4.3 Article

Single step aqueous synthesis of pure rare earth nanoparticles in biocompatible polymer matrices

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JOURNAL OF MATERIALS CHEMISTRY
卷 22, 期 25, 页码 12538-12546

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c2jm30971h

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  1. UGC-DAE [CSR-KC/CRS/09/RCO1/1461]
  2. DST [SR/S1/PC-63/2009]

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The room temperature synthesis of water soluble, stable rare earth (RE) metal nanoparticles (MNPs) with controlled size is a long standing interest. In the present work, we have established a synthetic strategy for the preparation of pure europium (Eu-0) metal nanoparticles (NPs) in aqueous solution employing a gamma-radiolytic reduction technique. Since radiolysis is the cleanest method amongst all other chemical routes, we preferentially choose this technique for the reduction of precursor Eu3+ ions to nanoscale metals in our work. This has been possible as hydrated electrons (e(aq)(-)) having a very high reduction potential (E-0(H2O/e(aq)(-)) = -2.87 V-NHE) produced in situ can efficiently reduce Eu3+ to Eu-0. Synthesized Eu-0 MNPs were stabilised within the matrices of biocompatible polymers, polyvinyl alcohol (PVA) and polyvinylpyrrolidone (PVP). Reduction of the metal ion has been conducted at different irradiation doses with a maximum dose of 83.88 kGy. The irradiated solution shows an absorption maximum at 266 +/- 2 nm and an emission maximum at 394 +/- 5 nm. Analysis of transmission electron microscopy (TEM) images shows that the average sizes of PVA and PVP encapsulated Eu-0 NPs are 13 +/- 0.6 nm and 17 +/- 1.01 nm, respectively ([Eu3+] = 5.0 x 10(-3) mol dm(-3), [polymer] = 1.0%). Formation of monodisperse pure Eu-0 MNPs was further characterised by dynamic light scattering (DLS), energy dispersive X-ray (EDX) as well as Fourier transformed infrared (FTIR) spectroscopy and cyclic voltammetry (CV) studies.

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