Iron Oxide Nanoclusters Incorporated into Iron Phthalocyanine as Highly Active Electrocatalysts for the Oxygen Reduction Reaction
© 2018 Wiley-VCH Verlag. Iron-nitrogen-carbon (Fe-N-C) composites have emerged as active and non-precious-metal electrocatalysts for the oxygen reduction reaction (ORR). Here, we developed a simple process to synthesize FeO x nanoclusters (NCs) incorporated with iron phthalocyanine (FePc) supported...
| Main Authors: | , , , , , , , , , |
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| Format: | Journal Article |
| Published: |
WILEY-V C H VERLAG GMBH,
2018
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| Online Access: | http://purl.org/au-research/grants/arc/DP150102044 http://hdl.handle.net/20.500.11937/65730 |
| Summary: | © 2018 Wiley-VCH Verlag. Iron-nitrogen-carbon (Fe-N-C) composites have emerged as active and non-precious-metal electrocatalysts for the oxygen reduction reaction (ORR). Here, we developed a simple process to synthesize FeO x nanoclusters (NCs) incorporated with iron phthalocyanine (FePc) supported on graphene (FeO x /FePc) as highly active electrocatalysts for the ORR by a self-assembly method. The electrochemical activity of FeO x /FePc depends on the loading or size of the FeO x NCs. The best results are obtained on FeO x /FePc with 10 wt % FeO x NCs of a size of approximately 2 nm and a thickness of approximately 0.6 nm, which achieves a half-wave potential of 0.888 V and current density of 37.6 Ag -1 at 0.9 V (vs. the reversible hydrogen electrode). This is 50 mV higher than that of FePc supported on graphene and 64 mV higher than that of Pt/C in 0.1 m KOH solution at a catalyst loading of 0.1 mg cm -2 . X-ray absorption spectroscopy and electrochemical cyclic voltammetry results indicate that the incorporated FeO x NCs interact with the active center of FePc, Fe-N 4 , to enhance the electron transition and reversibility of the Fe III /Fe II redox couple and promote the kinetics of the ORR. We demonstrate that the nature of the active center of FePc (i.e., Fe-N 4 ) is related closely to the activity of the Fe III /Fe II redox couple. |
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