4.8 Article

Flexible carbon nanofiber film with diatomic Fe-Co sites for efficient oxygen reduction and evolution reactions in wearable zinc-air batteries

Journal

NANO ENERGY
Volume 87, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.nanoen.2021.106147

Keywords

Carbon nanofiber; Dual-site catalyst; Electrospinning; Bifunctional electro-catalyst; Zn-air battery

Funding

  1. National Natural Science Foundation of China (NSFC) [22071137, 21701101]
  2. National Key Research and Development Project [2018YFE0118200, 2016YFF0204402]
  3. Fundamental Research Funds for the Central Universities [18CX06063A]
  4. Shandong Scientific Research Awards Foundation for Outstanding Young Scientists [ZR2018JL010]
  5. Shandong Key Research and Development Project [2019JZZY010506]
  6. Opening Fund of State Key Laboratory of Heavy Oil Processing [SKLOP202002007]
  7. Program for Tsingtao Al-ion Power and Energy-storage Battery Research Team in the University [17211zhc]
  8. China Scholarship Council [201806450091]

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This study developed a highly efficient strategy for preparing large-area flexible CNF films with excellent bifunctional catalytic performance, achieved optimal electronic properties for ORR and OER through abundant FeN3-CoN3 sites. The resulting ZAB not only has high specific power and cycling stability, but also the excellent mechanical properties of Fe1Co1-CNF make it suitable for manufacturing portable ZAB with deformability and stability.
Carbon nanofiber (CNF) papers have been widely used in many renewable energy systems, and the development of its catalytic function is of great significance and a major challenge. In this work, we pioneer a time- and costefficient strategy for the preparation of large-area flexible CNF films with uniformly distributed diatomic FeN3CoN3 sites (Fe1Co1-CNF). Due to the excellent compatibility and similar functionality of the pre-designed ZnFeCo-NC precursors (ZnFeCo-pre) with the electrospun polymer polyacrylonitrile (PAN), the mixture of ZnFeCo-pre and PAN can be co-electrospun and subject to a standard CNF fabrication process. The resulting Fe1Co1-CNF exhibits excellent bifunctional catalytic performance for both oxygen reduction reaction (ORR) and oxygen evolution reaction (OER), attributing to the abundant dual catalytic FeN3-CoN3 sites which are mutually beneficial for attaining optimal electronic properties for the adsorption/desorption of reaction intermediates. The assembled liquid-electrolyte ZAB provides a high specific power of 201.7 mW cm-2 and excellent cycling stability. More importantly, due to the good mechanical strength and flexibility of Fe1Co1-CNF, portable ZAB with exceptional shape deformability and stability can be demonstrated, in which Fe1Co1-CNF utility as an integrated free-standing membrane electrode. These findings provide a facile strategy for manufacturing flexible multi-functional catalytic electrodes with high production.

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