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CO2 Adsorption and Hydrogenation on Inverse InOx/Cu(111) Catalysts: Active Role of the Oxide–Metal Interface

Journal Article · · ACS Applied Materials and Interfaces
 [1];  [2];  [1];  [3];  [2];  [2];  [4]
  1. Brookhaven National Laboratory (BNL), Upton, NY (United States)
  2. Brookhaven National Laboratory (BNL), Upton, NY (United States). National Synchrotron Light Source II (NSLS-II)
  3. Stony Brook Univ., NY (United States)
  4. Brookhaven National Laboratory (BNL), Upton, NY (United States); Stony Brook Univ., NY (United States)
The direct conversion of carbon dioxide (CO2) into methanol via hydrogenation is essential for industrial applications. Recent studies on catalysts that contain an inverse oxide/metal configuration have shown very good catalytic performance for the CO2 hydrogenation to methanol process. Here, in this study, we investigated the behavior of indium oxide-Cu(111) interfaces under pure CO2 and CO2/H2 mixtures using synchrotron-based ambient-pressure X-ray photoelectron spectroscopy (AP-XPS). Initially, a single layer of copper oxide (CuxO) was grown on the Cu(111) surface by controlled oxidation. On this surface, indium was deposited at room temperature. Oxygen atoms transferred from CuxO/Cu(111) to the indium metal upon deposition, forming In-O-Cu bonds and active interfaces. Although Cu(111) is not very active for the binding and activation of CO2, the formed InOx-Cu(111) interfaces had no problem adsorbing and dissociating the molecule at room temperature. Reaction of CO2 with H2 on InOx-Cu(111) yielded surface-bound H3CO, CO2δ−, CO3, and CHx species that are typical intermediates in the production of methanol and other oxygenates. The InOx-Cu(111) interface underwent dynamic chemical changes under reaction conditions, forming In-Cu alloys at low indium coverages (< 0.05 monolayer), while at higher indium coverages a mixture of an In-Cu and InOx was detected in XPS. These findings indicate that InOx/In-Cu interfaces can play a key role in processes aimed at the trapping and valorization of CO2.
Research Organization:
Brookhaven National Laboratory (BNL), Upton, NY (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES). Chemical Sciences, Geosciences & Biosciences Division (CSGB); USDOE Office of Science (SC), Basic Energy Sciences (BES). Scientific User Facilities (SUF)
Grant/Contract Number:
SC0012704
OSTI ID:
2570558
Report Number(s):
BNL--228357-2025-JAAM
Journal Information:
ACS Applied Materials and Interfaces, Journal Name: ACS Applied Materials and Interfaces Journal Issue: 25 Vol. 17; ISSN 1944-8244; ISSN 1944-8252
Publisher:
American Chemical Society (ACS)Copyright Statement
Country of Publication:
United States
Language:
English

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