A Full Vacuum Approach for the Fabrication of Hybrid White-Light-Emitting Thin Films and Wide-Range In Situ Tunable Luminescent Microcavities
This study shows the fabrication by a dry approach at mild temperature (<150 °C) of a photoluminescence white light emitting hybrid layer. The white light emitter is obtained by evaporation of two photoluminescent small molecules, a blue (1,3,5-triphenyl-2-pyrazoline (TPP)) and an orange (Rubrene...
| Autores: | , , , , , , , , , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión aceptada para publicación |
| Fecha de publicación: | 2016 |
| País: | España |
| Institución: | Consejo Superior de Investigaciones Científicas (CSIC) |
| Repositorio: | DIGITAL.CSIC. Repositorio Institucional del CSIC |
| OAI Identifier: | oai:digital.csic.es:10261/149427 |
| Acceso en línea: | http://hdl.handle.net/10261/149427 |
| Access Level: | acceso abierto |
| Palabra clave: | Rubrene Photonic crystals Bragg microcavities White light emission GLAD |
| Sumario: | This study shows the fabrication by a dry approach at mild temperature (<150 °C) of a photoluminescence white light emitting hybrid layer. The white light emitter is obtained by evaporation of two photoluminescent small molecules, a blue (1,3,5-triphenyl-2-pyrazoline (TPP)) and an orange (Rubrene) dye within the porous of an SiO host film fabricated by glancing angle deposition. Fluorescence (Föster) resonant energy transfer between the two organic dyes allows the emission of the combined system upon excitation of the TPP molecule at wavelength of 365 nm. The distribution of the organic molecule within the host layer is analyzed as a function of the substrate temperature and vacuum conditions and the required conditions for the white emission determined by finely controlling the TPP:Rubrene ratio. The full vacuum processing of the hybrid layers provides a straightforward route for the incorporation of the white light emitters as optical defect within 1D Bragg microcavities. As a consequence, directional emission of the system is achieved which allows the development of wide-range in situ tunable photoluminescent devices. |
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