Nickel(ii) macrocycles: highly efficient electrocatalysts for the selective reduction of CO2 to CO

Abstract

A series of molecular materials that are structurally similar to the Ni^II macrocycle [Ni(cyclam)]²⁺ (cyclam = 1,4,8,11-tetraazacyclotetradecane) have been used as electrocatalysts for the reduction of CO₂ at a mercury pool working electrode in aqueous solution. At pH 5, with an applied potential of −0.96 V vs. NHE (overpotential of −0.55 V), the complexes are highly efficient, having both high rate constants and Faradaic efficiencies (F.E.s) for the selective reduction of CO₂ to CO. When the pH is below the pK_a (pH < 2) of the Ni(H) species (pK_as: 0.5–2), the F.E.s are still high but product selectivity changes to yield predominantly H₂ from the reduction of water. At least two of the complexes investigated are better electrocatalysts than [Ni(cyclam)]²⁺, probably due to: (i) surface geometries that are suitable for adsorption onto the mercury electrode surface, and (ii) electronic effects of methyl groups or cyclohexane rings on the cyclam backbone. Mechanistic studies by pulse radiolysis show evidence of Ni(CO₂) adducts for two of the catalysts, with K_CO2 ∼ 10 M⁻¹ for the reaction of Ni^I with CO₂ in aqueous solution.