Recently organic optics becomes a hot topic due to the rapid development of
organic light-emitting diodes, organic solar cells, and organic photon
detectors. The optical spectra of the molecular semiconductors are difficult to
solve an model from first-principles because (i) the very large number of atoms
in a unit cell and (ii) the accurate theoretical excited state is still under
development. Here we present a tight-binding model of an exciton band structure
in a molecular chain. We take into account the intra-molecule and
charge-transfer excitation within a molecular dimer in a unit cell, then we
apply the tight-binding model by including the coupling between two types of
excitations. We not only found that our calculations can explain a body of
UV-Vis optical spectra of transition-metal phthalocyanines, but also a
one-dimensional excitonic topological band structure if we fine-tune the
couplings in a dimerized molecular chain. We have found a large space to obtain
the topological Zak phase in the parameter space, in which there is a simple
linear relationship between the hopping integrals between cells and within
cell.Comment: 5 pages, 5 figure