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      Enabling Highly Robust Full‐Color Ultralong Room‐Temperature Phosphorescence and Stable White Organic Afterglow from Polycyclic Aromatic Hydrocarbons

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          Abstract

          In this work, full‐color and stable white organic afterglow materials with outstanding water, organic solvents, and temperature resistances have been developed for the first time by embedding the selected polycyclic aromatic hydrocarbons into melamine‐formaldehyde polymer via solution polymerization. The afterglow quantum yields and lifetimes of the resulting polymer films were up to 22.7 % and 4.83 s, respectively, under ambient conditions. For the coronene‐doped sample, its afterglow color could be linearly tuned between yellow and blue by adjusting the temperature, and it could still emit an intense blue afterglow with a lifetime of 0.68 s at 440 K. Moreover, the films showed a bright and stable white afterglow at 370 K with a lifetime of 2.80 s and maintained an excellent afterglow performance after soaking in water and organic solvents for more than 150 days. In addition, the application potential of the polymer films in information encryption and anti‐counterfeiting was also demonstrated.

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          Most cited references78

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          Aggregation-Induced Emission: Together We Shine, United We Soar!

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            Stabilizing triplet excited states for ultralong organic phosphorescence.

            The control of the emission properties of synthetic organic molecules through molecular design has led to the development of high-performance optoelectronic devices with tunable emission colours, high quantum efficiencies and efficient energy/charge transfer processes. However, the task of generating excited states with long lifetimes has been met with limited success, owing to the ultrafast deactivation of the highly active excited states. Here, we present a design rule that can be used to tune the emission lifetime of a wide range of luminescent organic molecules, based on effective stabilization of triplet excited states through strong coupling in H-aggregated molecules. Our experimental data revealed that luminescence lifetimes up to 1.35 s, which are several orders of magnitude longer than those of conventional organic fluorophores, can be realized under ambient conditions. These results outline a fundamental principle to design organic molecules with extended lifetimes of excited states, providing a major step forward in expanding the scope of organic phosphorescence applications.
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              Colour-tunable ultra-long organic phosphorescence of a single-component molecular crystal

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                Author and article information

                Contributors
                Journal
                Angewandte Chemie International Edition
                Angew Chem Int Ed
                Wiley
                1433-7851
                1521-3773
                March 04 2024
                February 05 2024
                March 04 2024
                : 63
                : 10
                Affiliations
                [1 ] School of Chemistry; Key Laboratory of Theoretical Chemistry of Environment, Ministry of Education South China Normal University Guangzhou 510006 China
                [2 ] School of Chemistry Sun Yat-sen University Guangzhou 510275 China
                Article
                10.1002/anie.202318516
                de4b30ff-c31e-49e9-a7e3-b11971fefeed
                © 2024

                http://onlinelibrary.wiley.com/termsAndConditions#vor

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