Organic Light Emitting Devices Based on Terbium Complex

Rare earth complex TbY(m-MOBA)6(phen)2·2H2O was synthesized,which was first used as an emitting material in electroluminescence.The properties of monolayer device with the rate of 1000 r·min-1 (70 nm) and the impure concentration of 1∶5 were the best.And the highest brightness of this device reached 21.8 cd·cm-2 at a fixed bias of 20 V.Bright green emission can be obtained from the optimized double-layer device,and the highest EL brightness of the device reached 289 cd·m-2 at the voltage of 21 V.     

Organic Light-Emitting Device Based on Terbium Complex

Organiclight emittingdevices(OLEDs)have beenattractingconsiderableinterestbecauseoftheir lowdrive voltage,potentialapplicationsinflatpanel displaysincethefirstdouble layerstructuredevice withhighefficiencyandluminancewasfabricatedby TangandVanSlykein1987[…     

Emission Characteristics of PVK Doped TbY（o-MBA）6（phen）2 Systems

Since the pioneering work of Tang and VanSlykeon organic light emitting diodes(OLEDs)in1987,OLEDs have been particularlyinterestedin because oftheir potential applications in next-generationflat-pan-el displays and large-area flexible displays[1~3].Rareearth complex materials have been widely used incathodoluminescent display phosphor screens,lasersand lamps because their photoluminescence PL ex-hibits high quantumefficiencies and very sharp spec-tral bands.Inthe1990s,Kido et al[4~6]first…     

Electroluminescence Based on Eu_(0.5)La_(0.5)(TTA)_3phen Doped Poly N-Vinylcarbazole

Organic electroluminescence (OEL) has been ex-tensively studied owing to its potential application inflat panel displays ever since the first double-layerOELdevice that has high efficiency and luminescencewas fabricated in 1987[1 ~4]. When compared withcommon smaller organic molecules and polymers ,rareearth (RE) complexes exhibit extremely sharp , well-defined spectral lines due to the emissions that origi-nate fromthe lanthanide metal ions .So the electrolu-minescence (EL) of REcomplexes…     

Luminescence Characteristic of a New Novel Coprecipitate Rare Earth Complexes

Organicelectroluminescence (OEL)hasbeenex tensivelystudiedbecauseoftheirpotentialapplicationinflatpaneldisplayssincethefirsttwo layerOELde vicewithhighefficiencyandluminancewasfabricatedin 1987[1～ 3] .Rareearth (RE)metalcomplexeshavesomegoodcharacteristics ,suchasextremelynarrowe missionbandsandhighinternalquantumefficiencies ,whicharesuitableforuseastheemissionmaterialsinOEL[4 ] .Tb3+complexwasfirstintroducedintoOELdevices ,andsharpgreenemissionfromTb3+ionhasbeenobserved[5] .Sincethen …     

Synthesis, Characterization and Fluorescence Properties of Europium, Terbium Complexes with Biphenyl-4-Carboxylic Acid and o-Phenanthroline

Two series of solid complexes of europium and terbium with biphenyl 4-carboxylic acid and phen were synthesized and characterized in this report. Their elemental analysis, molar conductivities and TG-DTA studies indicate that the complexes have the composition of Eu(phen)L3·1/2H2O, Eu0.5RE0.5(phen)L3·1/2H2O; Tb(phen)L3·H2O and Tb0.5RE0.5(Phen)L3·1/2H2O. (RE=Y3 , La3 and Gd3 ; L=biphenyl 4-carboxylic acid; phen=o-Phenanthroline). The studies of their IR, UV 1H NMR and molar conductivities demonstrate that biphenyl 4-carboylic acid is bounded with RE(Ⅲ) ion. Rare earth ions coordinate with two nitrogen atoms of phen molecules directly in these rare earth complexes. The fluorescence spectra and fluorescence lifetimes of the rare earth complexes show that the fluorescent intensity and lifetime of a series of europium complexes are longer than those of the series of terbium complexes as having the some ligands. There are better fluorescent intensity and lifetime of hetero-nuclear rare earth complexes than homo-nuclear rare earth complexes for europium complexes. The fluorescence emission intensity of Eu3 is raised by inert fluorescent rare earth ions (Y3 , Gd3 and La3 ), but in Tb3 hetero-nuclear rare earth complexes the intensity of Tb3 ions are quenched by the inert fluorescent rare earth ions.     

Doped Organic Electroluminescence from a Novel Rare Earth Complex Tb （3-metho） 3 phen

A novel rare earth complex Tb (3-metho)3phen was synthesized and characterized. The complex was doped into PVK to improve the conductivity and film-forming property of Tb(3-metho) 3phen. A device with a structure of ITO/PVK: Tb(3-metho)3phen/Al was fabricated to study the eleetrolumineseent properties of Tb(3-metho) 3 phen. And the optoluminescent and AFM properties of this device were also studied, which proved the existence of energy transfer from PVK to Tb(3-metho)3phen. As a result, a pure green emission with sharp spectral band at 547.5 nm was observed.     

Luminescent Properties of A Novel Terbium Complex Tb（o-BBA）3（phen）

A novel rare earth complex of terbium ion with 2-benzoylbenzoic acid and 1, 10-phenathroline （Tb（o-BBA）3 （phen）, o-BBA-2-benzoylbenzoic acid, phen = 1, 10-phenathroline） was used as an electroluminescent material for the first time. The Tb complex was blended with poly（N-vinylcarbazole） （PVK） in different weight ratios and spinn to coated into films （noted as PVK ：Tb films）. The photoluminescence （PL） properties of films were investigated and the optimum weight ratio between PVK and Tb（o-BBA）3（phen） was found to be 3：1. Monolayer devices with the structure ITO/PVK： Tb/AI were fabricated and emitted green light, which was characteristic of Tb^3＋ emission. The results show that mecha- nisms for PL and EL are different. The PL is considered to be caused because of energy transfer and direct excitation to the Tb（o-BBA）3（phen） molecule, while EL is mainly on charging trapping.     

Emission of Rare Earth Complex Tb0.5Eu0.5 （asprin）3phen

The coprecipitate Tho.sEuo.5(asprin)3phen was synthesized. By doping the rare earth complex into polymer PVK, the EL device was fabricated with the structure of ITO/PVK: RE/PBD/AI. Compared with the device using PVK/Eu (asprin)3phen blend as the light emitting layer, the emission of Eu^3 in the PVK/Th0.5Eu0.5(asprin)3 phen blend is great-ly enhanced along with the quenching of the emission of PVK.     

Preparation,Photo and Electroluminescence Properties of Novel Rare Earth Aromatic Carboxylates

ＳｉｎｃｅＫｉｄｏｅｔａｌ.ｈａｖｅｆｉｒｓｔｒｅｐｏｒｔｅｄｏｎｏｒｇａｎｉｃｅｌｅｃｔｒｏｌｕｍｉｎｅｓｃｅｎｃｅ (ＥＬ)ｕｓｉｎｇｒａｒｅｅａｒｔｈ (ＲＥ)ｃｏｍｐｌｅｘａｓｔｈｅｅｍｉｔｔｉｎｇｌａｙｅｒ[1] ,ｍｕｃｈｗｏｒｋｈａｓｂｅｅｎｆｏｃｕｓｅｄｏｎｔｈｉｓｆｉｅｌｄｄｕｅｔｏｉｔｓｈｉｇｈｃｏｌｏｒｐｕｒｉｔｙ[2～ 4] .Ｈｏｗｅｖｅｒ,ｔｈｅｋｅｙｐｒｏｂｌｅｍｗｉｔｈｒａｒｅｅａｒｔｈβ ｄｉｋｅｔｏｎｅｃｏｍｐｌｅｘｅｓｉｓｔｈｅｉｒｐｏｏｒｔｈｅｒｍａｌｓｔａｂｉｌｉｔｙａｎｄ…     

Electroluminescence Based on Eu0.5 La0.5 （TTA） a phen Doped Poly N-Vinylcarbazole

A novel rare earth complex Eu_0.5La_0.5(TTA)₃phen, displaying electroluminescent property, was synthesized, and monolayer and double-layer devices were fabricated by doping it into poly N-vinylcarbazole. The characteristics of these optimized devices were investigated, and the emitting mechanism was explained through the energy band diagram. Optimized double-layer devices with a turn-on voltage of 6.5 V were achieved. At the current density of 68.48 mA·cm⁻², the maximum brightness and the current efficiency of the device reached 238.4 cd·m⁻² and 0.35 cd·A⁻¹, respectively.     

