Photocatalysis
is a physiochemical effect arising from the relaxation
of photoinduced electrons from the conduction band to the valence
band. Controlling the electron relaxation to occur through photocatalytic
pathways and prohibiting other relaxations is the main scientific
thought for photocatalytic studies. It is needed to know the parallel
relaxation pathways that can compete with photocatalytic reactions.
By means of in situ photoconductances (PCs) and photoinduced absorptions
(PAs), the current research studied the photoinduced electron relaxations
of the Au/TiO2 in different atmospheres and at different
temperatures. The PC and PA relaxations became different and fast
when methanol, ethanol, isopropanol, and acetone were introduced;
they also tend to decrease as temperature increases, while that of
the undecorated TiO2 in all atmospheres and the Au/TiO2 in pure N2 increased. The results indicated that
the organic adsorptions over the Au/TO2 perimeters change
the relaxation pathway, and a hole-capturing organics adsorption-induced
recombination over the Au/TiO2 perimeter was proposed to
explain the relaxations. We found that this relaxation also exists
for Ag/TiO2, Pt/TiO2, and Au/ZnO, so it is a
commonly existing physical course for the metal/semiconductor (M/S)
materials. The effect of the organics and M/S structures on the relaxation
was discussed, and the relationship with photocatalytic reactions
was also analyzed. Our finding means that blocking this relaxation
pathway is an effective way to increase photocatalytic activities,
which might open a door for highly active photocatalyst developments.