Electron-Rich Pincer Ligand-Coupled Cobalt Porphyrin Polymer with Single-Atom Sites for Efficient (Photo)Electrocatalytic CO2 Reduction at Ultralow Overpotential.
Small
; 17(45): e2102957, 2021 Nov.
Article
em En
| MEDLINE
| ID: mdl-34585522
ABSTRACT
Porphyrin and phthalocyanine complexes bearing single-atom catalytic sites (M-N4 ) have been explored as promising electrocatalysts for CO2 reduction reaction (CO2 RR), whose activity can be improved by regulating the ligands and/or the metal centers. Moreover, their photosensitive features also provide the possibility for highly efficient photoelectrocatalytic CO2 RR. Herein, a novel N'NN'-pincer-ligand (N3 )-coupled cobalt porphyrin (CoPor-N3 ) polymer is developed for realizing efficient (photo)electrocatalytic CO2 RR. The unraveled electronic structure and (photo)electrocatalytic features suggest that a synergistic effect between the electron-rich N3 ligands and the Co-N4 single-atom sites in the CoPor-N3 polymer results in the Co centers attaining more electrons, which is beneficial to facilitating the electron transfer to CO2 for the activation and reduction processes. As expected, the resultant CoPor-N3 polymer delivers a good long-term durability and high CO faradaic efficiency (96%) at an ultralow overpotential (0.39 V), which outperforms the CoPor alone and most porphyrin-/phthalocyanine-based electrocatalysts reported so far. Moreover, the photosensitivity of CoPor units can further reduce the overpotential to 0.34 V with a CO faradaic efficiency over 90% under light illumination. The present findings offer a new approach to constructing porphyrin-based photosensitive electrocatalysts with high-efficiency photoelectrocatalytic CO2 RR.
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01-internacional
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MEDLINE
Idioma:
En
Revista:
Small
Assunto da revista:
ENGENHARIA BIOMEDICA
Ano de publicação:
2021
Tipo de documento:
Article