Sputtering and nitridation of transition metal surfaces under low energy, steady state nitrogen ion bombardment
[Display omitted] •Measured steady state sputter yields for Mo, Ru, Pd, W targets at energy range 50–500 eV.•Nitridation observed using X-ray photoelectron spectroscopy (XPS).•Nitrogen content was independent of incident ion energy over the range studied.•Reaction and sputtering competing processes...
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Veröffentlicht in: | Applied surface science 2020-03, Vol.505, p.144529, Article 144529 |
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Format: | Artikel |
Sprache: | eng |
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•Measured steady state sputter yields for Mo, Ru, Pd, W targets at energy range 50–500 eV.•Nitridation observed using X-ray photoelectron spectroscopy (XPS).•Nitrogen content was independent of incident ion energy over the range studied.•Reaction and sputtering competing processes explaining observations.•XPS and monte carlo code TRIDYN used to extract effective reaction cross-sections.
Transition metal surfaces exposed to low-energy reactive ions undergo dynamic changes in composition and density due to implantation and compound formation. We report measurements of nitrogen ion induced sputter yields for transition metals relevant to fusion and optics applications. Thin films of molybdenum, ruthenium, palladium and tungsten are bombarded by nitrogen ions of kinetic energies in the range of 50–500 eV at steady state fluences (1 × 1018ions/cm2). Measured sputter yields are explained through energy and momentum transfer under the binary collision approximation using the Monte Carlo code TRIDYN. X-ray Photoelectron spectroscopy (XPS) studies showed the nitrogen content in the films at the end of ion exposure is independent of incoming ion energy. This occurs due to competing implantation and preferential surface nitrogen sputtering processes within the XPS probing depth. All metals investigated showed evidence of a nitride formed due to energetic nitrogen impact. The combination of XPS and TRIDYN simulations were applied to extract effective reaction cross-sections for each metal. |
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ISSN: | 0169-4332 1873-5584 |
DOI: | 10.1016/j.apsusc.2019.144529 |