Due to their unusual physical and chemical properties, fullerenes and their derivatives appear to be attractive candidates for the construction of supramolecular assemblies and advanced materials [1]. The recent progress in the C 60 chemistry allows the preparation of many fullerene derivatives covalently bonded to donor moities. These systems provide entries into intramolecular processes such as energy and electron transfer [2]. It should be pointed out that the C 60 group appears to be a particularly interesting electron acceptor in photochemical molecular devices because of its symmetrical shape, its large size and the properties of its π-electron system.The efficient photogeneration of long lived charge-separated states by photoinduced electron transfer is of particular interest for initiating photocatalytical reactions or for solar energy conversion (photovoltaic cells). Photovoltaic devices using thin films of interpenetrating bicontinuous networks of C 60 itself or of a C 60 derivative and a number of conjugated polymers have been demonstrated to be promising for large-area photodetectors and solar cells [3]. The film morphology is of crucial importance for the device performance. It is also well known that donor and acceptor molecules are generally incompatible and tend to a strong and uncontrolled phase separation. An alternative approach which has been developed recently is to create the bicontinuous network by chemically connecting the donor and acceptor molecules.The compound under consideration, a fulleropyrrolidine derivative substituted by an oligophenylenevinylene (OPV) moiety has been used for the construction of a solar energy conversion cell [4]. The fullerene-OPV hybrid material leads to a photoinduced charge separation by combining the C 60 electron acceptor and the OPV moiety electron donnor within a unique molecular architecture (see chemical formula on figure 1). A photovoltaic cell has been prepared by spin-casting thin films of this C 60 -OPV derivative on a glass substrate coated with indium-tin-oxide. The 100 µm Al electrode was vacuum evaporated on the films. In such a configuration, this new material is not only able to generate electrons and holes when irradiated, but provides also pathways for their recombination on the electrodes, thus producing a photocurrent. This original chemical approach is in agreement with the basic concepts for obtaining a photocurrent, and is a good illustration of the large possibilities offered by organic chemistry to provide new materials able to be used in photovoltaic devices.The light-collecting and energy-conversion efficiencies of this molecular photovoltaic system is not yet optimized, but further improvements could be expected if using new fullerene derivatives with a strong absorption in the visible range, able to achieve very fast charge separation and slow charge recombination. Microelectronics based on semi-conductors plays an important role in information technology since several decades. However, for the high rates needed for todays highl...