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Related Concept Videos

IR Absorption Frequency: Delocalization01:04

IR Absorption Frequency: Delocalization

Electron delocalization refers to the distribution of electrons across multiple atoms within a molecule rather than being confined to a single atom or bond. This phenomenon is common in systems with conjugated bonds—structures where alternating single and double bonds allow π-electrons to move freely across the network. The movement of electrons stabilizes the molecule and can affect various chemical properties, including vibrational frequencies observed in IR spectroscopy.
In IR spectroscopy,...
IR Spectrum Peak Intensity: Dipole Moment01:20

IR Spectrum Peak Intensity: Dipole Moment

The dipole moment of a bond is the product of the partial charge on either atom and the distance between them. Dipole moments influence the efficiency of IR absorption and the peak intensity. When a bond with a dipole moment is placed in an electric field, the direction of the field determines if the bond is compressed or stretched. Electromagnetic radiation consists of an electric field component that rapidly reverses direction. It follows that polar bonds are alternately stretched and...
Atomic Emission Spectroscopy: Interference01:30

Atomic Emission Spectroscopy: Interference

In atomic emission spectroscopy (AES), high-temperature atomizers excite a broad range of elements and molecules that generate complex emissions from sources such as oxides, hydroxides, and flame combustion products in the flame or plasma. Several strategies can be employed to minimize spectral interferences caused by overlapping emission lines or bands. These include increasing instrument resolution, choosing alternative emission lines, optimally placing the detector in low-background regions,...
IR Spectrum Peak Splitting: Symmetric vs Asymmetric Vibrations01:08

IR Spectrum Peak Splitting: Symmetric vs Asymmetric Vibrations

Identical bonds within a polyatomic group can stretch symmetrically (in-phase) or asymmetrically (out-of-phase). Similar to hydrogen bonding, these vibrations also influence the shape of the IR peak. Generally, asymmetric stretching frequencies are higher than symmetric stretching frequencies. For example, primary amines exhibit two distinct IR peaks between 3300–3500 cm−1 corresponding to the symmetric and asymmetric N-H stretching, while secondary amines exhibit a single stretching vibration...
Atomic Absorption Spectroscopy: Interference01:25

Atomic Absorption Spectroscopy: Interference

Interference leads to systematic error in atomic absorption (AA) measurements by enhancing or diminishing the analytical signal or the background. These interferences can be grouped into three main categories: spectral interference, chemical interference, and physical interference.
Spectral interference occurs when signals from other elements or molecules overlap with the analyte signal, falsely elevating or masking the analyte's absorbance. This interference can be corrected using Zeeman,...
IR Spectrum Peak Broadening: Hydrogen Bonding01:23

IR Spectrum Peak Broadening: Hydrogen Bonding

The vibrational frequency of a bond is directly proportional to its bond strength. As a result, stronger bonds vibrate at higher frequencies, while weaker bonds vibrate at lower frequencies. The stretching vibration of the strong O–H bond in alcohols and phenols (very dilute solution or gas phase) appears as a sharp peak at 3600–3650 cm−1.
However, the extent of hydrogen bonding influences the observed stretching frequency and band broadening. Intermolecular or intramolecular hydrogen bonding...

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Related Experiment Video

Updated: May 16, 2026

Fabrication and Characterization of Disordered Polymer Optical Fibers for Transverse Anderson Localization of Light
09:19

Fabrication and Characterization of Disordered Polymer Optical Fibers for Transverse Anderson Localization of Light

Published on: July 29, 2013

Coherent forward scattering peak induced by Anderson localization.

T Karpiuk1, N Cherroret, K L Lee

  • 1Centre for Quantum Technologies, National University of Singapore, 3 Science Drive 2, Singapore 117543, Singapore.

Physical Review Letters
|December 11, 2012
PubMed
Summary

Numerical simulations reveal a new forward interference peak at Anderson localization onset. This peak, alongside coherent backscattering, confirms Anderson localization and is linked to Heisenberg time within the localization volume.

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Area of Science:

  • Condensed matter physics
  • Wave phenomena in disordered systems

Background:

  • Anderson localization describes the cessation of wave propagation in disordered media.
  • Coherent backscattering is a known signature of wave interference in random potentials.

Purpose of the Study:

  • To identify and characterize new signatures of Anderson localization.
  • To investigate the momentum distribution of wave packets in random potentials.

Main Methods:

  • Numerical simulations of wave packet propagation.
  • Analysis of momentum distributions.
  • Application of maximally crossed diagrams for theoretical explanation.

Main Results:

  • A novel interference peak observed in the forward direction of the momentum distribution.
  • This forward peak emerges at the localization time.
  • The signal's growth scales with the Heisenberg time of the localization volume.

Conclusions:

  • The forward interference peak, together with coherent backscattering, provides robust evidence for Anderson localization.
  • The observed phenomenon offers new insights into wave transport in disordered systems.