A bipolar charge transport molecule

Japanese Journal of Applied Physics, Part 1: Regular Papers and Short Notes and Review Papers

Volumn 35, Issue 10, 1996, Pages 5384-5388

  Murray, B J ^a   Kaeding, J E ^a   Gruenbaum, W T ^a   Borsenberger, P M ^a  

^a EASTMAN KODAK COMPANY   (United States)

Author keywords

Bipolar charge transport; Disorder controlled hopping; Molecular glasses

Indexed keywords

BIPOLAR CHARGE TRANSPORT; DISORDER CONTROLLED HOPPING; ELECTRON MOBILITIES; MOLECULAR GLASSES;

CHARGE CARRIERS; CHEMICAL VAPOR DEPOSITION; ELECTRON TRANSPORT PROPERTIES; MOLECULAR STRUCTURE; ORGANIC COMPOUNDS;

MOLECULAR PHYSICS;

EID: 0030259446     PISSN: 00214922     EISSN: None     Source Type: Journal    
DOI: 10.1143/jjap.35.5384     Document Type: Article

References (47)

1. G. Pfisler: Phys. Rev. B 16 (1977) 3676.
2. J. Mort and G. Pfister: Polym. Plast. Technol. Eng. 12 (1979) 89.
3. D. M. Pai, J. F. Yanus, M. Stolka, D. Renfer and W. W. Limburg: Philos. Mag. B 48 (1983) 505.
4. J. S. Facci and M. Stolka: Philos. Mag. B 54 (1986) 1.
5. D. M. Pai: J. Non-Cryst. Solids 59 & 60 (1983) 1255.
6. D. M. Pai and A. R. Melnyk: Proc. SPIE 617 (1986) 82.
7. M. A. Abkowitz and M. Stolka: Proc. Int. Symp. Polymers for Advanced Technologies, ed. M. Lewin (VCH Publishers, New York, 1988) p. 225.
8. D. M. Pai: Frontiers of Polymer Research, eds. P. N. Prasad and J. K. Nigam (Plenum Press, New York, 1991) p. 315.
9. P. M. Borsenberger and D. S. Weiss: Organic Photoreceptors for Imaging Systems (Marcel-Dekker, New York, 1993).
10. D. M. Pai and B. E. Springett: Rev. Mod. Phys. 65 (1993) 163.
11. M. Stolka and J. Mort: Kirk-Othmer Encyclopedia of Chemical Technology (J. Wiley and Sons, New York, 1994) Vol. 9, p. 245.
12. P. Di Marco and G. Giro: Organic Conductors, Fundamentals and Applications, ed. K.-P. Farges (Marcel Dekker, New York, 1994) p. 791.
13. D. M. Pai: Proc. Eleventh Int. Congr. Advances in Non-Impact Printing Technolgies, eds. J. Anderson (IS&T, Springfield, Virginia, 1995) p. 46.
14. C. W. Tang, S. A. Van Slyke and C. H. Chen: J. Appl. Phys. 65 (1989) 3610.
15. J. Kido, K. Hongawa, M. Kohda, K. Nagai and K. Okuyama: Jpn. J. Appl. Phys. 31 (1992) L960.
16. S. Saito, E. Aminaka, T. Tsutsui and M. Era: J. Lumin. 60 & 61 (1994) 902.
17. C. Adachi, K. Nagai and N. Tamoto: Appl. Phys. Lett. 66 (1995) 2679.
18. G. A. Chamberlin: Sol. Cells 8 (1983) 47.
19. C. W. Tang: Appl. Phys. Lett. 48 (1986) 183.
20. D. Wöhrle and D. Meisser: Adv. Mater. 3 (1991) 129.
21. N. Karl, A. Bauer, J. Holzäpfel, J. Marktanner, M. Möbus and F. Stölzle: Mol. Cryst. Liq. Cryst. 252 (1994) 252.
22. J. Mort and G. Pfister: Electronic Properties of Polymers, eds. J. Mort and G. Pfister (J. Wiley and Sons, New York, 1982) p. 215.
23. J. Mort and D. M. Pai: Noncrystalline Semiconductors, ed. M. Pollak (CRC Press, Boca Raton, FL, 1987) p. 35.
24. D. Haarer: Angew Makromol. Chem. 183 (1990) 197.
25. M. A. Abkowitz: Philos. Mag. B 65 (1992) 817.
26. A. V. Vannikov, A. D. Grishina and S. V. Novikov: Russ. Chem. Rev. 63 (1994) 103.
27. V. Mylinkov: Photoconducting Polymers and Metal-Containing Polymers, Advances in Polymer Science (Springer-Verlag, Berlin, 1994) p. 1.
28. W. D. Gill: J. Appl. Phys. 43 (1972) 5033.
29. W. D. Gill: Proc. Fifth Int. Conf. Amorphous and Liquid Semiconductors, eds. J. Stuke and W. Brenig, (Taylor and Francis, London, 1974) p. 901.
30. W. D. Gill: Photoconductivity and Related Phenomena, eds. J. Mort and D. M. Pai (Elsevier, Amsterdam, 1976) p. 303.
31. Y. Yamaguchi: Ph.U. Thesis, Faculty of Engineering, Osaka University, 1992.
32. Y. Yamaguchi, T. Fujiyama, H. Tanaka and M. Yokoyama: Chem. Mater. 2 (1990) 341.
33. Y. Yamaguchi, T. Fujiyama and M. Yokoyama: Can. J. Chem. 69 (1991) 759.
34. Y. Yamaguchi, T. Fujiyama and M. Yokoyama: J. Appl. Phys. 70 (1991) 855.
35. E. H. Magin, W. T. Gruenbaum and P. M. Borsenberger: Proc. Eleventh Int. Cong. Advances in Non-Impact Printing Technologies, ed. J. Anderson (IS&T, Springfield, Virginia, 1995) p. 64.
36. For doped polymers, the maximum dopant concentration that can be used without crystallization is typically 50% (by weight). For equal donor and acceptor concentrations, the maximum concentrations for ternary mixtures are thus approximately 25%.
37. H. Bässler: Phys. Status Solidi B 175 (1993) 15.
38. H. Bässler: Int. J. Mod. Phys. 8 (1994) 847.
39. H. Bssler: Disorder Effects on Relaxation Processes, eds. R. Richert and A. Blumen (Springer-Verlag, Berlin, 1994) p. 485.
40. H. Bässler: Mol. Cryst. Liq. Cryst. 252 (1995) 11.
41. P. M. Borsenberger, W. T. Gruenbaum and E. H. Magin: Phys. Status Solidi B 190 (1995) 555.
42. P. M. Borsenberger, W. T. Gruenbaum, J. E. Kaeding and E. H. Magin: Phys. Status Solidi B 191 (1995) 171.
43. A. R. Melnyk and D. M. Pai: Physical Methods of Chemistry, eds. B. W. Rossiter and R. C. Baetzold (J. Wiley and Sons, New York, 1993) Vol. 8, 2nd ed., p. 32.
44. J. C. Scott, L. Th. Pautmeier and L. B. Schein: Phys. Rev. B 46 (1992) 8603.
45. L. B. Schein: Philos. Mag. B 65 (1992) 795.
46. P. M. Borsenberger, L. Pautmeier and H. Bssler: J. Chem. Phys. 94 (1991) 5447.
47. P. M. Borsenberger, L. Pautmeier, R. Richert and H. Bässler: J. Chem. Phys. 94 (1991) 8276.