Photoinduced electron transfer processes in self-assembled zinc porphyrin (ZnP) or zinc phthalocyanine (ZnPc) with semiconducting (7,6)-and (6,5)-enriched SWCNTs were investigated. To bind photosensitizers to SWCNTs, first, pyrene covalently functionalized with a phenylimidazole (ImPyr) entity was treated with SWCNTs. Exfoliation of SWCNTs occurred due to π−π stacking of pyrene with nanotubes walls leaving the imidazole entity that was subsequently used to coordinate ZnP or ZnPc in o-dichlorobenzene (DCB). The donor-acceptor nanohybrids thus formed were characterized by TEM imaging, steady-state UV-visible-near IR absorption and fluorescence spectra. Free-energy calculations suggested possibility of electron transfer from the photoexcited ZnP or ZnPc to Im-Pyr/SWCNT(n,m) in the nanohybrids. Consequently, steady-state and time-resolved fluorescence studies revealed efficient quenching of the singlet excited state of ZnP or ZnPc with the rate constants of charge separation (k CS ) in the range of (3-6) × 10 9 s -1 . Nanosecond transient absorption technique confirmed the electron transfer products, ZnP •+ ←Im-Pyr/SWCNT •-and ZnPc •+ ←Im-Pyr/SWCNT •-(and opposite charged pairs) having characteristic absorptions with the decay rate constants due to charge recombination (k CR ) in the range of (1.4-2.4) × 10 7 s -1 , corresponding to lifetimes of radical ion-pairs in the 70-100 ns range. The SWCNT •-was further utilized to mediate electrons to hexyl-viologen dication (HV 2+ ) resulting in an electron-accumulation process in the presence of sacrificial electron donor, offering additional proof for the occurrence of photoinduced charge-separation and potential utilization of these materials in light energy harvesting applications. Further, photoelectrochemical cells have been constructed on FTO/SnO 2 electrodes to verify their ability to directly convert light into electricity. An IPCE efficiency of up to 7% has been achieved in case of ZnP←Im-Pyr/SWCNT modified electrode.