Pregled bibliografske jedinice broj: 1128176
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
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, 11 (2021), 10; 6210-6224 doi:10.1021/acscatal.0c05029 (međunarodna recenzija, članak, znanstveni)
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Naslov
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
Autori
Halder, Avik ; Lenardi, Cristina ; Timoshenko, Janis ; Mravak, Antonija ; Yang, Bing ; Kolipaka, Lakshmi K ; Piazzoni, Claudio ; Seifert, Sönke ; Bonačić-Koutecký, Vlasta ; Frenkel, Anatoly I. ; Milani, Paolo ; Vajda, Stefan
Izvornik
ACS Catalysis (2155-5435) 11
(2021), 10;
6210-6224
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
CO2conversion ; copper cluster ; DFT ; GISAXS ; reaction mechanism ; support effect ; XANES ; XPS
Sažetak
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 (∼3 nm thick film) and supersonic cluster beam deposition (nanostructured film, ∼100 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.
Izvorni jezik
Engleski
Znanstvena područja
Fizika, Kemija, Interdisciplinarne prirodne znanosti
POVEZANOST RADA
Projekti:
EK-KF-KK.01.1.1.01.0003 - STIM-REI (STIM-REI) (Bonačić-Koutecky, Vlasta; Smital, Tvrtko; Orlić, Sandi, EK - KK.01.1.1.01) ( CroRIS)
Ustanove:
Prirodoslovno-matematički fakultet, Split,
Sveučilište u Splitu
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus