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. 2015 Jul 6:5:11949.
doi: 10.1038/srep11949.

Core-shell Au@Pd nanoparticles with enhanced catalytic activity for oxygen reduction reaction via core-shell Au@Ag/Pd constructions

Affiliations

Core-shell Au@Pd nanoparticles with enhanced catalytic activity for oxygen reduction reaction via core-shell Au@Ag/Pd constructions

Dong Chen et al. Sci Rep. .

Abstract

Core-shell nanoparticles often exhibit improved catalytic properties due to the lattice strain created in these core-shell particles. Herein, we demonstrate the synthesis of core-shell Au@Pd nanoparticles from their core-shell Au@Ag/Pd parents. This strategy begins with the preparation of core-shell Au@Ag nanoparticles in an organic solvent. Then, the pure Ag shells are converted into the shells made of Ag/Pd alloy by galvanic replacement reaction between the Ag shells and Pd(2+) precursors. Subsequently, the Ag component is removed from the alloy shell using saturated NaCl solution to form core-shell Au@Pd nanoparticles with an Au core and a Pd shell. In comparison with the core-shell Au@Pd nanoparticles upon directly depositing Pd shell on the Au seeds and commercial Pd/C catalysts, the core-shell Au@Pd nanoparticles via their core-shell Au@Ag/Pd templates display superior activity and durability in catalyzing oxygen reduction reaction, mainly due to the larger lattice tensile effect in Pd shell induced by the Au core and Ag removal.

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Figures

Figure 1
Figure 1. Synthetic strategy.
Schematic illustration to show the synthesis of core-shell Au@Pd-I nanoparticles using core-shell Au@Ag/Pd with an Au core and an Ag/Pd alloy shell as intermediate template.
Figure 2
Figure 2. Core-shell Au@Ag/Pd nanoparticles.
TEM image (a), HRTEM image (b), STEM image (c), elemental profiles in STEM mode (c,d) and STEM-EDX analysis (c,e) of core-shell Au@Ag/Pd prepared via galvanic replacement reaction between Ag shell of core-shell Au@Ag nanoparticles and Pd(acac)2 precursors.
Figure 3
Figure 3. Core-shell Au@Pd-I nanoparticles.
TEM image (a), HRTEM image (b), STEM image (c), elemental profiles in STEM mode (c,d) and STEM-EDX analysis (c,e) of core-shell Au@Pd-I prepared using core-shell Au@Ag/Pd nanoparticles as parent template.
Figure 4
Figure 4. XPS spectra.
The 3d XPS spectra of Pd in commercial Pd/C catalysts (a), core-shell Au@Pd-I (b), and core-shell Au@Pd-II (c), respectively.
Figure 5
Figure 5. Electrochemical measurements.
Negative-going linear sweep voltammograms (a) and chronoamperograms at 0.45 V (b) of core-shell Au@Pd-I nanoparticles, core-shell Au@Pd-II nanoparticles, and commercial Pd/C-JM catalysts in O2 saturated 0.1 M HClO4 electrolyte at a scan rate of 10 mV s−1 and a rotating rate of 1600 rpm.

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