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Electrochemical Conversion of CO 2 to CO by a Competent Fe I Intermediate Bearing a Schiff Base Ligand
Author(s) -
Bonetto Ruggero,
Altieri Roberto,
Tagliapietra Mirko,
Barbon Antonio,
Bonchio Marcella,
Robert Marc,
Sartorel Andrea
Publication year - 2020
Publication title -
chemsuschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.412
H-Index - 157
eISSN - 1864-564X
pISSN - 1864-5631
DOI - 10.1002/cssc.202001143
Subject(s) - faraday efficiency , overpotential , catalysis , chemistry , electrochemistry , ligand (biochemistry) , inorganic chemistry , electrocatalyst , schiff base , selectivity , acetonitrile , photochemistry , electrode , polymer chemistry , organic chemistry , biochemistry , receptor
Iron complexes with a N 2 O 2 ‐type N,N ′ ‐bis(salicylaldehyde)‐1,2‐phenylenediamine salophen ligand catalyze the electrochemical reduction of CO 2 to CO in acetonitrile with phenol as the proton donor, giving rise to 90–99 % selectivity, faradaic efficiency up to 58 %, and turnover frequency up to 10 3 s −1 at an overpotential of 0.65 V. This novel class of molecular catalyst for CO 2 reduction operate through a mononuclear Fe I intermediate, with phenol being involved in the process with first‐order kinetics. The molecular nature of the catalyst and the low cost, easy synthesis and functionalization of the salophen ligand paves the way for catalyst engineering and optimization. Competitive electrodeposition of the coordination complex at the electrode surface results in the formation of iron‐based nanoparticles, which are active towards heterogeneous electrocatalytic processes mainly leading to proton reduction to hydrogen (faradaic efficiency up to 80 %) but also to the direct reduction of CO 2 to methane with a faradaic efficiency of 1–2 %.