Selective CO<sub>2</sub> electrolysis to CO using isolated antimony alloyed copper.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 36670129.
- Also identified by DOI 10.1038/s41467-023-35960-z and PMC identifier 9860050.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Renewable electricity-powered CO evolution from CO<sub>2</sub> emissions is a promising first step in the sustainable production of commodity chemicals, but performing electrochemical CO<sub>2</sub> reduction economically at scale is challenging since only noble metals, for example, gold and silver, have shown high performance for CO<sub>2</sub>-to-CO. Cu is a potential catalyst to achieve CO<sub>2</sub> reduction to CO at the industrial scale, but the C-C coupling process on Cu significantly depletes CO* intermediates, thus limiting the CO evolution rate and producing many hydrocarbon and oxygenate mixtures. Herein, we tune the CO selectivity of Cu by alloying a second metal Sb into Cu, and report an antimony-copper single-atom alloy catalyst (Sb<sub>1</sub>Cu) of isolated Sb-Cu interfaces that catalyzes the efficient conversion of CO<sub>2</sub>-to-CO with a Faradaic efficiency over 95%. The partial current density reaches 452 mA cm<sup>-2</sup> with approximately 91% CO Faradaic efficiency, and negligible C<sub>2+</sub> products are observed. In situ spectroscopic measurements and theoretical simulations reason that the atomic Sb-Cu interface in Cu promotes CO<sub>2</sub> adsorption/activation and weakens the binding strength of CO*, which ends up with enhanced CO selectivity and production rates.