4.8 Article

Green-/NIR-light-controlled rapid photochromism featuring reversible thermally activated delayed fluorescence and photoelectronic switching

Journal

CHEMICAL SCIENCE
Volume 13, Issue 32, Pages 9381-9386

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2sc02662g

Keywords

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Funding

  1. National Natural Science Foundation of China [21971100]
  2. Natural Science Foundation of Henan Province [222300420501]
  3. Science and Technology Project of Henan Province [212102210549]
  4. Key Scientific Research Project of Higher Education of Henan Province [22A430007]
  5. Innovation and Entrepreneurship Training Program for College students in China [202110482010]

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Fluorescent dithienylethene-based photochromic molecule BFBDTE exhibits visible light-controlled fluorescence and thermally activated delayed fluorescence (TADF) switching, as well as rapid and repeatable cyclization and cycloreversion reactions in PMMA. It also demonstrates a remarkable on-off photoelectronic response between the open- and closed-form and holds promise for applications in photoswitchable molecular devices and optical memory storage systems.
Fluorescent dithienylethene-based photochromic materials have been attracting considerable attention owing to their wide applications in biological and materials sciences. However, the limitations of detrimental UV irradiation for photocyclization, short emission lifetime, and inefficient photoresponsive speed still need to be addressed. Herein, a novel dithienylethene photochromic molecule, BFBDTE, has been prepared by the incorporation of a difluoroboron beta-diketonate (BF(2)bdk) unit. The strong electron acceptor BF(2)bdk not only reduces the energy gap of the open isomer, ensuring visible light-controlled fluorescence switching, but also promotes intersystem crossing for the generation of thermally activated delayed fluorescence (TADF). Upon alternating irradiation with green and NIR light, BFBDTE presents a rare example of photochromism, fluorescence and TADF switching in various polar solvents and a poly(methyl methacrylate) (PMMA) film. Meanwhile, it shows rapid and well repeatable cyclization (12 s) and cycloreversion reactions (20 s) in PMMA, accompanied by fast TADF switching within 11 s. Furthermore, photo-electrochemical measurements reveal a remarkable on-off photoelectronic response (photocurrent density ratio: I-light/I-dark = 684) between the open- and closed-form of BFBDTE. These remarkable merits make BFBDTE promising for photoswitchable molecular devices, optical memory storage systems, NIR detectors, and photoelectric switching.

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