Quantum dots (QDs) of InP strongly adsorb onto transparent, porous, na
nocrystalline TiO2 electrodes prepared by sintering 200-250 Angstrom d
iameter TiO2 colloidal particles. The interparticle space of the TiO2
electrodes is large enough to permit deep penetration of 65-Angstrom I
nP QDs into the porous TiO2 film. The absorption of light increases li
nearly with the thickness of the TiO2 film indicating that the InP QDs
are adsorbed homogeneously on the TiO2 surface. We found that large p
articles adsorb better than smaller ones probably due to less hindranc
e by the stabilizer. The solid films exhibit strong photoconductivity
in the visible region indicating photosensitization of TiO2 by InP QDs
. The photocurrent action spectrum of the TiO2/InP QD film at a potent
ial of +1 V is consistent with the absorption spectrum of the InP QDs.
A photoelectrochemical cell was formed that consisted of p-type InP Q
Ds loaded on TiO2, which was immersed in a I-/I-3(-) or hydroquinone/q
uinone acetonitrile solution, and a Pt counter electrode. These photoe
lectrochemical experiments show that electron transfer from InP QD int
o TiO2 nanoparticles occurs. p-Type InP/TiO2 electrodes are stable dur
ing illumination while n-type photocorrodes in an electrochemical cell
.