Theoretical study of electrochemical reduction of CO2 to CO using a nickel-N4-Schiff base complex.
Phys Chem Chem Phys
; 26(36): 24068-24077, 2024 Sep 18.
Article
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| MEDLINE
| ID: mdl-39248005
ABSTRACT
The electrochemical reduction (ECR) of CO2 to CO by nickel-N4-Schiff base complexes as catalysts was investigated using density functional theory (DFT). Three nickel complexes, 1-Ni, 2-Ni, and [2-Ni]Me were considered. Two CO2 reduction pathways, i.e., external and internal proton transfer, were proposed and their reaction energy profiles were computed. The external proton transfer pathway which includes three steps has no transition state. The reaction energies for all steps are exothermic and the reaction catalyzed by 1-Ni has the lowest overall reaction energy (-5.72 eV) followed by those by 2-Ni (-5.56 eV) and [2-Ni]Me (-5.54 eV). The internal proton transfer pathway is composed of four steps. The internal proton transfer step (carboxylic formation) includes a transition state. The CO2 reduction by [2-Ni]Me could not proceed via this mechanism, since [2-Ni]Me does not have an NH group in the ligand and 1-Ni has a lower activation energy (0.83 eV), which is in agreement with the experiment. The charge of the pre-adsorption nickel complex seems to be related to the activity of the catalysts. The catalyst with a less positive nickel charge is more active.
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1
Colección:
01-internacional
Base de datos:
MEDLINE
Idioma:
En
Revista:
Phys Chem Chem Phys
Asunto de la revista:
BIOFISICA
/
QUIMICA
Año:
2024
Tipo del documento:
Article
País de afiliación:
Tailandia
Pais de publicación:
Reino Unido