The photoelectrochemistry of single crystal C-60 and fullerene photoel
ectrochemical solar cells is studied. Illuminated and immersed, C-60 i
s shown to drive oxidation of several solution-phase redox couples. Ut
ilization of a photoelectrochemical solid/liquid junction, rather than
solid-state photovoltaic junction, improves the observed photocurrent
. Utilization of a single crystal, rather than a polycrystalline him,
of C-60 decreases dark current to the extent that light-driven charge
transfer dominates. The spectral response and current-voltage behaviou
r in several electrolytes is studied. A low-power fullerene photoelect
rochemical solar cell, utilizing a regenerative polyiodide and ferri/f
errocyanide redox couple, is demonstrated.