Magnetic field effects on the photoelectrochemical reactions of photosensitive electrodes modified with C 60 nanoclusters were examined, intended for the development of nanodevices where photofunctions were controllable with magnetic field. Mixed clusters of a C 60 derivative (C 60 N + ) containing a positive charge and methylphenothiazine (MePH) were prepared by dissolving them in the THF-H 2 O mixed solvent. Diameters of the clusters were estimated to be ca. 100 nm from dynamic light scattering and AFM measurements. Photofunctional electrodes with the nanoclusters of C 60 N + and MePH were fabricated on the electrodes modified with a self-assembled monolayer of HS(CH 2 ) 2 SO 3 À Na + on a gold substrate. The photocurrent action spectrum of the cluster-modified electrode strongly indicates that the photocurrents are ascribed to the photoexcitation of the nanoclusters of C 60 N + . Furthermore, the photocurrents increased with increasing an external magnetic field, typically 3% at 0.5 T. The profile of magnetic field dependence on the photocurrents is in good agreement with the results on the dynamics of radical pair in the nanoclusters of C 60 N + and MePH in the THF-H 2 O mixed solvent. This is suggested that the magnetic field effects are ascribable to the contribution of triplet radical pair that are generated by photoinduced intermolecular electron-transfer from MePH to triplet excited state of nanocluster of C 60 N + , and are explained in terms of spin-lattice relaxation mechanism in radical pair mechanism. r