Electronic and structural properties of single-crystal Jahn–Teller active Co1+xMn2−xO4 thin films. (12th January 2021)

• Record Type: Journal Article
• Authors: Blanchet, Miles D; Heath, Jonathan J; Kaspar, Tiffany C; Matthews, Bethany E; Spurgeon, Steven R; Bowden, Mark E; Heald, Steve M; Issacs-Smith, Tamara; Kuroda, Marcelo A; Comes, Ryan B
• Is Part Of: Journal of physics. Volume 33:Number 12(2021)
• Publication Date: 2021-01-12
• Subjects: CoMn2O4 -- molecular beam epitaxy -- x-ray photoelectron spectroscopy -- x-ray absorption spectroscopy -- density functional theory; Condensed matter -- Periodicals; Matière condensée -- Périodiques; Vaste stoffen; Vloeistoffen; Natuurkunde; Electronic journals; Computer network resources; 530.4105
• DOI: 10.1088/1361-648X/abd573
• Languages: English
• ISSNs: 0953-8984

Abstract

Abstract: Recent investigations on spinel CoMn2 O4 have shown its potential for applications in water splitting and fuel cell technologies as it exhibits strong catalytic behavior through oxygen reduction reactivity. To further understand this material, we report for the first time the synthesis of single-crystalline Co1+ x Mn2− x O4 thin films using molecular beam epitaxy. By varying sample composition, we establish links between cation stoichiometry and material properties using in-situ x-ray photoelectron spectroscopy, x-ray diffraction, scanning transmission electron microscopy, x-ray absorption spectroscopy, and spectroscopic ellipsometry. Our results indicate that excess Co ions occupy tetrahedral interstitial sites at lower excess Co stoichiometries, and become substitutional for octahedrally-coordinated Mn at higher Co levels. We compare these results with density functional theory models of stoichiometric CoMn2 O4 to understand how the Jahn–Teller distortion and hybridization in Mn–O bonds impact the ability to hole dope the material with excess Co. The findings provide important insights into CoMn2 O4 and related spinel oxides that are promising candidates for inexpensive oxygen reduction reaction catalysts.