Formation and microstructure of cubic metastable iron silicides synthesized during pulsed laser annealing View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2003-12

AUTHORS

A. Falepin, S. Cottenier, C. M. Comrie, O. Richard, H. Bender, G. Langouche, A. Vantomme

ABSTRACT

The phase formation and crystallization processes of metastable [CsCl]Fe1−xSi phases were investigated by irradiatingɛ-FeSi/Si(111) thin films with a pulsed excimer laser in the energy density range 300–900 mJ/cm2. The samples were analysed by Rutherford backscattering and channeling spectrometry (RBS/C), cross-sectional transmission electron microscopy (TEM) and conversion electron Mössbauer spectroscopy (CEMS). Laser irradiation results in mixing of the FeSi with the Si substrate, with the final concentration depending on the laser energy density. Due to the extremely rapid quench of the melt, a non-uniform Fe concentration is obtained. Analysis by cross-sectional transmission electron microscopy confirmed that this phase, which exhibits epitaxial ordering, corresponds to the metastable [CsCl]Fe1−xSi phase, which converts into the semiconductingβ-FeSi2 upon annealing at 600°C. CEMS indicates that no stable Fe-silicide phase nor a combination of stable phases have been formed. The CEM spectra consist of a distribution of quadrupole doublets and isomer shifts, in agreement with a [CsCl]Fe1−xSi phase that exhibits a (i) composition gradient and (ii) a random number of Fe vacancies in the neighbouring shells. These distributions make the CEM spectra hard to interpret. Full-Potential Linearized Augmented Plane Wave (FLAPW) calculations were performed to gain more insight in the hyperfine interaction parameters of the metastable [CsCl]Fe1−xSi phase and their dependence on a concentration variation. These calculations confirm the decreasing trend of the isomer shift with increasing number of laser pulses. More... »

PAGES

131-144

Identifiers

URI

http://scigraph.springernature.com/pub.10.1023/b:hype.0000020412.84450.6c

DOI

http://dx.doi.org/10.1023/b:hype.0000020412.84450.6c

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1006091905


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