How oxygen passivates polycrystalline nickel surfaces.

Autor: Wong CS; Sandia National Laboratories, Livermore, California 94550, USA., Wang CS; Sandia National Laboratories, Livermore, California 94550, USA., Whaley JA; Sandia National Laboratories, Livermore, California 94550, USA., Sugar JD; Sandia National Laboratories, Livermore, California 94550, USA., Kolasinski RD; Sandia National Laboratories, Livermore, California 94550, USA., Thürmer K; Sandia National Laboratories, Livermore, California 94550, USA.
Jazyk: angličtina
Zdroj: The Journal of chemical physics [J Chem Phys] 2021 Sep 07; Vol. 155 (9), pp. 094701.
DOI: 10.1063/5.0060352
Abstrakt: The passivation of polycrystalline nickel surfaces against hydrogen uptake by oxygen is investigated experimentally with low energy ion scattering (LEIS), direct recoil spectroscopy (DRS), and thermal desorption spectroscopy (TDS). These techniques are highly sensitive to surface hydrogen, allowing the change in hydrogen adsorption in response to varying amounts of oxygen exposure to be measured. The chemical composition of a nickel surface during a mixed oxygen and hydrogen exposure was characterized with LEIS and DRS, while the uptake and activation energies of hydrogen on a nickel surface with preadsorbed oxygen were quantified with TDS. By and large, these measurements of how the oxygen and hydrogen surface coverage varied in response to oxygen exposure were found to be consistent with predictions of a simple site-blocking model. This finding suggests that, despite the complexities that arise due to polycrystallinity, the oxygen-induced passivation of a polycrystalline nickel surface against hydrogen uptake can be approximated by a simple site-blocking model.
Databáze: MEDLINE