Related Experiment Video
Updated: Sep 16, 2025

06:08
Time-resolved Photophysical Characterization of Triplet-harvesting Organic Compounds at an Oxygen-free Environment Using an iCCD Camera
Published on: December 27, 2018
9.0K
Spectrally Resolved Dynamics of Delayed Luminescence in Dense Scattering Media
Mahshid Zoghi1, Ernesto Jimenez-Villar1, Aristide Dogariu1
1CREOL, The College of Optics & Photonics, University of Central Florida, 4304 Scorpius Street, Orlando, FL 32816, USA.
Materials (Basel, Switzerland)
|July 12, 2025
Summary
We studied delayed luminescence (DL) in highly scattering titanium dioxide (TiO2) films. The material
Area of Science:
- Materials Science
- Optics
- Condensed Matter Physics
Background:
- Highly scattering media are crucial for applications like solar cells and photocatalysis.
- Understanding light-matter interactions in these materials is key for photonic device development.
Purpose of the Study:
- To investigate spectrally and time-resolved delayed luminescence (DL) in highly scattering rutile TiO2 films.
- To elucidate the influence of mesoscale structure on DL kinetics and spectral properties.
Main Methods:
- Measurements of spectrally and time-resolved delayed luminescence (DL).
- Analysis of non-exponential photon density decay and spectral composition evolution.
- Modeling of DL emission from dense scattering media.
Main Results:
- DL kinetics in TiO2 films exhibit complex, non-exponential decay.
- DL intensity and duration are significantly affected by scattering processes within the mesoscale structure.
- Observed DL lifetimes up to 6 seconds, linked to reabsorption processes and spectral redshift.
Conclusions:
- The mesoscale structure of scattering media critically influences delayed luminescence.
- A model is proposed to predict DL properties, aiding the design of advanced composite materials.
- Findings provide insights into light propagation and energy transfer in disordered photonic materials.
More Related Videos
Related Concept Videos
Protein Dynamics in Living Cells
2.3K
Different fluorescence-based techniques are used to study the protein dynamics in living cells. These techniques include FRAP, FRET, and PET.
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
2.3K
Photoluminescence: Fluorescence and Phosphorescence
2.3K
Photoluminescence is a process where a molecule absorbs light energy and re-emits it in the form of light. This phenomenon occurs when a substance absorbs photons, promoting its electrons to higher energy level excited states, followed by a relaxation process in which the electrons return to their original ground state energy levels and emit light. Photoluminescence is widely observed in various materials, including semiconductors, and organic and inorganic compounds.
A pair of electrons in a...
A pair of electrons in a...
2.3K
Photoluminescence: Applications
491
Photoluminescence offers a wide range of applications due to its inherent sensitivity and selectivity. This technique allows for both direct and indirect analyses of the analyte. Direct quantitative analysis is possible when the analyte exhibits a favorable quantum yield for fluorescence or phosphorescence. However, an indirect analysis may be feasible if the analyte is not fluorescent or phosphorescent, or if the quantum yield is unfavorable. Indirect methods include reacting the analyte with...
491
Super-resolution Fluorescence Microscopy
7.7K
Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been...
7.7K

