Sol-gel synthesis and luminescent properties of red-emitting Y(P,V)O4:Eu(3+) phosphors.

Eu(3+)-activated Y(P,V)O4 phosphors were prepared by the EDTA sol-gel method, and the corresponding morphologies and luminescent properties were investigated. The sample particles were relatively spheroid with size of 2-3 µm and had a smooth surface. The excitation spectra for Y(P,V)O4:Eu(3+) consisted of three strong excitation bands in the 200-350 nm range, which were attributed to a Eu(3+)- O(2-) charge-transfer band and (1)A1-(1) T1/(1) T2 transitions in VO4(3-). The as-synthesized phosphors exhibited a highly efficient red luminescence at 613 nm due to the Eu(3+5) D0-(7) F2 electric dipole transition. With the increase in the V(5+)/P(5+) ratio, the luminescence intensity of the red phosphor under UV excitation was greatly improved due to enhanced VO4(3-) → Eu(3+) energy transfer.

Thermal quenching of luminescence of LiSr4 (BO3)3:Eu2+ orange-emitting phosphor.

An orange-emitting phosphor, Eu(2+)-activated LiSr4(BO3)3, was synthesized using the conventional solid-state reaction. The photoluminescence excitation and emission spectra, and temperature dependence of the luminescence intensity of the phosphor were investigated. The results showed that LiSr4(BO3)3:Eu(2+) could be efficiently excited by incident light of 250-450 nm, and emits a strong orange light. With increasing temperature, the emission bands of LiSr4(BO3)3:Eu(2+) show an abnormal blue-shift with broadening bandwidth and decreasing emission intensity.

Synthesis and photophysical properties of europium(III)-ß-diketonate complexes applied in LEDs.

Six ß-diketonate ligands were used to prepare the corresponding antenna europium(III) ternary complexes using 1,10-phenanthroline as an ancillary ligand. All the complexes exhibited high decomposition temperatures. Photophysical properties such as FT-IR spectra, UV-Vis absorption spectra, excitation and emission spectra, relative luminescent intensity ratios, luminescence decay curves and quantum yields based on the complexes were systematically studied and compared with each other. The energy-transfer mechanism was proposed as a ligand-sensitized luminescence process. Bright red light-emitting diodes (LEDs) were then fabricated by coating the complexes onto 395 nm-emitting InGaN chips. The light emission from the InGaN chips could be completely absorbed in the spectra of LEDs. The Commission International de I'Eclairage (CIE) chromaticity coordinates are close to the National Television Standard Committee (NTSC) standard value for the red color. All these findings indicate that these Eu(III) complexes are promising red phosphors for fabrication of near UV-based white LEDs.

Single-phased white-light-emitting NaCaBO3:Ce3+,Tb3+,Mn2+ phosphors for LED applications.

A series of NaCaBO3:Ce(3+),Tb(3+),Mn(2+) borate phosphors were prepared via a high-temperature solid-state reaction. The obtained phosphors exhibit a strong excitation band between 250 and 400 nm, matching well with the dominant emission band of a NUV light-emitting-diode (LED) chip. The phosphors can generate light from blue to green, and from blue to red by Ce(3+)→Tb(3+) and Ce(3+)→Mn(2+), respectively. Furthermore, a wide-range-tunable white light emission was obtained by precisely controlling the contents of Ce(3+), Mn(2+), Tb(3+). The results show that this phosphor has potential applications as a single-phased phosphor for NUV white LEDs.

Highly-photoluminescent ZnSe nanocrystals via a non-injection-based approach with precursor reactivity elevated by a secondary phosphine.

Highly-photoluminescent ZnSe quantum dots with 72% quantum yield and 22 nm full width at half maximum were synthesized with more reactive precursors via a non-injection approach with high synthetic reproducibility; (31)P NMR provided insight into the formation mechanisms of ZnSe monomers.

[Synthesis and luminiescence of Eu(III) complex based on 4,4,4-trifluoro-1-(4'-m-terphenyl)-1, 3-butanedione and 1,10-phenanthroline].

