116results about How to "High Luminous Quantum Efficiency" patented technology

The invention discloses a dye / metal-organic framework composite material for white light emission. The dye / metal-organic framework composite material for white light emission is composed of 70-90% of indium-containing metal-organic framework, 5-15% of pyridine hemicyanine dye and 5-15% of acridine dye by molar percent. The preparation method comprises the steps of: firstly, synthesizing the indium-containing metal-organic framework from a benzene polycarboxylic acid organic ligand and an indium salt through a solvothermal reaction, and secondly, introducing the pyridine hemicyanine dye and the acridine dye into the indium-containing metal-organic framework by the ion exchange method to obtain the dye / metal-organic framework composite material. The synthetic method is simple in process and mild in conditions; the raw materials are easy to get and the yield of the dye / metal-organic framework composite material is high; the prepared dye / metal-organic framework composite material is high in chemical stability; the chromaticity coordinates of the emitted color are quite close to the chromaticity coordinates of the ideal white light; the color rendering index of the composite material is higher than 80 and the luminous quantum efficiency of the composite material is greater than 20%; therefore, the dye / metal-organic framework composite material for white light emission is expected to be applied to the fields of display and light emitting devices and the like as a novel white light emitting material.

The invention discloses a preparation method of a composite luminescent fiber nanomaterial. The preparation method comprises the steps: reacting a rare earth complex or a rare-earth-doped nanocrystal with a polymer monomer to form a core-shell structured compound; demulsifying, separating and drying the compound to obtain a rare-earth complex-polymer or rare-earth-doped nanocrystal-polymer composite nanoparticle powder; and preparing the composite nanoparticle power into an electrospinning solution, and preparing the electrospinning solution into the composite luminescent fiber nanomaterial with an electrospining method. The invention provides a new approach to preparation of a rare-earth organic-inorganic composite fiber nanomaterial with good dispersity, high orientation property, strong chemical stability and high luminous efficiency. The composite luminescent fiber nanomaterial is about to achieve important application values in the fields of optical communication, laser, communication and transportation, sailing fire fighting, raining working, bioinstrumentation and biochip, submarine signal transmission and solar photovoltaic cells.

An Organic Light Emitting Diode (OLED) which is adapted to inhibit the formation and growth of non-emissive areas known as “dark spots.” The OLED comprises an anode disposed on a substrate, a cathode, an electroluminescent (EL) layer disposed between the anode and the cathode and a hole transport layer disposed between the anode and the EL layer. The OLED has one or more dielectric organic barrier layers disposed between one or more of the OLED's layers. These barrier layers are made from an organic polymer and are adapted to resist permeation by oxygen and moisture and to inhibit metal migration.

The invention provides bio-based carbon nano dot fluorescent powder, a preparation method and applications thereof, belongs to the scientific field of nano materials, and aims to solve the problems that in the prior art the luminescent quantum efficient of conventional carbon nano dot based luminescent materials is low and the luminescent materials are difficult to process. The bio-based carbon nano dot fluorescent powder takes the carbon nano dots as the central luminescent materials; biological products such as starch, agar powder, and the like are taken as the dispersing medium; the carbon nano dots are evenly bonded to the selected particle surfaces of the biological product powder through hydrogen bonds, thus the carbon nano dots are highly dispersed in space, the solid-state luminescence quenching caused by conglomeration is effectively avoided, and the high efficient luminescence of carbon nano dots in a solid-state system is achieved. The invention further provides a preparation method of the bio-based carbon nano dot fluorescent powder, and the provided fluorescent powder can be applied to the industries such as temperature sensor, illumination and display, fluorescent paint, and the like.

The invention provides a conjugated polymer with a side chain containing a triazine group as well as a preparation method and application of the conjugated polymer. The conjugated polymer provided by the invention has a structure represented by formula (I) (as shown in the description). By selecting a specific polymer unit and a proportion of the specific polymer unit, the concentration quenching effect of light-emitting kernel with an E-form delayed fluorescence emitting effect is adequately inhibited, and therefore, the photoluminescence quantum efficiency is remarkably improved; and an electroluminescence device prepared from the conjugated polymer is improved, meanwhile, a roll-off effect of the electroluminescence device under a high light condition is effectively inhibited. Besides, the preparation method of the polymer is simple, and when the polymer is used for preparing a device, the device can be prepared by virtue of simple solution processing manners such as spinning and spray ink printing, so that the preparation method of the electroluminescence device is greatly simplified.

