Ionic Liquid Crystalline Based on Amino Acid and Gemini Surfactant: Tunable Phase Structure, Circular Polarized Luminescence and Emission Color

Circularly polarized luminescence (CPL)-active ionic liquid crystalline (ILC) featuring excitation wavelength-dependent (Ex-De) photoluminescence have latent application prospects in display devices. In addition, materials with tunable CPL responses are quite attractive...

Compatibility of Photoluminescence Properties in ScPO4:Eu3+, Tb3+ Phosphor for White Light Emitting Diodes

ScPO4:Eu3+, Tb3+ phosphors with tuned emission color were prepared through high temperature solid-state reaction. The structure, morphology and photoluminescence properties of the title samples were collected by XRD, SEM and fluorescence spectrophotometer, respectively. Co-doping Eu3+ and Tb3+ in ScPO4 does not change the body-centered tetragonal structure of the host. And the morphology remains essentially unchanged except for slight agglomeration. Changing the ratio of Tb3+/Eu3+, the tuned emission can be achieved, the color could be adjusted from green through yellow to orange-red. The ScPO4:0.03Tb3+, 0.03Eu3+ phosphor with high thermal stability as the single matrix phosphor can be suitable for the NUV-pumped white LED. The white LED with a color rendering index of 86.5 and a correlated color temperature of 3470 K has been generated by packaging BAM:Eu2+ with ScPO4:0.03Tb3+, 0.03Eu3+ on an NUV-InGaN chip.

CdSe and CsPbBr3 Quantum Dots Co-doped Monolithic Glasses as Tunable Wavelength Convertors

CdSe and CsPbBr3 quantum dots are well studied photoluminescent materials due to their extraordinary emission properties. However, their vulnerability against environmental conditions limits their integration into further applications. At this point, glass encapsulation offers promising durability features due to its robust and dense structure. In this study, CdSe and CsPbBr3 QDs are successfully synthesized in the same glass host through melt-quenching technique followed by a single heat-treatment process. Excitation wavelength dependent photoluminescence properties are investigated and emission color tunability of monolithic glasses from yellow-green to red is demonstrated. Favorable quantum yield values are obtained as 21.78% and 16.63% under 345 and 365 nm excitation wavelengths, respectively. Prepared glasses demonstrate high potential to be used as tunable wavelength convertors for state-of-the-art photonic and opto-electronic applications.

New Multicolor Tungstate-Molybdate Microphosphors as an Alternative to LED Components

Due to the ongoing need to create phosphors with the appropriate emission color for the production of light emitting diodes, we decided to synthesize a series of multicolour microphosphors with tunable visible emissions, depending on the composition of dopant ions. In this work, we investigated the structure, morphology, and luminescent properties of new molybdate–tungstate phosphors co-doped with Tb3+ and Eu3+ ions. The conventional high temperature solid state method was used to prepare a series of CaMoyW1−yO4:Eu3+x/Tb3+1−x materials. In order to obtain phosphors with the most promising luminescent properties, the experiment was planned by taking into account the different composition of the matrix and the concentration of the particular dopant ions (Eu3+x/Tb3+1−x, x = 0.001, 0.003, 0.005, 0.007, 0.009). As a result, luminescent materials were obtained with a pure tetragonal crystal structure, the space group of I41/a, confirmed by X-ray diffraction (XRD). The size and shape of the particles obtained from the materials were analyzed based on scanning electron microscopy images. Luminescence spectroscopy (excitation and emission spectra, decay lifetimes) was utilized to characterize the luminescence properties of the as-prepared phosphors. The color change of the emission from green-yellow to orange-red was confirmed using the 1931 Comission Internationale de l’Eclairage (CIE) chromaticity coordinates and color correlated temperature (CCT).

Tetraphenylethenyl-Modified 1,8-Naphthalimide Dye with Efficient Aggregation-Enhanced Emisssion, Solvatochromism and Intramolecular Charge Transfer Characteristics

1,8-naphthalimide (NI) dyes are one class of important organic luminophores with good photo-stability, high fluorescent quantum yields and broad emission color-tunability, which are widely used in biological and chemical fields. However, they exhibit bad ACQ property, which heavily limits their application in real word. Contrary to ACQ, tetraphenylethene (TPE) is an AIE luminogen. To eliminate the ACQ effect of NI, TPE was used as core and NI chromophores was used as peripheries to obtain a new dye TPEDNI. TPEDNI dye demonstrates typical aggregation-enhanced emission (AEE) characteristic with high fluorescence Φ>F, solid up to 100% in the film state, which is 24 times of that for its THF solution. Besides, TPEDNI exhibits marked solvatochromism, and the emission peak red-shifts from 505 nm in hexane to 610 nm in acetonitrile. TPENI also displays evident intramolecular charge transfer property in THF/water mixtures

Fluorinated Dibenzo[a,c]-phenazine-Based Green to Red Thermally Activated Delayed Fluorescent OLED Emitters

Purely organic thermally activated delayed fluorescence (TADF) emitting materials for organic light-emitting diodes (OLEDs) enable a facile method to modulate the emission color through judicious choice of donor and acceptor units. Amongst purely organic TADF emitters, the development of TADF molecules that emit at longer wavelengths and produce high-efficiency devices that show low efficiency roll-off remains a challenge. We report a modular synthesis route that delivers three structurally related fluorinated dibenzo[a,c]-phenazine-based TADF molecules, each bearing two donor moieties with different electron-donating strengths, namely 3,6-bis(3,6-di-tert-butyl-9H-carbazol-9-yl)-10-fluorodibenzo[a,c]phenazine (2DTCz-BP-F), 3,6-bis(9,9-dimethylacridin-10(9H)-yl)-10-fluorodibenzo[a,c]phenazine (2DMAC-BP-F) and 10,10'-(10-fluorodibenzo[a,c]phenazine-3,6-diyl)bis(10H-phenoxazine) (2PXZ-BP-F). They exhibit donor strength-controlled color-tuning over a wide color range from green to deep-red with photoluminescence maxima, PL, of 505 nm, 589 nm, and 674 nm in toluene solution. OLED devices using these TADF materials showed excellent to moderate performance with an EQEmax of 21.8% in the case of 2DMAC-BP-F, 12.4% for 2PXZ-BP-F and 2.1% with 2DTCZ-BP-F, and associated electroluminescence (EL) emission maxima, EL, of 585 nm, 605 nm and 518 nm in mCBP host, respectively.

Copper(I) iodide-based organic–inorganic hybrid compounds as phosphor materials

Two photoluminescent copper(I) iodide inorganic-organic hybrid materials have been synthesized and structurally characterized as 1D-Cu2I2(bpoe)2 (1) and 1D-Cu2I2(bbtpe-m)2 (2) (bpoe = 1,2-bis(pyridin-3-yloxy)ethane, bbtpe-m = 1,1′-(3-methylpentane-1,5-diyl)bis(1H-benzo[1,2,3]triazole). Both are chain-like structures composed of Cu2I2 rhomboid dimers connected by bidentate ligands. Their emission colors range from cyan to yellow with relatively high internal quantum yields in the solid state. The tunable band gap and emission color is achieved by varying the LUMO energies of the ligands. The structures are robust and remain stable up to T = 260 °C, and coupled with their efficient and adjustable luminescence, facile synthesis, and non-toxic nature, these compounds demonstrate potential as rare earth element (REE)-free phosphors.