MÖSSBAUER SPECTROSCOPY OF METAL SANDWICH COMPOUNDS *
MÖSSBAUER SPECTROSCOPY OF METAL SANDWICH COMPOUNDS *
复制标题
金属夹层化合物的穆斯堡尔谱*
DOI:
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发表时间:
1974
影响因子:
5.2
通讯作者:
D. Foyt
中科院分区:
文献类型:
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作者:
M. Good;John Buttone;D. Foyt
The application of Mossbauer spectroscopy to problems of chemical interest involves two steps: the extraction of the basic Mossbauer parameters (isomer shift, electric field gradient tensor at the nucleus, and so forth) from the experimental data and the interpretation of these parameters in terms of structure and bonding. In the special case of iron spectroscopy, the extraction of the isomer shift and quadrupole splitting parameters is relatively straightforward because Ipw nuclear spin states in the Mossbauer transition give rise to rather simple spectra. In the absence of an electric field gradient at the nucleus, the I = 3/2 to I = 1/2 transition is observed as a single line resonance where the isomer shift reflects the effect of the chemical (electronic) environment of the absorbing nucleus. The Mossbauer effect is observed by allowing the gamma’ rays from the decay of an excited nucleus to be resonantly absorbed by the same nucleus (in the ground state) in an absorber matrix of interest. The isomer shift arises from the fact that the electronic environments of the Mossbauer nuclide in the source. and absorber are different; thus, electrostatic interactions with the nuclear levels are such that the energy of the emitted gamma ray from the source is slightly different from the energy required for resonance absorption in the absorber. The spectrum is developed by mounting the source. on a movable drive and “scanning” the energy range of interest by means of the Doppler effect. Thus, the usual Mossbauer spectrum is displayed as counts (gamma ray density) vs velocity (directly proportional to the energy perturbation of the gamma rays by the Doppler effect). The isomer shift is defined as: