Iron Oxide Nanoclusters Incorporated into Iron Phthalocyanine as Highly Active Electrocatalysts for the Oxygen Reduction Reaction
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This is the peer reviewed version of the following article: Y. Cheng, J. Liang, J.-P. Veder, M. Li, S. Chen, J. Pan, L. Song, H.-M. Cheng, C. Liu, S. P. Jiang, ChemCatChem 2018, 10, 475, which has been published in final form at https://doi.org/10.1002/cctc.201701183. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.
© 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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