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Enhancing the optical emission of cerium oxide nanoparticles is essential for potential biomedical applications. In the present work, we report a simple chemical precipitation technique to synthesize europium-doped cerium oxide nanostructures to enhance the emission properties. Structural and optical properties showed an acute dependence on the concentration of oxygen ion vacancy and trivalent cerium, which, in turn, could be modified by dopant concentration and the annealing temperature. Results from X-ray photoelectron spectroscopy showed an increase in tetravalent cerium concentration to 85% on annealing at 900 degrees C. The concentration of oxygen ion vacancy increased from 1.7x10(20) cm(-3) to 4.1x10(20) cm(-3) with the increase in dopant concentration. Maximum emission at room temperature was obtained for 15 mol % Eu-doped ceria, which improved with annealing temperature. The role of oxygen ion vacancies and trivalent cerium in modifying the emission properties is discussed.

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Thermo-responsive polymers undergo a reversible coil-to-globule transition in water after which the chains collapse and aggregate into bigger globules when passing to above its lower critical solution temperature (LCST). The hydrogen bonding with the amide groups in the side chains has to be contrasted with the hydration interaction of the hydrophobic main-chain hydrocarbons. In the present investigation we study molecular changes in the polymer poly(N-isopropyl acrylamide) (PNIPAM) and in its monomer N-isopropyl acrylamide (NIPAM) in solution across the LCST transition. Employing Fourier-transform infrared spectroscopy we probe changes in conformation and hydrogen bonding. We observe a nearly discontinuous shift of the peak frequencies and areas of vibrational bands across the LCST transition for PNIPAM whereas NIPAM exhibits a continuous linear change with temperature. This supports the crucial role of the polymer backbone with respect to hydration changes in the amide group in combination with cooperative interactions of bound water along the backbone chain.

ZnO nanorods doped with Ag and Sb have been synthesized by a facile hydrothermal technique. Crystal quality, morphology, chemical/electronic composition, local structure, and vibrational mode properties are investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and micro-Raman spectroscopy. Evidence of dopant incorporation is demonstrated in the XPS measurements of both Sb-doped and Ag-doped ZnO nanorods. From XRD data, it was found that the doped ZnO nanorods have a lower degree of crystallinity. The lattice constants of doped ZnO nanorods were slightly larger than that of the pure samples.