X-ray fluorescence is Characteristic X-ray emission following excitation by incident photons. In a simple initially unexcited chemical atom, photoionization can eject an inner Electron if the incident photon supplies its binding energy. An outer Electron can then fill the vacancy, releasing an emitted photon with the difference of shell binding energies. Nonradiative relaxation competes with this route, so one absorbed incident photon need not yield one escaping characteristic photon.
Choose a separate stipulated electron shell model with values , and , all in . Ignore subshell splitting, recoil and changes of binding energy during relaxation. The possible shell differences areThese labels denote simplified shell groups, not resolved subshell electronic transitions. With , their calculated wavelengths are respectively , and . An incident photon exceeds both K-line energies but cannot directly create the K vacancy in this initially unexcited model. A photon can, leaving approximately of photoelectron kinetic energy. This comparison fixes neither the excitation probability nor the radiative branching probability.
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X-ray fluorescence (XRF) is a non-destructive analytical technique used to determine the elemental composition of materials. When a sample is irradiated with X-rays, it absorbs some of the energy, causing the inner-shell electrons of the atoms in the sample to be ejected. As a result, electrons from higher energy levels within the atom fill these vacancies, and energy is released in the form of characteristic X-rays.