Dye-sensitization processes for the (001) surface of n-type titanium o
xide (n-TiO2) single crystal coated with vacuum-deposited titanylphtha
locyanine (TiOPc) were investigated by means of photoelectrochemical m
easurements and X-ray and ultraviolet photoelectron spectroscopy (XPS,
UPS). The electrode of n-TiO2 coated with TiOPc exhibited two photoox
idation current bands in an aqueous electrolyte including hydroquinone
(H(2)Q), due to direct excitation of n-TiO2 below 420 nm and electron
transfer from TiOPc to n-TiO2 under the Q-band absorption of TiOPc at
600-800 nm, respectively, The former photocurrent process due to n-Ti
O2 excitation was remarkably decreased by presence of surface states,
which originated from defects of oxygen induced by Ar ion bombardment
of the n-TiO2 surface. The photooxidation process sensitized by the la
tter was evaluated from the determined energy levels of electronic ban
ds for n-TiO2 and TiOPc. The LUMO level of TiOPc was located 0.3 eV ab
ove that of n-TiO2, which enabled electrons to transfer from TiOPc to
n-TiO2. The excited state of TiOPc was not quenched by the surface sta
tes of n-TiO2 but was efficiently transferred to n-TiO2 at the n-TiO2/
TiOPc interface.