Microlasers from AIE-Active BODIPY Derivative.

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State Key Laboratory of Luminescent Materials and Devices, South China University of Technology, Guangzhou, 510640, P. R. China.

Published: February 2020

AI Article Synopsis

  • Organic microlasers are gaining interest for their flexibility, easy material doping, and low-cost production, but traditional organic gain materials face issues like aggregation-caused quenching (ACQ).
  • A new microlaser design using aggregation-induced emission (AIE) materials has been created, which allows for high-quality performance through a unique self-assembly process.
  • AIE microlasers can achieve higher doping concentrations and improved performance metrics, opening doors for applications in fields like chemical sensing and biology.

Article Abstract

Organic microlasers have attracted much attention due to their unique features such as high mechanical flexibility, facile doping of gain materials, high optical quality, simplicity and low-cost fabrication. However, organic gain materials usually suffer from aggregation-caused quenching (ACQ), preventing further advances of organic microlasers. Here, a new type of microlaser from aggregation-induced emission (AIE) material is successfully demonstrated. By introducing a typical noncrystalline AIE material, a high quality microlaser is obtained via a surface tension-induced self-assembly approach. Distinct from conventional organic microlasers, the organic luminescent material used here is initially nonluminescent but can shine after aggregation under optical pumping. Further investigations demonstrate that AIE-based microlasers exhibit advantages to enable much higher doping concentrations, which provides an alternative way to improved lasing performance including dramatically reduced threshold and favorable lasing stability. It is believed that these results could provide a promising way to extend the content of microlasers and open a new avenue to enable applications ranging from chemical sensing to biology.

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Source
http://dx.doi.org/10.1002/smll.201907074DOI Listing

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