Hybridization of an unoccupied molecular orbital with an image potential state at a lead phthalocyanine/graphite interface.

The interaction of a molecular orbital with a surface state is important to understand the spatial distribution of the wave function at the molecule/substrate interface. In this study, we focus on hybridization of an unoccupied state of lead phthalocyanine (PbPc) with the image potential state (IPS) on a graphite surface. The hybridization modifies the energy-momentum dispersions of the IPS on PbPc films as observed by angle-resolved two-photon photoemission. On the PbPc 1 monolayer film, the IPS band forms a band gap and back-folding appears at the first Brillouin zone boundary due to the periodic potential by the adsorbate lattice. The modification of the dispersion is accompanied by the intensity enhancement of the IPS. We attributed the origin of the modified dispersion and intensity enhancement to a hybridization of the IPS with a molecule-derived unoccupied level. From the photon energy-dependent measurement on multilayer films, we have found the diffuse unoccupied molecular level in the vicinity of the IPS. The tail part of the IPS wave function in the substrate is enhanced by the hybridization with the unoccupied state, and thus strengthens the transition from the occupied substrate band to the hybridized IPS.

Efficient Cycloreversion Reaction of a Diarylethene Derivative in Higher Excited States Attained by Off-Resonant Simultaneous Two-Photon Absorption.

Off-resonant excitation of the closed-ring isomer of a photochromic diarylethene derivative at 730 nm induced the efficient cycloreversion reaction with a yield of ∼20%, while the reaction yield was only 2% under one-photon excitation at 365 nm. Excitation wavelength dependence of the one-photon cycloreversion reaction yield under steady-state irradiation in a wide wavelength range showed that the specific electronic state leading to the large cycloreversion reaction yield, which is originally forbidden in the optical transition but partially allowed owing to the low symmetry of the molecule, is spectrally overlapped with the electronic state accessible by the allowed one-photon optical transition in the UV region. Femtosecond transient absorption spectroscopy also revealed that the off-resonant two-photon excitation preferentially pumped the molecule into the specific state, leading to the 10-fold enhancement of the cycloreversion reaction.