Cyclic voltammetry has been used to characterize the Ti4+/Ti3+ redox s
ystem in titanosilicalite TS-1. The charge imbalance resulting from th
e reduction of Ti4+ to Ti3+ is compensated by the electrolyte cations
migrating through the porous structure of the zeolite. The maximum ele
ctrochemical current was found to be proportional to the fraction of f
ramework Ti and independent of the structure and the crystal size of t
he material. The technique was very sensitive to the coordination of t
itanium and was used to characterize titanium-peroxo species formed by
framework titanium in the presence of hydrogen peroxide.