Gold-supported two-dimensional cobalt oxyhydroxide (CoOOH) and multilayer cobalt oxide islands. Issue 3 (6th January 2017)

• Record Type: Journal Article
• Authors: Fester, Jakob; Walton, Alex; Li, Zheshen; Lauritsen, Jeppe V.
• Is Part Of: Physical chemistry chemical physics. Volume 19:Issue 3(2017)
• Page Start: 2425
• Page End: 2433
• Publication Date: 2017-01-06
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c6cp07901f
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : Synthesis and characterization of layered cobalt oxides for model studies of electrochemical water splitting catalysts. Abstract : In the present study, we investigate the facile conversion of Co–O bilayer islands on a Au(111) surface into preferentially O–Co–O trilayers in an oxygen atmosphere and O–Co–O–Co–O multilayers at elevated temperature. We characterize and compare the island morphologies with scanning tunneling microscopy, X-ray photoemission spectroscopy (XPS) and valence band spectroscopy, and show that the cobalt oxidation state changes from Co 2+ in bilayers to purely Co 3+ in trilayers and a mixture of Co 2+ and Co 3+ in the multilayer morphology. In contrast to bilayers and multilayers, the trilayer structure appears to grow pseudomorphic with the Au(111) substrate, and in addition we reveal the presence of a hydroxyl overlayer on this island type as evidenced by the appearance of a superstructure in STM correlated with the fingerprints of OH species in XPS and valence band spectroscopy. The obtained layered morphology consisting of hydroxylated trilayer islands is identical to an exfoliated sheet of the β-CoOOH which is proposed to be the active phase of the cobalt oxide oxygen evolution reaction catalyst present in the electrochemical environment, and we note that this synthesized structure thus could serve as a valuable model catalyst.