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Updated: Feb 12, 2026

Compact Quantum Dots for Single-molecule Imaging
Published on: October 9, 2012
Two Mechanisms Determine Quantum Dot Blinking
Gangcheng Yuan1, Daniel E Gómez2, Nicholas Kirkwood1
1ARC Centre of Excellence in Exciton Science, School of Chemistry , University of Melbourne , Parkville , Victoria 3010 , Australia.
Abstract:
Many potential applications of quantum dots (QDs) can only be realized once the luminescence from single nanocrystals (NCs) is understood. These applications include the development of quantum logic devices, single-photon sources, long-life LEDs, and single-molecule biolabels. At the single-nanocrystal level, random fluctuations in the QD photoluminescence occur, a phenomenon termed blinking. There are two competing models to explain this blinking: Auger recombination and surface trap induced recombination. Here we use lifetime scaling on core-shell chalcogenide NCs to demonstrate that both types of blinking occur in the same QDs. We prove that Auger-blinking can yield single-exponential on/off times in contrast to earlier work. The surface passivation strategy determines which blinking mechanism dominates. This study summarizes earlier studies on blinking mechanisms and provides some clues that stable single QDs can be engineered for optoelectronic applications.
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