Doping electrochemical

Fig. 5. Evolution of optical spectra of polypyrrole during electrochemical doping.

The other way to produce EL devices is based on a pin junction [47]. A pin junction with conjugated polymers was realized by electrochemical doping of the... 

One idea to realize a pin junction with conjugated polymers is to create it in situ by electrochemical doping. By using the conjugated polymer in a solid slate electrochemical cell, the production of bipolar light-emitting pin junction devices can be realized [69, 70]. 

Table 5.3 Examples of electronically conducting polymers, y is the level of electrochemical doping and k is the maximum electrical conductivity. Except for poly acetylene and polyparaphenylene, only p-doping is considered... 

This contribution reviews recent results on [Si(Pc)0]n (Pc = phthalocyaninato) solid state electrochemistry and the structural interconversions that accompany electrochemical doping/undoping processes. In aceto-nitrile/(a-Bu)4N+BF4, it is found that a significant overpotential accompanies initial oxidation of as-polymerized [Si(Pc)0]n. This can be associated with an ortho rhomb ic- te tr agonal structural transformation. 

Figure 4. Structural transformations accompanying electrochemical doping and undoping of [Si(Pc)0](BF4)y n materials, y = 0.00-0.50...

It is a convenient aspect of electrochemical doping of the polymer that the electrolyte can provide the counter ion, although a similar result can be achieved via chemical doping under certain circumstances, e.g., Using a radical ion containing species such as sodium naphthalide, Na+ npthT, i.e.,... 

NB. Where only a current density was given in the original Ref. this is quoted in place of the polymerisation potential. c Counter ions are as incorporated during the electrochemical polymerisation process or by subsequent electrochemical doping unless suffixed with (chem.) which indicates the use of chemical doping. d Conductivities f-film, p-pressed pellet. 

Fig. 25. Absorption coefficient vs. photon frequency for PITN. The data were obtained in situ during the injection part of the electrochemical doping cycle with (CI04 ) as the dopant. The cell voltages and corresponding dopant concentrations (in mol%) are indicated. Reproduced from [456b],...

The speed of p- and n-type doping and that of p-n junction formation depend on the ionic conductivity of the solid electrolyte. Because of the generally nonpolar characteristics of luminescent polymers like PPV, and the polar characteristics of solid electrolytes, the two components within the electroactive layer will phase separate. Thus, the speed of the electrochemical doping and the local densities of electrochemically generated p- and n-type carriers will depend on the diffusion of the counterions from the electrolyte into the luminescent semiconducting polymer. As a result, the response time and the characteristic performance of the LEC device will highly depend on the ionic conductivity of the solid electrolyte and the morphology and microstructure of the composite. 

On one hand, the ionic conductor was unique in creating dynamic junction in LEC. On the other hand, the slow ionic motion and irreversibly electrochemical doping under high biasing field were two of the challenges for polymer LECs to be used in practical applications. More recent works have been focusing on the following directions ... 

An optical microcavity produced by the latter process has been applied to tune the emission from erbium-doped PS [Zh6], Erbium compounds like Er203 are known to exhibit a narrow emission band at 1.54 pm, which is useful for optical telecommunications. Several methods have been used to incorporate erbium in PS. A simple and economical way is cathodic electrochemical doping. External quantum efficiencies of up to 0.01% have been shown from erbium-doped PS films under electrical excitation [Lo2]. The emission band, however, is much broader than observed for Er203. This drawback can be circumvented by the use of an optical cavity formed by PS multilayers. In this case the band is narrowed and the intensity is increased because emission is only allowed into optical cavity modes [Lo3]. 

It has been shown that the chemical and electrochemical doping of polymers may be described as a redox reaction which involves the... 

The occurrence of bipolaronic states in the polymer chains promotes optical absorption prior to the n-n gap transitions. In fact, referring to the example (9.30) of the band structure of doped heterocyclic polymers, transitions may occur from the valence band to the bipolaronic levels. These intergap transitions are revealed by changes in the optical absorptions, as shown by Fig. 9.8 which illustrates the typical case of the spectral evolution of polydithienothiophene upon electrochemical doping (Danieli et al., 1985). 

Considerable attention is presently devoted to heterocyclic polymers, such as polypyrrole, polythiophene and their derivatives. The kinetics of the electrochemical doping processes of these polymers has been extensively studied in electrochemical cells using non-aqueous electrolytes. 

---