CO2 Methanation on Cu-Cluster Decorated Zirconia Supports with Different Morphology: A Combined Experimental In Situ GIXANES/GISAXS, Ex Situ XPS and Theoretical DFT Study

0543566 - ÚFCH JH 2022 RIV US eng J - Journal Article
Halder, A. - Lenardi, C. - Timoshenko, J. - Mravak, A. - Yang, B. - Kolipaka, L. K. - Piazzoni, C. - Seifert, S. - Bonačić-Koutecký, V. - Frenkel, A. I. - Milani, P. - Vajda, Štefan
CO2 Methanation on Cu-Cluster Decorated Zirconia Supports with Different Morphology: A Combined Experimental In Situ GIXANES/GISAXS, Ex Situ XPS and Theoretical DFT Study.
ACS Catalysis. Roč. 11, č. 10 (2021), s. 6210-6224. ISSN 2155-5435. E-ISSN 2155-5435
EU Projects: European Commission(XE) 810310
Institutional support: RVO:61388955
Keywords : CO conversion 2 * copper cluster * dft * gisaxs * reaction mechanism * support effect * xanes * xps
OECD category: Physical chemistry
Impact factor: 13.700, year: 2021
Method of publishing: Limited access

Subnanometer copper tetramer-zirconia catalysts turn out to be highly efficient for CO2 hydrogenation and its conversion to methane. The cluster size and substrate morphology are controlled to optimize the catalytic performance. The two types of zirconia supports investigated are prepared by atomic layer deposition (μ3 nm thick film) and supersonic cluster beam deposition (nanostructured film, μ100 nm thick). The substrate plays a crucial role in determining the activity of the catalyst as well as its cyclability over repeated thermal ramps. A temperature-programmed reaction combined with in situ X-ray characterization reveals the correlation between the evolution in the oxidation state and catalytic activity. Ex situ photoelectron spectroscopy indicates Cu clusters with stronger interactions with the nanostructured film, which can be the cause for the higher activity of this catalyst. Density functional theory calculations based on the Cu4O2 cluster supported on a ZrOx subunit reveal low activation barriers and provide mechanism for CO2 hydrogenation and its conversion to methane. Altogether, the results show a new way to tune the catalytic activity of CO2 hydrogenation catalysts through controlling the morphology of the support at the nanoscale.
Permanent Link: http://hdl.handle.net/11104/0320753