The invention relates to novel luminescent material synthesis technologies, in particular to a novel binuclear copper (I) complex blue-light material and a method for preparing the same. The molecular formula of the blue-light material, namely a perchlorate di-[5-tertiary butyl-3-(2-pyridyl)-1,2,4-triazole] di-[N,N-dual(diphenyl phosphorous) amine] dimeric copper (I) complex, is C<70>H<70>Cl<2>Cu<2>N<10>O<8>P<4>, and the molecular weight of the blue-light material is 1501.26. The novel binuclear copper (I) complex blue-light material and the method have the advantages that as shown by luminescence test results, the novel binuclear copper (I) complex blue-light material is excellent in solid photo-luminescence performance, a powerful blue-light emission property can be realized, the maximum blue-light emission value is 439nm, and the luminescent quantum efficiency is 34%.

The invention discloses bivalent manganese-doped full inorganic perovskite quantum dot glass. The bivalent manganese-doped full inorganic perovskite quantum dot glass is prepared from 25 to 45 percentof B2O3, 25 to 45 percent of SiO2, 1 to 10 percent of MCO3, 1 to 10 percent of Al2O3, 1 to 5 percent of ZnO, 1 to 10 percent of Cs2CO3, 1 to 10 percent of PbCl2, 1 to 10 percent of NaCl and 1 to 10 percent of MnCl2, wherein M is Ca, Sr or Ba. The preparation method of the quantum dot glass comprises the following steps: grinding all raw material components of the glass and melting after uniform mixing; then carrying out compression molding on a melt, annealing and carrying out heat treatment, thus obtaining the bivalent manganese-doped full inorganic perovskite quantum dot glass by carrying out heat treatment with different temperatures. The quantum dot-doped glass prepared by the invention has the advantages of good chemical stability and higher fluorescence quantum efficiency, and is aluminescent material with a promising application prospect.

The invention relates to a Li / Mg-codoped bi-perovskite red fluorescent powder and preparation method of same, wherein the red fluorescent powder is characterized by being represented as the following formula: Na(Gd<1-x-y-z>Eu<x>Li<y>Mg<z>)MgWO6, wherein 0.05 <= x <= 0.2, 0.02 <= y <= 0.1 and 0.02 <= z <= 0.2. The red fluorescent powder is prepared through a solid-phase method. In the invention, bi-perovskite NaGdMgWO6 is employed as a basic structure material, europium is employed as a red luminescent center and the codoped lithium and magnesium are employed as sensitization sources and are used for providing a fluxing effect, wherein the three mentioned above substitute the position of gadolinium in the bi-perovskite NaGdMgWO6 to generate low crystal lattice symmetry, thereby ensuring stability, high efficiency and high color rendering property of the fluorescent powder. In addition, the fluorescent powder is prepared through a conventional solid-phase method which is simple in operation and is controllable in process.

The invention belongs to the technical field of perovskite-like nanocrystals. The invention discloses a preparation method of Cs<3>Cu<2>X<5> nanocrystalline and a product. The preparation method comprises the steps that indium halide InX3 or zinc halide ZnX2 is additionally introduced into a precursor solution for preparing Cs<3>Cu<2>X<5> nanocrystalline through a thermal injection method, preparing the Cs<3>Cu<2>X<5> nanocrystalline through a thermal injection method, wherein X is selected from Cl, Br and I. According to the preparation method, a key precursor for regulating and controlling the growth of the nanocrystalline in the preparation method of the nanocrystalline is improved; indium halide or zinc halide is used as an additive in a precursor, and a copper element is used as a substitute of a lead element, so that the preparation of the lead-free metal halide light-emitting nanocrystal is completed, the preparation process is easy to implement, the cost is low, and meanwhile,the defects of the lead-containing halogen perovskite nanocrystal can be overcome.

The invention relates to a water-soluble high-efficiency rare-earth luminescent material and a preparation method of a transparent film made from the same. The water-soluble high-efficiency rare-earth luminescent material comprises LAPONITE RD nano-clay, ionic liquid and water, wherein the LAPONITE RD nano-clay contains a luminescent rare-earth organic complex; the ionic liquid contains oxygen; the mass ratio of the LAPONITE RD nano-clay which contains the luminescent rare-earth organic complex to the ionic liquid which contains the oxygen is 1:(1-3); the mass of the water accounts for 80%-85% of the rare-earth luminescent material; the average particle diameter of the LAPONITE RD nano-clay is 30 nanometers, and the mass percentage of rare-earth ions contained in the LAPONITE RD nano-clay is 6%-7.5%. The water-soluble high-efficiency rare-earth luminescent material disclosed by the invention takes a large amount of water as a medium, can not only increase the efficiency of luminous quantum, but also enhance the dissolution concentration of the rare-earth ions in an inorganic matrix and the luminescent property.

The invention relates to a micro-crystal glass capable of precipitating La2O3 nanometer crystal, particularly to a La2O3 micro-crystal glass doped with rare earth ions or transition metal ions. The micro-crystal glass comprises (mol %) SiO2 45, Al2O3 25, Na2O or Na2CO3 15-20, LaF3 7-12, rare earth ions including ErF3 0.1-7.9 and YbF3 0.1-7.9, and transition metal ions including NiO 0.05-2. The preparation method comprises the steps of preparing SiO2-Al2O3-Na2O-LaF3 glass doped with rare earth ions or transition metal ions by fusion method, and performing heat treatment to obtain micro-crystal glass. The inventive micro-crystal glass has the advantages of low production cost, good transparency, and good physicochemical properties; and can realize effective upconversion luminescence and near-infrared wideband light amplification, and can be used in the fields of laser, optical fiber amplifier and three-dimensional display.

The invention relates to a flexible rare-earth transparent light-emitting film and a preparation method thereof. The film is composed of a rare-earth light-emitting material and polyvinyl alcohol (PVA) in a mass ratio of 1:(1-4). The rare-earth light-emitting material comprises LAPONITE RD nano clay containing light-emitting rare-earth organic complex, an oxygen-containing ionic liquid and water, wherein the mass ratio of the LAPONITE RD nano clay containing light-emitting rare-earth organic complex to the oxygen-containing ionic liquid is 1:(1-3); the water accounts for 80-85 wt% of the rare-earth light-emitting material; the average particle size of the nano clay is 30nm; and the mass percent of the rare earth ions in the nano clay is 6-7.5%. The novel high-efficiency flexible rare-earth transparent light-emitting film is peelable and thin, and has the advantages of large area, excellent flexibility, excellent heat stability, excellent photostability and high mechanical strength.

The invention belongs to the nano mesoporous material preparation technology field, in particular to the synthesis technology of rare earth aromatic carboxylic acids mesoporous red luminescent material. The invention adopts a two-step method, firstly synthesizing complex which has distinct and stable structure and bright light-emitting, then assembling to the pore passage of MCM-41 mesoporous material, thereby synthesizing red mesoporous material which has stable and high ordered chemical and thermodynamic properties. The process which is provided by the invention is simple and easy to operate, has the characteristics of controllability and quantification. And the rare earth aromatic carboxylic acids mesoporous red luminescent material has long service life and high light-emitting quantum efficiency, regular ordered microcosmic topography, which can be extensively applied on the fields of luminescent material, catalyst material, sorbent material, nano reactor and photoelectric sensor and the like.

The invention relates to a new luminescent material, in particular to a novel mononuclear copper (I) complex blue light material and a preparation method thereof. The novel mononuclear copper (I) complex blue light material is perchlorate 5-tertiary butyl-3-[2-pyridyl]-1, 2, 4-triazole-bis [triphenylphosphine] copper [I] complex, the molecular formula is C47H44ClCuN4O4P2, and the molecular weight is 889.82. The mononuclear copper (I) complex blue light material provided by the invention is mainly used for luminescent materials in daily lighting, luminescent display and optical sensors. Photoluminescence property test results show that the copper (I) complex has good photoluminescence property in the solid state, strong pure blue light emission is represented, and the maximum value is located at 455 nm.

