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Ultrafast upconversion superfluorescence with a sub-2.5 ns lifetime at room temperature

Author

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  • Mengwei Zhou

    (Chinese Academy of Sciences
    Fujian Science & Technology Innovation Laboratory for Optoelectronic Information of China
    University of Chinese Academy of Sciences)

  • Ping Huang

    (Chinese Academy of Sciences
    Fujian Science & Technology Innovation Laboratory for Optoelectronic Information of China
    University of Chinese Academy of Sciences)

  • Xiaoying Shang

    (Chinese Academy of Sciences
    Fujian Science & Technology Innovation Laboratory for Optoelectronic Information of China)

  • Ruihuan Zhang

    (Chinese Academy of Sciences)

  • Wen Zhang

    (Chinese Academy of Sciences
    University of Chinese Academy of Sciences)

  • Zhiqing Shao

    (Chinese Academy of Sciences
    University of Chinese Academy of Sciences)

  • Shuo Zhang

    (Chinese Academy of Sciences)

  • Wei Zheng

    (Chinese Academy of Sciences
    Fujian Science & Technology Innovation Laboratory for Optoelectronic Information of China
    University of Chinese Academy of Sciences)

  • Xueyuan Chen

    (Chinese Academy of Sciences
    Fujian Science & Technology Innovation Laboratory for Optoelectronic Information of China
    University of Chinese Academy of Sciences)

Abstract

Photon upconversion through lanthanide-doped nanoparticles is of great significance for various applications. However, the current development of upconversion nanoparticles is hindered by the low quantum efficiency and long radiative lifetimes of lanthanide ions, restricting their applications in time-dependent nanophotonics. Herein, we report ultrafast upconversion superfluorescence with a lifetime of sub-2.5 ns in lanthanide-doped nanoparticles at room temperature. Upon excitation with an 800-nm fs-pulsed laser, we achieve a large number (N = 912) of correlated dipoles in Nd3+-concentrated nanoparticles, resulting in collective coherent emission with two orders of magnitude amplification in intensity and more than three orders of magnitude improvement in the radiative decay rate. Furthermore, we demonstrate that the control of excitation power and emitting sample length enables the lifetime manipulation of upconversion emission in a wide range from μs to sub-ns, accompanied by the typical superfluorescence signature of Burnham-Chiao ringing. These findings may benefit applications in many advanced technologies such as quantum counting and high-speed super-resolution bioimaging.

Suggested Citation

  • Mengwei Zhou & Ping Huang & Xiaoying Shang & Ruihuan Zhang & Wen Zhang & Zhiqing Shao & Shuo Zhang & Wei Zheng & Xueyuan Chen, 2024. "Ultrafast upconversion superfluorescence with a sub-2.5 ns lifetime at room temperature," Nature Communications, Nature, vol. 15(1), pages 1-8, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-54314-x
    DOI: 10.1038/s41467-024-54314-x
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    References listed on IDEAS

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    3. Gabriele Rainò & Michael A. Becker & Maryna I. Bodnarchuk & Rainer F. Mahrt & Maksym V. Kovalenko & Thilo Stöferle, 2018. "Superfluorescence from lead halide perovskite quantum dot superlattices," Nature, Nature, vol. 563(7733), pages 671-675, November.
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