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Related Concept Videos

Raman Spectroscopy Instrumentation: Overview01:26

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...
Raman Spectroscopy: Overview01:20

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...
Atomic Absorption Spectroscopy: Instrumentation01:22

Atomic Absorption Spectroscopy: Instrumentation

An atomic absorption spectrophotometer (AAS) comprises several components: a radiation source, an atomizer, a monochromator, and a detector. The radiation source can be a hollow-cathode lamp (HCL) or an electrodeless-discharge lamp (EDL), both of which provide a narrow emission line of the required wavelength. However, some instruments use continuum sources and high-resolution monochromators to achieve a narrow range of radiation.
The atomizer used in AAS can be either a flame atomizer or an...
IR Spectrometers01:25

IR Spectrometers

There are two main infrared (IR) spectrophotometers: dispersive IR spectrometers and Fourier transform infrared (FTIR) spectrometers. In a dispersive IR spectrometer, a beam of infrared radiation produced by a hot wire is divided into two parallel equal-intensity beams using mirrors. One beam passes through the sample, while another is a reference beam. The beams then move through the monochromator, which separates the radiations into a continuous spectrum of different frequencies. The...
UV–Vis Spectrometers01:14

UV–Vis Spectrometers

The absorbance of UV and visible (UV–visible) radiations is measured using a UV–visible spectrophotometer. Deuterium lamps, which emit UV radiation, and tungsten lamps, which produce radiation in the visible region, are used as light sources in UV–visible spectrophotometers. A monochromator or prism is used for diffraction grating, i.e., to split the incoming radiation into different wavelengths. A system of slits is used to focus the desired wavelength on the sample cell. Samples for...

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Related Experiment Video

Updated: Jul 13, 2026

Rejection of Fluorescence Background in Resonance and Spontaneous Raman Microspectroscopy
15:04

Rejection of Fluorescence Background in Resonance and Spontaneous Raman Microspectroscopy

Published on: May 18, 2011

Device for Raman difference spectroscopy.

Torsten Frosch1, Tobias Meyer, Michael Schmitt

  • 1Institut für Physikalische Chemie, Friedrich-Schiller-Universität Jena, Helmholtzweg 4, D-07743 Jena, Germany.

Analytical Chemistry
|July 14, 2007
PubMed
Summary

A novel Raman difference spectroscopy (RDS) setup enhances sensitivity for detecting minute molecular changes. This versatile instrument precisely analyzes biomolecules and their interactions, offering significant advancements in chemical analysis.

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Area of Science:

  • Spectroscopy
  • Analytical Chemistry
  • Physical Chemistry

Background:

  • Raman difference spectroscopy (RDS) is highly accurate for detecting small spectral shifts.
  • Conventional RDS requires strict prevention of environmental perturbations for accurate difference spectra.
  • Resonance Raman enhancement and CCD detectors offer advantages in sensitivity and efficiency.

Purpose of the Study:

  • To present a new, versatile Raman difference spectroscopy setup.
  • To combine the benefits of rotating cells, RDS, and CCD detectors.
  • To improve the accuracy and sensitivity of spectral shift detection.

Main Methods:

  • A double-beam layout was implemented to simultaneously detect Raman signals from two sample cells.
  • A Y-fiber bundle combined signals, which were then imaged onto a CCD detector.
  • The setup utilized resonance Raman enhancement with excitation wavelengths from UV to NIR.

Main Results:

  • The new apparatus significantly increased accuracy in detecting frequency shifts and minor sample components compared to conventional Raman spectroscopy.
  • A previously undetected shift of <0.02 cm(-1) in the CCl4 band at 218 cm(-1) was resolved in binary mixtures of CHCl3 and CCl4.
  • The setup demonstrated versatility for various samples with minor optical arrangement changes.

Conclusions:

  • The new RDS setup offers a versatile, sensitive, selective, and precise method for analyzing biomolecules and their interactions.
  • The device is crucial for fast and gentle investigations.
  • Initial results show promise for studying interactions like chloroquine with hematin.