376 results about "Luminophore" patented technology

The present invention provides organic light emitting devices having a combined emission from at least two emissive materials, a fluorescent blue emissive material and a phosphorescent emissive material. The device may further comprise additional fluorescent or phosphorescent emissive materials. In preferred embodiments, the invention provides OLEDs having three different emissive materials—a red emissive material, a green emissive material and a blue emissive material. The invention provides a device architecture which is optimized for efficiency and lifetime by using a combination of fluorescent and phosphorescent emitters. Further, in preferred embodiments the device architecture provides a high color-stability of the light emission over a wide range of currents or luminances.

A white light-emitting organic-inorganic hybrid electroluminescence device which has nanocrystals as illuminants. According to the device, a semiconductor nanocrystal layer composed of at least one kind of nanocrystals, a hole transport layer and/or an electron transport layer simultaneously emit light to produce white light, or a semiconductor nanocrystal layer composed of at least two kinds of nanocrystals emits light at different wavelengths to produce white light. The device can be used as a backlight unit for a liquid crystal display, or can be used to manufacture an illuminator.

The present invention relates to organic light emitting devices (OLEDs), and more specifically to OLEDS that emit light using a combination of fluorescent emitters and phosphorescent emitters for the efficient utilization of all of the electrically generated excitons.

An OLED device for emitting white light comprises adjacent layers 1 and 2 wherein layer 1 contains a host and a yellow, orange, or red emitter and layer 2 contains a host and a blue or blue-green light emitter wherein the host in layer 2 comprises an anthracene material bearing an aromatic ring bonded to the 2-, 9-, and 10-positions of the anthracene nucleus.

The invention relates to a light source comprising a light-emitting element, which emits light in a first spectral region, and comprising a luminophore, which comes from the group of alkaline-earth orthosilicates and which absorbs a portion of the light emitted by the light source and emits light in another spectral region. According to the invention, the luminophore is an alkaline-earth orthosilicate, which is activated with bivalent europium and whose composition consists of: (2-x-y)SrOx(Ba, Ca)O(1-a-b-c-d)SiO2aP2O5bAl2O3cB2O3dGeO2:yEu<2+> and/or (2-x-y)BaOx((Sr, Ca)O(1-a-b-c-d)SiO2aP2O5bAl2O3cB2O3dGeO2:yEu<2+>. The desired color (color temperature) can be easily adjusted by using a luminophore of the aforementioned type. The light source can contain an additional luminophore selected from the group of alkaline-earth aluminates, activated with bivalent europium and/or manganese, and/or can contain an additional red-emitting luminophore selected from the group Y(V, P, Si)O4:Eu or can contain alkaline-earth magnesium disilicate.

A colour tunable lighting module is described which includes at least three solid state lighting emitters (such as light emitting diodes) and at least two wavelength converting elements (such as phosphors). The three solid state lighting emitters are formed of the same semiconductor material system and the light generated by them has dominant wavelengths in the blue-green-orange range of the optical spectrum. The two wavelengths converters are used re-emit some of the light from two of the emitters in broader spectra having longer dominant wavelengths, while the third emitter is selected to emit light at a wavelength between the dominant wavelengths of the light from the two emitters and the two converters. A control system may be employed to monitor and control the module and the lighting module can be optimised for tunable high colour quality white light applications.

Device, kit and method of using same to detect analytes such as nucleic acids are described. An excitation source, preferably a nitride-based LED, emits light capable of being absorbed by luminophores. Sensors are stably attached, preferably via covalent or ionic bonds, to a surface within the device, such as the surface of the excitation source that is exposed to the sample. When a complex is formed between the sensors and the analyte, the luminophores emit light or emit light of a different wavelength, thereby signaling the presence or quantity of the analyte.

Improved carbon dioxide sensors are disclosed which are less sensitive to the moisture content of the environment and which are substantially insensitive to oxygen levels under normal working conditions. The CO₂ sensor comprises a pH indicator and long-lived reference luminophore and a porous sol-gel matrix. Combined CO₂ and O₂sensors are also described. Further disclose are methods of printing sensor onto substrates.

A system (20) of the present invention includes light source instrumentation (30) to selectively illuminate a light scattering medium including a luminophore and detection instrumentation (50) to detect multiply scattered light output from the medium in response to illumination by the light source instrumentation (30). A processor (70) is operatively coupled to the detection instrumentation (50) to determine a first optical characterization of the medium from a first multiply scattered light output of a first illumination light wavelength and a second optical characterization of the medium from a second multiply scattered light output of a second illumination light wavelength different than the first illumination light wavelength. The processor (70) is operable to calculate lifetime of the luminophore from the first optical characterization, the second optical characterization, and a multiply scattered emission of the luminophore from the medium in response to excitation.

