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
Hauptverfasser: Zhang, Sike, Zhou, Qixing, Fang, Linya, Wang, Rui, Lu, Tingyu, Zhao, Qun, Gu, Xuefang, Tian, Shu, Xu, Lin, Pang, Huan, Yang, Jun, Tang, Yawen, Sun, Shuhui
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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. [Display omitted] •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.
ISSN:0926-3373
1873-3883
DOI:10.1016/j.apcatb.2023.122489