Synthesis and characterization of terbium（Ⅲ）-pyromellitic acid（H4L）-1,10-phenanthroline （phen） luminescent complex

The terbium(Ⅲ)-pyromellitic acid(H4L)-1,10-phenanthroline(phen) luminescent complex was synthesized using a co-precipitation method.The chemical composition of the synthesized complex was speculated to be Tb4L3(phen)0.075·10H2O by elemental analysis,inductively coupled plasma-atomic emission spectroscopy(ICP-AES),and Fourier-transform infrared spectroscopy(FT-IR).The X-ray diffraction analytic results indicated that the synthesized complex is a new crystalline complex,whose structure was different from those of other two ligands.The scanning electron microscopy analytic results showed that the product was of spherical crystals with good dispersion property,and the mean diameter of the spheres was about 1-2 μm.The TG-DTA result showed that the complex had good stability below 489 °C.PL spectra showed that the complex emitted characteristic green fluorescence of Tb(Ⅲ) ion under ultraviolet excitation.     

Synthesis and Fluorescence Property of Eu^3 ＋ , Tb^3＋ Perchlorate Complexes with Diphenyl Sulfoxide and 1,10-Phenanthroline

Eu3 ,Tb3 canemitfluorescenceinconjugatedsystemcontainingorganicligand[1,2 ] ,forexample ,1 ,1 0 phenanthroline ,becauseithasbettercoordina tionabilityandbiggerconjugationsystem ,soitcantransmitenergyeffectivelytoEu3 ,Tb3 ,leadingtofluorescenceemission ,andthestabilityisveryhigh ,butsolubilityisverypoor .Inaddition ,diphenylsul foxidehasbettercoordinationabilityandbiggerconju gationsystem ,too .Soitcanalsotransmitenergyef fectivelytoEu3 ,Tb3 ,resutlinginfluorescencee mission ,andsolubi…     

Thermochemical studies on complex of [Sm(o-NBA)_3phen]_2

A ternary complex [Sm(o-NBA)3phen]2 (o-NBA: o-Nitrobenzoate; phen: 1,10-phenanthroline) was synthesized and characterized by elemental analysis, IR, molar conductance, and thermogravimetric analysis. The dissolution enthalpies of SmCl3·6H2O(s), o-HNBA(s) and phen·H2O(s) in mixed solvent (VHCl :VDMF :VDMSO=2:2:1) were determined by calorimetry at 298.15 K. The enthalpy change of the reaction was determined to be rHmΔθ=252.49±1.60 kJ/mol. Using the relevant data in the literature and a thermochemical recycle according to Hess’s Law, the standard molar enthalpy of formation of [Sm(o-NBA)3 phen]2 (s) was estimated to be f mHΔθ=–4109.2±7.3 kJ/mol.     

Magnetic Properties and Phase Transformation of Tb1-xPrxFe1.96 （x=0 to 0.7） Compounds

In recent years,the fields of application of the(Tb,Dy)Fe2giant magnetostrictive materials,as ad-vancedfunctional materials,have become wider.Suchmaterials can be composed by pseudo-binaryRExRE′1-xFe2compounds that have the same sign ofmagnetostriction but the opposite sign of anisotropy,inorder to mini mize the magnetic anisotropy while stillmaintaining a large positive magnetostriction[1].Ac-cordingto Steven′s calculation,inthe magnetocrystal-line anisotropy and mangetostriction of rare…     

Luminescence of Terbium Complexes Incorporated into Silica Matrix

Ｔｈｅｓｏｌ ｇｅｌｍｅｔｈｏｄｈａｓｓｈｏｗｎａｓｕｉｔａｂｌｅａｐｐｒｏａｃｈｆｏｒｔｈｅｐｒｅｐａｒａｔｉｏｎｏｆｎｏｖｅｌｌｕｍｉｎｅｓ ｃｅｎｔｍａｔｅｒｉａｌｓ .Ｍａｎｙｒｅｃｅｎｔｗｏｒｋｓｈａｖｅｆｏ ｃｕｓｅｄｏｎｔｈｅｄｅｖｅｌｏｐｍｅｎｔｏｆｓｏｌｉｄ ｓｔａｔｅｔｕｎａｂｌｅｄｙｅｌａｓｅｒｍｅｄｉａｕｓｉｎｇｏｒｇａｎｉｃｄｙｅｄｏｐａｎｔｓ[1 ,2 ]ａｎｄｔｒｉｓ( 2 ,2′ ｂｉｐｙｒｉｄｉｎｅ)ｒｕｔｈｅｎｉｕｍ (Ⅱ )ｃｏｍ ｐｌｅｘ[3 ,4 ] ｗｈｉｃｈｃａｎｈａｖｅｓｏｍｅｐｏ…     

Hydrothermal Synthesis and Characterization of Pyrochlore Titanate R2Ti2O7(R=Gd3+, Tb3+, Dy3+)

