Summary
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 catalyst’s 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.
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 catalyst’s 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.
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| Web resources: | https://cordis.europa.eu/project/id/101117270 |
| Start date: | 01-12-2023 |
| End date: | 30-11-2028 |
| Total budget - Public funding: | 1 500 000,00 Euro - 1 500 000,00 Euro |
Cordis data
Original description
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 catalyst’s 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.
Status
SIGNEDCall topic
ERC-2023-STGUpdate Date
12-03-2024
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