ĮDS is often contrasted with its spectroscopic counterpart, wavelength dispersive X-ray spectroscopy (WDS). Information on the quantity and kinetic energy of ejected electrons is used to determine the binding energy of these now-liberated electrons, which is element-specific and allows chemical characterization of a sample. X-ray photoelectron spectroscopy (XPS) is another close relative of EDS, utilizing ejected electrons in a manner similar to that of AES. This ejected species is called an Auger electron, and the method for its analysis is known as Auger electron spectroscopy (AES). Often, instead of X-ray emission, the excess energy is transferred to a third electron from a further outer shell, prompting its ejection. The excess energy of the electron that migrates to an inner shell to fill the newly created hole can do more than emit an X-ray. Now, newer systems are often equipped with silicon drift detectors (SDD) with Peltier cooling systems. The most common detector used to be a Si(Li) detector cooled to cryogenic temperatures with liquid nitrogen. A detector is used to convert X-ray energy into voltage signals this information is sent to a pulse processor, which measures the signals and passes them onto an analyzer for data display and analysis. X-ray beam excitation is used in X-ray fluorescence (XRF) spectrometers. the excitation source (electron beam or x-ray beam)Įlectron beam excitation is used in electron microscopes, scanning electron microscopes (SEM) and scanning transmission electron microscopes (STEM).Equipment įour primary components of the EDS setup are As the energies of the X-rays are characteristic of the difference in energy between the two shells and of the atomic structure of the emitting element, EDS allows the elemental composition of the specimen to be measured. The number and energy of the X-rays emitted from a specimen can be measured by an energy-dispersive spectrometer. An electron from an outer, higher-energy shell then fills the hole, and the difference in energy between the higher-energy shell and the lower energy shell may be released in the form of an X-ray. The incident beam may excite an electron in an inner shell, ejecting it from the shell while creating an electron hole where the electron was. At rest, an atom within the sample contains ground state (or unexcited) electrons in discrete energy levels or electron shells bound to the nucleus. To stimulate the emission of characteristic X-rays from a specimen a beam of electrons is focused into the sample being studied. The peak positions are predicted by the Moseley's law with accuracy much better than experimental resolution of a typical EDX instrument. Its characterization capabilities are due in large part to the fundamental principle that each element has a unique atomic structure allowing a unique set of peaks on its electromagnetic emission spectrum (which is the main principle of spectroscopy). It relies on an interaction of some source of X-ray excitation and a sample. One peak is from the L shell of iron.Įnergy-dispersive X-ray spectroscopy ( EDS, EDX, EDXS or XEDS), sometimes called energy dispersive X-ray analysis ( EDXA or EDAX) or energy dispersive X-ray microanalysis ( EDXMA), is an analytical technique used for the elemental analysis or chemical characterization of a sample. EDS spectrum of the mineral crust of the vent shrimp Rimicaris exoculata Most of these peaks are X-rays given off as electrons return to the K electron shell ( K-alpha and K-beta lines).
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