Reaching the 5% theoretical limit of fluorescent OLEDs with push-pull benzophospholes
We report the synthesis and characterization of benzophosphole oxides featuring an ethoxy substituent on the P atom and electro-donating amino groups on the lateral phenyl groups. The optical and redox properties of these compounds are studied experimentally and computationally (TD-DFT). In particul...
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Published in | Journal of materials chemistry. C, Materials for optical and electronic devices Vol. 11; no. 11; pp. 3826 - 3831 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
16.03.2023
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Subjects | |
Online Access | Get full text |
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Summary: | We report the synthesis and characterization of benzophosphole oxides featuring an ethoxy substituent on the P atom and electro-donating amino groups on the lateral phenyl groups. The optical and redox properties of these compounds are studied experimentally and computationally (TD-DFT). In particular, we show how the nature of the donor allows fine-tuning the internal charge transfer (ICT) and, thus, the optical properties. Considering the intense fluorescence in the solid state (powder or thin film) and the favorable redox and thermal properties, these compounds were introduced in multilayered organic light emitting devices. All compounds display high efficiency and one compound even exhibits an external quantum efficiency (EQE) of 5%, which represents the theoretical limit of the EQE of purely fluorescent emitters. These results highlight the potential of this novel family of fluorophores to develop next generation optoelectronic/photonic devices.
Push-pull benzophospholes were synthesized and characterized. They could reach the 5% theoretical limit of external quantum efficiency of fluorescent OLEDs. |
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Bibliography: | Electronic supplementary information (ESI) available. See DOI https://doi.org/10.1039/d3tc00245d |
ISSN: | 2050-7526 2050-7534 |
DOI: | 10.1039/d3tc00245d |