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Molecular Electrochemical Catalysis of CO-to-Formaldehyde Conversion with a Cobalt Complex.
Singh, Ajeet; Zamader, Afridi; Khakpour, Reza; Laasonen, Kari; Busch, Michael; Robert, Marc.
Afiliación
  • Singh A; Université Paris Cité, CNRS, Laboratoire d'Electrochimie Moléculaire (LEM), F-75013 Paris, France.
  • Zamader A; Université Paris Cité, CNRS, Laboratoire d'Electrochimie Moléculaire (LEM), F-75013 Paris, France.
  • Khakpour R; Department of Chemistry and Material Science, School of Chemical Engineering, Aalto University, 02150 Espoo, Finland.
  • Laasonen K; Department of Chemistry and Material Science, School of Chemical Engineering, Aalto University, 02150 Espoo, Finland.
  • Busch M; Division of Materials Science, Department of Engineering Sciences and Mathematics, Luleå University of Technology, 971 87 Luleå, Sweden.
  • Robert M; Wallenberg Initiative Materials Science for Sustainability (WISE), Luleå University of Technology, 971 87 Luleå, Sweden.
J Am Chem Soc ; 146(32): 22129-22133, 2024 Aug 14.
Article en En | MEDLINE | ID: mdl-39083037
ABSTRACT
Formox, a highly energy-intensive process, currently serves as the primary source of formaldehyde (HCHO), for which there is a crucial and steadily growing chemical demand. The alternative electrochemical production of HCHO from C1 carbon sources such as CO2 and CO is still in its early stages, with even the few identified cases lacking mechanistic rationalization. In this study, we demonstrate that cobalt phthalocyanine (CoPc) immobilized on multiwalled carbon nanotubes (MW-CNTs) constitutes an excellent electrocatalytic system for producing HCHO with productivity through the direct reduction of CO, the two-electron reduction product of CO2. By carefully adjusting both the pH and the applied potential, we identified conditions that enable the production of HCHO with a partial current density of 0.64 mA cm-2 (17.5% Faradaic efficiency, FE) and a total FE of 61.2% for the liquid products (formaldehyde and methanol). A reduction mechanism is proposed.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2024 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2024 Tipo del documento: Article País de afiliación: Francia