The invention discloses an ionic rare-earth complex luminescent material, a preparation method therefor and application therefor. The structural formula of the rare-earth complex is [Ln(ND)4]M, wherein ND is a 4-hydroxyl-1,5-naphthyridine anionic ligand; Ln represents rare earth ions comprising yttrium, lanthanum, europium, gadolinium, terbium, ytterbium ions; M is counter cations comprising alkali metal ions, alkyl substituted quaternary ammonium ions, alkyl substituted quaternary phosphonium ions, l,3-dialkyl substituted imidazolium ions and N-alkyl substituted pyridinium ions. According to the europium complex provided by the invention, the ligand is hardly dissociated and the complex is high in thermal decomposition temperature; furthermore, the europium complex further has a high-efficiency photoluminescent quantum yield and good resistance to ultraviolet light, and can be used as photoluminescent and electroluminescent materials.

The invention belongs to the field of organic light-emitting materials, and particularly relates to a nitrogen-containing compound and an electronic element and an electronic device using the same, and the nitrogen-containing compound has a structure as shown in a chemical formula 1. When the nitrogen-containing compound is applied to the organic electroluminescent device, the performance of the device can be effectively improved.

The invention discloses a method for synthesizing a polyhedron oligomerization silsesquioxane macromolecule composite luminescent material containing rare earth. The method comprises the following steps: firstly, coordinating organic ligand modified polyhedron oligomerization silsesquioxane of a cage-shaped structure with a first ligand rare earth ion by using a sol-gel method according to the coordination chemistry principle, subsequently introducing polymethyl methacrylate as a second ligand which can be coordinated with the rare earth ion, and coordinating, thereby obtaining the polyhedron oligomerization silsesquioxane macromolecule composite luminescent material which is good in fluorescence property and thermal stability, contains rare earth and is of the cage-shaped structure. The synthesis method is gentle in experiment condition, the whole preparation system is easy to establish and simple and convenient to operate, the conditions are easy to control, and a product is stable in quality.

The invention provides a wide color gamut backlight source for display of LED combined with perovskite quantum dot glass-ceramics, and is used for providing a light source for the displayer. The backlight source comprises the LED and the perovskite quantum dot glass-ceramics. The perovskite quantum dot glass-ceramics comprises red light, green light and blue light perovskite quantum dot glass-ceramics. The perovskite quantum dot glass-ceramics material is CsPbX3 (X=Cl, Br, I) or CsPb (ClxBr1-x) 3 or CsPb (BrxI1-x) 3. The backlight source spectrum contains its own blue light component of the blue LED, the narrow linewidth green light component produced by exciting CsPbBr3 or CsPb (BrxI1-x) 3 quantum dot glass-ceramics by the blue LED and the narrow linewidth red light component produced byexciting CsPbI3 or CsPb (BrxI1-x) 3 quantum dot glass-ceramics by the blue LED. The backlight source spectrum can also contain the narrow linewidth blue light component produced by exciting the blue light CsPb (ClxBr1-x)3 quantum dot glass-ceramics by the short wavelength LED of which the wavelength is less than the absorption cutoff wavelength of the quantum dot, the narrow linewidth green lightcomponent produced by exciting the CsPbBr3 or CsPb (ClxBr1-x)3 quantum dot glass-ceramics by the short wavelength or blue LED and the narrow linewidth red light component produced by exciting the CsPbI3 or CsPb (ClxBr1-x)3 quantum dot glass-ceramics by the short wavelength or blue LED.

The invention relates to medium-infrared gain sulfide optical fibers and a preparation method thereof, and belongs to laser gain optical fibers and a preparation method thereof. According to the present invention, the optical fiber core material is a rare earth ion doped Ga-Sb-As-S glass, the optical fiber cladding material is a Ga-Sb-As-S glass, the refractive index of the optical fiber core glass is greater than the refractive index of the cladding glad, the chemical formula of the Ga-Sb-As-S glass is Ga(1-x-y-z)SbxAsySz, x is 0.26-0.32, y is 0.02-0.06, z is 0.55-0.65, the rare earth ion is one selected from Dy<3+>, Er<3+> and Tm<3+>, and the molar concentration of the doped rare earth ions is 0.05-1%; the optical fibers are prepared through a rod tube method, wherein the fiber core glass and the cladding glass are respectively prepared into the thin rod and the bushing, the fiber core glass thin rod is inserted into the cladding glass bushing, and drawing is performed to obtain the optical fibers having the final size; and the gain sulfide optical fibers have strong luminescence at a wavelength of 2.5-5 [mu]m, the luminescence quantum efficiency is greater than 70%, and the gain sulfide optical fibers can be adopted as the core gain medium of the low-cost and compact medium-infrared optical fiber laser.

