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Iron Oxide Nanoclusters Incorporated into Iron Phthalocyanine as Highly Active Electrocatalysts for the Oxygen Reduction Reaction

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Authors
Cheng, Yi
Liang, J.
Veder, Jean-Pierre
Li, Meng
Chen, S.
Pan, Jian
Song, L.
Cheng, H.
Liu, C.
Jiang, San Ping
Date
2018
Type
Journal Article

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Cheng, Y. and Liang, J. and Veder, J. and Li, M. and Chen, S. and Pan, J. and Song, L. et al. 2018. Iron Oxide Nanoclusters Incorporated into Iron Phthalocyanine as Highly Active Electrocatalysts for the Oxygen Reduction Reaction. ChemCatChem. 10 (2): pp. 475-483.
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ChemCatChem
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John de Laeter Centre
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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.

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Abstract

© 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.