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Polymer Matrix Electrolytes

Electrolytes used in lithium batteries can be liquid or polymer-based electrolytes. Lithium batteries including liquid electrolytes have been on the market for several years. Lithium ion rechargeable batteries having liquid electrolytes are mass produced for applications such as notebook computers, camcorders and cellular telephones. Lithium batteries based on liquid electrolytes technology have some drawbacks. [Pg.498]

The liquid electrolyte generally requires hermetic sealing, which may reduce the energy density. In addition, for safety reasons, lithium ion rechargeable batteries and lithium-metal primary batteries having liquid electrolytes are designed to vent automatically when certain abuse conditions exist, sucb as a substantial increase in internal pressure which can be caused by internal or external overheating. If the cell is not vented under extreme pressure, it can explode because the liquid electrolyte used in liquid Li cells is extremely flammable. [Pg.498]

An alternative to lithium batteries with liquid electrol5des are those with solid polymer electrolytes. Solid polymer electrodes are generally gel type electrolytes which trap solvent and salt in pores of the polymer to provide a medium for ionic conduction. Typical polymer electrolytes are shown in Table 15.8. [Pg.498]

The polymer electrolyte generally functions as a separator, being in- [Pg.498]

Poly(ethylene oxide) PolyCacrylonitrile) Poly(methyl metbacrylate) PolyCvinyUdene fluoride) Poly(imide) [Pg.499]


Incorporation into a Polymer Layer In recent years a new electrode type is investigated which represents a layer of conducting polymer (such as polyaniline) into which a metal catalyst is incorporated by chemical or electrochemical deposition. In some cases the specific catalytic activity of the platinum crystallites incorporated into the polymer layer was found to be higher than that of ordinary dispersed platinum, probably because of special structural features of the platinum crystallites produced within the polymer matrix. A variant of this approach is that of incorporating the disperse catalyst directly into the surface layer of a solid polymer electrolyte. [Pg.536]

Polymeric conducting systems were also prepared by in situ polymerization of vinyl monomers in ionic liquids [22], with a conductivity of 1 mS/cm. A conductive polymer electrolytes were also prepared by polymerization in liquid EMIm(HF)nF leading to a composite poly(2-hydroxyethyl methacrylate)-EMIm(HF)nF. Recently, polymer electrolytes were prepared in the form of thin foils, by incorporating ionic liquids in a polymer matrix [13-15], Conductivities of polymer-IL or polymer-IL-solvent systems are collected in Table 4. [Pg.102]

The solid polymer electrolyte approach provides enhanced safety, but the poor ambient temperature conductivity excludes their use for battery applications. which require good ambient temperature performance. In contrast, the liquid lithium-ion technology provides better performance over a wider temperature range, but electrolyte leakage remains a constant risk. Midway between the solid polymer electrolyte and the liquid electrolyte is the hybrid polymer electrolyte concept leading to the so-called gel polymer lithium-ion batteries. Gel electrolyte is a two-component system, viz., a polymer matrix... [Pg.202]

We have studied the oxygenation of ferroheme bound to a polymer ligand in the solid state98. The profiles of oxygen uptake by powders of polymer-heme complexes were measured by volumetry, as shown in Fig. 22. The heme complex embedded in the porous polymer matrix or in the poly(electrolyte) aggregate takes up... [Pg.50]

Batteries. Many 7t-conjugated polymers can be reversibly oxidized or reduced. This has led to interest in these materials for charge-storage batteries, since polymers are lightweight compared to metallic electrodes and liquid electrolytes. Research on polymer batteries has focused on the use of polymers as both the electrode and electrolyte. Typical polymer electrolytes are formed from complexes between metal-ion salts and polar polymers such as poly(ethyleneoxide). The conductivity is low at room temperature due to the low mobility of cations through the polymer-matrix, and the batteries work more efficiendy when heated above the glass-transition temperature of the polymer. Advances in the development of polymer electrolytes have included polymers poly(ethylene oxide) intercalated into layered silicates (96). These solid-phase electrolytes exhibit significantly improved conductance at room temperature. [Pg.246]

Ion exchange can be an effective method for the controlled release of ionizable drugs that are coupled with the oppositely charged ionic groups on a polymer matrix, as in ion-exchange resins used in gastrointestinal (Gl) applications. The drug release from such a system depends on the ionic environment, that is, pH and electrolyte concentration within the Gl tract, as well as the properties of the resin (5). [Pg.269]

One area where the relationship between the structure of the polymer matrix and the physical processes of the thin layer has been studied in detail is that of electrodes modified with polymer films. The polymer materials investigated in these studies include both conducting and redox polymers. Such investigations have been driven by the many potential applications for these materials. Conducting polymers have been applied in sensors, electrolytic capacitors, batteries, magnetic storage devices, electrostatic loudspeakers and artificial muscles. On the other hand, the development of electrodes coated with redox polymers have been used extensively to develop electrochemical sensors and biosensors. In this discussion,... [Pg.244]