A new europium (III) complex, EuL3 phen, [HL = 4,4,4-trifluoro-1-(4'-m-terphenyl)-1,3-butanedione, phen = 1, 10-phenanthroline] was synthesized. Its structure was characterized by elemental analysis, IR and FAB-MS. The complex exhibits strongly red emission due to the 5D0-7F(J) (J = 0-4) transitions of Eu3+ ions under irradiation of UV or 395 nm emission light of InGaN chip. The strongest emission peak is located at 613 nm. The luminescence quantum yield is 13%. The lifetime of the complex is 470 micros. The decay curve can be fit with a single exponential. The thermogravimetric analyses curve for the complex shows that the complex is stable up to 220 degrees C, which meets the requirement of fabrication of LED device. A red luminescent LED was successfully fabricated by coating complex EuL3 phen onto 395 nm emitting InGaN chip. The mass ratio of complex to the silicone is related to the chromaticity coordinates and efficiency of fabricated LED. When the mass ratio of complex to the silicone is 1 : 25, the chromaticity coordinates of the fabricated LED with the europium complex are x = 0.64 and y = 0.35 and the efficiency achieves 0.89 lm x W(-1). The results indicate that the complex may act as a potential red component in the fabrication of white LEDs.

Effect of different alkyl groups at the N-position on the luminescence of carbazole-based beta-diketonate europium(III) complexes.

A series of carbazole-based beta-diketone derivatives and their europium(III) ternary complexes Eu(N-Cx)(3)phen were designed and synthesized, where N-Cx denotes carbazole-based beta-diketonates with different alkyl substituents at N-position of the carbazole ring and phen is 1,10-phenethroline. Thermogravimetric analysis (TGA) shows that the decomposition temperature of the complexes is over 360 degrees C. UV-visible absorption spectroscopy, photoluminescence (PL), and the luminescence quantum yield of the Eu(III) complexes were measured and compared with each other, and the effect of different substituted-alkyls at N-position in the carbazole ring on the photoluminescence was discussed in details, indicating there exists a competition between the absorption capacity and the energy transfer efficiency for the complexes when the structure of the substituted-alkyls changes. The triplet state energy levels of the beta-diketonate ligands in the complexes are higher than that of the lowest excited level of Eu(3+) ion, (5)D(0), so the photoluminescence mechanism of the Eu(III) complexes was proposed as a ligand-sensitized luminescence process. Red LEDs were fabricated by precoating the complexes onto 395 nm emitting InGaN chips. All the results show that this series of Eu(III) complexes is a promising candidate as a red component in fabrication of NUV-based white LEDs.

A luminescent Eu(III) complex based on 2-(4', 4', 4'-trifluoro-1', 3'-dioxobutyl)-dibenzothiophene for light-emitting diodes.

Complex Eu(dbt)(3)(phen) (Hdbt=2-(4', 4', 4'-trifluoro-1', 3'-dioxobutyl)-dibenzothiophene, phen=1,10-phenanthroline) was synthesized. The complex emits red luminescence, characteristic of the (5)D(0)-->(7)F(J) (J=0-4) emission bands of Eu(3+) under near ultraviolet. A red conversion light-emitting diode (LED) device was fabricated by coating complex onto InGaN-based-LED chip that emits 395nm ultraviolet light. When the mass ratio of the red phosphor to the silicone is 1:25, the LED device's CIE chromaticity coordinates are x=0.5835, y=0.2857, and the luminescence efficiency is 1.29 lm/w. All the results show that this europium complex may act as a red component in fabrication of white LEDs with high color-rendering index.

A single red InGaN-based light-emitting diode with a europium (III) ternary complex as mono-phosphor.

A novel europium (III) ternary complex, Eu(TPBDTFA)(3)Phen, was designed and synthesized. Photoluminescence measurements show that the energy absorbed by the organic ligands was efficiently transferred to the central Eu(3+) ions, and the complex exhibits strongly red emission due to the (5)D(0)-(7)F(j) transitions of Eu(3+) ions with appropriate CIE (Commission Internationale de l'Eclairage, International Commission on Illumination) chromaticity coordinates (x=0.66, y=0.33) under 310-420 nm light excitation. The luminescence quantum yield for the Eu(3+) complex is 0.18. Thermogravimetric analysis (TGA) confirms a high thermal stability of the complex with a decomposition temperature of 341 degrees C. All the characteristics indicate that the Eu(3+) complex is a highly efficient red phosphor suitable to be excited by near UV light. An intense red-emitting LED was fabricated by combining the mono-phosphor Eu(TPBDTFA)(3)Phen with a approximately 395 nm emitting InGaN chip.

