2.7 µm emission in Er3+:CaF2 nanocrystals embedded oxyfluoride glass ceramics.

Using conventional melt-quenching and subsequent thermal treatment, Er(3+) doped CaF(2) transparent glass ceramic (GC) was prepared. X-ray diffraction and high-resolution transmission electron microscopy confirmed the formation and microstructure of CaF(2) nanocrystals in glass. An energy-dispersive spectrometer was used to investigate the distribution of Er(3+) ions and CaF(2) nanocrystals in glass. It was found that Er(3+) ions prefer to concentrate in the CaF(2) nanocrystals rather than in a glass matrix, and the amount of Er(3+) ions plays a key role in the formation of CaF(2) nanocrystals in a glass matrix with the Er(3+) ions as nucleating agent. An intense 2.7 µm emission due to Er(3+): I(11/2)4 → I(13/2)4 was achieved upon excitation at 980 nm with a laser diode, while the 2.7 µm emission can be neglected in the as-prepared glass counterpart, which confirmed the incorporation of Er(3+) ions into CaF(2) nanocrystals. An obvious enhancement of 2.7 µm emerged in the GC doped with 3% Er(3+) and heat-treated at 620 °C.

Anisotropic vanadium dioxide sculptured thin films with superior thermochromic properties.

VO2 (M) STF through reduction of V2O5 STF was prepared. The results illustrate that V2O5 STF can be successfully obtained by oblique angle thermal evaporation technique. After annealing at 550 °C/3 min, the V2O5 STF deposited at 85° can be easily transformed into VO2 STF with slanted columnar structure and superior thermochromic properties. After deposition SiO2 antireflective layer, Tlum of VO2 STF is enhanced 26% and ΔTsol increases 60% compared with that of normal VO2 thin films. Due to the anisotropic microstructure of VO2 STF, angular selectivity transmission of VO2 STF is observed and the solar modulation ability is further improved from 7.2% to 8.7% when light is along columnar direction. Moreover, the phase transition temperature of VO2 STF can be depressed into 54.5 °C without doping. Considering the oblique incidence of sunlight on windows, VO2 STF is more beneficial for practical application as smart windows compared with normal homogenous VO2 thin films.

Synthesis and luminescence mechanism of multicolor-emitting g-C3N4 nanopowders by low temperature thermal condensation of melamine.

Graphite like C3N4 (g-C3N4) was synthesized facilely via the low temperature thermal condensation of melamine between 300-650°C. The results showed that the products maintained as melamine when the temperature is below 300°C. With the increase of temperature, the products were transformed into carbon nitride and amorphous g-C3N4 successively. The morphology of products was changed from spherical nanoparticles of melamine into layer carbon nitride and g-C3N4 with the increase of temperature. The photoluminescence spectra showed that the carbon nitride products have continuous tunable photoluminescence properties in the visible region with increasing temperature. With the help of steady state, transient state time-resolved photoluminescence spectra and Raman microstructural characterization, a novel tunable photoluminescence mechanism was founded systematically, which is mainly related to the two dimensional π-conjugated polymeric network and the lone pair of the carbon nitride.

Phase transformation and intense 2.7†µm emission from Er3+ doped YF3/YOF submicron-crystals.

Yttrium fluoride YF3:Er(3+) and yttrium oxyfluoride YOF:Er(3+) submicron-crystals with mid-infrared fluorescent emissions were synthesized for the first time. The rhombohedral phase YOF submicron-crystals were synthesized by the crystalline phase transformation from pure orthorhombic YF3 submicron-crystals, which were prepared by co-precipitation method. The composition and morphology were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM) and transmission electron microscopy (TEM), which showed that submicron-crystals were quasi-spherical with the particle size of ~400 nm. A novel formation mechanism of YOF submicron-crystals was proposed. Photoluminescence (PL) spectra indicated the 2.7 µm emission of Er(3+) has remarkably enhanced with the increase of Er(3+) doping concentration, and a novel dynamic circulatory energy transfer mechanism was proposed. Fourier transform infrared spectra (FTIR) were used to demonstrate the change of hydroxyl content. These oxyfluoride submicron-crystals provide a new material for nano/submicron-crystals-glass composites, and open a brand new field for the realization of mid-infrared micro/nano-lasers.

Controllable fabrication and broadband near-infrared luminescence of various Ni2+-activated ZnAl2O4 nanostructures by a single-nozzle electrospinning technique.

By finely tuning the electrospun parameters (feeding rate of solution, working voltage and distance, etc.) and concentration of inorganic salts, various ZnAl(2)O(4) nanostructures (nanoparticles, nanonecklaces, nanofibers, nanotubes and hollow micromelts) were controllably synthesized by a single-nozzle electrospinning technique. The formation mechanisms of different ZnAl(2)O(4) nanostructures, including 'oriented attachment' mechanism, 'gas-push' mechanism, etc., were proposed to elucidate the morphology of the nanostructures and microstructure evolvement process. The morphology and microstructure of calcined electrospun nanostructures were considered to be mainly dependent on two factors, i.e. concentration of inorganic salts and size of as-prepared electrospun nanofibers. Using Ni(2+) ions as activators, broadband near infrared (NIR) emission covering 1000-1400 nm peaking at about 1176 nm was detected in Ni(2+)-doped ZnAl(2)O(4) nanostructures. The broadband NIR emission at around 1.3 µm optical communication window with a long lifetime of ~640 µs makes Ni(2+)-doped ZnAl(2)O(4) nanostructures as a promising candidate for micro/nano-broadband optical amplifiers, fibers, etc.

Morphology and phase control of fluorides nanocrystals activated by lanthanides with two-model luminescence properties.

The morphology, size and phase control of luminescent fluoride nanocrystals through doping has become a new research hotspot due to their improved properties. In this work, Yb(3+) ions, as one of the most efficient sensitizers for various lanthanide activators, were doped in NaGd(Y)F(4) nanocrystals. The results show that no obvious influence was observed for Yb(3+)-doped NaYF(4) nanocrystals, while the influence of Yb(3+) doping on NaGdF(4) nanocrystals was remarkable. The NaGd(1-x)Yb(x)F(4) nanocrystals were synthesized by a hydrothermal route and had a morphology of rice-like nanorods. By controlling the synthesis parameters, the average size and slenderness of the nanocrystals increased gradually with addition of Yb(3+) ions. In contrast, the NaGd(1-x)Yb(x)F(4) nanocrystals maintained a hexagonal phase, which is more beneficial for application as a luminescent host, until the content of Yb(3+) ions reached x = 0.9. The growth and transformation mechanism of NaGd(1-x)Yb(x)F(4) nanocrystals was proposed to be a result of the competition between ion diffusion and an Oswald ripening process. Photoluminescence (PL) spectra confirm the efficient up-conversion and near-infrared (NIR) two-model luminescence properties of Er(3+) (Tm(3+)) activated NaGd(Y)(1-x)Yb(x)F(4) nanocrystals. Simulated analysis results indicate that a colloidal solution of mixed luminescent nanocrystals is expected to find application as the activated medium of three dimensional displays and a broadband optical amplifier.