Gram-scale synthesis and unraveling the activity origin of atomically dispersed Co-N4O sites toward superior electrocatalytic oxygen reduction
Exploring highly efficient nonprecious metal-based single-atom catalysts (SACs) toward the electrocatalytic oxygen reduction reaction (ORR) is critical for the sustainable development of ORR-related energy conversion and storage systems. However, the scalable synthesis, delicate regulation of the co...
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Veröffentlicht in: | Applied catalysis. B, Environmental Environmental, 2023-07, Vol.328, p.122489, Article 122489 |
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Sprache: | eng |
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Zusammenfassung: | Exploring highly efficient nonprecious metal-based single-atom catalysts (SACs) toward the electrocatalytic oxygen reduction reaction (ORR) is critical for the sustainable development of ORR-related energy conversion and storage systems. However, the scalable synthesis, delicate regulation of the coordination environment and molecular-level elucidation of the electrocatalytic mechanism remain challenging. Herein, we report a facile gram-scale synthesis of atomically dispersed Co sites anchored on N-doped carbon nanofibers (noted as Co-SA@N-CNFs) via a reliable predesigned phenolic resin-mediated strategy for efficient oxygen reduction electrocatalysis. The local coordination configuration of the single-atomic Co sites is proposed as the Co-N4O moiety with one O atom in the axial direction perpendicular to the Co-N4 plane. Theoretical calculations uncover that, compared with the common Co-N4 single sites, the formation of Co-N4O configuration is beneficial to reduce the reaction energy barrier, adjust the bond length between the metal sites and the intermediates, and also increase the electric conductivity. Therefore, the Co-SA@N-CNFs demonstrated distinguished ORR activity, outstanding electrochemical stability and methanol tolerance in KOH electrolyte. Furthermore, when assembled in liquid and flexible solid-state rechargeable zinc-air batteries (ZABs), the Co-SA@N-CNFs-equipped ZABs exhibited higher power densities, larger specific capacities and extraordinary cycling performance, compared with the Pt/C-based ZABs. The simple and robust methodology for the mass production of SACs and the engineered coordination environment for performance optimization inspire the future design of a wide range of SACs for energy devices.
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•A facile and robust “phenolic resin-bridged” synthesis of single-atom catalysts is developed.•The Co-SA@N-CNFs exhibit excellent ORR activity and high methanol tolerance.•The axial O atom modulates the coordination environment of center Co atoms•The Zn-air battery equipped with Co-SA@N-CNFs shows superior cycling stability. |
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ISSN: | 0926-3373 1873-3883 |
DOI: | 10.1016/j.apcatb.2023.122489 |