Abstract
The photocatalytic reduction of carbon dioxide (CO2) represents an attractive approach for solar-energy storage and leads to the production of renewable fuels and valuable chemicals. Although some osmium (Os) photosensitizers absorb long wavelengths in the visible-light region, a self-photosensitized, mononuclear Os catalyst for red-light-driven CO2 reduction has not yet been exploited. Here, we discovered that the introduction of an Os metal to a PNNP-type tetradentate ligand resulted in the absorption of light with longer-wavelength (350–700 nm) and that can be applied to a panchromatic self-photosensitized catalyst for CO2 reduction to give mainly carbon monoxide (CO) with a total turnover number (TON) of 625 under photoirradiation (λ≥400 nm). CO2 photoreduction also proceeded under irradiation with blue (λ0=405 nm), green (λ0=525 nm), or red (λ0=630 nm) light to give CO with >90 % selectivity. The quantum efficiency using red light was determined to be 12 % for the generation of CO. A catalytic mechanism is proposed based on the detection of intermediates using various spectroscopic techniques, including transient absorption, electron paramagnetic resonance, and UV/Vis spectroscopy.
Original language | English |
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Article number | e202403886 |
Journal | Angewandte Chemie - International Edition |
Volume | 63 |
Issue number | 22 |
DOIs | |
State | Published - 27 May 2024 |
Bibliographical note
Publisher Copyright:© 2024 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH.
Keywords
- Carbon monoxide
- CO photoreduction
- Laser flash photolysis
- Osmium complex
- Photocatalyst