Published August 9, 2019 | Version v1
Journal article

Electrospun Fe2C-loaded carbon nanofibers as efficient electrocatalysts for oxygen reduction reaction

  • 1. State Key Laboratory of Organic-Inorganic Composites, Beijing Key Laboratory of Advanced Functional Polymer Composites, and College of Materials Science and Engineering, Beijing University of Chemical Technology, Beijing, 100029 (China)
  • 2. Institute for Frontier Materials, Deakin University, Waurn Ponds, Vic 3216 (Australia)

Description

Carbon-based non-precious metal catalysts have been regarded as the most promising alternatives to the state-of-art Pt/C catalyst for the oxygen reduction reaction (ORR). However, there are still some unresolved challenges such as agglomeration of nanoparticles, complex preparation process and low production efficiency, which severely hamper the large-scale production of non-precious metal catalysts. Herein, a novel carbon-based non-precious metal catalyst, i.e. iron carbide nanoparticles embedded on carbon nanofibers (Fe2C/CNFs), prepared via the direct pyrolysis of carbon- and iron-containing Janus fibrous precursors obtained by electrospinning. The Fe2C/CNF catalyst shows uniform dispersion and narrow size distribution of Fe2C nanoparticles embedded on the CNFs. The obtained catalyst exhibits positive onset potential (0.87 V versus RHE), large kinetic current density (1.9 mA cm−2), and nearly follows the effective four-electron route, suggesting an outstanding electrocatalytic activity for the ORR in 0.1 M of KOH solution. Besides, its stability is better than that of the commercial Pt/C catalyst, due to the strong binding force between Fe2C particles and CNFs. This strategy opens new avenues for the design and efficient production of promising electrocatalysts for the ORR. (paper)

Availability note (English)

Available from http://dx.doi.org/10.1088/1361-6528/ab1777

Additional details

Identifiers

Publishing Information

Journal Title
Nanotechnology (Print)
Journal Volume
30
Journal Issue
32
Journal Page Range
[8 p.]
ISSN
0957-4484