Tailoring the Composition of Eu3+-Doped Y3NbO7 Niobate: Structural Features and Luminescent Properties Induced by Spark Plasma Sintering.

The defective fluorite-related Y3NbO7 host lattice was doped with Eu3+ ions to understand the influence of spark plasma sintering (SPS) process on this host lattice. The intrinsic disorder due to the occurrence of oxygen vacancies results in amorphous-type responses of the luminescent cations, and the spectral distribution varies as a function of the niobium content. Two spectral fingerprints of europium emissions were clearly enhanced. The correlation between luminescence, X-ray diffraction, and electron diffraction characterizations shows the existence of local inhomogeneity. Indeed, the particular nonequilibrium sintering conditions allowed pointing out a lack of miscibility within the Y3NbO7 solid solution domain. Thus, the SPS pellet is a composite of two extreme compositions. This phase demixing is mainly induced by the pressure coupled with a current effect that makes possible ionic migration in this Y3NbO7 ionic conductive matrix.

Near-field probing of Mie resonances in single TiO2 microspheres at terahertz frequencies.

We show experimentally that poly-crystalline TiO2 spheres, 20-30 µm in diameter, exhibit a magnetic dipole Mie resonance in the terahertz (THz) frequency band (1.0-1.6 THz) with a narrow line-width (<40 GHz). We detect and investigate the magnetic dipole and electric dipole resonances in single high-permittivity TiO2 microspheres, using a near-field probe with a sub-wavelength (~λ/50) size aperture and THz time-domain spectroscopy technique. The Mie resonance signatures are observed in the electric field amplitude and phase spectra, as well as in the electric field distribution near the microspheres. The narrow line-width and the sub-wavelength size (λ/10) make the TiO2 microspheres excellent candidates for realizing low-loss THz metamaterials.

Structural, thermal, spectroscopic, specific-heat, and magnetic studies of (C5H18N3)[Fe3(HPO3)6].3H2O: a new organically templated iron(III) phosphite with a pillared structure formed by the interpenetration of two subnets.

A new open framework iron(III) phosphite with formula (C5H18N3)[Fe3(HPO3)6].3H2O has been prepared by hydrothermal synthesis with N-(2-aminoethyl)-1,3-propanediamine as a templating agent. The crystal structure was solved from single-crystal X-ray diffraction data in the trigonal space group R. The unit cell parameters are a= 8.803(1) A and c= 25.292(2) A with Z = 3. The complex pillared structure can be described as two interpenetrating subnets, one organic, [(C5H18N3).3H2O]3+, and one inorganic, [Fe3(HPO3)6]3-. In the inorganic subnet, the pillars are formed by FeO6 trimers linked by vertex sharing phosphite groups, while in the cationic subnet the organic molecules act like pillars. With increasing temperature, the flexibility of the structure allows contraction due to dehydration followed by thermal expansion before reaching the thermal stability limit. The Dq and Racah parameters calculated for (C5H18N3)[Fe3(HPO3)6].3H2O are Dq = 965, B = 1080, and C = 2472 cm(-1). Mössbauer spectroscopy confirms the trivalent oxidation state of iron cations and the crystallographic multiplicities of their sites. The ESR spectra show isotropic signals with a g-value of 2.00(1). Specific-heat measurements show a three-dimensional (lambda-type) peak at a critical temperature Tc = 32 K. The value of the entropy at saturation is 46 J/mol K, very near the expected value of 44.7 J/mol K for the iron(III) cations with S = 5/2. Magnetic measurements indicate a three-dimensional antiferromagnetic ordering below 32 K and a reorientation of spins below 15 K with an incomplete cancellation of spins due to triangular interactions inherent to the structure.