The influence of the organic layer thickness on short-circuit photocurrent spectra and efficiency is investigated in heterojunction photovoltaic cells with the electron donor materials poly͑p-phenylenevinylene͒ ͑PPV͒ and Cu-phthalocyanine ͑CuPc͒, respectively, together with C 60 as electron acceptor material. The main process of photocurrent generation after light absorption, exciton generation, and exciton diffusion in the bulk of the absorbing material is given by the exciton dissociation at the donor-acceptor interface. We determined a strong dependence of the optimum layer thickness of the absorbing material on the exciton diffusion length by systematically varying the layer thickness of the electron donor material. Additionally, a significant photocurrent contribution occurred due to light absorption and exciton generation in the C 60 layer with a subsequent hole transfer to PPV, respectively, CuPc at the dissociation interface. Using a simple rate equation for the exciton density we estimated the exciton diffusion lengths from the measured photocurrent spectra yielding ͑12Ϯ3͒ nm in PPV and ͑68Ϯ20͒ nm in CuPc. By systematically varying the layer thickness of the C 60 layer we were able to investigate an optical interference effect due to a superposition of the incident with backreflected light from the Al electrode. Therefore both the layer thickness of the donor and of the acceptor layer significantly influence not only the photocurrent spectra but also the efficiencies of these heterolayer devices. With optimized donor and acceptor layer thicknesses power conversion efficiencies of about 0.5% under white light illumination were obtained.