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Selective CO2 Reduction to CO and Alcohols without Platinum or Noble Group Electrodes

Project description

Improved electrochemical conversion of CO2: cost-effective, highly selective and sustainable

Carbon-containing compounds are the feedstock for a plethora of chemicals and polymers including plastics, rubbers and detergents. Greener alternatives are a key goal of the chemical industry as most are sourced from fossil resources. Electrochemical conversion of CO2 is one of the most promising pathways, yet it faces challenges. These include the need to use iridium-based anodes to avoid the acidification of CO2 electrolysers and the difficulty in achieving high selectivity in the production of high-energy-density alcohols. The ERC-funded RECALLCO2 project will attempt to remove these obstacles. They will develop a novel electrochemical cell design, molecular catalytic architectures that overcome current limitations, and coupling with metal rather than carbon electrodes.

Objective

The electrochemical conversion of CO2 to carbon-based feedstocks represents one of few technological routes capable of replacing fossil fuel derivatives. Despite substantial advancements, however, major challenges impair CO2 electrolysis from matching its promise. Critically, steady acidification of CO2 electrolyzers during operation currently necessitates the use of iridium-based anodes. This is unacceptable from a cost and resource availability perspective. More fundamentally, while CO2 reduction to CO, formate and ethylene has become highly selective, the production of high-energy density alcohols with high selectivity has been elusive. To overcome these barriers, new scientific approaches are needed.

RECALLCO2 will resolve iridium dependencies and non-selective alcohol production in CO2 electrolysis through a combination of novel electrochemical cell design and the development of molecular catalytic architectures which break existing fundamental limitations. On the system design front, I will micro manipulate reagent, ionic and water fluxes to inhibit nickel corrosion pathways which presently necessitate iridium anodes. This will be the first-ever intrinsically stable CO2 electrolyzer capable of using nickel anodes.

A second pillar is the conceptualization that strong electronic-coupling of metal complexes to metal electrodes can eliminate redox-controlled reaction pathways on molecular catalysts. This counters decades of work using carbon electrodes as supports. Coupling with a metal electrode will delink electron transfers from a molecular catalysts oxidation states, and fundamentally change catalytic behaviour that currently restricts reactions to 2 electrons. Thus, CO2 reduction products such as methanol (6 electrons) and ethanol (12 electrons) will become viable. Utilizing this counterintuitive approach, I will push alcohol synthesis well beyond state-of-the-art selectivity and reaction rates, giving renewed promise for producing these compounds.

Fields of science (EuroSciVoc)

Keywords

Programme(s)

Topic(s)

Funding Scheme

HORIZON-ERC - HORIZON ERC Grants

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Call for proposal

(opens in new window) ERC-2023-STG

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Host institution

TECHNISCHE UNIVERSITEIT DELFT
Net EU contribution
€ 1 500 000,00
Total cost
€ 1 500 000,00

Beneficiaries (1)