Synthesis of Fe Nanoparticles Functionalized with Oleic Acid Synthesized by Inert Gas Condensation

Author:

Silva L. G.1,Solis-Pomar F.1,Gutiérrez-Lazos C. D.1,Meléndrez Manuel F.2,Martinez E.3,Fundora A.4,Pérez-Tijerina E.1

Affiliation:

1. Facultad de Ciencias Físico-Matemáticas, Universidad Autónoma de Nuevo León, 66451 San Nicolás de los Garza, NL, Mexico

2. Hybrid Materials Laboratory (HML), Department of Materials Engineering (DIMAT), Faculty of Engineering, University of Concepcion, 270 EdmundoLarenas, Casilla 160-C, 4070409 Concepcion, Chile

3. Centro de Investigación en Materiales Avanzados S. C., Unidad Monterrey-PIIT, 66600 Apodaca, NL, Mexico

4. Instituto de Ciencia y Tecnología de Materiales (IMRE), Universidad de La Habana, Zapata y G, Vedado, CP 10400 La Habana, Cuba

Abstract

In this work, we study the synthesis of monodispersed Fe nanoparticles (Fe-NPs)in situfunctionalized with oleic acid. The nanoparticles were self-assembled by inert gas condensation (IGC) technique by using magnetron-sputtering process. Structural characterization of Fe-NPs was performed by transmission electron microscopy (TEM). Particle size control was carried out through the following parameters: (i) condensation zone length, (ii) magnetron power, and (iii) gas flow (Ar and He). Typically the nanoparticles generated by IGC showed diameters which ranged from ~0.7 to 20 nm. Mass spectroscopy of Fe-NPs in the deposition system allowed the study ofin situnanoparticle formation, through a quadrupole mass filter (QMF) that one can use together with a mass filter. When the deposition system works without quadrupole mass filter, the particle diameter distribution is around +/−20%. When the quadrupole is in line, then the distribution can be reduced to around +/−2%.

Funder

CONACYT Mexico

Publisher

Hindawi Limited

Subject

General Materials Science

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