Thermodynamics of nano- and macrocrystalline anatase using cell voltage measurements

In view of increasing scientific and technological interest in nanomaterials, it is important to examine whether or, more exactly, to what extent the thermodynamic parameters change with size. Electrochemical e.m.f. measurements which provide a direct and elegant access to these thermodynamic data have been used in this study to investigate the excess contributions of anatase due to nano-size. The e.m.f. measurements are carried out (250-450 degrees C) on different particle sizes (1.2 mu m-5 nm) using the cell: Au, O-2, Na2Ti6O13, TiO2 (anatase) vertical bar Na-beta '' alumina vertical bar TiO2 (rutile), Na2Ti6O13, O-2, Au. The e.m.f. observed is closely related to the difference of the Gibbs energies of formation (Delta(f)G degrees) of the titania crystals on both sides. Such cell voltage measurements with various sizes of anatase (1200, 100, 15, and 5 nm) as working electrodes enable us to calculate the excess enthalpy and entropy due to surface contributions and to provide refined data for the macroscopic anatase. No electrochemical Ostwald ripening or chemical Ostwald ripening was observed in the case of anatase nanoparticles up to 500 degrees C.