1968
DOI: 10.1116/1.1492596
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X-Ray Measurement of Faulting in Evaporated α Cu–Ge Films

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Cited by 6 publications
(3 citation statements)
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“…An x-ray study of silver films (thickness 2000 and 6000 A) prepared at different residual gas pressures has been made by Light and Wagner (1966) to determine particle size, strains and faulting from the lattice parameter measurements and Fourier analysis of line shapes. The lattice parameter and stacking fault probabilities in a-Cu-Ge films as a function of composition have been measured by Marchetto et al (1968) by an x-ray diffraction method. An x-ray line broadening analysis in gold films less than 1000 A thick has been made by Atasagun and Vook (1970) to determine the crystallite size and non-uniform strains in the films.…”
Section: Introductionmentioning
confidence: 99%
“…An x-ray study of silver films (thickness 2000 and 6000 A) prepared at different residual gas pressures has been made by Light and Wagner (1966) to determine particle size, strains and faulting from the lattice parameter measurements and Fourier analysis of line shapes. The lattice parameter and stacking fault probabilities in a-Cu-Ge films as a function of composition have been measured by Marchetto et al (1968) by an x-ray diffraction method. An x-ray line broadening analysis in gold films less than 1000 A thick has been made by Atasagun and Vook (1970) to determine the crystallite size and non-uniform strains in the films.…”
Section: Introductionmentioning
confidence: 99%
“…The partially annealed specimen also shows considerable faulting (p -45.6 x 10-3). The high incidence of growth faults (p) in these alloy films is inconsistent withMarchetto et al (1968), for a-Cu-Ge films.…”
mentioning
confidence: 75%
“…The microstructure of powder samples of metals and alloys has been extensively studied [3][4][5], by x-ray diffraction method over the period of last two decades and many important advancements have been made in the theory and application by such studies. However, only a few corresponding studies [6][7][8][9][10][11][12][13][14][15] have been reported in the thin films of metals and alloys. The main reasons are that (i) the microcrystallites in thin films are not randomly deposited such as found in powders, (ii) films should be very uniform, sufficiently thick and good quality for XDS measurement, and (iii) the corrections due to geometrical effect and preferred orientation are not easy to perform experimentally.…”
Section: Introductionmentioning
confidence: 99%