The charge carrier transport in liquid-crystalline triphenylenes is complet
ely different from the transport in amorphous photoconductors. The high deg
ree of order leads to quasi-one-dimensional transport. In this paper we are
proposing a model for a field-assisted incoherent hopping process in one-d
imensional systems based on Monte Carlo simulations. The numerically determ
ined field and temperature dependences were compared with experimental resu
lts of a butyloxy-substituted triphenylene dimer. In this glass-forming mat
erial the mobility could be measured by a conventional time-of-flight techn
ique in the very large temperature range between 128 and 410K. This dimer i
s, at room temperature, ordered in a discotic hexagonal plastic phase with
a very high hole mobility of 10(-2) cm(2) V-1 s(-1). We have observed a tra
nsition from a nonactivated to a thermally activated behaviour of the charg
e carrier mobility at -20 degrees C, which we assign to a phase transition
from the liquid-crystalline phase to the anisotropic glassy state. The temp
erature dependence in the low-temperature state is in good agreement with o
ur model with a calculated energy distribution of the hopping sites of 48 m
eV. The field dependence is found to be much stronger than theoretically ex
pected.