Related Experiment Video
Updated: Jun 18, 2026

17:14
Compact Quantum Dots for Single-molecule Imaging
Published on: October 9, 2012
18.6K
Sub-10 nm upconversion nanocrystals for long-term single-particle tracking.
Xiaochen Qiu1,2, Daoming Guan1, Xiaojing Xia3
1Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai, PR China.
Nature Communications
|October 24, 2025
Summary
We developed ultra-small, bright upconversion nanoparticles for single-molecule imaging. These probes overcome size-brightness challenges, enabling long-term tracking of cell surface receptors.
Area of Science:
- Nanotechnology
- Biomedical Imaging
- Materials Science
Background:
- Lanthanide-doped upconversion nanoparticles (UCNPs) offer high photostability and anti-Stokes luminescence for bioimaging.
- A key challenge is balancing small particle size with high emission brightness, as smaller UCNPs are often dimmer.
- Surface defects and energy leakage commonly reduce UCNP efficiency, especially in smaller particles.
Purpose of the Study:
- To engineer sub-10 nm upconversion nanoparticles with enhanced brightness and efficiency.
- To investigate methods for minimizing surface quenching and energy loss in UCNPs.
- To demonstrate the utility of these novel UCNPs for long-term single-molecule tracking in live cells.
Main Methods:
- Fabrication of sub-10 nm cascade actively protected UCNPs using NaYbF4 and NaLuF4 layers.
- Utilizing theoretical modeling and time-resolved measurements to analyze energy transfer pathways and loss mechanisms.
- Employing single-particle level efficiency measurements and live-cell imaging of epidermal growth factor receptor (EGFR) molecules.
Main Results:
- Achieved a 33-fold increase in upconversion efficiency at the single-particle level compared to ~19 nm conventional UCNPs.
- Identified and minimized energy leakage from Er3+ ions to surface defects using a NaYbF4 intermediate layer.
- Demonstrated effective suppression of Yb3+ surface quenching with a NaLuF4 monolayer.
- Successfully tracked single EGFR molecules on live cells for up to one hour, observing dynamic diffusion mode switching.
Conclusions:
- Developed ultra-small (<10 nm) and highly bright UCNPs by actively protecting the cascade structure.
- Mitigated surface-related emission quenching, significantly boosting UCNP efficiency.
- Enabled unprecedented long-term single-molecule tracking of cell surface dynamics, providing insights into receptor behavior.