The invention discloses a rare earth oxyfluoride near-infrared luminescent glass and a preparation method thereof. The glass is composed of the following components: 48.5 to 49.5 mol of SiO2, 20 to 40 mol of BaF2, 10 to 30 mol of ZnF2, 0.5 to 1.5 mol of RE2O3, wherein the RE2O3 represents one or more components selected from Ho2O3, Er2O3, Tm2O3, Dy2O3 and Nd2O3. The preparation method comprises the following steps: mixing the raw materials according to the ratio mentioned above, smelting the raw materials for one hour at a temperature of 1220 to 1250 DEG C; pouring the molten glass into a mould which has been heated in advance, annealing for 6 to 8 hours at a temperature of 470 to 500 DEG C; then cooling the glass in the furnace to the room temperature; and finally cutting, burnishing and polishing the obtained glass so as to obtain the required samples. The products prepared through the preparation method are non-toxic, environment-friendly, and cheap, and are capable of generating near infrared lights in a plurality of wave bands.

The invention discloses a Cr<3+> doped near-infrared wide-spectrum luminescent material and a preparation method thereof, which belong to the technical field of near-infrared luminescent materials. The general chemical formula is Ca3Y2-xGe3O12: xCr<3+>, and x is greater than or equal to 0.01 mol% and less than or equal to 20 mol%. The near-infrared luminescent material belongs to a cubic crystal system and has a garnet type space crystal structure the same as Ca3Y2Ge3O12, the space group is Ia3d, Ca<2+> occupies dodecahedron octa-coordination, Y<3+> occupies octahedron hexa-coordination, and Ge<4+> occupies tetrahedron tetra-coordination. The material is wide in excitation spectrum, the optimal excitation wavelength ranges from 400 nm to 550 nm, and the emission wavelength ranges from 700nm to 1200 nm. The material is matched with a blue-light LED chip, can be used for manufacturing a wide-spectrum near-infrared light source, and is applied to the fields of plant illumination, biological probes, military affairs and the like. The method is simple in preparation process, low in raw material price and easy to synthesize.

A phosphor includes a host crystal including Sr3MgSi2O8 crystal and SrMgSiO4 crystal and also includes Eu2+, or Eu2+ and Mn2+ as luminescent centers. Alternatively, a phosphor includes a host crystal including Sr3MgSi2O8 crystal and SrMgSiO4 and also includes Eu2+ as a luminescent center, the phosphor being free from Mn2+ as a luminescent center. A light-emitting device includes a phosphor layer containing the phosphor. A projector and a vehicle include the light-emitting device.

The invention provides a kinetic cause light emitting device and a preparation method thereof. The light emitting device comprises a kinetic cause light emitting layer made of an organic light emitting material having an amorphous kinetic cause light emitting property, the organic light emitting material employed by the kinetic cause light emitting layer contains a charge transfer (CT) molecule consisting of a benzophenone electron withdrawing group and an aromatic amine electron donating group, and the color of the kinetic cause light emitting can be adjusted and controlled by adjusting the intensity of the CT state, and beneficial to study the kinetic cause light emitting property and widen the application of the same in different environments. In addition, according to the kinetic causelight emitting device and preparation method thereof, the light emitting materials have very high light emitting quantum efficiency and typical thermal activation delayed fluorescence (TADF) property, which can be used in the preparation of optoelectronic devices.

The invention provides a novel garnet-based high efficiency green phosphor, a chemical formula is [(Gd1-xLux)1-yTby]Al5O12 (short for (Gd, Lu)AG:Tb<3+>), wherein x is Lu / (Gd+Lu+Tb) and y is Tb / (Gd+Lu+Tb)(x is 0-1.0, y is 0-0.15). The phosphor takes rare earth nitrate and an ammonium aluminium sulfate according to stoichiometric ratio to prepare a mother salting liquid, the mother salting liquid is dropped into a NH4HCO3 precipitating agent solution, the obtained deposition is centrifuged, washed, and dried to obtain the white precursor powder, and phosphor (Gd, Lu)AG:Tb<3+> can be obtained through calcining at different temperature. non radiation energy transmission of Gd<3+> to Tb<3+> is existed, the fluorescence quantum efficiency is high, addition of Lu can obvious improve the stability of a system, and is more suitable for a scintillator material.

