Related Experiment Video
Updated: Jun 16, 2026

15:04
Rejection of Fluorescence Background in Resonance and Spontaneous Raman Microspectroscopy
Published on: May 18, 2011
A low cost time-resolved Raman spectroscopic sensing system enabling fluorescence rejection
Joseph V Sinfield1, Oliver Colic, Daniel Fagerman
1School of Civil Engineering, Purdue University, West Lafayette, Indiana 47907-2051, USA. jvs@purdue.edu
Applied Spectroscopy
|February 13, 2010
Summary
A new, low-cost, time-resolved Raman spectroscopy system uses pulsed lasers to minimize fluorescence interference. This enables more affordable and accessible in situ chemical analysis for various applications.
Area of Science:
- Analytical Chemistry
- Spectroscopy
- Chemical Sensing
Background:
- Fluorescence often interferes with Raman spectroscopy, complicating chemical analysis.
- Traditional continuous wave (CW) Raman systems can be limited by fluorescence, especially in complex samples.
- Advancements in laser and data acquisition technology offer new possibilities for improving Raman spectroscopy.
Purpose of the Study:
- To develop a novel, compact, and low-cost time-resolved Raman spectroscopy system.
- To minimize the impact of fluorescence on Raman observations for enhanced chemical analysis.
- To create a foundation for affordable in situ and fieldable chemical sensing devices.
Main Methods:
- Utilized a 6.4 kHz repetition rate, 900 ps pulsed diode laser (532 nm).
- Employed time-resolved photon counting with custom and off-the-shelf hardware/software.
- Compared long- and short-gated acquisition scenarios for signal-to-noise ratio (SNR) improvement.
Main Results:
- Demonstrated reduced fluorescence interference in Raman observations.
- Achieved an approximately 15-fold SNR improvement for benzene with a fluorophore using time-resolved photon counting.
- Successfully analyzed complex mixtures like gasoline and identified various compounds (e.g., trichloroethylene, benzene, olive oil).
Conclusions:
- The developed time-resolved Raman system effectively enhances Raman signature quality, particularly in the presence of fluorescence.
- The system offers a cost-effective solution for in situ and fieldable chemical analysis.
- Efficient signal averaging enables low-concentration detection, expanding its utility in diverse settings.
Related Concept Videos
Raman Spectroscopy Instrumentation: Overview
A conventional Raman spectrophotometer includes a laser source, a sample holding system, a wavelength selector, and a detector.
The monochromatic laser source, typically using visible or near-infrared radiation, generates a highly focused beam of light. This light interacts with the molecules of the sample, scattering some of the light. Liquid and gaseous samples are usually tested in ordinary glass capillaries, while solids can be analyzed as powders packed in capillaries or as potassium...
The monochromatic laser source, typically using visible or near-infrared radiation, generates a highly focused beam of light. This light interacts with the molecules of the sample, scattering some of the light. Liquid and gaseous samples are usually tested in ordinary glass capillaries, while solids can be analyzed as powders packed in capillaries or as potassium...
Raman Spectroscopy: Overview
The underlying principle of Raman spectroscopy is based on the interaction between light and matter, specifically molecules' inelastic scattering of photons. When a monochromatic beam of light, typically from a laser source, interacts with a sample, most scattered light has the same frequency as the incident light. This is known as Rayleigh scattering.
However, a small fraction of the scattered light exhibits a frequency shift due to the exchange of energy between the incident photons and the...
However, a small fraction of the scattered light exhibits a frequency shift due to the exchange of energy between the incident photons and the...

