The Mossbauereffect was discovered in 1956 by R.L.Mossbauer. He
showed that nuclear radiation can be emitted and absorbed recoilless if
the atoms are placed in a solid state. For this experiment, also called
nuclear resonant absorbtion, one neads a radioactive source which decays
via an excited state into the so-called Mossbauer isotope. Depending on
the lifetime of the excited state, the energy of the radiation can be extremly
sharp. In the case of the iron 57 isotope the energy uncertaincy, called
natural linewidth, is 5 *10^-9 eV compared to the energy of 14.4 *10^3
eV of the radiation. Because the energy of the nuclear state is so well
defined, the difference between the hyperfine interaction of the isotopes
in the source and the sample can be studied . The influence of the hyperfine
interaction in the case of iron 57 is shown in the picture. The spectra
resulting from these interactions are also shown. They can be measured
by moving the source. Via the Doppler-effect the energy increases if the
source moves towards the sample and vice versa. A velocity of 1 mm/s corresponds
to an energy of 50 *10^-9 eV. Absorbtion can only occure, if the spectrum
of source overlapps with energy levels of the sample. So the Mossbauer
spectrum is a picture of the hyperfine interaction of the sample.
Several parameters can be extracted from the spectrum. These parameters
can determine the chemical and magnetical phases of the sample like a fingerprint.


Transmission Geometry is the standard Method. The experimental
set-up is very easy, but it is limited to powders or thin foils. The countrate
decreases in resonance, because the radiation can be preferred absorbed.
The whole sample contributes to the spectrum.
Backscattering Geometry measures either the emitted gamma or
x-ray radiation or the emitted electrons. As this radiation has to leave
the sample, only a layer at the surface contributes to the backscattered
spectrum. The thickness of this layer depends on the range of the radiation.
In the case of Fe 57 the gamma or x-rays have a range of approx. 10 e-6
m. If ones uses electrons ( CEMS = conversion electron Mossbauer spectroscopy
) the range is smaller. Furthermore the thickness of the contributing layer
can be varied by detecting the electrons energy dispersive. DCEMS
Courtesy of University of Damstadt