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      Recent development of phenanthroimidazole-based fluorophores for blue organic light-emitting diodes (OLEDs): an overview

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          Abstract

          Full color displays (white OLEDs) require all the primary colors: blue, green, and red. In recent decades, numerous phenanthroimidazole-based emitting materials have been developed for efficient blue OLEDs.

          Abstract

          The imminent global energy crisis and continuing inefficient energy utilization are driving the development of smart energy-efficient devices for display and lighting applications. Energy-efficient organic light-emitting diodes (OLEDs) are considered one of the most competitive candidates for next-generation smart displays and particularly for future energy-saving lighting sources. Recently, much effort has been devoted to attempts to generate white OLEDs comprising both fluorescent and phosphorescent materials. Efficient blue-emitting materials are extremely essential for the commercialization of white OLEDs and play a vital role in energy-efficient solid-state lighting and smart display devices. The molecular designing of efficient deep-blue materials is limited due to their intrinsic wide bandgap, poor carrier charge balance, and low efficiency in the solid state. In recent decades, phenanthroimidazole (PI)-based materials have attracted tremendous interest (due to the ease of their chemical/structural modification at the N1 and C2 positions) to produce efficient deep-blue OLEDs (satisfying the color purity criteria given by the National Television System Committee (NTSC)) (CIE: 0.14, 0.08) and European Broadcasting Union (EBU) (CIE: 0.15, 0.06). This review mainly focuses on the design of PI-based blue/deep-blue emitting materials and their applications in OLEDs. Here at first, some of the PI-based blue-fluorescence emitters endowed with unipolar and bipolar-transporting abilities are comprehensively reviewed. Then attention is focused on the typical PI-based host materials for phosphorescent OLEDs. Finally, PI-based hybridized local and charge-transfer (HLCT) active fluorescent emitters are presented in brief. The rational molecular design concepts and general synthetic routes for PI-based materials are briefly discussed.

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          Highly efficient organic light-emitting diodes from delayed fluorescence.

          The inherent flexibility afforded by molecular design has accelerated the development of a wide variety of organic semiconductors over the past two decades. In particular, great advances have been made in the development of materials for organic light-emitting diodes (OLEDs), from early devices based on fluorescent molecules to those using phosphorescent molecules. In OLEDs, electrically injected charge carriers recombine to form singlet and triplet excitons in a 1:3 ratio; the use of phosphorescent metal-organic complexes exploits the normally non-radiative triplet excitons and so enhances the overall electroluminescence efficiency. Here we report a class of metal-free organic electroluminescent molecules in which the energy gap between the singlet and triplet excited states is minimized by design, thereby promoting highly efficient spin up-conversion from non-radiative triplet states to radiative singlet states while maintaining high radiative decay rates, of more than 10(6) decays per second. In other words, these molecules harness both singlet and triplet excitons for light emission through fluorescence decay channels, leading to an intrinsic fluorescence efficiency in excess of 90 per cent and a very high external electroluminescence efficiency, of more than 19 per cent, which is comparable to that achieved in high-efficiency phosphorescence-based OLEDs.
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            Organic electroluminescent diodes

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              Highly efficient phosphorescent emission from organic electroluminescent devices

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                Author and article information

                Contributors
                (View ORCID Profile)
                (View ORCID Profile)
                Journal
                JMCCCX
                Journal of Materials Chemistry C
                J. Mater. Chem. C
                Royal Society of Chemistry (RSC)
                2050-7526
                2050-7534
                October 4 2018
                2018
                : 6
                : 38
                : 10138-10173
                Affiliations
                [1 ]Optoelectronic Laboratory
                [2 ]Department of Chemistry
                [3 ]National Institute of Technology Rourkela
                [4 ]India
                Article
                10.1039/C8TC03689F
                781a4ee6-52a3-40c6-9426-1d872ac407bb
                © 2018

                http://rsc.li/journals-terms-of-use

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