Sample-shape dependent energy levels in organic semiconductors

Abstract

Energy levels in an organic semiconductor are mainly determined by the molecular orbital energies of the constituent molecules. Recent studies, however, have revealed that the energy levels can be altered as much as 1 eV by the molecular orientation in the film or the molecular mixing ratio in the binary film, owing to the intermolecular electrostatic interaction. Because of the long-range nature of Coulomb interaction, theory predicts that the electrostatic energy should depend on the sample shape. In this article, we examine the coverage-dependent energy levels of zinc phthalocyanine and per-fluorinated zinc phthalocyanine in the submonolayer region with ultraviolet photoelectron spectroscopy (UPS) and low-energy inverse photoelectron spectroscopy (LEIPS). Using the procedure we reported previously, we separately evaluated the electronic polarization energy and electrostatic energy as a function of coverage. Unlike the electronic polarization, which contributes only as much as 10 meV, the electrostatic energy contributes as much as 120 meV to the coverage-dependent energy shift. We conclude that the shift in energy levels by changing the coverage is attributed to the sample shape-dependent energy level, owing to the long-range nature of the charge--permanent quadrupole interaction.