4.8 Article

Earth-Abundant Photocatalytic CO2 Reduction by Multielectron Chargeable Cobalt Porphyrin Catalysts: High CO/H2 Selectivity in Water Based on Phase Mismatch in Frontier MO Association

Journal

ACS CATALYSIS
Volume 11, Issue 16, Pages 10436-10449

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.1c02475

Keywords

CO2 reduction; earth-abundant photosynthesis; water-soluble copper photosensitizer; multielectron chargeable cobalt porphyrin catalysts; DFT studies; effective MO association

Funding

  1. JSPS KAKENHI [JP18H01996, JP18H05171, JP21H01952]
  2. China Scholarship Council [201706650009]

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Efforts have been made to reduce CO2 emissions through photocatalytic and electrocatalytic CO2 reduction into fuels. A recent study focuses on developing environmentally friendly photo-catalytic systems, using non-precious-metal molecular CO2 reduction catalysts in aqueous conditions, and suppressing hydrogen evolution during CO2 reduction.
To stop global warming and climate changes, substantial efforts have been made to diminish CO2 emission. Photocatalytic and electrocatalytic CO2 reduction into fuels has thus become a highly important topic. Our recent interest has been to develop earth-abundant and environmentally friendly photo-catalytic systems consisting of a non-precious-metal molecular CO2 reduction catalyst combined with subcomponents, especially using aqueous conditions without any organic solvents. However, CO2 reduction in water suffers from a drawback of decreasing its reaction yield due to concomitant H-2 evolution, which can be driven by an overpotential less than that for CO2 reduction. Herein, we demonstrate a strategy to suppress H-2 evolution using a cobalt porphyrin CO2 reduction catalyst possessing four N-methylpyridinium acceptors. The H-2 evolution path is not favored by the active intermediate possessing a low-spin d(7) Co-II center because of its mismatch in forming an effective MO association with a 1s(H+) orbital. This is a rare example of catalysts avoiding the standard path relying on a filled (d(z2))(2) orbital in binding CO2. Instead, both pi- and sigma-type frontier MO associations are simultaneously formed by two degenerated p*(CO2) orbitals using a filled (d(xz))(2) and a half-filled (d(z2))(1) orbital. We also find that highly electron charged intermediates show switching in configuration from (d(xz))(2)(d(z2))(1) to (d(xz))(1)(d(z2))(2), leading us to allow the standard sigma-type interaction with CO2. Correlation between the multielectron charging behaviors of cobalt porphyrins and the mechanism of photo- and electrocatalytic CO2 reduction is rationalized using our electrochemical and DFT results. This study sheds a light on strategies to rationally control the reaction rates and pathways based on the frontier MO engineering.

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