The magnetocaloric properties of a composite material consisting of isolated Gd2O3 nanoparticles with a diameter of 6–8 nm embedded in the pores of a mesoporous silica matrix have been studied. The fascinating nanostructure and composition were properly characterized by small angle X-ray scattering, X-ray absorption near edge structure, and TEM. Almost ideal paramagnetic behavior of the material was observed in the temperature range of 1.8–300 K. When compared to various nanosystems, the presented composite exhibits an extraordinarily large magnetic entropy change of 40 J/kg K for a field variation of 0–5 T at cryogenic temperature (3 K). Considering only the mass of the Gd2O3 nanoparticle fraction, this corresponds to 120 J/kg K. Calculated refrigerant capacities are 100 J/kg and 400 J/kg for the composite and nanoparticles, respectively. Our findings suggest that the combination of the unique porous structure of amorphous silica with fine gadolinium oxide nanoparticles and high value of magnetic entropy change enables to extend the application of the Gd2O3@SiO2 composite, to cryomagnetic refrigeration. In addition, the characteristics of the thermomagnetic behavior have been studied using the scaling analysis of the magnetic entropy change.

A stimuli-responsive drug delivery system consisting of mesoporous silica with its surface modified by p-coumaric acid derivatives (CA) as photo-switchable ligands was studied for the delivery of the non-steroidal anti-inflammatory drug (NSAID) naproxen. For this purpose, MCM-41 mesoporous silica material was prepared and post-synthetically modified by the grafting of a triethoxysilyl derivative of p-coumaric acid, which undergoes a reversible photo-dimerization under UV irradiation and creates the “valves” on the surface of silica allowing targeted opening/closing of the pores. Naproxen was encapsulated into grafted MCM-41 and drug release studies were performed in two different media, in a simulated gastric fluid (pH = 2) and in a simulated body fluid (pH = 7.4). Differences in drug release were observed after irradiation of the material using UV light at λ = 365 nm (closed pore configuration) and UV light at λ = 254 nm (opened pore configuration).