The potential of Lu(3)N@C(80) and its analogues as electron acceptors in the areas of photovoltaics and artificial photosynthesis is tremendous. To this date, their electron-donating properties have never been explored, despite the facile oxidations that they reveal when compared to those of C(60). Herein, we report on the synthesis and physicochemical studies of a covalently linked Lu(3)N@C(80)-perylenebisimide (PDI) conjugate, in which PDI acts as the light harvester and the electron acceptor. Most important is the unambiguous evidence--in terms of spectroscopy and kinetics--that corroborates a photoinduced electron transfer evolving from the ground state of Lu(3)N@C(80) to the singlet excited state of PDI. In stark contrast, the photoreactivity of a C(60)-PDI conjugate is exclusively governed by a cascade of energy-transfer processes. Also, the electron-donating property of the Lu(3)N@C(80) moiety was confirmed through constructing and testing a bilayer heterojunction solar cell device with a PDI and Lu(3)N@C(80) derivative as electron acceptor and electron donor, respectively. In particular, a positive photovoltage of 0.46 V and a negative short circuit current density of 0.38 mA are observed with PDI/Ca as anode and ITO/Lu(3)N@C(80) as cathode. Although the devices were not optimized, the sign of the V(OC) and the flow direction of J(SC) clearly underline the unique oxidative role of Lu(3)N@C(80) within electron donor-acceptor conjugates toward the construction of novel optoelectronic devices.