J. Mater. Sci. Technol. ›› 2014, Vol. 30 ›› Issue (11): 1071-1077.DOI: 10.1016/j.jmst.2014.07.018

• Orginal Article • Previous Articles     Next Articles

Facile Synthesis of Bimetallic Au@Pd Nanoparticles with Core-shell Structures on Graphene Nanosheets

Nanting Li,Shaochun Tang,Xiangkang Meng*   

  1. Institute of Materials Engineering,National Laboratory of Solid State Microstructures,College of Engineering and Applied Sciences,Nanjing University,Nanjing 210093,China
  • Received:2014-04-09 Online:2014-11-20 Published:2014-12-12
  • Contact: *Corresponding author.Prof,Ph.D.; Tel.:t86 25 8368 5585; Fax:t86 25 8359 5535; E-mail address:mengxk@nju.edu.cn (X.Meng).
  • Supported by:
    This work was supported by the PAPD (No.50831004),the Innovation Fund of Jiangsu Province (No.BY2013072-06),the Natural Science Foundation of Jiangsu Province (No.2012729),the National Natural Science Foundation of China (No.51171078,11374136),and the State Key Program for Basic Research of China (No.2010CB631004).

Abstract: In this paper,we report a simple one-step thermal reducing method for synthesis of bimetallic Au@Pd nanoparticles with core-shell structures on the graphene surface.This new type of Au@Pd-G composites is characterized by transmission electron microscopy,high resolution transmission electron microscopy,X-ray photoelectron spectroscopy and X-ray diffraction.It is found that Au@Pd nanoparticles with an average diameter of 11 nm are well dispersed on the graphene surface,and the Au core quantity as well as the Pd shell thickness can be quantitatively controlled by loading different amounts of metallic precursors,and the involved core-shell structure formation mechanism is also discussed.The ternary Pt/Au@Pd-G composites can also be synthetized by the subsequent Pt doping.The catalytic performance of Au@Pd-G composites toward methanol electro-oxidation in acidic media is investigated.The results show that Au@Pd-G composites exhibit higher catalytic activity,better stability and stronger tolerance to CO poisoning than Pd-G and Au-G counterparts.