Carsten Giebeler

Bio: Carsten Giebeler is an academic researcher from University of Sheffield. The author has contributed to research in topics: Phosphorescence & Photoluminescence. The author has an hindex of 6, co-authored 17 publications receiving 1108 citations.

Electrochemical determination of the ionization potential and electron affinity of poly(9,9-dioctylfluorene)

Abstract: We report cyclic voltammetry measurements for the blue electroluminescent conjugated polymer poly(9,9-dioctylfluorene). Both oxidation and reduction potentials are determined and thus estimates of both the ionization potential Ip and electron affinity Ea of the polymer are obtained for the same sample under the same experimental conditions. We estimate Ip=5.80 eV and Ea=2.12 eV. These results disagree with the common assumption that Ea is, to good approximation, given by the difference between Ip and the optical gap. Measurements on indium tin oxide/polyfluorene/calcium light emitting diode structures are consistent with the deductions from the electrochemical data.

Origin of electrophosphorescence from a doped polymer light emitting diode

Abstract: The origin of electrophosphorescence from a doped polymer light emitting diode (LED) has been investigated. A luminescent polymer host, poly(9,9-dioctylfluorene) (PFO), was doped with a red phosphorescent dye, 2,3,7,8,12,13,17,18-octaethyl-21H,23H-porphyrin platinum(II) (PtOEP). The maximum external quantum efficiency of 3.5% was obtained at a concentration of 4% PtOEP by weight. Energy transfer mechanisms between PFO and PtOEP were studied by absorption, photoluminescence, and photoinduced absorption spectroscopy. Even though electroluminescence spectra were dominated by PtOEP at a concentration of only 0.2 wt% PtOEP, Forster transfer of singlet excitons was weak and there was no evidence for Dexter transfer of triplet excitons. We conclude that the dominant emission mechanism in doped LED{close_quote}s is charge trapping followed by recombination on PtOEP molecules.

Device degradation of polymer light emitting diodes studied by electroabsorption measurements

Abstract: We have studied the device degradation of single layer poly(2,5-dialkoxy-p-phenylenevinylene) light emitting diodes by electroabsorption spectroscopy The applied direct current (dc) bias generates an opposing internal field This internal field rises as the applied dc bias is increased The development of the internal field is less pronounced in vacuum than in an ambient atmosphere and is no longer apparent for devices that were prepared and tested under an inert atmosphere in a glovebox For the devices that were tested in air and under dynamic vacuum conditions we have also observed a change in the flat band voltage of the devices due to an aging effect on the electrodes The combination of these two processes leads to an increase in the device turn-on voltage with increasing operating time

Electroluminescence in conjugated polymers

Abstract: Research in the use of organic polymers as the active semiconductors in light-emitting diodes has advanced rapidly, and prototype devices now meet realistic specifications for applications. These achievements have provided insight into many aspects of the background science, from design and synthesis of materials, through materials fabrication issues, to the semiconductor physics of these polymers.

Synthesis of Light-Emitting Conjugated Polymers for Applications in Electroluminescent Devices

Abstract: A review was presented to demonstrate a historical description of the synthesis of light-emitting conjugated polymers for applications in electroluminescent devices. Electroluminescence (EL) was first reported in poly(para-phenylene vinylene) (PPV) in 1990 and researchers continued to make significant efforts to develop conjugated materials as the active units in light-emitting devices (LED) to be used in display applications. Conjugated oligomers were used as luminescent materials and as models for conjugated polymers in the review. Oligomers were used to demonstrate a structure and property relationship to determine a key polymer property or to demonstrate a technique that was to be applied to polymers. The review focused on demonstrating the way polymer structures were made and the way their properties were controlled by intelligent and rational and synthetic design.

The electroluminescence of organic materials

Abstract: This article provides a review about electroluminescence from organic materials and deals in detail with organic light-emitting diodes (OLEDs), light-emitting electro-chemical cells (LECs) and electrogenerated chemilumi-nescence (ECL) reflecting different electrooptical appli-cations of conjugated materials. It is written from an organic chemist's point of view and pays particular attention to the development of organic materials involved in corresponding devices. In recent years a substantial amount of both academic and industrial research has been directed to organic electroluminescence in an effort to improve the processability and tunability of organic materials and the longevity of OLEDs and LECs. On the eve of the commercialization of organic electrolumi-nescence this review provides an overview of lifetimes and efficiencies attained and reflects materials and device concepts developed over the last decade. In this context electrogenerated chemiluminescence is discussed with respect to its importance as a versatile tool to simulate the fundamental electrochemical processes in OLEDs.

Electron Transport Materials for Organic Light-Emitting Diodes

Abstract: A comprehensive review of the literature on electron transport materials (ETMs) used to enhance the performance of organic light-emitting diodes (OLEDs) is presented. The structure−property−performance relationships of many classes of ETMs, both small-molecule- and polymer-based, that have been widely used to improve OLED performance through control of charge injection, transport, and recombination are highlighted. The molecular architecture, electronic structure (electron affinity and ionization potential), thin film processing, thermal stability, morphology, and electron mobility of diverse organic ETMs are discussed and related to their effectiveness in improving OLED performance (efficiency, brightness, and drive voltage). Some issues relating to the experimental procedures for the estimation of relevant material properties such as electron affinity and electron mobility are discussed. The design of multifunctional electroluminescent polymers whereby light emission and electron- and hole-transport pro...