that Eq. 47 will have similar influence in the development of all the cross-interactions of electrochemistry and polymer science by the use of the ESCR model. A second point is that Eq. 47 provides us with an efficient tool to obtain this constant in electroactive... [Pg.403]


See other pages where Electroactive polymer is mentioned: [Pg.33]    [Pg.8]    [Pg.198]    [Pg.74]    [Pg.434]    [Pg.915]    [Pg.14]    [Pg.38]    [Pg.9]    [Pg.33]    [Pg.8]    [Pg.198]    [Pg.74]    [Pg.434]    [Pg.915]    [Pg.14]    [Pg.38]    [Pg.9]    [Pg.1939]    [Pg.135]    [Pg.135]    [Pg.333]    [Pg.407]    [Pg.41]    [Pg.231]    [Pg.21]    [Pg.151]    [Pg.313]    [Pg.321]    [Pg.324]    [Pg.324]    [Pg.324]    [Pg.325]    [Pg.325]    [Pg.325]    [Pg.330]    [Pg.368]    [Pg.381]    [Pg.427]   
See also in sourсe #XX -- [ Pg.135 ]




SEARCH



Advantages of Electroactive Polymers

Artificial muscles ionic electroactive polymer

Biomedical Applications of Electroactive Polymer Actuators Edited by Federico Carpi and Elisabeth Smela

Biomedical Applications of Electroactive Polymer Actuators Edited by Federico Carpi and Elisabeth Smela 2009 John Wiley Sons Ltd. ISBN

Catalytic Systems Using Electroactive Polymer Films

Conducting polymers electroactive

Conductive Electroactive Polymers

Conductive Electroactive Polymers mechanism

Conductive Electroactive Polymers molecular structure

Conductive Electroactive Polymers monomer type

Conductive Electroactive Polymers morphology

Conductive Electroactive Polymers oxidant

Conductive Electroactive Polymers solvent

Conductive Electroactive Polymers structure

Conductive Electroactive Polymers substitution

Conductive Electroactive Polymers temperature

Dielectric Elastomers as Electroactive Polymers (EAPs) Fundamentals

Doped poly Electroactive polymers

Electroactive

Electroactive Fluorene Copolymers and Devices Made with Such Polymers

Electroactive Polymer Actuators and Devices

Electroactive Polymers as Mixed Conductors

Electroactive Polymers as Sensors

Electroactive conducting polymers electrochromism

Electroactive layers polymers

Electroactive polymer , IPMCs

Electroactive polymer actuators

Electroactive polymer actuators (ionic

Electroactive polymer actuators (ionic actuation

Electroactive polymer actuators (ionic actuation mechanism

Electroactive polymer actuators (ionic actuation strain

Electroactive polymer actuators (ionic applications

Electroactive polymer actuators (ionic artificial muscles

Electroactive polymer actuators (ionic performance

Electroactive polymer actuators (ionic sensors

Electroactive polymer artificial muscle

Electroactive polymer artificial muscle sensors

Electroactive polymer blends

Electroactive polymer film dynamics

Electroactive polymer films

Electroactive polymer materials

Electroactive polymer redox conduction

Electroactive polymer redox switching

Electroactive polymers conductive coating methods

Electroactive polymers doping

Electroactive polymers electrochromic devices

Electroactive polymers microelectronics

Electroactive polymers ordered thin films

Electroactive polymers polymeric electrolytes

Electroactive polymers properties

Electroactive polymers rechargeable batteries

Electroactive polymers redox process

Electroactive polymers, applications

Electroactivity

Electrodiffusional Transport in Electroactive Polymer Films

Electronic electroactive polymers

Electropolymerized electroactive polymer

Ionic electroactive polymer

Light-Emitting Polymers and Electroactive Materials

Membranes electroactive polymer

Menten Substrate Kinetics in Electroactive Polymer Films

Percolation in Electroactive Polymers Basic Concepts

Percolation in Electroactive Polymers Experimental Techniques

Poly electroactive polymer

Polymer electrodes electroactive

The field of electroactive polymers

The future of electroactive polymers

Voltammetry, electroactive polymers

Wave-Shape Pattern Control of Electroactive Polymer Gel

Wave-Shape Pattern Formation of Electroactive Polymer Gel

© 2024 chempedia.info