Dispersion relation in the context of Phase velocity


Dispersion relation in the context of Phase velocity

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⭐ Core Definition: Dispersion relation

In the physical sciences and electrical engineering, dispersion relations describe the effect of dispersion on the properties of waves in a medium. A dispersion relation relates the wavelength or wavenumber of a wave to its frequency. Given the dispersion relation, one can calculate the frequency-dependent phase velocity and group velocity of each sinusoidal component of a wave in the medium, as a function of frequency. In addition to the geometry-dependent and material-dependent dispersion relations, the overarching Kramers–Kronig relations describe the frequency-dependence of wave propagation and attenuation.

Dispersion may be caused either by geometric boundary conditions (waveguides, shallow water) or by interaction of the waves with the transmitting medium. Elementary particles, considered as matter waves, have a nontrivial dispersion relation, even in the absence of geometric constraints and other media.

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Dispersion relation in the context of Rayleigh scattering

Rayleigh scattering (/ˈrli/ RAY-lee) is the scattering or deflection of light, or other electromagnetic radiation, by particles with a size much smaller than the wavelength of the radiation. For light frequencies well below the resonance frequency of the scattering medium (normal dispersion regime), the amount of scattering is inversely proportional to the fourth power of the wavelength (e.g., a blue color is scattered much more than a red color as light propagates through air). The phenomenon is named after the 19th-century British physicist Lord Rayleigh (John William Strutt).

Rayleigh scattering results from the electric polarizability of the particles. The oscillating electric field of a light wave acts on the charges within a particle, causing them to move at the same frequency. The particle, therefore, becomes a small radiating dipole whose radiation we see as scattered light. The particles may be individual atoms or molecules; it can occur when light travels through transparent solids and liquids, but is most prominently seen in gases.

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Dispersion relation in the context of Fast magnetosonic wave

In physics, magnetosonic waves, also known as magnetoacoustic waves, are low-frequency compressive waves driven by mutual interaction between an electrically conducting fluid and a magnetic field. They are associated with compression and rarefaction of both the fluid and the magnetic field, as well as with an effective tension that acts to straighten bent magnetic field lines. The properties of magnetosonic waves are highly dependent on the angle between the wavevector and the equilibrium magnetic field and on the relative importance of fluid and magnetic processes in the medium. They only propagate with frequencies much smaller than the ion cyclotron or ion plasma frequencies of the medium, and they are nondispersive at small amplitudes.

There are two types of magnetosonic waves, fast magnetosonic waves and slow magnetosonic waves, which—together with Alfvén waves—are the normal modes of ideal magnetohydro­dynamics. The fast and slow modes are distinguished by magnetic and gas pressure oscillations that are either in-phase or anti-phase, respectively. This results in the phase velocity of any given fast mode always being greater than or equal to that of any slow mode in the same medium, among other differences.

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Dispersion relation in the context of Density of states

In condensed matter physics, the density of states (DOS) of a system describes the number of allowed modes or states per unit energy range. The density of states is defined as , where is the number of states in the system of volume whose energies lie in the range from to . It is mathematically represented as a distribution by a probability density function, and it is generally an average over the space and time domains of the various states occupied by the system. The density of states is directly related to the dispersion relations of the properties of the system. High DOS at a specific energy level means that many states are available for occupation.

Generally, the density of states of matter is continuous. In isolated systems however, such as atoms or molecules in the gas phase, the density distribution is discrete, like a spectral density. Local variations, most often due to distortions of the original system, are often referred to as local densities of states (LDOSs).

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Dispersion relation in the context of Dispersion (water waves)

In fluid dynamics, dispersion of water waves generally refers to frequency dispersion, which means that waves of different wavelengths travel at different phase speeds. Water waves, in this context, are waves propagating on the water surface, with gravity and surface tension as the restoring forces. As a result, water with a free surface is generally considered to be a dispersive medium.

For a certain water depth, surface gravity waves – i.e. waves occurring at the air–water interface and gravity as the only force restoring it to flatness – propagate faster with increasing wavelength. On the other hand, for a given (fixed) wavelength, gravity waves in deeper water have a larger phase speed than in shallower water. In contrast with the behavior of gravity waves, capillary waves (i.e. only forced by surface tension) propagate faster for shorter wavelengths.

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Dispersion relation in the context of Electron energy loss spectroscopy

Electron energy loss spectroscopy (EELS) is a form of electron microscopy in which a material is exposed to a beam of electrons with a known, narrow range of kinetic energies. Some of the electrons will undergo inelastic scattering, which means that they lose energy and have their paths slightly and randomly deflected. The amount of energy loss can be measured via an electron spectrometer and interpreted in terms of what caused the energy loss. Inelastic interactions include phonon excitations, inter- and intra-band transitions, plasmon excitations, inner shell ionizations, and Cherenkov radiation. The inner-shell ionizations are particularly useful for detecting the elemental components of a material. For example, one might find that a larger-than-expected number of electrons comes through the material with 285 eV less energy than they had when they entered the material. This is approximately the amount of energy needed to remove an inner-shell electron from a carbon atom, which can be taken as evidence that there is a significant amount of carbon present in the sample. With some care, and looking at a wide range of energy losses, one can determine the types of atoms, and the numbers of atoms of each type, being struck by the beam. The scattering angle (that is, the amount that the electron's path is deflected) can also be measured, giving information about the dispersion relation of whatever material excitation caused the inelastic scattering.

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