作者: M.P. Seah
DOI: 10.1016/0039-6028(73)90147-7
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摘要: Abstract Three independent approaches are discussed for the quantitative calibration of tin adsorbed on surface iron monitored by Auger electron spectroscopy. Two involved measurement substrate and condensate intensities at stages during condensation or stannic oxide pure iron. The quantity was directly a quartz crystal oscillator growth form measurements elastic scattering. Allowances were made changes in peak structure due to its combination with oxygen condensate. These two calibrations compare very closely obtained from cleavage face single α-iron containing 7.9 wt % solid solution. A terms relative is it concluded that quantifica- tion procedures applicable, even strongly bonded compounds.