Jurado A., David A., Higham, Michael D., Catlow, C. Richard A. ![]() ![]() |
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Abstract
The mechanism of CO2 hydrogenation to methanol is modelled using plane‐wave DFT applied to a representative Cu8‐ZnO(CZ) model, reported previously, with aluminium substituting a bulk Zn (= Cu/ZnO/Al2O3(CZA)). On CZA, CO2 adsorption and activation are enhanced at the active Cu/ZnO interface compared to systems with a Cu‐based or CZ‐based interface, demonstrating Al's electronic effect. Methanol formation at CZA follows the formate path: CO2*→ HCOO*→ H2COO*→ H2COOH*→ H2CO*→ H2COH*→ H3COH, with small contributions from the RWGS mechanism. Methoxy's binding is enhanced, making it a dead‐end and not an intermediate as on CZ. Formate intermediate at the Cu/Zn interface in CZA is electronically destabilized through Al. By contrast, other surface formates are stabilized and act as spectators. The most energy demanding step is the hydrogenation of formate to dioxomethylene (Ea = 1.08 eV) and not methoxy hydrogenation as on CZ. Multiple species are able to scavenge O* regenerating the active interfacial site. OH* was found to poison the active site, although its formation is energy demanding, making the CZA system overall more selective to MeOH than CZ. Water formation occurs on the Cu site as on the CZ system, although Zn sites can stabilize adsorbed water consistent to on experiments at CZA.
Item Type: | Article |
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Date Type: | Published Online |
Status: | In Press |
Schools: | Schools > Chemistry |
Additional Information: | License information from Publisher: LICENSE 1: URL: http://creativecommons.org/licenses/by/4.0/ |
Publisher: | Wiley |
ISSN: | 1867-3880 |
Date of First Compliant Deposit: | 18 August 2025 |
Date of Acceptance: | 22 July 2025 |
Last Modified: | 18 Aug 2025 09:45 |
URI: | https://orca.cardiff.ac.uk/id/eprint/180477 |
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