The invention relates to an organic blue fluorescent material and a preparation method and application thereof. The material adopts a delta bond as a bridge chain to connect two anthracene molecule luminescence units and regulate the conjugation state of organic molecules; meanwhile, a steric hindrance group is introduced onto the delta bond to inhibit a pi-pi accumulation effect among the organicmolecules, and correspondingly the organic blue fluorescent material is prepared and has high thermal stability and high luminous quantum efficiency. The specific preparation method and application mainly include the steps of adopting 9-benzanthracene-10 borate and 4,4'-dibromo diphenyl bis-substituted methane for conducting a Suzuki coupling reaction to prepare the organic blue fluorescent material. The material is adopted as a luminous layer and achieves a non-doped deep blue OLED device with high performance.

The invention provides a laser taking perovskite quantum dot microcrystalline glass as a gain medium. The laser comprises a pump source, a laser gain medium and a resonant cavity. The pump source is apump light source which is shorter than a quantum dot absorption cut-off wavelength and is used to excite the laser gain medium. The laser gain medium is the perovskite quantum dot microcrystalline glass and is used to receive radiation from the pump source and emit photons. The resonant cavity is a periodic structure resonant cavity and is used for amplifying the photon emitted by the laser gainmedium to output continuous lasers or a pulsed laser. A perovskite quantum dot microcrystalline glass material of the laser gain medium is CsPbX3 (X=Cl, Br, I), or CsPb (ClxBr1-x)3, or CsPb (BrxI1-X)3, or CsPb2Br5. Pb ions in the perovskite quantum dot microcrystalline glass material can be completely or partially replaced with tin ions, or bismuth ions, or manganese ions. A luminous wavelength of the perovskite quantum dot microcrystalline glass can be adjusted in a range of 400-800 nm, environmental and mechanical stability is good, and optical transmission losses are low.

An organic electroluminescent device comprises an anode substrate, an organic light-emitting functional layer, a buffer layer, a pn node layer and a cathode layer which are sequentially laminated, wherein the pn node layer comprises an n-type layer laminated on the buffer layer and a p-type layer laminated on the n-type layer; the cathode layer is laminated on the p-type layer; the anode substrate is made of transparent conductive glass; the buffer layer is made of lithium fluoride, cesium fluoride or sodium fluoride; the n-type layer is made of zinc oxide, tin oxide or cerium dioxide; the p-type layer is made of nickel oxide or copper oxide; the cathode layer is made of an indium tin oxide conductive thin film, an aluminum zinc oxide conductive thin film or an indium zinc oxide conductive thin film. The organic electroluminescent device has relatively high luminous performance and is uniform in luminescence. The invention further provides a manufacturing method of the organic electroluminescent device.

The invention relates to a preparation method of a transition metal microcrystal-doped chalcogenide glass composite material. The method comprises the following steps: (1) preparing a TM<2+>: ZnX material (wherein TM<2+> is a transition metal ion, and X is S or Se): putting TMX powder and ZnX powder into a ball mill, fully and evenly mixing, putting the evenly mixed powder into a smelting furnace, and carrying out heat preservation at the temperature of 850-1100 DEG C for 72-168 hours to obtain the TM<2+>: ZnX material; (2) putting the TM<2+>: ZnX material and chalcogenide glass into the ball mill according to a certain mass proportion, and fully grinding to prepare evenly mixed powder; (3) putting the mixed powder into a quartz tube, vacuumizing the quartz tube, sealing the vacuumized quartz tube, putting the sealed quartz tube into the smelting furnace, and carrying out heat preservation at the temperature of 270-400 DEG C for 2-20 hours to obtain the TM<2+>: ZnX-doped chalcogenide glass composite material. The composite material prepared by the invention is stable in thermal property and high in conversion efficiency, and is excellent in intermediate infrared fluorescence emission, thus providing a new working medium material for development of an intermediate infrared laser.