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Showing posts with label Mossbauer Spectroscopy. Show all posts
Showing posts with label Mossbauer Spectroscopy. Show all posts

Saturday, 14 June 2014

Introduction to Mossbauer Spectroscopy

In 1957 Rudolf Mossbauer achieved the first experimental observation of the resonant absorption and recoil-free emission of nuclear γ-rays in solids during his graduate work at the Institute for Physics of the Max Planck Institute for Medical Research in Heidelberg Germany. Mossbauer received the 1961 Nobel Prize in Physics for his research in resonant absorption of γ-radiation and the discovery of recoil-free emission a phenomenon that is named after him (http://nobelprize.org/nobel_prizes/physics/laureates/1961 for more information about Rudolf Mossbauer and his nobel prize). The Mossbauer effect is the basis of Mossbauer spectroscopy.
The Mossbauer effect can be described very simply by looking at the energy involved in the absorption or emission of a γ-ray from a nucleus. When a free nucleus absorbs or emits a γ-ray to conserve momentum the nucleus must recoil, so in terms of energy:
Eγ-ray = Enuclear transition - Erecoil
When in a solid matrix the recoil energy goes to zero because the effective mass of the nucleus is very large and momentum can be conserved with negligible movement of the nucleus. So, for nuclei in a solid matrix:
Eγ-ray = Enuclear transition
This is the Mossbauer effect which results in the resonant absorption/emission of γ-rays and gives us a means to probe the hyperfine interactions of an atoms nucleus and its surroundings.
A Mossbauer spectrometer system consists of a γ-ray source that is oscillated toward and away from the sample by a “Mossbauer drive”, a collimator to filter the γ-rays, the sample, and a detector.
Figure 1: Schematic of Mossbauer Spectrometers. A = transmission; B = backscatter set up. Adapted from M. D. Dyar, D. G. Agresti, M. W. Schaefer, C. A. Grant, and E. C. Sklute, Annu. Rev. Earth. Planet. Sci., 2006, 34 , 83. Copyright Annual Reviews (2006).
Figure 1 (zeb1.jpg)
Figure 1 shows the two basic set ups for a Mossbauer spectrometer. The Mossbauer drive oscillates the source so that the incident γ-rays hitting the absorber have a range of energies due to the doppler effect. The energy scale for Mossbauer spectra (x-axis) is generally in terms of the velocity of the source in mm/s. The source shown (57Co) is used to probe 57Fe in iron containing samples because 57Co decays to 57Fe emitting a γ-ray of the right energy to be absorbed by 57Fe. To analyze other Mossbauer isotopes other suitable sources are used. Fe is the most common element examined with Mossbauer spectroscopy because its 57Fe isotope is abundant enough (2.2), has a low energy γ-ray, and a long lived excited nuclear state which are the requirements for observable Mossbauer spectrum. Other elements that have isotopes with the required parameters for Mossbauer probing are seen in Table 1.

Mossbauer spectra

The primary characteristics looked at in Mossbauer spectra are isomer shift (IS), quadrupole splitting (QS), and magnetic splitting (MS or hyperfine splitting). These characteristics are effects caused by interactions of the absorbing nucleus with its environment.
Isomer shift is due to slightly different nuclear energy levels in the source and absorber due to differences in the s-electron environment of the source and absorber. The oxidation state of an absorber nucleus is one characteristic that can be determined by the IS of a spectra. For example due to greater d electron screening Fe2+ has less s-electron density than Fe3+ at its nucleus which results in a greater positive IS for Fe2+.
For absorbers with nuclear angular momentum quantum number I > ½ the non-spherical charge distribution results in quadrupole splitting of the energy states. For example Fe with a transition from I=1/2 to 3/2 will exhibit doublets of individual peaks in the Mossbauer spectra due to quadrupole splitting of the nuclear states as shown in red in Figure 2.
In the presence of a magnetic field the interaction between the nuclear spin moments with the magnetic field removes all the degeneracy of the energy levels resulting in the splitting of energy levels with nuclear spin I into 2I + 1 sublevels. Using Fe for an example again, magnetic splitting will result in a sextet as shown in green in Figure 2. Notice that there are 8 possible transitions shown, but only 6 occur. Due to the selection rule ІΔmIІ = 0, 1, the transitions represented as black arrows do not occur.
Figure 2: Characteristics of Mossbauer spectra related to nuclear energy levels. Adapted from M. D. Dyar, D. G. Agresti, M. W. Schaefer, C. A. Grant, and E. C. Sklute, Annu. Rev. Earth. Planet. Sci., 2006,34 , 83. Copyright Annual Reviews (2006).
Figure 2 (zeb2.jpg)

Bibliography

  • G. Wertheim. Mossbauer Effect: Principles and Applications. New York: Academic Press Inc. (1964).
  • D. P. E. Dickson and F. J. Berry. Mossbauer Spectroscopy. New York: Cambridge University Press (1986).
  • A. G. Maddock. Mossbauer Spectroscopy: Principles and Applications of the Techniques. England: Horwood Publishing Limited (1997).
  • M. D. Dyar, D. G. Agresti, M. W. Schaefer, C. A. Grant, and E. C. Sklute, Annu. Rev. Earth. Planet. Sci., 2006, 34 , 83.
Fisher, E.; Barron, A. Introduction to Mossbauer Spectroscopy, OpenStax-CNX Web site. http://cnx.org/content/m22328/1.7/, Aug 14, 2009.


TABLE 1: Elements with known Mossbauer isotopes and most commonly examined with Mossbauer spectroscopy.

Most commonly examined elements

Fe, Ru, W, Ir, Au, Sn, Sb, Te, I, W, Ir, Au, Eu, Gd, Dy, Er, Yb, Np

Elements that exhibit Mossbauer effect

K, Ni, Zn, Ge, Kr, Tc, Ag, Xe, Cs, Ba, La, Hf, Ta, Re, Os, Pt, Hg, Ce, Pr, Nd, Sm, Tb, Ho, Tm, Lu, Th, Pa, U, Pu, Am