image: A Co porphyrin with a tethered imidazole for Co axial binding is synthesized, which outperforms its imidazole-free analog in electrocatalytic oxygen reduction and evolution reactions in alkaline aqueous solutions. view more
Credit: Journal of Energy Chemistry
Electrocatalytic oxygen reduction and evolution reactions occur in various fuel cells, metal-air batteries, and in water splitting devices. Large-scale use of noble metals and their complexes in industries are limited by their low abundance and high cost. Recently, several first-row transition metal complexes have been identified as active electrocatalysts for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). Nevertheless, only a few catalysts are efficient for both ORR and OER under identical conditions, which is crucial for use in rechargeable metal-air batteries.
Co porphyrins have been largely studied as catalysts for O2 reduction. In addition to ORR, Co porphyrins have been shown to be efficient electrocatalysts for OER. Despite these achievements, however, developing Co porphyrins with high activity and stability for both electrocatalytic oxygen reduction and evolution reactions under the same conditions is still required.
Recently Rui Cao and Weiqiang Zhang of Shaanxi Normal University, Shunichi Fukuzumi and Wonwoo Nam of Ewha Womans University and others published a letter titled “A cobalt(II) porphyrin with a tethered imidazole for efficient oxygen reduction and evolution electrocatalysis” in Journal of Energy Chemistry.
In cytochrome c oxidases (CcOs), Fe porphyrins with an axial histidine imidazole group catalyze the selective reduction of O2 to water. The axial imidazole group can increase the electron density of Fe, and thus improve O2 binding and activation at the Fe center through an electronic “push effect” (Fig. 1a). Inspired by nature, the authors report Co porphyrin 1 with an imidazole group appended to the porphyrin backbone for Co axial binding as an active bifunctional electrocatalyst for oxygen reduction and evolution reactions (Fig.1b). In addition, 1 was used as a catalyst in air electrodes for Zn-air batteries. The resulting Zn-air battery exhibited comparable performance to batteries made using commercial Pt/C and Ir/C materials. This work is significant as it highlights the important role of axial ligands in enhancing ORR and OER and shows the potential applications of molecular catalysts in electrocatalysis-based energy conversion and storage technologies.
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The Journal of Energy Chemistry is a publication that mainly reports on creative researches and innovative applications of chemical conversions of fossil energy, carbon dioxide, electrochemical energy and hydrogen energy, as well as the conversions of biomass and solar energy related with chemical issues to promote academic exchanges in the field of energy chemistry and to accelerate the exploration, research and development of energy science and technologies.
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