4.8 Review

Thermodynamics and kinetics of CO2, CO, and H+ binding to the metal centre of CO2 reduction catalysts

Journal

CHEMICAL SOCIETY REVIEWS
Volume 41, Issue 6, Pages 2036-2051

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c1cs15278e

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Funding

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

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In our developing world, carbon dioxide has become one of the most abundant greenhouse gases in the atmosphere. It is a stable, inert, small molecule that continues to present significant challenges toward its chemical activation as a useful carbon end product. This tutorial review describes one approach to the reduction of carbon dioxide to carbon fuels, using cobalt and nickel molecular catalysts, with particular focus on studying the thermodynamics and kinetics of CO2 binding to metal catalytic sites.

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