A new concept of photoresponsive composites has been elaborated by intimately connecting a Photochromic Phase (PP), (H(2)DABCO)(2)(HDMA)(0.5)Na(0.75)(H(3)O)(0.75)[Mo(8)O(27)]·3H(2)O (1), with a second hybrid organic-inorganic molybdate material, (H(2)DABCO)(HDABCO)[Fe(OH)(6)Mo(6)O(18)]·4H(2)O (2) acting as an Oxidation Catalytic Phase (OCP) toward the former once photoexcited. The association of both the PP and the OCP in the composite drastically improves the bleaching process of the PP alone because of efficient electronic transfers through the OCP-PP interface without affecting significantly its photoinduced color change characteristic. Two OCP-PP composites with different PP weight percents have been obtained by associating 1 with 2. The optical properties of these composites before and after UV irradiation have been investigated by Diffuse Reflectance Spectroscopy, and the strong impact of the OCP on the fading kinetics of the PP has been clearly highlighted.

The preparation of Th1-xYxO2-x/2 ceramics, to be used as electrolyte in oxygen sensors for sodium-cooled nuclear reactors, was successfully undertaken from oxalate precursors. Such method was found to provide quantitative precipitation of the cations into Th1-xYx(C2O4)2.2H2O solid solutions up to x = 0.15 while a polyphase system was obtained for x = 0.22. The corresponding oxides were obtained through heat treatment in air at 500°C and characterized by the means of PXRD, SEM and statistical X-EDS measurements. The conditions for the densification of Th1-xYxO2-x/2 ceramics were further determined by dilatometry (T = 1575°C, t = 8 hours) resulting in densification rates up to 99%. Finally, a first estimation of the electric properties of the solids was undertaken by impedance spectroscopy. Electrical conductivity was found to increase linearly with the incorporation of Y 3+ content while the associated values of activation energy decreased, with a minimum value of 1.1 eV for Th0.85Y0.15O1.925.