Abstract

This report describes the formation of gold-coated silver bimetallic nanoparticles prepared by the one-pot synthetic approach which involves the subsequent reduction of silver and gold ions at ambient conditions. The reduction of silver ions by excess L-ascorbic acid initially led to the formation of silver cores. This step was followed by the addition of gold ions into the preformed cores, resulting in the formation of silver-core gold-shell type bimetallic nanoparticles at room temperature. This process systematically allowed for the formation of various bimetallic nanoparticles which exhibited tunable absorption properties corresponding to the visible and near-IR regions. The thickness of the gold shells and the diameter of the silver-core nanoparticles were readily controlled; the morphological and structural properties of the resulting bimetallic nanoparticles were thoroughly analyzed by SEM/TEM, DLS, and UV–Vis spectrophotometry. The overall results demonstrated not only that these gold-coated silver nanoparticles were reliably prepared by our one-pot synthetic approach, but also that their optical properties were tunable in the visible and near-IR areas as a function of the core size and shell thickness.

Highlights

  • The preparation of metal nanoparticles in small sizes that absorb in the visible and near-IR spectral regions remains an ongoing challenge to colloidal science [1, 2]

  • We demonstrate a simple one-pot synthetic method that allows for the reliable preparation of stable core–shell type bimetallic nanoparticles with strong and tunable optical properties at ambient conditions

  • Characterization methods All nanoparticles were characterized by ultraviolet–visible (UV–Vis) spectroscopy for the absorption properties, by environmental scanning electron microscopy (SEM) and transmission electron microscopy (TEM) for the morphology and structure, and by dynamic light scattering (DLS) for the size distribution

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Summary

Introduction

The preparation of metal nanoparticles in small sizes that absorb in the visible and near-IR spectral regions remains an ongoing challenge to colloidal science [1, 2] Access to these broad absorption areas is especially important for solar energy based and/or biological applications because optically driven solar cells and therapies represent some of the most promising advances in the emerging field of renewable energy systems and nanomedicine [3, 4]. These developing nanotechnologies take advantage of the fact that there are not many chromophores in biological tissue that broadly absorb in the visible and near-IR regions [5, 6].

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