The invention discloses a chemiluminescence reagent, and relates to a chemiluminescence reagent which is mainly applied to a biotechnology, bioscience, medical diagnosis, food safety, and environment-friendly detection. The chemiluminescence reagent is prepared from the materials by mass percent: at least one 0.001-0.1% luminous reagent, at least one 0.001-0.2% oxidant, at least one 0.01-0.5% luminous enhancer, at least one 0.000001-0.05% background control agent, and a buffer solution of which the pH value is 8-11. The key is as follows: chemiluminescence is adjusted by utilizing the background control agent (particularly the antioxidant); the chemiluminescence reagent is valid on background control of enhanced chemiluminescence enzyme immunoassay detection, improvement of the signal to noise ratio and the like. The basis is how to control luminol free radical and concentration of related free radical in a horse radish peroxidase-luminol luminescence system.

The invention relates to an optochemical sensor functioning in accordance with the FRET-principle and exhibiting an acceptor (chromophore or luminophore) responsive to an analyte contained in a sample medium as well as a donor (luminophore), characterized in that acceptor and donor are located in separate chemical phases, whereby the phase containing the donor is essentially impermeable to the sample medium or to components of the sample medium affecting the luminescence characteristics of the luminophore. The invention further relates to a method for qualitative and/or quantitative determination of at least one analyte and/or component of a gaseous or liquid measuring medium according to the FRET-principle, characterized by the use of the sensor according to the invention.

This invention describes a method of use surface plasmon of nanoparticles to enhance CRT, LCD, OLED, Plasma and other display technologies. The plasmon-enhanced nanoparticles interacting with nearby luminophores, liquid crystals or other materials improve in display technologies brightness, contrast, and longevity of luminophores; make faster response time and better direction emission display. The plasmon-enhanced nanoparticles like quantum dots can be also used directly as a luminophores in quantum display technologies.

This optical coding device comprises a plurality of aggregates suitable for emitting infrared, visible or ultraviolet rays by luminescence, at least one of the said aggregates comprising at least one luminophore. This aggregate further comprises at least one particle consisting of a surface plasmon effect material, the said luminophore and the said particle being suitable for entering into interaction.

The invention discloses a preparation method of an unmarked electrochemiluminescent tumor marker immunosensor and application of the immunosensor in detection of tumor markers, and belongs to the field of novel nano functional materials and biosensors. According to the preparation method of the unmarked electrochemiluminescent tumor marker immunosensor, a novel micro-nano material NH4CoPO4 is taken as a substrate so that the luminescence stability of a luminol-hydrogen peroxide luminescent system can be greatly enhanced, and meanwhile, rod-like gold@siver core-shell nanoparticles are taken as a biomimetic catalytic luminescent system, and therefore, an unmarked electrochemiluminescent immunosensor, which is low in cost, high in sensitivity, good in specificity, fast in detection and simple to prepare and is used for detecting tumor makers, can be prepared.

The diode is comprised of the luminous chip electrode, phosphor and sealing material. The phosphor is comprised of the silicon chloride acid Mg Zn Ca (CMZSC) and alkali earth silicate and pyrosilicate phosphor. This phosphor with the other phosphor of the visible light combines the UV white light and LD. The CMZSC green phosphor can transform the blue light transmitted by the semiconductor compound into yellow light. Thus the transmitting spectrum covered area is broadened and the optical transform effect is improved.

An oxygen-quenching luminophore constituting part of a pressure-sensitive luminophore is directly bonded by a covalent bond to an organic polymer compound having trimethylsilyl groups, so the luminophore molecules are retained in the polymer and free aggregation is inhibited when the organic solvent is evaporated. It is therefore possible to prevent light response from being reduced by the aggregation of the luminophore molecules during evaporation of the organic solvent, which is a drawback of forming films from conventional mixed-type pressure-sensitive paints. A thin-film sensor with uniform characteristics can be formed by spraying or application from a pressure-sensitive paint obtained by mixing a functional polymer with a solvent. In addition, a coating solution that has high reproducibility and is suitable for spraying or application can be obtained merely by dissolving the functional polymer as a single component in a suitable solvent. It is possible to obtain a functional polymer, a pressure-sensitive paint, and a pressure-sensitive element in which a reduction in light response due to luminophore aggregation can be prevented, and a thin sensor film having uniform characteristics can be formed, even when the organic solvent has evaporated.

In the illuminator, the following layers are prepared between the anode and cathode in sequence: hole transport layer, electron barrier layer, the first subject material layer, the second subject material layer, the hole barrier layer and electron transport layer. With the first object luminiferous material being intermixed in, the first subject material layer shoots the first color light (B) under bias voltage being added. The second object luminiferous material shooting the second color light (G) and the third object luminiferous material shooting the third color light (R) is intermixed in the second subject material layer. Moreover, the second and the third object luminiferous materials are phosphorescent materials, therefore besides the continuous all wave band true color light source can be obtained.