Electron transfer (ET) processes are of fundamental importance
in many photochemical processes in biological and chemical systems.
Here, semiconductor nanoparticles of ZnS (as electron relay) and trans-stilbene molecules (t-St) (as electron
donor), both confined within the porous volume of mordenite (MOR),
are combined to mimic photosynthetic processes. ZnS nanoparticles
were synthesized by cationic exchange between the counterion of the
zeolite and ZnS precursors in solution. The characterization of the
ZnS/Na-MOR composite was performed by powder X-ray diffraction (XRD),
diffuse reflectance UV–vis spectroscopy, X-ray photoelectron
spectroscopy (XPS), and transmission electron microscopy (TEM) coupled
with energy-dispersive X-ray spectroscopy (EDS). These complementary
techniques highlight the successful formation of ZnS nanoparticles
at the surface of Na-MOR. The electron transfer mechanisms taking
place after the incorporation and photoionization of t-St molecules were evaluated using diffuse reflectance UV–vis
spectroscopy. The results show the formation of long-lived t-St•+@ZnS/Na-MOR•– charge-separated states (lifetime = 18 min; k =
0.0553 min–1) whose stability is linked to the nature
of the new charge compensating cation and to the close proximity of
the ZnS nanoparticles, which are probably located within the zeolite
framework. Indeed, the augmentation of the transient species lifetime
was attributed to an electron transfer from the t-St molecule toward the ZnS conduction band.