Hydrothermal Synthesis, Microstructure and Photoluminescence of Eu3+-Doped Mixed Rare Earth Nano-Orthophosphates

Eu3+-doped mixed rare earth orthophosphates (rare earth = La, Y, Gd) have been prepared by hydrothermal technology, whose crystal phase and microstructure both vary with the molar ratio of the mixed rare earth ions. For LaxY1–xPO4: Eu3+, the ion radius distinction between the La3+ and Y3+ is so large that only La0.9Y0.1PO4: Eu3+ shows the pure monoclinic phase. For LaxGd1–xPO4: Eu3+ system, with the increase in the La content, the crystal phase structure of the product changes from the hexagonal phase to the monoclinic phase and the microstructure of them changes from the nanorods to nanowires. Similarly, YxGd1–xPO4: Eu3+, Y0.1Gd0.9PO4: Eu3+ and Y0.5Gd0.5PO4: Eu3+ samples present the pure hexagonal phase and nanorods microstructure, while Y0.9Gd0.1PO4: Eu3+ exhibits the tetragonal phase and nanocubic micromorphology. The photoluminescence behaviors of Eu3+ in these hosts are strongly related to the nature of the host (composition, crystal phase and microstructure)

Impact of 1,10-Phenanthroline-Induced Intermediate Valence on the Luminesence of Divalent Europium Halides

Starting from EuX2 (X = Cl, Br, I), we systematically investigated a variety of divalent europium complexes containing bidentate 1,10-phenanthroline (Phen) ligands. Depending on the Eu/Phen ratio, mono-, di-, and polynuclear complexes are formed, with the latter yielding one-dimensional infinity 1[EuBr2(phen)] chains. Seven new divalent europium complexes, [Eu(phen)4(H2O)]Br2 center dot 2MeCN, [Eu(phen)4]I2 center dot 1.7Tol, [EuBr(phen)3]2Br2 center dot 4MeCN, [EuCl2(phen)2]2 center dot 2MeCN, [EuBr2(phen)2]2, [EuI2(phen)2]2, and [EuBr2(phen)]x, are presented in this work. All species show remarkable optical properties based on a partial electron transfer from the EuII center to the Phen ligand. The photophysical characterization is further supported by electrochemistry studies in order to describe the intermediate valence of the Eu center

Selenous Acid in an Aromatic Framework: Insights Into a Temperature-Sensitive Internal Redox System from the Solid State

We report on a new compound composed of a phenanthroline network in which emerging channels are alternately occupied by selenous acid (H2SeO3) and dioxane molecules. The material undergoes a variety of structural changes due to both its redox activity as well as its thermal decomposition. We investigate an internal redox system of the incorporated selenous acid and the aldehyde groups of the phenanthroline framework. The reduction process of the selenium species was further elucidated by cyclic voltammetry, while the oxidation process was also monitored by H-1 NMR spectra. The thermal behavior reveals that the material can undergo a reversible, topotactic transition due to dioxane and water (de)intercalation

Growing Gold Nanostars on SiO2 Nanoparticles: Easily Accessible, NIR Active Core–Shell Nanostructures from PVP/DMF Reduction

A new synthesis strategy towards gold-coated silica nanoparticles is presented. The method provides an efficient, reliable and facile-coating process of well-defined star-shaped shell structures, characterized by UV-Vis, TEM, PXRD, DLS and zeta-potential measurements. A marked red shift of the Au-based plasmonic band to the region of the first biological window is observed offering great potential for future research of biological applications

Growing Gold Nanostars on SiO2 Nanoparticles: Easily Accessible, NIR Active Core-Shell Nanostructures from PVP/DMF Reduction

A new synthesis strategy towards gold-coated silica nanoparticles is presented. The method provides an efficient, reliable and facile-coating process of well-defined star-shaped shell structures, characterized by UV-Vis, TEM, PXRD, DLS and zeta-potential measurements. A marked red shift of the Au-based plasmonic band to the region of the first biological window is observed offering great potential for future research of biological applications

Luminescent Study on Nd3+ Complexes Containing Carboxylate-Dithiolene and Alkoxide-Dithiolene Ligands

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