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Brightness-equalized quantum dots

Author

Listed:
  • Sung Jun Lim

    (University of Illinois at Urbana-Champaign
    Micro and Nanotechnology Laboratory, University of Illinois at Urbana-Champaign)

  • Mohammad U. Zahid

    (University of Illinois at Urbana-Champaign
    Micro and Nanotechnology Laboratory, University of Illinois at Urbana-Champaign)

  • Phuong Le

    (University of Illinois at Urbana-Champaign
    Micro and Nanotechnology Laboratory, University of Illinois at Urbana-Champaign)

  • Liang Ma

    (Micro and Nanotechnology Laboratory, University of Illinois at Urbana-Champaign
    University of Illinois at Urbana-Champaign)

  • David Entenberg

    (Albert Einstein College of Medicine of Yeshiva University
    Integrated Imaging Program, Albert Einstein College of Medicine of Yeshiva University
    Gruss-Lipper Biophotonics Center, Albert Einstein College of Medicine of Yeshiva University)

  • Allison S. Harney

    (Albert Einstein College of Medicine of Yeshiva University
    Integrated Imaging Program, Albert Einstein College of Medicine of Yeshiva University
    Gruss-Lipper Biophotonics Center, Albert Einstein College of Medicine of Yeshiva University
    Albert Einstein College of Medicine of Yeshiva University)

  • John Condeelis

    (Albert Einstein College of Medicine of Yeshiva University
    Integrated Imaging Program, Albert Einstein College of Medicine of Yeshiva University
    Gruss-Lipper Biophotonics Center, Albert Einstein College of Medicine of Yeshiva University)

  • Andrew M. Smith

    (University of Illinois at Urbana-Champaign
    Micro and Nanotechnology Laboratory, University of Illinois at Urbana-Champaign
    University of Illinois at Urbana-Champaign)

Abstract

As molecular labels for cells and tissues, fluorescent probes have shaped our understanding of biological structures and processes. However, their capacity for quantitative analysis is limited because photon emission rates from multicolour fluorophores are dissimilar, unstable and often unpredictable, which obscures correlations between measured fluorescence and molecular concentration. Here we introduce a new class of light-emitting quantum dots with tunable and equalized fluorescence brightness across a broad range of colours. The key feature is independent tunability of emission wavelength, extinction coefficient and quantum yield through distinct structural domains in the nanocrystal. Precise tuning eliminates a 100-fold red-to-green brightness mismatch of size-tuned quantum dots at the ensemble and single-particle levels, which substantially improves quantitative imaging accuracy in biological tissue. We anticipate that these materials engineering principles will vastly expand the optical engineering landscape of fluorescent probes, facilitate quantitative multicolour imaging in living tissue and improve colour tuning in light-emitting devices.

Suggested Citation

  • Sung Jun Lim & Mohammad U. Zahid & Phuong Le & Liang Ma & David Entenberg & Allison S. Harney & John Condeelis & Andrew M. Smith, 2015. "Brightness-equalized quantum dots," Nature Communications, Nature, vol. 6(1), pages 1-10, November.
  • Handle: RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms9210
    DOI: 10.1038/ncomms9210
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    Cited by:

    1. Yanyu Xiong & Qinglan Huang & Taylor D. Canady & Priyash Barya & Shengyan Liu & Opeyemi H. Arogundade & Caitlin M. Race & Congnyu Che & Xiaojing Wang & Lifeng Zhou & Xing Wang & Manish Kohli & Andrew , 2022. "Photonic crystal enhanced fluorescence emission and blinking suppression for single quantum dot digital resolution biosensing," Nature Communications, Nature, vol. 13(1), pages 1-14, December.

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