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Conducting composite electrodes

Figure 3.2. Scanning electron micrographs of mechanically polished rigid conducting composite electrodes based on (A) Araldite-M-graphite (73.2%3, [B) Araldite-CW2215-graphite (45.8%), (C) silicone-graphite (61,0%), (D) epoxy-H77-graphite (20.0%) (Adapted with permission from Analyst 2002, 127, 1512-1519. Copyright 2002, The Royal Society of Chemistry). Figure 3.2. Scanning electron micrographs of mechanically polished rigid conducting composite electrodes based on (A) Araldite-M-graphite (73.2%3, [B) Araldite-CW2215-graphite (45.8%), (C) silicone-graphite (61,0%), (D) epoxy-H77-graphite (20.0%) (Adapted with permission from Analyst 2002, 127, 1512-1519. Copyright 2002, The Royal Society of Chemistry).
Graphene attracts enormous interest because of its unique properties. Giant intrinsic charge mobility at room temperature makes it a potential material for nanoelectronics. Its optical and mechanical properties are ideal for micro- and nanomechanical systems, thin-film transistors, transparent and conductive composites, electrodes and for photonics. This Chapter will show that Raman Spectroscopy is a very powerful tool for the investigation of graphene, being very sensitive to phonons, electronic states, defects and to the interaction between the fundamental excitations of graphene. [Pg.29]

Electrochemical polymeriza tion of heterocycles is useful in the preparation of conducting composite materials. One technique employed involves the electro-polymerization of pyrrole into a swollen polymer previously deposited on the electrode surface (148—153). This method allows variation of the physical properties of the material by control of the amount of conducting polymer incorporated into the matrix film. If the matrix polymer is an ionomer such as Nation (154—158) it contributes the dopant ion for the oxidized conducting polymer and acts as an effective medium for ion transport during electrochemical switching of the material. [Pg.39]

Composite structures that consist of carbon particles and a polymer or plastic material are useful for bipolar separators or electrode substrates in aqueous batteries. These structures must be impermeable to the electrolyte and electrochemical reactants or products. Furthermore, they must have acceptable electronic conductivity and mechanical properties. The physicochemical properties of carbon blacks, which are commonly used, have a major effect on the desirable properties of the conductive composite structures. Physicochemical properties such as the surface... [Pg.237]

A quite different approach was introduced in the early 1980s [44-46], in which a dense solid electrode is fabricated which has a composite microstructure in which particles of the reactant phase are finely dispersed within a solid, electronically conducting matrix in which the electroactive species is also mobile. There is thus a large internal reactant/mixed-conductor matrix interfacial area. The electroactive species is transported through the solid matrix to this interfacial region, where it undergoes the chemical part of the electrode reaction. Since the matrix material is also an electronic conductor, it can also act as the electrode s current collector. The electrochemical part of the reaction takes place on the outer surface of the composite electrode. [Pg.375]

We believe that new type of conducting polymer / expanded graphite composite electrodes as gas-diffusion cathodes will find in perspective a practical application for some types of batteries and fuel cells. [Pg.124]

The seven papers in Chapter 6 are focused on cathode materials for lithium and lithium-ion batteries. Carbon is used as a conductive additive in composite electrodes for batteries. The type of carbon and the amount can have a large effect on the electrochemical performance of the electrode. [Pg.451]

Among those several different types of transducers based on CNTs, the CNT-composite electrode, which was the first CNT electrode tested in 1996, is still widely used with different composite materials such as conducting polymers, nanoparticles, sol-gel, etc. The usefulness of these electrodes is based on their high sensitivity, quick response, good reproducibility, and particularly long-term stability. We expect to see continued research activities using CNT-composite electrodes. [Pg.516]

The addition of an ionic conductive phase, such as GDC, also promotes the elec-trocatalytic activity of an MIEC cathode. Hwang et al. [108] studied the electrochemical activity of LSCF6428/GDC composites for the 02 reduction and found that the activation energy decreased from 142 kJmol-1 for the pure LSCF electrode to 122 kJmol1 for the LSCF/GDC composite electrodes. Thus, the promotion effect of the GDC is most effective at low-operation temperatures (Figure 3.12). This is due to the high ionic conductivity of the GDC phase at reduced temperatures. [Pg.153]

Besides the aforementioned, preliminary investigations showed that synthesized oligomers and polymers, in combination with phenolformaldehyde resin, were successfully used as binding component for polymer/graphite electro-conducting composites (ECC) [15, 16], Obtained ECC were recommended for creation of electrode material for electrolytic section and the chemical (fuel) sources of electrical energy (on the basis of analogous material) [16],... [Pg.78]

The final step entailed coating both the inner and outer surfaces of the LiMn204 tubules with the conductive polymer polypyrrole [125]. It has been shown that such LiMn204/polypyrrole composite electrodes have lower resistance and higher capacity than electrodes prepared from LiMn204 alone [125]. Furthermore, the high porosity and fast (relative to... [Pg.51]

Figure 48. Kenjo s ID macrohomogeneous model for polarization and ohmic losses in a composite electrode, (a) Sketch of the composite microstructure, (b) Description of ionic conduction in the ionic subphase and reaction at the TPB s in terms of interpenetrating thin films following the approach of ref 302. (c) Predicted overpotential profile in the electrode near the electrode/electrolyte interface, (d) Predicted admittance as a function of the electrode thickness as used to fit the data in Figure 47. (Reprinted with permission from refs 300 and 301. Copyright 1991 and 1992 Electrochemical Society, Inc. and Elsevier, reepectively.)... Figure 48. Kenjo s ID macrohomogeneous model for polarization and ohmic losses in a composite electrode, (a) Sketch of the composite microstructure, (b) Description of ionic conduction in the ionic subphase and reaction at the TPB s in terms of interpenetrating thin films following the approach of ref 302. (c) Predicted overpotential profile in the electrode near the electrode/electrolyte interface, (d) Predicted admittance as a function of the electrode thickness as used to fit the data in Figure 47. (Reprinted with permission from refs 300 and 301. Copyright 1991 and 1992 Electrochemical Society, Inc. and Elsevier, reepectively.)...
The resulting pastes, for all cases, were placed into a PVC cylindrical sleeve body. The conducting composite material glued to the copper contact was cured at 40°C during a week. Before each use, the surface of the electrode was wet with doubly distilled water and then thoroughly smoothed, first with abrasive paper and then with alumina paper (see more details on the preparation of GECE in Procedure 7). [Pg.147]


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See also in sourсe #XX -- [ Pg.418 , Pg.432 , Pg.434 ]




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Composite electrode

Compositions conductive

Conductance electrodes

Conducting composite electrodes with graphite powder

Conductive composites

Conductivity composite

Electrode composition

Electrodes conductivity

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