Abstract
A local (probe-hole) mass-to-charge resolved retarding potential analysis of N 2 + emitted from a few surface sites of the apex plane of a [111]-oriented W tip is carried out and corresponding field ion appearance energies are obtained. A comparison of the results of N 2 + W(111) field ion appearance energy spectroscopy with independently obtained field-free nitrogen adsorption data reveals a noble-gas-like mechanism for the localized field ionization of N 2, supplied as imaging gas in the field ion microscope. The differences in the physical nature of the field-dependent terms of the appearance energy of N 2 + and CO + field ions are discussed in relation to the peculiarities of the high-field modified interaction of nitrogen and carbon monoxide with the tungsten surface.
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