Manganese Electrocatalysts with Bulky Bipyridine Ligands: Utilizing Lewis Acids To Promote Carbon Dioxide Reduction at Low Overpotentials

• Published in: Journal of the American Chemical Society Vol. 138; no. 4; pp. 1386 - 1393
• Main Authors: Sampson, Matthew D, Kubiak, Clifford P
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 03-02-2016
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/jacs.5b12215

Earth-abundant manganese bipyridine (bpy) complexes are well-established molecular electrocatalysts for proton-coupled carbon dioxide (CO2) reduction to carbon monoxide (CO). Recently, a bulky bipyridine ligand, 6,6′-dimesityl-2,2′-bipyridine (mesbpy), was utilized to significantly lower the potential necessary to access the doubly reduced states of these manganese catalysts by eliminating their ability to dimerize after one-electron reduction. Although this Mn mesbpy catalyst binds CO2 at very low potentials, reduction of a resulting Mn­(I)–COOH complex at significantly more negative potentials is required to achieve fast catalytic rates. Without reduction of Mn­(I)–COOH, catalysis occurs slowly via a alternate catalytic pathway–protonation of Mn­(I)–COOH to form a cationic tetracarbonyl complex. We report the use of Lewis acids, specifically Mg2+ cations, to significantly increase the rate of catalysis (by over 10-fold) at these low overpotentials (i.e., the same potential as CO2 binding). Reduction of CO2 occurs at one of the lowest overpotentials ever reported for molecular electrocatalysts (η = 0.3–0.45 V). With Mg2+, catalysis proceeds via a reductive disproportionation reaction of 2CO2 + 2e– → CO and CO3 2–. Insights into the catalytic mechanism were gained by using variable concentration cyclic voltammetry, infrared spectroelectrochemistry, and bulk electrolysis studies. The catalytic Tafel behavior (log turnover frequency vs overpotential relationship) of [Mn­(mesbpy)­(CO)3(MeCN)]­(OTf) with added Mg2+ is compared with those of other commonly studied CO2 reduction catalysts.