Abstract
Ultraviolet photoelectron spectra were measured for ultrathin films of OTi-phthalocyanine (OTiPc), which has an electric dipole perpendicular to the molecular plane, prepared on highly oriented pyrolytic graphite in order to study effects of the molecular orientation and the electric dipole layer on the organic electronic states. For the as-grown films, the observed highest occupied molecular orbital (HOMO) band consists of two prominent peaks that can be assigned to different molecular orientations. For the oriented monolayer obtained by annealing the as-grown film, we detected a very sharp HOMO band at 290 K. The binding-energy ( E B) difference between the HOMO bands of the as-grown and annealed films was found to agree with the shift in the vacuum level. For the oriented monolayer, the observed sharp HOMO band involves at least four components that are ascribed to the coupling between the HOMO hole and the molecular vibration. Upon cooling the sample to 95 K, the HOMO bandwidth became sharper than that at 290 K. From the peak fitting using Voigt function, additional components are expected in the HOMO band at 95 K. Moreover, we detected the E B shift in the HOMO band for the oriented monolayer upon cooling, which can be originated from decrease in the HOMO-hole screening due to the change in the film structure and/or the molecule-substrate interaction.
Published Version
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