X-ray absorption spectroscopy


X-ray absorption spectroscopy is a set of advanced techniques used for probing the local environment of matter at atomic level and its electronic structure. The experiments require access to synchrotron radiation facilities for their intense and tunable X-ray beams. Samples can be in the gas phase, solutions, or solids.

Background

XAS data are obtained by tuning the photon energy, using a crystalline monochromator, to a range where core electrons can be excited. The edges are, in part, named by which core electron is excited: the principal quantum numbers n = 1, 2, and 3, correspond to the K-, L-, and M-edges, respectively. For instance, excitation of a 1s electron occurs at the K-edge, while excitation of a 2s or 2p electron occurs at an L-edge.
There are three main regions found on a spectrum generated by XAS data, which are then thought of as separate spectroscopic techniques :
  1. The absorption threshold determined by the transition to the lowest unoccupied states:
  2. The X-ray absorption near-edge structure, introduced in 1980 and later in 1983 and also called NEXAFS, which are dominated by core transitions to quasi bound states for photoelectrons with kinetic energy in the range from 10 to 150 eV above the chemical potential, called "shape resonances" in molecular spectra since they are due to final states of short life-time degenerate with the continuum with the Fano line-shape. In this range, multi-electron excitations and many-body final states in strongly correlated systems are relevant;
  3. In the high kinetic energy range of the photoelectron, the scattering cross-section with neighbor atoms is weak, and the absorption spectra are dominated by EXAFS, where the scattering of the ejected photoelectron of neighboring atoms can be approximated by single scattering events. In 1985, it was shown that multiple scattering theory can be used to interpret both XANES and EXAFS; therefore, the experimental analysis focusing on both regions is now called XAFS.
XAS is a type of absorption spectroscopy from a core initial state with a well-defined symmetry; therefore, the quantum mechanical selection rules select the symmetry of the final states in the continuum, which are usually a mixture of multiple components. The most intense features are due to electric-dipole allowed transitions to unoccupied final states. For example, the most intense features of a K-edge are due to core transitions from 1s → p-like final states, while the most intense features of the L3-edge are due to 2p → d-like final states.
XAS methodology can be broadly divided into four experimental categories that can yield complementary results: metal K-edge, metal L-edge, ligand K-edge, and EXAFS.
The most obvious means of mapping heterogeneous samples beyond x-ray absorption contrast is through elemental analysis by x-ray fluorescence, similar to EDX methods in electron microscopy.

Applications

XAS is a technique used in various scientific fields, including molecular and condensed matter physics, materials science and engineering, chemistry, earth science, and biology. In particular, its unique sensitivity to the local structure, as compared to x-ray diffraction, has been exploited for studying: