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The formation mechanism of Cd–S–Se quantum dots (QDs) with a CdS/CdSe core–shell structure within a silicate glass system was investigated by monitoring the change in the first excitonic absorption peak of CdSe, CdS, and Cd–S–Se QDs as a function of the heat‐treatment (HT) duration. When a silicate glass containing QD formation components for CdSe or CdS single‐phased QDs was heat‐treated, CdSe QDs grew via Ostwald ripening, whereas CdS QDs hardly formed within the given silicate glass matrix. When the glass, including CdO, ZnSe, and ZnS, was utilized for the synthesis of Cd–S–Se QDs within the glass matrix, Cd–S–Se QDs were successfully formed and exhibited similar growth behavior to CdSe QDs during the initial stage of HT. The structural changes in the QD‐embedded glasses during HT were also monitored by Raman spectroscopy and discussed, and a possible formation mechanism of CdSe/CdS core–shell‐structured QDs within silicate glasses is suggested. [ABSTRACT FROM AUTHOR]

Cd‐S‐Se quantum dot embedded glasses (QDEGs) with dual‐band emissions of green and red were synthesized by assembling two QDEGs, to obtain a color converter for white LEDs (wLEDs) with a wide color gamut and long‐term stability. Each QDEG, possessing different sizes of QD, was prepared by adjusting heat‐treatment conditions. They were then bonded to each other by an additional heat treatment to fabricate a pattern structured QDEG (pQDEG). The fabrication conditions of the pQDEGs, such as their heat‐treatment condition and thickness, were varied to improve the color gamut. pQDEG‐based WLEDs were demonstrated and their optical properties such as color coordinates, luminous efficiency, and color rendering index (CRI) were monitored. The effect of pQDEG fabrication conditions on the resultant emission spectra and color gamut were discussed. [ABSTRACT FROM AUTHOR]

Quantum dot embedded glasses (QDEGs) were prepared by the conventional melt‐quenching method to enhance its color conversion efficiency via optimizing the concentration of ZnS, ZnSe, and CdO within the silicate‐based glass matrix. The QDEG, which contained 0.875 ZnS, 0.625 ZnSe, and 0.75 CdO (in mol%) and was heat treated at 500°C for 10 hours showed promising color conversion with an improved quantum yield of up to 25%. Color coordination of light‐emitting diodes (LEDs) mounted with the QDEGs could be adjusted by tuning heat‐treatment conditions and thickness control of QDEGs. The practical feasibility of the QDEG for a white LED is demonstrated with a reasonable glass thickness for LED packaging process. The formation of Cd‐S‐Se quantum dots within a glass matrix was identified by Raman and HR‐TEM analyses. The effect of ZnSe and CdO on the formation of Cd‐S‐Se quantum dots within silicate glass is also discussed. [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]

Silicate glasses with CdS and CdSe quantum dots ( QDs) were synthesized for application as an inorganic color converter for a 450-nm blue light-emitting diode ( LED). CdO and ZnS (or ZnSe) were added, and heat treatment conditions were changed to control QD formation within the silicate matrix. Absorption spectra and high-resolution transmission electron microscopy confirmed the QD formation. Variations in absorption and photoluminescence ( PL) spectra were observed with CdSe QD-embedded glasses when heat treatment conditions varied, whereas glasses with CdS QDs did not show noticeable variation. QD-embedded glasses were then mounted on top of a 450-nm LED chip to make a color-converted LED, and their electroluminescence and PL spectra as well as CIE color coordinates were investigated. The practical potential of QD-embedded glasses as an inorganic color converter has been observed, and their spectral properties were discussed. [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]