Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

The de Broglie Wavelength02:32

The de Broglie Wavelength

34.7K
In the macroscopic world, objects that are large enough to be seen by the naked eye follow the rules of classical physics. A billiard ball moving on a table will behave like a particle; it will continue traveling in a straight line unless it collides with another ball, or it is acted on by some other force, such as friction. The ball has a well-defined position and velocity or well-defined momentum, p = mv, which is defined by mass m and velocity v at any given moment. This is the typical...
34.7K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Scalable Super-Localization Optical Probing of Individual Josephson Junctions in Superconducting Devices.

Nano letters·2026
Same author

Synthesis and Optical Levitation of Ellipsoidal Silica Particles.

ACS omega·2026
Same author

Modulation of Semiconductor Quantum Dot Photoluminescence by Photochromic Molecules.

Nano letters·2026
Same author

Locating the atoms at the hard-soft interface of gold nanoparticles.

Nature communications·2026
Same author

Optical Properties of CdSe/CdZnS Core/Shell Nanoplatelets at High Pressure.

Journal of the American Chemical Society·2025
Same author

Wavefront Shaping of Scattering Forces Enhances Optical Trapping of Levitated Nanoparticles.

Nature communications·2025
Same journal

Precursor-Directed Self-Assembly in Hydrothermal Carbon Nitride Nanostructures Revealed by Nano-FTIR.

The journal of physical chemistry letters·2026
Same journal

Correction to "Equation-of-Motion Block-Correlated Coupled Cluster Method for Excited Electronic States of Strongly Correlated Systems".

The journal of physical chemistry letters·2026
Same journal

Rationalizing Stacking-Dependent Charge Injection Dynamics in Radical-Based Organic Light-Emitting Diodes.

The journal of physical chemistry letters·2026
Same journal

Bottom-Up Formation of the Simplest Geminal Thiol─Methanedithiol (CH<sub>2</sub>(SH)<sub>2</sub>)─and the Methyl Hydrodisulfide (H<sub>3</sub>CSSH) Isomer in Interstellar Analogue Ices.

The journal of physical chemistry letters·2026
Same journal

Trion Mediated Sequential Charge Separation in Functionalized CsPbBr<sub>3</sub>/AgInS<sub>2</sub> Hybrid Nanocrystals.

The journal of physical chemistry letters·2026
Same journal

Linking Local Water Electrostatic Potentials to Measured Hydrogen Evolution Onset in Aqueous Electrolytes.

The journal of physical chemistry letters·2026
See all related articles

Related Experiment Video

Updated: Apr 5, 2026

Compact Quantum Dots for Single-molecule Imaging
17:14

Compact Quantum Dots for Single-molecule Imaging

Published on: October 9, 2012

18.9K

Spontaneous Spectral Diffusion in CdSe Quantum Dots.

Mark J Fernée1, Taras Plakhotnik2, Yann Louyer3

  • 1†Université Bordeaux, LP2N, F-33405 Talence, France.

The Journal of Physical Chemistry Letters
|August 20, 2015
PubMed
Summary
This summary is machine-generated.

Spectral diffusion in colloidal nanocrystals is not random. We found that nanocrystal emission lines remember previous spectral positions, showing a "two steps forward, one step back" pattern in their spectral jumps.

Keywords:
CdSe nanocrystalsCdSe quantum dotscryogenic photoluminescencesingle quantum dot photoluminescencesingle quantum dot spectroscopyspectral diffusionsurface phenomena

More Related Videos

High Resolution Phonon-assisted Quasi-resonance Fluorescence Spectroscopy
10:40

High Resolution Phonon-assisted Quasi-resonance Fluorescence Spectroscopy

Published on: June 28, 2016

8.0K
Resonance Fluorescence of an InGaAs Quantum Dot in a Planar Cavity Using Orthogonal Excitation and Detection
12:57

Resonance Fluorescence of an InGaAs Quantum Dot in a Planar Cavity Using Orthogonal Excitation and Detection

Published on: October 13, 2017

9.7K

Related Experiment Videos

Last Updated: Apr 5, 2026

Compact Quantum Dots for Single-molecule Imaging
17:14

Compact Quantum Dots for Single-molecule Imaging

Published on: October 9, 2012

18.9K
High Resolution Phonon-assisted Quasi-resonance Fluorescence Spectroscopy
10:40

High Resolution Phonon-assisted Quasi-resonance Fluorescence Spectroscopy

Published on: June 28, 2016

8.0K
Resonance Fluorescence of an InGaAs Quantum Dot in a Planar Cavity Using Orthogonal Excitation and Detection
12:57

Resonance Fluorescence of an InGaAs Quantum Dot in a Planar Cavity Using Orthogonal Excitation and Detection

Published on: October 13, 2017

9.7K

Area of Science:

  • Physical Chemistry
  • Materials Science
  • Nanotechnology

Background:

  • Spectral diffusion in single colloidal nanocrystals is typically modeled as a random process.
  • Understanding the dynamics of charge distribution is crucial for nanocrystal applications.

Purpose of the Study:

  • To investigate the underlying dynamics of spectral diffusion in colloidal nanocrystals.
  • To determine if spectral diffusion exhibits memory effects.

Main Methods:

  • Analysis of time series data of spectral jumps in single colloidal nanocrystals.
  • Statistical analysis to identify correlations in spectral position changes.

Main Results:

  • Observed persistent anticorrelations in spectral jump time series, indicating memory effects.
  • Demonstrated that spectral diffusion progresses with a "two steps forward, one step back" pattern.
  • Showed spontaneous relaxation in spectral position in the absence of optical pumping.

Conclusions:

  • Spectral diffusion in colloidal nanocrystals is not purely random, but influenced by memory effects.
  • The observed memory suggests a tendency for charge configurations to revert to previous states.
  • These findings offer new insights into nanocrystal photophysics and potential control mechanisms.