Figure 18 Various models proposed for the surface films that cover Li electrodes in nonaqueous solutions. The relevant equivalent circuit analog and the expected (theoretical) impedance spectrum (presented as a Nyquist plot) are also shown [77]. (a) A simple, single layer, solid electrolyte interphase (SEI) (b) solid polymer interphase (SPI). Different types of insoluble Li salt products of solution reduction processes are embedded in a polymeric matrix (c) polymeric electrolyte interphase (PEI). The polymer matrix is porous and also contains solution. Note that the PEI and the SPI may be described by a similar equivalent analog. However, the time constants related to SPI film are expected to be poorly separated (compared with a film that behaves like a PEI) [77]. (With copyrights from The Electrochemical Society Inc., 1998.)... Figure 18 Various models proposed for the surface films that cover Li electrodes in nonaqueous solutions. The relevant equivalent circuit analog and the expected (theoretical) impedance spectrum (presented as a Nyquist plot) are also shown [77]. (a) A simple, single layer, solid electrolyte interphase (SEI) (b) solid polymer interphase (SPI). Different types of insoluble Li salt products of solution reduction processes are embedded in a polymeric matrix (c) polymeric electrolyte interphase (PEI). The polymer matrix is porous and also contains solution. Note that the PEI and the SPI may be described by a similar equivalent analog. However, the time constants related to SPI film are expected to be poorly separated (compared with a film that behaves like a PEI) [77]. (With copyrights from The Electrochemical Society Inc., 1998.)...
In the case of ion conductive polymers, gel polymer electrolytes which consist of a polymer matrix, organic solvents and supporting electrolyte, were introduced as novel nonaqueous electrolyte systems in electrochemical applications, such as rechargeable batteries and electric double layer capacitors [3-5], Recently, considerable attention has been devoted to the application of gel poly-... [Pg.417]

The Ni and Pt complexes can also be incorporated into polymer films of quaternized poly(vinylpyridine) (PVP) and deposited onto the transparent electrode (84). Photocurrents are enhanced to microamps (pA), an increase that may be attributed to either the effect of immobilization of the complexes near the electrode surface or an increase of the excited-state lifetimes in the polymer matrix. However, the effective concentrations of the complexes in this study were much greater than for the acetonitrile solutions in their earlier work. The polymer films are not stable to continuous photolysis, and voltammograms of the films are quite sensitive to anions used in the supporting electrolyte. The system can be stabilized by using a polymer blend of PVP and a copolymer containing quaternary ammonium ion and including [Fe(CN)6]4- in the electrolyte solution (85). Upon irradiation of the visible MLCT bands of [M(mnt)2]2 (M = Ni, Pt), photocurrents are produced. The mechanism (Scheme 4) is believed to involve photooxidation of the metal bis(dithiolene) triplet state by the Sn02 electrode, followed by [Fe(CN)6]4 reduction of the monoanion, with completion of the ET cycle as ferricyanide, Fe(CN)6 3, diffuses to the other electrode and is reduced. [Pg.333]

Figure 9 Electroactive Polymer/Lithium battery, (a) During charging of the battery, CIO4 anions enter into the polymer matrix, while Li+ cations move to the lithium cathode where they are reduced to the metallic state Li+ + e — Li. (b) During the discharge, both CIO4 and Li+ ions move back into the electrolyte. Figure 9 Electroactive Polymer/Lithium battery, (a) During charging of the battery, CIO4 anions enter into the polymer matrix, while Li+ cations move to the lithium cathode where they are reduced to the metallic state Li+ + e — Li. (b) During the discharge, both CIO4 and Li+ ions move back into the electrolyte.

See other pages where Polymer Matrix Electrolytes is mentioned: [Pg.498]    [Pg.499]    [Pg.357]    [Pg.358]    [Pg.418]    [Pg.1320]    [Pg.498]    [Pg.499]    [Pg.357]    [Pg.358]    [Pg.418]    [Pg.1320]    [Pg.246]    [Pg.41]    [Pg.42]    [Pg.46]    [Pg.382]    [Pg.101]    [Pg.640]    [Pg.240]    [Pg.120]    [Pg.237]    [Pg.25]    [Pg.203]    [Pg.57]    [Pg.221]    [Pg.241]    [Pg.127]    [Pg.41]    [Pg.260]    [Pg.657]    [Pg.246]    [Pg.419]    [Pg.426]    [Pg.80]    [Pg.166]    [Pg.53]    [Pg.574]    [Pg.331]    [Pg.363]    [Pg.264]    [Pg.1827]   


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Polymer matrices

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