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Core‐shell structure in Cd‐Zn‐Se quantum dots (QDs) precipitated in the silicate glass matrix by continuous wave laser (λ = 532 nm) were demonstrated using transmission electron microscopy (TEM) and local electrode atom probe (LEAP) tomography. TEM images of the QDs in glasses after 60 min of irradiation at 9 W/cm2 show two portions with different contrasts, and diameters of 5.97 and 22.49 nm, respectively; 3D elemental distribution in these glasses from LEAP tomography shows areas of high Zn concentration near the CdSe QDs. Iso‐concentration images obtained using visualization software show that Cd‐rich clusters were not completely covered by the Zn‐rich shells in the glass after 15 min irradiation that resulted emission due to the surface defects of CdSe QDs. As the irradiation time increased to 60 min, the Zn‐rich cluster gradually surrounded the Cd‐rich core to form shells that eliminated the surface defects. During laser irradiation, CdSe QDs precipitated first due to the high degree of supersaturation of Cd and Se followed by the sequential incorporation of Zn on the Cd‐rich QDs forming shells. [ABSTRACT FROM AUTHOR]

CdSe QDs with Cd1−xZnxSe shell structures were precipitated inside silicate glasses by continuous‐wave laser irradiation (λ = 532 nm) without any heat‐treatment process. Emission from the surface defects (λ ≈ 620 nm) was quenched significantly and the lifetimes of the band‐edge emission was increased. During the laser irradiation, Zn ions were gradually incorporated into the outer region of CdSe QDs to form Cd1−xZnxSe (0.76 ≤ x ≤ 0.8) alloy shells. [ABSTRACT FROM AUTHOR]

A complete inorganic quantum dot color converter for a white LED is achieved using silicate-based quantum-dot-embedded glasses (QDEGs). The white LED exhibits a high CRI of 90 and highly improved thermal stability up to 200 °C, demonstrating its robustness and practicality. The CdSe/CdS core/shell structure within the silicate glass is expected to enhance the colour converting efficiency. [ABSTRACT FROM AUTHOR]

Abstract: We experimentally verify that a color center in the form of takes shape in silicate glasses containing relatively small amount of ZnSe which are prepared via a conventional melt-quenching process. Samples also produce broad photoluminescence when excited with UV light source, suggesting potential applications in the visible range. Analyses based on X-ray diffraction patterns, high resolution transmission electron microscopy, and Raman spectroscopy support the formation of color centers in addition to Se nanocrystals. [Copyright &y& Elsevier]

Silicate glasses containing CdS and Ag2O were made by the melt-quenching method. CdS quantum dots ( QDs) were precipitated inside the glass matrix by heat treatment at 570-590 °C for 10 h, and the influence of Ag on photoluminescence ( PL) of CdS QDs was investigated. The emission located at 478-493 nm in wavelength originated from the direct recombination of electron/hole pairs was quenched due to charger transfer between Ag and CdS QDs. Modification of PL from CdS QDs by Ag provides potentials toward developing the color changing materials for light-emitting diodes ( LEDs). [ABSTRACT FROM AUTHOR]

Various rare earth (RE) oxides such as Pr 2 O 3 , Dy 2 O 3 , Ho 2 O 3 , and Er 2 O 3 were introduced into Cd–S–Se quantum dot embedded glasses (QDEGs) to investigate their effect on the color conversion properties of the Cd–S–Se QDEGs. The absorption and emission peak wavelengths due to the excitonic transition of the Cd–S–Se QDs were modified by the introduction of RE oxides, implying their influence on QD formation. The photoluminescence of the various QDEGs RE oxides under 450 nm excitation were monitored and compared with the un-doped QDEGs. White LEDs (wLEDs) were also fabricated with the RE-doped QDEGs and their color conversion properties, such as quantum yield (QY), luminous efficacy, correlated color temperature (CCT) and color rendering index (CRI) were examined. Transmission electron microscope (TEM) revealed that the size and spatial distribution of the QDs were improved by the RE-oxides. Their effect on QD formation within the silicate glass was discussed using Raman spectroscopy. • Cd–S–Se quantum dot embedded glasses (QDEG) with various rare earth (RE) ions were fabricated. • RE ions reduced QD size and modified spectral properties of QDEGs. • RE ions improved size and spatial distribution of QDs within glass matrix. • White LED was successfully achieved with RE-doped QDEGs. [ABSTRACT FROM AUTHOR]

