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              Polymers, Electronic Properties                                                             657

              carrier ranges because of their very long deep-trapping  technological promise, although, because of the infancy
              lifetimes.                                        of this class of electronic polymers, further advances lead-
                For systems in which the photogeneration occurs by  ing to other innovations cannot be ruled out.
              photoexcitation within a polymer, such as the charge-
              transfer complexes or dye-sensitized systems, the pho-
              togeneration efficiency can be controlled by a geminate  SEE ALSO THE FOLLOWING ARTICLES
              recombination mechanism. This type of carrier recombi-
              nation in molecular systems can lead to quantum efficien-  ELECTRONS IN SOLIDS • FULLERENES AND CARBON
              cies for photogeneration that are substantially less than  NANOTUBES • ORGANIC CHEMICAL SYSTEMS,THEORY
                                                                • PHOTOGRAPHIC PROCESSES AND MATERIALS • POLY-
              unity and are strongly field dependent. This may result in
              a photosensitivity limitation, depending on the particular  MERS,FERROELECTRIC • POLYMERS,SYNTHESIS
              system, and can be overcome to some degree by increasing
              the light exposure in a machine.
                For other electronic applications, the magnitudes of the  BIBLIOGRAPHY
              carrier mobilities are of paramount importance, since they
              determine the frequency response of devices or, through  Chiang, C. K., Druy, M. A., Gau, S. C., Heeger, A. J., Louis, E. J.,
                                                                 MacDiarmid, A. J., Park, Y. W., and Shirakawa, H. (1978). “Synthesis
              the related diffusion lengths, determine ultimate collection
                                                                 of highly conducting films of derivatives of poyacetylene (CH) x ,”
              efficiencies in devices such as photovoltaic cells. Pendant-  J. Am. Chem. Soc. 100, 1013.
              group polymers and disordered molecularly doped sys-  Farges, J.-P. (1994). “Organic Conductors: Fundamentals and Applica-
              tems are not likely to find applications in these areas be-  tions,” Marcel Dekker, New York.
              cause of their low mobilities and the probable importance  Kahol, P. K., Harbeke, G., and Clark, G. C. (1992). “Conjugated Con-
                                                                 ducting Polymers,” Springer-Verlag, Berlin/New York.
              of geminate recombination processes.
                                                                Kroschwitz, J., ed. (1988). “Electrical and Electronic Properties of Poly-
                A major commercial application of highly conductive  mers: A State-of-the-Art Compendium,” Wiley, New York.
              polymers, such as doped polyacetylene, has yet to be re-  Nalwa, H. S. (1997). “Handbook of Organic Conductive Molecules and
              alized. Potential uses that have been explored or are cur-  Polymers: Vol. 1, Charge-Transfer Salts, Fullerenes and Photocon-
              rently under study include experimental photovoltaic and  ductors,” Vol. 1, Wiley, New York.
                                                                Okamura, S., and Ranby, B. (1994). “Photoconducting Polymers/Metal-
              photoelectrochemical cells and lightweight rechargeable
                                                                 Containing Polymers,” Springer-Verlag, Berlin/New York.
              batteries. Organic batteries, based on reversible electro-  Skotheim, T. A., and Elsenbaumer, R. L. (1997). “Handbook of Con-
              chemical doping, in particular, appear to hold the most  ducting Polymers,” 2nd ed., Marcel Dekker, New York.
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