Abstract:
The present invention generally relates to organic photodetectors. Further, it is directed to an optimized organic photodetector having reduced dark current and high efficiency and response time.
Abstract:
Organic light emitting devices are described wherein the emissive layer comprises a host material containing an emissive molecule, which molecule is adapted to luminesce when a voltage is applied across the heterostructure, and the emissive molecule is selected from the group of phosphorescent organometallic complexes, including cyclometallated platinum, iridium and osmium complexes. The organic light emitting devices optionally contain an exciton blocking layer. Furthermore, improved electroluminescent efficiency in organic light emitting devices is obtained with an emitter layer comprising organometallic complexes of transition metals of formula L2MX, wherein L and X are distinct bidentate ligands. Compounds of this formula can be synthesized more facilely than in previous approaches and synthetic options allow insertion of fluorescent molecules into a phosphorescent complex, ligands to fine tune the color of emission, and ligands to trap carriers.
Abstract:
A photonic integrated circuit comprises a first waveguide with a first mode of light propagating therein and a second waveguide with a second mode of light propagating therein. The first and second modes of light have different effective indices of refraction. A taper formed in the second waveguide facilitates communication of light between waveguides. Each of the first and second waveguides operate to perform at least one of the generating light, detecting light, and transporting light.
Abstract:
Organic photosensitive optoelectronic devices (“OPODs”) which include an exciton blocking layer to enhance device efficiency. Single heterostructure, stacked and wave-guide type embodiments. Photodetector OPODs having multilayer structures and an exciton blocking layer. Guidelines for selection of exciton blocking layers are provided.
Abstract:
An organic light emitting device (OLED) is disclosed for which the hole transporting layer, the electron transporting layer and/or the emissive layer, if separately present, is comprised of a non-polymeric material. A method for preparing such OLED's using vacuum deposition techniques is further disclosed.
Abstract:
An asymmetric twin waveguide (ATG) structure is disclosed that significantly reduces the negative effects of inter-modal interference in symmetric twin-waveguide structures and which can be effectively used to implement a variety of optical devices. The ATG structure of the invention can be monolithically fabricated on a single epitaxial structure without the necessity of epitaxial re-growth. To achieve the ATG structure of the invention, the effective index of the passive waveguide in the ATG is varied from that of a symmetric twin waveguide such that one mode of the even and odd modes of propagation is primarily confined to the passive waveguide and the other to the active waveguide. The different effective indices of the two coupled waveguides result in the even and odd modes becoming highly asymmetric. As a result, the mode with the larger confinement factor in the active waveguide experiences higher gain and becomes dominant. In a further embodiment, the active waveguide is tapered to reduce coupling losses of the optical energy between the passive waveguide and the active waveguide. In a further embodiment, a grating region is incorporated atop the passive waveguide to select certain frequencies for transmission of light through the passive waveguide.
Abstract:
Highly efficient photon recycling photosensitive optoelectronic device (POD) structures are disclosed which may include optical concentrating non-imaging collectors. Such device structures may be utilized with both organic and inorganic photoconverting heterostructures to enhance photoconversion efficiency. These photo recycling POD structures are particularly well suited for use with organic photoactive materials.
Abstract:
A photonic integrated circuit (PIC) device comprising two or more vertically stacked asymmetric waveguides is provided. A photo-detector PIC device comprises a coupling waveguide for providing low-coupling loss with an external optical fiber and for guiding primarily a first mode of light, a second waveguide vertically coupled to the first waveguide for guiding primarily a second mode of light having an effective index of refraction different from the first mode, and a photo-detector vertically coupled to the second waveguide. Light received at the coupling waveguide is moved into the second waveguide via a lateral taper in the second waveguide. The photo-detector PIC device may further comprise a third waveguide having an optical amplifier therein and positioned between the coupling waveguide and the second waveguide.
Abstract:
Dopant compounds of Formula I below for use in organic light emitting devices (OLED's) as device elements capable of emitting light of wavelengths associated with saturated red emissions. OLED's utilize device elements comprising the above compounds and display devices are based on those OLED's.
Abstract:
A new method for tuning the emission spectrum of OLEDs while retaining a high luminescence efficiency wherein the emission spectrum of a polar luminescent molecule is wavelength shifted by as much as 70 nm when doped into a conductive host in a vacuum-deposited molecular organic light emitting device. The effect may be attributed to changes in the average dipole moment of the host thin film that are induced by the addition of highly dipolar dopant molecules. This phenomenon may be referred to as a “solid state solvation effect” in analogy to similar effects previously identified in solution chemistry. In experiments using singly doped devices, different concentrations of a polar laser dye known as DCM2 are doped in non-polar triaryl amine conductive host films. In these experiments, DCM2 performs the dual role of functioning both as the luminescent center and as the source of the increased spatially averaged dipole moment. In a second set of experiments using dual-doped devices, DCM2 is employed only as the luminescent center in a non-polar host, while a second polar dopant, aluminum tris(8-hydroxyquinoline) (Alq3), is introduced to generate the local dipole moment. By changing the concentration of Alq3, while keeping the DCM2 concentration fixed, the OLED emission may be tuned over a range of 30 nm. For the singly doped devices, the external luminescence quantum efficiency, &eegr;, decreases with dopant concentration due to aggregation induced quenching. However, for the dual-doped devices, &eegr; increases with an increase in the bathochromic shift.