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Microstructural characterization of iron implanted sapphire nanocomposites
Author(s) -
S.X. Ren,
C.J. McHargue,
L.F. Allard,
Y. Chen,
J.D. Hunn,
B.N. Lucas,
R.K. Williams
Publication year - 1994
Publication title -
osti oai (u.s. department of energy office of scientific and technical information)
Language(s) - English
Resource type - Reports
DOI - 10.2172/102181
Subject(s) - materials science , sapphire , nanocomposite , annealing (glass) , crystallinity , analytical chemistry (journal) , transmission electron microscopy , amorphous solid , ion implantation , fluence , crystallography , ion , nanotechnology , composite material , optics , chemistry , laser , physics , organic chemistry , chromatography
Nanocomposites of iron in sapphire ({alpha}-Al{sub 2}O{sub 3}) prepared by ion implantation have been studied as a model to investigate the potential of such materials for applications in high technology areas. The implantation was performed with 160 keV ions at several doses; the nanocomposites were then annealed at selected temperatures between 700 and 1,400 C in an Ar-4%H{sub 2} atmosphere for 1 hour. Rutherford backscattering spectroscopy and high resolution transmission electron microscopy (TEM) were used to characterize the structure of these nanocomposites. Measurements showed that damage depth extended to about 300 nm and the embedded iron extended to about 200 nm. This region became amorphous when the fluence reaches 2 {times} 10{sup 17} Fe/cm{sup 2} at this energy. Thermal annealing could be used to restore the crystallinity to the damaged near-surface region, to form the metallic colloids, and also to coarsen the precipitates. In the case of high dose implantation, oriented precipitates with diameters of 2 to 3 nm were identified by TEM techniques as {alpha}-Fe which had the following orientation relationship with the sapphire matrix: <111>{sub Fe} {parallel} <310>{sub Sapphire} and {l_brace}01{bar 1}{r_brace}{sub Fe} {parallel} {l_brace}006{r_brace}{sub Sapphire}. The optical density and luminescence spectra were also measured. The predominant defects were oxygen vacancies with two electrons (F center) at the known absorption peak of 200 nm

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