Abstract

Colloidal Cu@CuAlO2-Al2O3 bimetallic nanoparticles were prepared by a gamma irradiation method in an aqueous system in the presence of polyvinyl pyrrolidone (PVP) and isopropanol respectively as a colloidal stabilizer and scavenger of hydrogen and hydroxyl radicals. The gamma irradiation was carried out in a 60Co gamma source chamber with different doses up to 120 kGy. The formation of Cu@CuAlO2-Al2O3 nanoparticles was observed initially by the change in color of the colloidal samples from colorless to brown. Fourier transform infrared spectroscopy (FTIR) confirmed the presence of bonds between polymer chains and the metal surface at all radiation doses. Results of transmission electron microscopy (TEM), energy dispersive X-ray spectrometry (EDX), and X-ray diffraction (XRD) showed that Cu@CuAlO2-Al2O3 nanoparticles are in a core-shell structure. By controlling the absorbed dose and precursor concentration, nanoclusters with different particle sizes were obtained. The average particle diameter increased with increased precursor concentration and decreased with increased dose. This is due to the competition between nucleation, growth, and aggregation processes in the formation of nanoclusters during irradiation.

Highlights

  • Investigation on bimetallic nanoparticles in colloidal solution is of great interest due to their applications in catalysis [1,2,3,4], electronics [5], optics [5,6], and the change in the surface plasmon band energy [7,8] relative to the component monometallic particles [9]

  • An oversimplified scheme of the interactions between the polyvinyl pyrrolidone (PVP) capping agent and metal ions before irradiation is shown in Figure 1, which shows that the Al (III) and Cu (II) ions are bound by the ionic bonds between the metallic ions and the amide group in a polymeric chain

  • We have succeeded in synthesizing Cu@CuAlO2-Al2O3 nanoparticles in core-shell structure from a

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Summary

Introduction

Investigation on bimetallic nanoparticles in colloidal solution is of great interest due to their applications in catalysis [1,2,3,4], electronics [5], optics [5,6], and the change in the surface plasmon band energy [7,8] relative to the component monometallic particles [9]. Isopropanol scavenged OH and H radicals and at the same time isopropanol changed into isopropanol radicals, which eventually reduced Al3+ and Cu2+ into zero-valent atoms of Al0 and Cu0 as shown in the following reactions [3]: OH

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