Pyrochlore titanate oxides, R2Ti2O7(R=Gd3+, Tb3+, Dy3+), were synthesized under mild hydrothermal conditions. The crystal growth of pyrochlore titanate oxides and taking place of chemical reaction in the hydrothermal processing were sensitive to the alkalinity, temperature, reaction time, the nature of the rare earth ion and the composition of initial reaction mixture. The as-prepared samples were characterized by powder X-ray diffraction, scanning electron microscopy, Raman spectrum and variable temperature dc magnetic susceptibility(Superconductivity quantum interference device, SQUIDS). The magnetic studies gave 7.29×10-23 A·m2/Gd3+ and -8.28 K, 8.75×10-23 A·m2/Tb3+ and -19.7 K, and 8.85×10-23 A·m2/Dy3+ and 0.84 K effective moments and Weiss constants for Gd2Ti2O7,Tb2Ti2O7 and Dy2Ti2O7, respectively.     

Effect of light conversion agent on luminous properties of a new down-converting material SrAl_2O_4:Eu~(2+),Dy~(3+)/light conversion agent

A new luminous material SrAl_2O_4:Eu~(2+),Dy~(3+)/light conversion agent that can emit red light in the darkness after being excited was fabricated by combining light conversion agent on to SrAl_2O_4:Eu~(2+),Dy~(3+) particles through YsiX3.The morphology of the luminous materials was analyzed by scan electron microscopy(SEM).The emission behavior was evaluated by fluorescence spectrophotometric analysis and the results demonstrated that the emission spectra of samples had a redshift compared to SrAl_2O_4:Eu~(2+),Dy~(3+) and the emission intensity rose dramatically at first and then decreased when the ratio of light conversion agent doping was over 1.4 wt.%.And the emission color of SrAl_2O_4:Eu~(2+),Dy~(3+)/light conversion agent was tuned from green(SrAl_2O_4:Eu~(2+),Dy~(3+))to orange-red.Furthermore,the afterglow property was also investigated,and the results indicated that the afterglow brightness reached 6.5 cd/m~2,and as the light conversion agent concentration increased the brightness intensity decreased.     

稀土铕,铽β-二酮配合物的合成与发光性能

采用Claisen缩合反应合成了一种新型的β-二酮化合物1-(4-溴苯)-3-苯基丙烷-1,3-二酮(L),并以其为第一配体,邻菲罗啉(phen)为第二配体,合成出新型稀土铕,铽二元及三元配合物。通过元素分析、红外光谱、紫外光谱、荧光光谱对合成的配体及配合物进行了表征。元素分析确定了配合物的组成。红外光谱的分析表明第一配体L中的氧原子以及第二配体phen中的氮原子与稀土离子进行了配位。紫外光谱表明第一配体L为能量的给体,第二配体phen起协同作用。通过荧光光谱研究了配合物的发光性质,结果显示三元配合物的发光强度大于二元配合物,三元配合物Eu(L)3phen表现出Eu3+的特征发射,在593,615,653,701 nm处的发射峰分别归属于Eu3+的5D0→7Fj(j=1,2,3,4)能级间的跃迁,并且以位于615 nm处的5D0→7F2电子跃迁所发出的荧光强度最大;而铽配合物中并没有出现Tb3+的特征发射。进一步的研究表明,这是由于配体L的最低三重态能级较适合Eu3+的发射能级,配体L吸收的能量可以有效的通过Antenna效应传递给稀土中心离子,使得三元配合物Eu(L)3phen的发光强度较大。     

Synthesis and crystal structure of a novel double 1：11 series arsenotungstate： [Cu^I（phen）2]5H6[Sm（AsW11O39）2]·6H2O

A novel double 1：11 series arsenotungstate, [Cu^I（phen）2]5H6[Sm（AsW11O39）2]·6H2O （phen=1, 10-phenanthroline） was synthesized by the hydrothermal method and characterized by elemental analysis, 1R spectra, and single-crystal X-ray diffraction. The title compound was monoclinic, space group P2 1/c, a=3.75710（2） nm, b=1.39776（8） nm, c=-3.33735（18） nm, β=96.967（10）°, V=17.3969（17） nm^3, Z=4. Single crystal X-ray structural analyses revealed that the dimeric polyanion, [SmAs2W22O78]^1-, consisted of one central Sm^3＋ ion and two tetradentate heteropoly ligands [ASW11O39]^7-. The Sm^3＋ ion and two tetradentate defective [AsW11O39]^7- anions were joined together by the sharing of four oxygen atoms from each heteropoly ligand. The bond valence sum （BVS） calculations of the title compound suggested that all four Cu atoms were in the ＋1 oxidation sate.