4.8 Article

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

Journal

ENERGY & ENVIRONMENTAL SCIENCE
Volume 5, Issue 11, Pages 9502-9510

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2ee22528j

Keywords

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Funding

  1. U.S. Department of Energy [DE-AC02-98CH10886]
  2. Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences
  3. Toyota Motor Engineering & Manufacturing North America, Inc.

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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(a)s: 0.5-2), the F.E.s are still high but product selectivity changes to yield predominantly H-2 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 similar to 10 M-1 for the reaction of Ni-I with CO2 in aqueous solution.

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