Published January 15, 2012 | Version v1
Journal article

CuO nanoparticles: Synthesis, characterization, optical properties and interaction with amino acids

  • 1. Nanochemistry Laboratory, Chemistry Department, Faculty of Science, Kafrelsheikh, University, 33516 Kafr ElSheikh (Egypt)

Description

Cupric oxide (CuO) nanoparticles with an average size of 6 nm have been successfully prepared by an alcothermal method. The prepared CuO nanoparticles were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier-transform infrared (FT-IR) and UV-visible absorption spectroscopy. A strong sharp emission under UV excitation is reported from the prepared CuO nanoparticles. The results show that the CuO nanoparticles have high dispersion and narrow size distribution. The fluorescence emission spectra display an intense sharp emission at 365 nm and weak broad intensity emission at 470 nm. Picosecond fluorescence measurements of the nanoparticles suggest bi-exponential function giving time constants of τ1 (330 ps, 94.21%) and τ2 (4.69 ns, 5.79%). In neutral and alkaline solutions, Zeta potential values of CuO nanoparticles are negative, due to the adsorption of COO- group via the coordination of bidentate. At low pH the zeta potential value is positive due to the increased potential of H+ ions in solution. Comparative UV-visible absorption experiments with the model amino acid compounds of positive and negative charges as arginine and aspartic acid, respectively confirmed the negative surface of CuO nanoparticles. The results should be extremely useful for understanding the mode of the interaction with biological systems. This binding process also affects the particle's behavior inside the body.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.apsusc.2011.11.025

Additional details

Identifiers

DOI
10.1016/j.apsusc.2011.11.025;
PII
S0169-4332(11)01776-4;

Publishing Information

Journal Title
Applied Surface Science
Journal Volume
258
Journal Issue
7
Journal Page Range
p. 2997-3001
ISSN
0169-4332
CODEN
ASUSEE

Optional Information

Copyright
Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.