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PDI-Re FINAL (paper+supporting).pdf (7.41 MB)

Electron-Reservoir Effect on a Perylene Diimide Tethered Rhenium Bipyridine Complex for CO2 Reduction

preprint
submitted on 30.10.2020, 21:00 and posted on 02.11.2020, 10:04 by Josh D. B. Koenig, Zachary Dubrawski, Keerthan Rao, Janina Willkomm, Benjamin S. Gelfand, Chad Risko, Warren Piers, Gregory C. Welch
Here we report on a molecular catalyst with a built-in electron-reservoir for enhanced CO2 conversion. The synthesis and characterization of this N-annulated perylene diimide (PDI) photosensitized Re(bpy) supramolecular dyad [Re(bpy-TAz-PDI)], as well as successful electro- and photocatalytic CO2-to-CO conversion, are detailed herein. Upon electrochemical reduction in the presence of CO2 and a proton source, Re(bpy-TAz-PDI) exhibited significant current enhancement, where the onset of electrocatalytic CO2 reduction for Re(bpy-TAz-PDI) occurred at a much less negative potential than standard Re(bpy) complexes. At an applied potential of -1.8 V vs. Fc+/0, 400 mV lower than the benchmark Re(dmbpy) catalyst, Re(bpy-TAz-PDI) was able to achieve the same catalytic activity (TONco = 24) and Faradaic efficiency (FE = 92 %) during controlled potential electrolysis (CPE) experiments. Through a combination of UV-visible-nearIR spectroelectrochemistry (SEC), FTIR SEC, and chemical reduction experiments, it was shown that the PDI-moiety served as an electron-reservoir for Re(bpy), thereby allowing catalytic activity at lower overpotentials. Density functional theory (DFT) studies probing the optimized geometries, frontier molecular orbitals, and spin-densities of various catalytic intermediates revealed that the geometric configuration of PDI, relative to the Re(bpy)-moiety, plays a critical role in accessing electrons from the electron-reservoir. The near identical performance of Re(bpy-TAz-PDI) at lower overpotentials relative to the benchmark Re(dmbpy) catalyst highlights the utility of organic chromophore electron-reservoirs as a method for lowering the required overpotential for CO2 conversion.

History

Email Address of Submitting Author

wpiers@ucalgary.ca

Institution

University of Calgary

Country

Canada

ORCID For Submitting Author

0000-0003-2278-1269

Declaration of Conflict of Interest

No conflict of interest

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