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Statements

Subject Item
dbr:Surface_science
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dbr:Surface-extended_X-ray_absorption_fine_structure
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Surface-extended X-ray absorption fine structure
rdfs:comment
Surface-extended X-ray absorption fine structure (SEXAFS) is the surface-sensitive equivalent of the EXAFS technique. This technique involves the illumination of the sample by high-intensity X-ray beams from a synchrotron and monitoring their photoabsorption by detecting in the intensity of Auger electrons as a function of the incident photon energy. Surface sensitivity is achieved by the interpretation of data depending on the intensity of the Auger electrons (which have an escape depth of ~1–2 nm) instead of looking at the relative absorption of the X-rays as in the parent method, EXAFS.
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1045514341
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Surface-extended X-ray absorption fine structure (SEXAFS) is the surface-sensitive equivalent of the EXAFS technique. This technique involves the illumination of the sample by high-intensity X-ray beams from a synchrotron and monitoring their photoabsorption by detecting in the intensity of Auger electrons as a function of the incident photon energy. Surface sensitivity is achieved by the interpretation of data depending on the intensity of the Auger electrons (which have an escape depth of ~1–2 nm) instead of looking at the relative absorption of the X-rays as in the parent method, EXAFS. The photon energies are tuned through the characteristic energy for the onset of core level excitation for surface atoms. The core holes thus created can then be filled by nonradiative decay of a higher-lying electron and communication of energy to yet another electron, which can then escape from the surface (Auger emission). The photoabsorption can therefore be monitored by direct detection of these Auger electrons to the total photoelectron yield. The absorption coefficient versus incident photon energy contains oscillations which are due to the interference of the backscattered Auger electrons with the outward propagating waves. The period of this oscillations depends on the type of the backscattering atom and its distance from the central atom. Thus, this technique enables the investigation of interatomic distances for adsorbates and their coordination chemistry. This technique benefits from long range order not being required, which sometimes becomes a limitation in the other conventional techniques like LEED (about 10 nm). This method also largely eliminates the background from the signal. It also benefits because it can probe different species in the sample by just tuning the X-ray photon energy to the absorption edge of that species. Joachim Stöhr played a major role in the initial development of this technique.
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