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Research Article

Dendritic platinum–copper bimetallic nanoassemblies with tunable composition and structure: Arginine-driven self-assembly and enhanced electrocatalytic activity

Gengtao Fu1,2Huimin Liu3Nika You1Jiayan Wu1Dongmei Sun1Lin Xu1Yawen Tang1( )Yu Chen3 ( )
Key Laboratory of Macromolecular Science of Shaanxi ProvinceSchool of Materials Science and EngineeringShaanxi Normal UniversityXi'an710062China
Jiangsu Key Laboratory of New Power BatteriesJiangsu Collaborative Innovation Centre of Biomedical Functional MaterialsSchool of Chemistry and Materials ScienceNanjing Normal UniversityNanjing210023China
Materials Science and Engineering Program & Texas Materials InstituteThe University of Texas at AustinAustinTexas78712USA
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Abstract

Novel self-assembled architectures have received a growing amount of attention and have significant potential for application in catalysis/electrocatalysis. Herein, we take advantage of the unique coordination and self-assembly properties of arginine for the preparation of dendritic PtCu bimetallic nanoassemblies with tunable chemical composition and structure. Strong interactions between the arginine molecules are key in driving the self-assembly of primary nanocrystals. In addition, the strong coordination interactions between arginine and metal ions is responsible for the formation of Pt–Cu alloys. We also investigated the electrocatalytic activity of various dendritic PtCu bimetallic nanoassemblies towards the methanol oxidation reaction. Pt3Cu1 nanoassemblies exhibited excellent electrocatalytic activity and stability in comparison with other PtCu bimetallic nanoassemblies (Pt1Cu3, Pt1Cu1) and commercial Pt black, due to their unique dendritic structures and the synergistic effect between the Pt and Cu atoms.

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Nano Research
Pages 755-765

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Cite this article:
Fu G, Liu H, You N, et al. Dendritic platinum–copper bimetallic nanoassemblies with tunable composition and structure: Arginine-driven self-assembly and enhanced electrocatalytic activity. Nano Research, 2016, 9(3): 755-765. https://doi.org/10.1007/s12274-015-0954-0

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Received: 03 October 2015
Revised: 15 November 2015
Accepted: 21 November 2015
Published: 13 January 2016
© Tsinghua University Press and Springer‐Verlag Berlin Heidelberg 2015