ABSTRACT
High-brightness, color-tunable colloidal quantum dots are incorporated in 3D nanoporous GaN to create a nanocomposite material (CQD/NP-GaN), which is demonstrated to be an effective approach for a wavelength down-conversion nanomaterial in solid-state lighting. The white-light-emitting diode (LED) made from a blue GaN-based LED and the CQD/NP-GaN shows an increase of extraction efficiency by a factor of 2, a controllable white color, and a down-conversion quantum efficiency as high as 82%.
Subject(s)
Colloids/chemistry , Lighting/instrumentation , Luminescent Measurements/instrumentation , Nanostructures/chemistry , Quantum Dots , Semiconductors , Color , Equipment Design , Equipment Failure Analysis , Systems IntegrationABSTRACT
Colloidal quantum dots exhibit efficient photoluminescence with widely tunable bandgaps as a result of quantum confinement effects. Such quantum dots are emerging as an appealing complement to epitaxial semiconductor laser materials, which are ubiquitous and technologically mature, but unable to cover the full visible spectrum (red, green and blue; RGB). However, the requirement for high colloidal-quantum-dot packing density, and losses due to non-radiative multiexcitonic Auger recombination, have hindered the development of lasers based on colloidal quantum dots. Here, we engineer CdSe/ZnCdS core/shell colloidal quantum dots with aromatic ligands, which form densely packed films exhibiting optical gain across the visible spectrum with less than one exciton per colloidal quantum dot on average. This single-exciton gain allows the films to reach the threshold of amplified spontaneous emission at very low optical pump energy densities of 90 µJ cm(-2), more than one order of magnitude better than previously reported values. We leverage the low-threshold gain of these nanocomposite films to produce the first colloidal-quantum-dot vertical-cavity surface-emitting lasers (CQD-VCSEL). Our results represent a significant step towards full-colour single-material lasers.
ABSTRACT
Blue poly(phenylene-ethynylene) (PPE) electroluminescence is achieved in a single layer organic light emitting device. The polymeric system consists of an oxadiazole grafted PPE, which combines the necessary charge transport properties while maintaining the desirable efficient, narrow light-emitting properties of the PPE. Incorporation of a pentiptycene scaffold within the PPE structure prevents ground-state and excited-state interactions between the pendent oxadiazole units and the conjugated backbone.
Subject(s)
Electrochemistry/instrumentation , Luminescent Measurements/instrumentation , Nanostructures/chemistry , Polymers/chemistry , Color , Electrochemistry/methods , Equipment Design , Equipment Failure Analysis , Materials Testing , Nanostructures/analysis , Polymers/analysisABSTRACT
A new approach based on a conjugated polymer/block copolymer guest/host system for the generation of polarized photoluminescence is reported. Synthetic modification of a poly(p-phenylene-ethynylene) (PPE) conjugated polymer is used for domain-specific incorporation into a cylindrical morphology block copolymer host matrix. Subsequent ordering of the host nanostructure via roll cast processing templates uniaxial alignment of the guest PPE. The ordered films are optically anisotropic displaying both polarized absorption with a dichroic ratio of 3.0 at 440 nm and polarized emission with a polarization ratio of 7.3 at 472 nm.
