Related Experiment Video
Updated: May 18, 2026

13:00
Hot Biological Catalysis: Isothermal Titration Calorimetry to Characterize Enzymatic Reactions
Published on: April 4, 2014
Creating, characterizing, and controlling chemistry with SERS hot spots
Samuel L Kleinman1, Renee R Frontiera, Anne-Isabelle Henry
1Northwestern University, Department of Chemistry, 2145 Sheridan Rd., Evanston, IL 60208, USA.
Physical Chemistry Chemical Physics : PCCP
|October 9, 2012
Summary
This perspective reviews hot spots in surface-enhanced Raman spectroscopy (SERS). It explores how these
Area of Science:
- Nanotechnology and Spectroscopy
- Surface-enhanced Raman spectroscopy (SERS)
- Plasmonics
Background:
- Hot spots are crucial for amplifying signals in SERS.
- Understanding hot spots is key to optimizing SERS substrates.
- Substrate design significantly influences hot spot formation and properties.
Purpose of the Study:
- To discuss the critical roles of hot spots in SERS.
- To evaluate various SERS substrates and their hot spot characteristics.
- To analyze hot spot contributions to SERS signals under different conditions.
Main Methods:
- Review of existing literature on SERS substrates and hot spots.
- Comparative analysis of different SERS substrate properties.
- Theoretical and experimental considerations of hot spot effects on SERS signals.
Main Results:
- Hot spots are essential for both ensemble-averaged and single-molecule SERS.
- Substrate morphology and dielectric environment dictate hot spot effectiveness.
- Clear rules for calculating the SERS enhancement factor (EF) are enumerated.
Conclusions:
- Hot spots are fundamental to achieving high SERS enhancement.
- Controlling hot spots enables precise nanoscale chemical manipulation.
- Future applications lie in advanced SERS-based sensing and chemistry.
Related Concept Videos
Supercritical Fluid Chromatography
Supercritical fluid chromatography (SFC) provides a beneficial substitute for gas chromatography (GC) and liquid chromatography (LC) for certain samples because it merges the top attributes of both techniques. SFC allows the separation and analysis of compounds that GC or LC does not easily manage. These compounds are traditionally nonvolatile or thermally unstable, making GC unsuitable and lacking functional groups required for HPLC analysis.
SFC utilizes a supercritical fluid mobile phase,...
SFC utilizes a supercritical fluid mobile phase,...
Gas Chromatography–Mass Spectrometry (GC–MS)
Gas chromatography–mass spectrometry (GC–MS) is the combination of analytical techniques of gas chromatography and mass spectrometry in a single instrument for analyzing a mixture of compounds. The gas chromatograph separates the compounds in the mixture, and the mass spectrometer analyzes each compound separately to determine the molecular masses and molecular structures.
A gas chromatograph consists of a long, narrow capillary column with a polysiloxane coating on the inner wall. The coating...
A gas chromatograph consists of a long, narrow capillary column with a polysiloxane coating on the inner wall. The coating...
Atomic Absorption Spectroscopy: Atomization Methods
Atomic Absorption Spectroscopy (AAS) atomizes samples through flame atomization or electrothermal atomization. Flame atomization typically involves a nebulizer and spray chamber assembly to combine the sample with a fuel–oxidant mixture, creating a fine aerosol mist that enters a burner. Typically, the fuel and oxidant are combined in an approximately stoichiometric ratio. However, for atoms that are easily oxidized, a fuel-rich mixture may be more advantageous. Only about 5% of the aerosol...
Chemical Ionization (CI) Mass Spectrometry
The molecular ion peak of a molecule in the mass spectrum provides vital information for molecular identification. However, conventional electron impact ionization can lead to the rapid dissociation of some molecular ions before they reach the detector. A milder ionization method is required to increase the lifetime of such ionized analyte molecules. Chemical ionization (CI) is a gas-phase protonation reaction useful for mass-analyzing analyte molecules that are easily protonated to yield the...
Washing, Drying, and Ignition of Precipitates
After filtration, the precipitate is washed to remove coprecipitated impurities and any remaining mother liquor. Colloidal precipitates, such as silver chloride, are washed with an electrolyte (such as dilute nitric acid) to prevent the peptization of the precipitate. In the case of slightly soluble precipitates, the wash solution contains a common ion to reduce solubility. Lead sulfate, which is slightly soluble in water, is washed with dilute sulfuric acid. Similarly, wash solutions may be...

