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Research Article

N-doped carbon-stabilized PtCo nanoparticles derived from Pt@ZIF-67: Highly active and durable catalysts for oxygen reduction reaction

Nana Du1,2Chengming Wang1( )Ran Long1Yujie Xiong1 ( )
Hefei National Laboratory for Physical Sciences at the Microscale, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials)School of Chemistry and Materials Science, and National Synchrotron Radiation LaboratoryUniversity of Science and Technology of ChinaHefei230026China
School of Chemistry and Materials EngineeringFuyang Normal CollegeFuyang236041China
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Abstract

The development of catalysts with high activity and durability for the cathodic oxygen reduction reaction (ORR) in both alkaline and acidic media is important for improving the performance of the proton exchange membrane (PEM) fuel cells. This can be achieved by dispersing Pt-based alloy nanoparticles inside N-doped porous carbon frameworks. However, it still requires the development of a facile method towards synthesizing this unique hybrid structure. In this work, we demonstrate that N-doped carbon-stabilized PtCo nanoparticles (PtCo@NC) can be facilely synthesized via thermal decomposition of Pt-incorporated Co-based zeolitic imidazolate framework (Pt@ZIF-67). The thickness of the carbon framework can be optimized to enable excellent durability, in sharp contrast to a commercial Pt/C catalyst. The mass activities achieved by optimizing the thickness of the carbon framework are 0.80 and 0.82 A·mgPt–1 at 0.9 V vs. RHE in alkaline and acidic electrolytes, respectively, which are nearly 8 times greater than those of the Pt/C. This work provides an alternative approach to low-cost and high-performance catalysts for both alkaline and acidic fuel cells.

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Nano Research
Pages 3228-3237

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Cite this article:
Du N, Wang C, Long R, et al. N-doped carbon-stabilized PtCo nanoparticles derived from Pt@ZIF-67: Highly active and durable catalysts for oxygen reduction reaction. Nano Research, 2017, 10(9): 3228-3237. https://doi.org/10.1007/s12274-017-1611-6

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Received: 24 February 2017
Revised: 28 March 2017
Accepted: 01 April 2017
Published: 06 June 2017
© Tsinghua University Press and Springer-Verlag Berlin Heidelberg 2017