Hydrogen-induced atomic structure evolution of the oxygen-chemisorbed Cu(110) surface

Weitao Shan; Qianqian Liu; Jonathan Li; Na Cai; Wissam A Saidi; Guangwen Zhou

doi:10.1063/1.4972070

Hydrogen-induced atomic structure evolution of the oxygen-chemisorbed Cu(110) surface

J Chem Phys. 2016 Dec 21;145(23):234704. doi: 10.1063/1.4972070.

Authors

Weitao Shan¹, Qianqian Liu¹, Jonathan Li², Na Cai¹, Wissam A Saidi³, Guangwen Zhou¹

Affiliations

¹ Department of Mechanical Engineering and Materials Science and Engineering Program, State University of New York, Binghamton, New York 13902, USA.
² Department of Physics, Applied Physics and Astronomy and Materials Science and Engineering Program, State University of New York, Binghamton, New York 13902, USA.
³ Department of Mechanical Engineering and Materials Science, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, USA.

PMID: 28010088
DOI: 10.1063/1.4972070

Abstract

Using a combination of scanning tunneling microscopy (STM) and density functional theory (DFT) modeling, we determine the mechanism of the atomic structural evolution of the oxygenated Cu(110) surface induced by the reaction of adsorbed hydrogen with chemisorbed oxygen in the Cu(110)-c(6 × 2)-O structure. Our STM observations show that the reconstructed Cu(110)-c(6 × 2)-O surface undergoes a phase transition to the (2 × 1)-O reconstruction in the course of oxygen loss induced by the reaction with H₂ gas. Using DFT modeling, we find that the surface phase transition is initiated via the adsorption of molecular hydrogen on the chemisorbed oxygen, which results in the formation of H₂O molecules that desorb spontaneously from the surface. The loss of chemisorbed oxygen induces the c(6 × 2) → (2 × 1) transition that involves the diffusion of Cu-O-Cu chains along the ⟨1¯10⟩ direction.