Preparation and photoluminescence of a novel beta-diketone ligand containing electro-transporting group and its europium(III) ternary complex.

A novel beta-diketone with an electro-transporting oxadiazole group, 1-(4'-(5-(4-methylphenyl)-1,3,4-oxadiazol-2-yl)biphenyl-4-yl)-4,4,4-trifluorobutane-1,3-dione (MPBDTFA), was prepared with high yield. With this synthesized ligand as the first ligand and 1,10-phenanthroline (Phen) as the secondary ligand, a new europium(III) ternary complex, Eu(MPBDTFA)(3)Phen, was synthesized. The new beta-diketone and its europium(III) ternary complex were characteristized by elemental analysis, thermo-gravimetric analysis, IR and UV-visible spectroscopies. Photoluminescence measurements indicated that the energy absorbed by the organic ligands was efficiently transfered to the central Eu(3+) ions, and the complex showed intensely and characteristically red emissions due to the (5)D(0)-->(7)F(j) transitions of the central Eu(3+) ions. With an electro-transporting group in molecule and highly thermal stability, the synthesized Eu(III) ternary complex is expected as a red-emitting candidate material for fabrication of organic light-emitting diodes (OLEDs).

Synthesis and luminescence of a novel conjugated europium complex with 6-aniline carbonyl 2-pyridine carboxylic acid.

A novel organic ligand, 6-aniline carbonyl 2-pyridine carboxylic acid (HAP), and the corresponding europium complex, tris(6-aniline carbonyl 2-pyridine carboxylato) europium (III) (Eu-AP) have been designed and synthesized. The results showed that Eu-AP was a conjugated complex, emitting strong red luminescence. The lifetimes of (5)D(0) of Eu(3+) in the complex were examined using time-resolved spectroscopic analysis, and the lifetime value was 0.55 +/- 0.01 ms for solid Eu(AP)(3). Thermogravimetric analysis showed that the europium complex had good thermal stability.

Syntheses, crystal structures, and physical properties of dinuclear copper(I) and tetranuclear mixed-valence copper(I,II) complexes with hydroxylated bipyridyl-like ligands.

Four copper complexes with hydroxylated bipyridyl-like ligands, namely [Cu(2)(ophen)(2)] (1), [Cu(4)(ophen)(4)(tp)] (2), [Cu(4)(obpy)(4)(tp)] (3), and [Cu(4)(obpy)(4)(dpdc)].2H(2)O (4), (Hophen=2-hydroxy-1,10-phenanthroline, Hobpy=6-hydroxy-2,2'-bipyridine, tp=terephthalate, dpdc=diphenyl-4,4'-dicarboxylate) have been synthesized hydrothermally. X-ray single-crystal structural analyses of these complexes reveal that 1,10-phenanthroline (phen) or 2,2'-bipyridine (bpy) ligands are hydroxylated into ophen or obpy during the reaction, which provides structural evidence for the long-time argued Gillard mechanism. The dinuclear copper(I) complex 1 has three supramolecular isomers in the solid state, in which short copper-copper distances (2.66-2.68 A) indicate weak metal-metal bonding interactions. Each of the mixed-valence copper(i,ii) complexes 2-4 consists of a pair of [Cu(2)(ophen)(2)](+) or [Cu(2)(obpy)(2)](+) fragments bridged by a dicarboxylate ligand into a neutral tetranuclear dumbbell structure. Dinuclear 1 is an intermediate in the formation of 2 and can be converted into 2 in the presence of additional copper(II) salt and tp ligands under hydrothermal conditions. In addition to the ophen-centered pi-->pi* excited-state emission, 1 shows strong emissions at ambient temperature, which may be tentatively assigned as an admixture of copper-centered d-->s,p and MLCT excited states.