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Aqueous Processing CdSe/TGA Quantum dots For Potential Bio-Medical Applications

Published online by Cambridge University Press:  11 June 2015

Raquel Feliciano-Crespo ,
José A Rodriguez-Gonzalez ,
Chuan-Jian Zhong  and
Oscar Perales-Perez
Raquel Feliciano-Crespo
Affiliation:
Department of Chemistry, University of Puerto Rico, Mayaguez, PR, USA.
José A Rodriguez-Gonzalez
Affiliation:
Department of Engineering Science & Materials, University of Puerto Rico, Mayaguez, PR, USA.
Chuan-Jian Zhong
Affiliation:
Department of Chemistry, State University of New York, Binghamton, NY, USA
Oscar Perales-Perez
Affiliation:
Department of Chemistry, University of Puerto Rico, Mayaguez, PR, USA. Department of Engineering Science & Materials, University of Puerto Rico, Mayaguez, PR, USA.
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Abstract

The size-dependent optical properties of CdSe nanoparticles are desirable in bio-imaging and cell sorting applications because of their tunable photoluminescence in the visible range. Previous studies have already suggested that CdSe QDs could be utilized for pathogen detection by using suitable capping agents to make it biocompatible; however, systematic works on the effect of crystallite size and composition of the nanocrystals are scarce. The present research will be focused on the effect of CdSe crystal size and composition (pure and doped systems) to systematically evaluate its applicability in detecting pathogens, like Escherichia coli (E. coli). Highly luminescent water-soluble CdSe QDs were firstly synthesized in the aqueous phase, in the presence of thioglycolic acid (TGA) as a capping agent. CdSe/TGA molar ratios, reaction temperature, time, and pH were evaluated in order to optimizer the QDs optical properties. X-Ray diffraction (XRD) measurements confirmed the formation of CdSe exhibiting hexagonal structure with an estimated averaged crystallite size in the 4-6 nm range. Transmission electron microscopy (TEM) analyses evidenced the formation of CdSe nanocrystals with particle sizes between 3-5 nm. UV-Vis measurements showed a strong exciton peak between 390-400 nm with an estimated band gap of 2.64 eV (bulk: 1.74 eV); additionally, a strong fluorescence peak was observed between 500-550 nm using an excitation wavelength of 400 nm. Fourier Transform Infrared Spectroscopy (FT-IR) analyses suggested the actual functionalization of the CdSe surface with TGA functional groups. Preliminary results of the CdSe/TGA coupling with the selected bacteria, E. coli, are presented and discussed.

Keywords

optical propertiesphotoemissionsurface chemistry
Type
Articles
Information
MRS Online Proceedings Library (OPL) , Volume 1797: Symposium KK – Nanomaterials in Translational Medicine , 2015 , mrss15-2137557
Copyright
Copyright © Materials Research Society 2015 

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References

REFERENCES

Ingole, P.P. et al. , K.Materials Science and Engineering B, 168, 60–65, (2010).CrossRefGoogle Scholar
Thanh, N.T., Green, L.A. Nano Today, 5, 213–230, (2010).CrossRefGoogle Scholar
Sun, et al. , Molecules, 17(7), 8430–8438, (2012).CrossRefGoogle Scholar
Dethlefsen, J.R. and Døssing, A. Nano letters, 11, pp. 1964–1969, (2011).CrossRefGoogle Scholar
Masashi, F. et al. J. Phys. Chem. C, 113, 38, (2009).Google Scholar
Yu, W.W. et al. , Biochemical and Biophysical Research, 348, 781, (2006).CrossRefGoogle Scholar
Melacon, M.P. et al. , J. Am. Chem. Soc., vol. 44, 10, pp. 947, (2011).Google Scholar
Zhou, et al. , J. Am. Chem. Soc., 132, 15351, (2010).CrossRefGoogle Scholar
Hessel, C.M., Nano Lett., 11, pp. 947–956, (2011).CrossRefGoogle Scholar
Tian, Q. et al. , J. Am. Chem. Soc, 5, 12, 9761, (2011).Google Scholar
Chen, J. et al. , Nano Lett.,7, 5, 1318, (2007).CrossRefGoogle Scholar
Huang, et al. , Nanomater, 10, 1–6, (2010).Google Scholar
Vider, et al. , Nano Lett., 9, 442–448, (2009).Google Scholar
Fujii, et al. . Asian J Androl, 5, 231–242, (2003).Google Scholar
Dong, W. et al. , Spectromic Acta Part A, 78, 537–542, (2011).CrossRefGoogle Scholar