Ferroelectric K0.5Na0.5NbO3 (KNN) thin films were prepared by a chemical solution deposition approach with polyvinylpyrrolidone (PVP) of different molecular weights introduced in the precursor solutions. The volatilization of the alkali ions and the effects of the molecular weight of PVP were examined with x-ray diffraction (XRD), thermal analysis, mass spectrometry, and x-ray photoelectron spectroscopy (XPS). The results clearly showed that the volatilization of the alkali ions mainly happened at moderate temperatures before the crystallization of the KNN perovskite phase. Loss of Na was more significant than K ions during the heating process of KNN. The introduction of PVP with the appropriate molecular weight could effectively promote the crystallization of the KNN perovskite phase at reduced temperature and substantially suppress the loss of the alkali ions before crystallization. Therefore, a high dielectric constant, piezoelectric coefficient, and well saturated ferroelectric hysteresis loops were obtained in the KNN films in which PVP of the right molecular weight were introduced.

This paper reports findings of an investigation of the synthesis of monolayer-capped iron oxide and core (iron oxide)-shell (gold) nanocomposite and their assembly towards thin films as sensing materials. Pre-synthesized and size-defined iron oxide nanoparticles were used as seeding materials for the reduction of gold precursors, which was shown to be effective for coating the iron oxide cores with gold shells (Fe oxide@Au). The unique aspect of our synthesis is the formation of Fe oxide@Au core-shell nanoparticles with controllable surface properties. By controlling the reaction temperatures and manipulating the capping agent properties and solution compositions, the size, shape, composition, and monodispersity can be tailored. The core-shell nanoparticles were shown to form molecularly-mediated thin film assemblies using molecular mediators. The sensing properties of the nanostructures on piezoelectric devices were examined for the detection of volatile organic compounds. The preliminary results have provided important insights into the design of core-shell nanocomposites as sensing materials.

This paper reports the preliminary results of an investigation of the synthesis of monolayer-capped GaAs nanoparticles using different surface capping molecules. Our approach focuses on the surface encapsulation using alkanethiolates. The organic shell can effectively block the aggregation during nanoparticle synthesis, providing molecular-level control of the core-shell structure. The results have demonstrated the effect of surface alkanethiolate modification on the interparticle spatial properties and particle sizes, which upon further refinement could lead to the ability in controlling the size of GaAs nanoparticles.

This paper describes the results of an investigation of modified synthetic protocols to produce monodispersed magnetic ferrite nanoparticles, γ-Fe2O3 and Fe3O4, and their magnetic properties. The synthesis involved thermal decomposition of organometallic precursors followed by oxidation or reduction. In the synthesis of γ-Fe2O3, iron pentacarbonyl was used as the precursor and trimethylamine oxide as the oxidant. In the synthesis of Fe3O4, iron (III) acetylacetonate was reduced by 1, 2-hexadecanediol. The particle sizes ranged from 5–15 nm with high monodispersity. Results from TEM, XPS, and SQUID characterizations of these iron oxide nanoparticles are discussed.

The application of molecularly-capped gold nanoparticles (1–5 nm) in catalysis (e.g., electrocatalytic oxidation of CO and methanol) requires a thorough understanding of the surface composition and structural properties. Gold nanoparticles consisting of metallic or alloy cores and organic encapsulating shells serve as an intriguing model system. One of the challenges for the catalytic application is the ability to manipulate the core and the shell properties in controllable ways. There is a need to understand the relative core-shell composition and the ability to remove the shell component under thermal treatment conditions. In this paper, we report results of a thermogravimetric analysis of the alkanethiolate monolayer-capped gold nanoparticles. This investigation is aimed at enhancing our understanding of the relative core-shell composition and thermal profiles.

The radiation effect in hydrolyzed BaF2 was investigated through tile changes in their optical absorption and EPR spectra before and after γ-irradiation. The resulti demonstrated that hydroxyl and oxygen can be easily introduced into BaF2by means of a hydrolysis, the most likely modes are OH— ions substituting for fluorine and O2– ions substituting for fluorine associated with charge-compensating fluorine vacancies O2– — F+. Combining with the Hartree-Fock-Slater local-density discrete variational (HFS-Xα-DV) cluster calculation on some possible defects related to hydrogen and oxygen impurities, we propose that the radiation damage observed in hydrolyzedBaF2 can be explained in terms of OH— and O2– — F+ dissociation through a radiolysis.

The electronic structures of pure BaF2 crystal and lanthanum doped BaF2 crystal have been calculated in a self-consistent molecular-cluster model. The cluster is embedded in the crystal lattice and the entire system treatediteratively in the Hartree-Fock-Slater local-density theory. As lanthanum doped BaF2 is concerned, the obtained results revealed that the F1–i which is introduced by the lanthanum may contribute to the suppression ofthe slow component in the scintillation light of BaF2 crystal.