Infrared photoluminescence (PL) properties of Sn-modified PbSe quantum dots (QDs) in silicate glass were investigated. The QDs' sizes were controlled by changing the heat treatment temperatures. The longest absorption peak from Sn-modified PbSe QDs was centered at 2590 nm, and the PL band extended to 2650 nm. X-ray diffraction peaks indicated that the PbSe QDs formed in the glass matrix although low Sn content resulted in no obvious difference between PbSe QDs and Sn-modified PbSe QDs. Sn was found in QDs that proves the incorporation of Sn into PbSe QDs. The proposed composition of the Sn-modified PbSe QDs was Pb 0.92 Sn 0.08 Se with a band gap of ~ 0.13 eV; the small amount of Sn changed the energy structure of QDs, narrowed the band-gap, and increased the PL emission wavelength. [ABSTRACT FROM AUTHOR]

Effects of SnO addition on the optical properties of Pb 1 − x Sn x Se quantum dots (QDs) were investigated as a function of GeO 2 content [GeO 2 ] in germanosilicate glasses. Addition of SnO resulted in a red-shift of the absorption bands from QDs at [GeO 2 ] < 20 mol%, but in a blue-shift at [GeO 2 ] ≥ 20 mol%. Addition of GeO 2 to the glass caused a large decrease in its viscosity, so it increased diffusion coefficient ( D ); as a result the amount of Sn in Pb 1 − x Sn x Se QDs increased. D of Sn 2 + was ~ 560 times higher in the glasses with [GeO 2 ] = 40 mol% than in the glass with no GeO 2 . The differences in Sn content in QDs affected their bandgap. [ABSTRACT FROM AUTHOR]

Lead selenide (PbSe) quantum dots (QDs) doped with Sr 2 + were precipitated in silicate glasses. The absorption and photoluminescence (PL) bands of the glasses blue-shifted as SrO concentration increased. These changes resulted mainly because Sr incorporation increased the band gap of PbSe nanocrystals. After heat treatment at 520 °C for 10 h, mean QD diameters were similar before and after the addition of SrO: ~ 7.2 nm with 0% SrO and ~ 6.9 nm with 10 mol% SrO. However, these two glasses show the absorption bands at 1743 nm and 1246 nm, and PL bands at 1803 and 1370 nm, respectively. These large shifts are due to the increase in the band gap through the formation of Pb 1 − x Sr x Se mixed-type QDs. One typical chemical composition of QDs formed in a glass with 10 mol% SrO after heat treatment at 520 °C for 10 h is Pb 0.89 Sr 0.11 Se with a band gap of ~ 0.58 eV. [ABSTRACT FROM AUTHOR]

Lead selenide quantum dots (QDs) were precipitated in germanosilicate glasses to investigate the effect of GeO 2 content on the precipitation and optical properties. The absorption and photoluminescence (PL) bands red-shifted strongly as GeO 2 concentration increased. After heat-treatment at 470 °C for 10 h, the first excitonic absorption bands red-shifted from 801 nm to 2593 nm as GeO 2 content increased from 0 to 40 mol%, and thus PL at 2619 nm was achieved. The corresponding average QD diameters were 2.48–12.54 nm. The precipitation of large PbSe QDs resulted from the enhancement of diffusion with the increase of GeO 2 concentration, and is the main reason for these red-shifts. [ABSTRACT FROM AUTHOR]

Phosphor-in-glasses (PiGs) with rare earth (RE) doped SiO 2 –B 2 O 3 –RO glasses were prepared by embedding YAG:Ce 3+ as the yellow phosphor. Eu 3+ and Pr 3+ were used to dope the glass, varying their concentrations in order to provide red emissions for possible chromaticity-control of white-light emitting diodes (WLEDs). The glass-to-phosphor mixing ratio was also varied to find the proper combination for color-controlled white LEDs. PiGs with RE-doped glasses were sintered at 750 °C and polished to 250 μm in thickness for blue LED color conversion. The photoluminescence spectra of the PiGs were monitored after they were mounted on commercial blue LED chips. Variation of color coordination, color rendering index and correlated color temperature were observed due to red emissions from the doped RE-ions. The spectral contribution of Eu 3+ and Pr 3+ ions to white LEDs under 450 nm LED excitation was discussed. The spatial distribution of phosphors within the glass matrix, and their possible interaction, was inspected by SEM. The thermal quenching effect was also investigated. [ABSTRACT FROM AUTHOR]

Abstract: We experimentally verified, within silicate glasses, the formation of Se2 − color centers that are responsible for a broad visible emission under optical excitation at UV wavelengths. In addition to Raman spectra, all the spectroscopic analyses on absorption, photoluminescence, and photoluminescence excitation unanimously confirm the formation of Se2 − color centers. However, the visible absorption due to Se2 − color centers disppeared upon increasing concentration of Na2O, which implies that their formation would depend on the compositions of silicate glasses. The role of Na2O in the formation mechanism in relation to glass structure is then discussed in terms of various analyses on X-ray diffraction patterns, X-ray photoelectron spectroscopy, and Raman spectroscopy. [Copyright &y& Elsevier]