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      Regioisomerism vs Conformation: Impact of Molecular Design on the Emission Pathway in Organic Light-Emitting Device Emitters

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          Abstract

          Despite the design and proposal of several new structural motifs as thermally activated delayed fluorescent (TADF) emitters for organic light-emitting device (OLED) applications, the nature of their interaction with the host matrix in the emissive layer of the device and their influence on observed photophysical outputs remain unclear. To address this issue, we present, for the first time, the use of up to four regioisomers bearing a donor–acceptor–donor electronic structure based on the desymmetrized naphthalene benzimidazole scaffold, equipped with various electron-donating units and possessing distinguished conformational lability. Quantum chemical calculations allow us to identify the most favorable conformations adopted by the electron-rich groups across the entire pool of regioisomers. These conformations were then compared with conformational changes caused by the interaction of the emitter with the Zeonex and 4,4′-bis( N-carbazolyl)-1,1′-biphenyl (CBP) matrices, and the correlation with observed photophysics was monitored by UV–vis absorption and steady-state photoluminescence spectra, combined with time-resolved spectroscopic techniques. Importantly, a CBP matrix was found to have a significant impact on the conformational change of regioisomers, leading to unique TADF emission mechanisms that encompass dual emission and inversion of the singlet–triplet excited-state energies and result in the enhancement of TADF efficiency. As a proof of concept, regioisomers with optimal donor positions were utilized to fabricate an OLED, revealing, with the best-performing dye, an external quantum emission of 11.6%, accompanied by remarkable luminance (28,000 cd/m 2). These observations lay the groundwork for a better understanding of the role of the host matrix. In the long term, this new knowledge can lead to predicting the influence of the host matrix and adopting the structure of the emitter in a way that allows the development of highly efficient and efficient OLEDs.

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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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            Recent advances in organic thermally activated delayed fluorescence materials.

            Organic materials that exhibit thermally activated delayed fluorescence (TADF) are an attractive class of functional materials that have witnessed a booming development in recent years. Since Adachi et al. reported high-performance TADF-OLED devices in 2012, there have been many reports regarding the design and synthesis of new TADF luminogens, which have various molecular structures and are used for different applications. In this review, we summarize and discuss the latest progress concerning this rapidly developing research field, in which the majority of the reported TADF systems are discussed, along with their derived structure-property relationships, TADF mechanisms and applications. We hope that such a review provides a clear outlook of these novel functional materials for a broad range of scientists within different disciplinary areas and attracts more researchers to devote themselves to this interesting research field.
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              Purely Organic Thermally Activated Delayed Fluorescence Materials for Organic Light-Emitting Diodes

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                Author and article information

                Journal
                ACS Appl Mater Interfaces
                ACS Appl Mater Interfaces
                am
                aamick
                ACS Applied Materials & Interfaces
                American Chemical Society
                1944-8244
                1944-8252
                26 April 2024
                08 May 2024
                : 16
                : 18
                : 23654-23667
                Affiliations
                []Institute of Organic Chemistry, Polish Academy of Sciences , Kasprzaka 44/52, 01-224 Warsaw, Poland
                []Department of Molecular Physics, Faculty of Chemistry, Łódź University of Technology , Stefana Żeromskiego 114, 90-543 Łódź, Poland
                [§ ]Institute of Physical Chemistry, Polish Academy of Sciences , Kasprzaka 44/52, 01-224 Warsaw, Poland
                Author notes
                Author information
                https://orcid.org/0000-0002-4658-7922
                https://orcid.org/0000-0002-5508-0533
                https://orcid.org/0000-0002-1831-971X
                https://orcid.org/0000-0002-5514-674X
                Article
                10.1021/acsami.3c19212
                11082840
                38668584
                16c1a9ac-b0bf-4304-8eba-f7bfd11b3aab
                © 2024 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 22 December 2023
                : 17 April 2024
                : 14 April 2024
                Funding
                Funded by: H2020 Marie Sklodowska-Curie Actions, doi 10.13039/100010665;
                Award ID: 847413
                Funded by: Narodowe Centrum Badan i Rozwoju, doi 10.13039/501100005632;
                Award ID: POLBER/5/63/PrintedQDD/2022
                Funded by: Narodowe Centrum Badan i Rozwoju, doi 10.13039/501100005632;
                Award ID: LIDER/21/0077/L-11/19/NCBR/2020
                Funded by: Ministerstwo Edukacji i Nauki, doi 10.13039/501100004569;
                Award ID: 5005/H2020-MSCA-COFUND/2019/2
                Funded by: Ministerstwo Edukacji i Nauki, doi 10.13039/501100004569;
                Award ID: 2/DSP/2021
                Funded by: Narodowe Centrum Nauki, doi 10.13039/501100004281;
                Award ID: 2022/45/B/ST5/03712
                Funded by: Narodowe Centrum Nauki, doi 10.13039/501100004281;
                Award ID: 2020/39/B/ST4/01952
                Categories
                Research Article
                Custom metadata
                am3c19212
                am3c19212

                Materials technology
                tadf,rtp,s-t inversion,regioisomerism,oled,tict,charge transfer
                Materials technology
                tadf, rtp, s-t inversion, regioisomerism, oled, tict, charge transfer

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