The suitable interfacial combination of CeO2 and oxidized carbon nanohorns (CeO2@oxCNHs) is instrumental to the control of the activity and selectivity in CO2 reduction reaction (CO2RR). This study presents a newly developed synthetic approach that integrates the CeO2 and CNH to form extended interfacial domains, resulting in a higher performance for CO2RR as compared with previously reported ceria-nanocarbon catalysts. In particular, detailed electrochemical characterization reveals that the CeO2@oxCNHs nanocomposite synthesized with this newly developed solvothermal method exhibits up to ten times higher current density (j) than its counterpart prepared by conventional sol-gel method and can be effectively integrated into a state-of-the-art gas diffusion electrode (GDE) device. The combination of high-surface area oxCNH with the gas diffusion electrode configuration boosts the CeO2 efficiency in converting CO2 to products involving C─C couplings as ethanol and acetaldehyde, even at very low overpotentials, offering a promising pathway for developing nanocomposite materials for CO2 reduction.

Exploiting the Functionality of Cerium Oxide‐Modified Carbon Nanohorns Catalysts Toward Enhanced CO2 Reduction Performance / Pollice, Alessia; Cacioppo, Michele; Marchi, Miriam; Moro, Miriam; Paolucci, Francesco; Bonchio, Marcella; Prato, Maurizio; Valenti, Giovanni; Melchionna, Michele; Fornasiero, Paolo. - In: ADVANCED FUNCTIONAL MATERIALS. - ISSN 1616-301X. - ELETTRONICO. - (2025), pp. e09299.1-e09299.8. [10.1002/adfm.202509299]

Exploiting the Functionality of Cerium Oxide‐Modified Carbon Nanohorns Catalysts Toward Enhanced CO2 Reduction Performance

Cacioppo, Michele;Marchi, Miriam;Prato, Maurizio;Valenti, Giovanni
;
Melchionna, Michele
;
Fornasiero, Paolo
2025-01-01

Abstract

The suitable interfacial combination of CeO2 and oxidized carbon nanohorns (CeO2@oxCNHs) is instrumental to the control of the activity and selectivity in CO2 reduction reaction (CO2RR). This study presents a newly developed synthetic approach that integrates the CeO2 and CNH to form extended interfacial domains, resulting in a higher performance for CO2RR as compared with previously reported ceria-nanocarbon catalysts. In particular, detailed electrochemical characterization reveals that the CeO2@oxCNHs nanocomposite synthesized with this newly developed solvothermal method exhibits up to ten times higher current density (j) than its counterpart prepared by conventional sol-gel method and can be effectively integrated into a state-of-the-art gas diffusion electrode (GDE) device. The combination of high-surface area oxCNH with the gas diffusion electrode configuration boosts the CeO2 efficiency in converting CO2 to products involving C─C couplings as ethanol and acetaldehyde, even at very low overpotentials, offering a promising pathway for developing nanocomposite materials for CO2 reduction.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11368/3124822
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