P. Alnot, D.J. Auerbach, et al.
Surface Science
Extensive characterization of the hole mobilities in dispersions of p-diethylamino- benzaldehyde-diphenyl hydrazone (DEH) in polycarbonate has been carried out. We report the effect of varying the electric field E, temperature T, and spacing between DEH molecules on . These data are analyzed by a procedure that allows proper separation of the functional dependencies of the mobility on E, T, and . It is found that ln is proportional to En(T-1-T0-1), where n=0.5 and T0 is a fitted parameter which decreases with increasing , behavior opposite to the dependence of the glass transition temperature on . These experimental results are not yet understood theoretically. Our procedure for separating the and T dependence is applied to data taken on DEH-polycarbonate and to data taken from the literature on another molecularly doped polymer system, N,N diphenyl-N,N-bis (3-methylphenyl)-(1,1-biphenyl)-4,4-diamine (TPD) in polycarbonate. For DEH-polycarbonate, the activation energy is found to be independent of . In contrast, for TPD-polycarbonate the activation energy is strongly dependent on . Our data suggest that small-polaron hopping is occurring in molecularly doped polymers; this different dependence of the activation energy on is consistent with different small-polaron hopping regimes, adiabatic and nonadiabatic, in these two systems. © 1989 The American Physical Society.
P. Alnot, D.J. Auerbach, et al.
Surface Science
William Hinsberg, Joy Cheng, et al.
SPIE Advanced Lithography 2010
T.N. Morgan
Semiconductor Science and Technology
Michiel Sprik
Journal of Physics Condensed Matter