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CHEMICAL VAPOR DEPOSITION OF THIN FILM MATERIALS FOR ...

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1.2.3.3 X-ray Diffraction (XRD)<br />

X-ray diffraction is a classic technique for crystal structure characterization. X-rays that<br />

can be used to probe the material structures in atomic scale (few angstroms) have wavelengths in<br />

the same order. They usually possess much larger energies than those used for XPS analysis and<br />

are thus called hard X-rays. Generation of these X-rays starts from the bombardment of anode<br />

source materials, such as Cu, Co, Ag, Cr, or Fe etc., with a focused high energy (tens to hundreds<br />

of keV) electron beam. When electrons strike these materials, they are decelerated and a<br />

continuous spectrum of X-ray is emitted known as Bremsstrahlung radiation. High energy<br />

electrons can also knock inner shell electrons out of the atoms and leave vacancies in those shells.<br />

When an outer shell electron falls into the inner shell to fill the vacancy, the excessive energies<br />

left will be relieved by emission of characteristic X-ray photons. The as emitted X-ray possess<br />

the energy (wavelength) characteristic of the shell energy gap of atoms of the source material.<br />

For example, Cu Kα X-ray frequently used in XRD measurement has a wavelength of ~1.5418Å<br />

(~8.04 keV) and Kα here represents the X-ray originating from the action of filling up a vacancy<br />

in K shell by a L shell electron.<br />

Fig. 6. Geometric derivation of Bragg's law.<br />

nλ 2d sin θ (1.12)<br />

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