Hostname: page-component-586b7cd67f-rcrh6 Total loading time: 0 Render date: 2024-11-23T12:58:21.463Z Has data issue: false hasContentIssue false

Magneto-optic Response of Functionalized vs. Uncoated Fe2O3 (Maghemite) Nanoparticles

Published online by Cambridge University Press:  03 June 2014

Maarij Syed
Affiliation:
Rose-Hulman Institute of Technology, Terre Haute, IN 47803, USA
Thomas Foulkes
Affiliation:
Rose-Hulman Institute of Technology, Terre Haute, IN 47803, USA
Erwann Guenin
Affiliation:
University of Paris, 74 rue Marcel Cachin, F-93017 Bobigny Cedex, France
Laurence Motte
Affiliation:
University of Paris, 74 rue Marcel Cachin, F-93017 Bobigny Cedex, France
Get access

Abstract

Iron oxide nanoparticles (NPs) have attracted a lot of interest due to their many potential applications in areas including optoelectronics, magneto-optics, high density data storage, etc. In particular, iron oxides (Fe3O4 and γ –Fe2O3) are also well suited for biomedical applications [1]. We have investigated Faraday Rotation (FR) response for two types of Fe2O3 NPs (in aqueous suspension) that are of the same average diameter (10 nm) but differ in one important respect; one group consists of uncoated particles whereas the other group is functionalized with caffeic acid. This system is being investigated and characterized for use in tumor imaging applications. Faraday rotation (FR) refers to the rotation of the polarization vector of a light beam as it passes through a sample in the presence of a magnetic field. FR can reveal interesting material properties such as saturation magnetization and wavelength dependent Verdet constant of the material under investigation. The latter is a measure of the magnetically induced birefringence of the material. Typically FR setups rely on AC or DC magnetic fields. While these are valuable techniques with their own advantages, this work focuses on a pulsed field setup that can reveal dynamic information about the resulting magnetization, as the magnetic response of the sample is measured in the presence of short intense fields on the order of 0.6 Tesla and lasting approximately 100 milliseconds. All experiments are carried out at excitation wavelength of 633 nm (He-Ne wavelength).

The two NP samples show very different response to the field pulses. The NP systems investigated in this work show very unique short term and long term behavior revealing various time scales of interest. These unique characteristic times for the functionalized vs. uncoated particles provide valuable clues about the magnetization response of the NP and its relationship to the detailed structure of the NPs (core vs. shell). Magnetic response from these systems persists long after the magnetic field pulse has subsided. This can be related to the relaxation modes (Néel vs. Brownian) and as possible evidence of NP size dispersion. Additionally, the possibility of agglomeration is also discussed. While more detailed quantitative analysis will be dealt with in a more comprehensive publication that is under preparation, we hope to show in this preliminary report both that the AC and pulsed FR measurements can reveal complimentary information and that FR in general can be a reliable technique, which can be used to develop a detailed picture of the magnetic response of these NP systems.

Type
Articles
Copyright
Copyright © Materials Research Society 2014 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Gupta, A. K. and Gupta, M., Biomaterials, 26, 39954021 (2005).CrossRefGoogle Scholar
Xia, T. K., Hui, P. M., and Stroud, D., Journal of Applied Physics, 67, 27362741 (1990).CrossRefGoogle Scholar
Jain, A., Kumar, J., Zhou, F., Li, L., and Tripathy, S., Am. J. Phys. 67, 714717 (1999).CrossRefGoogle Scholar
Chung, S., et al. ., J. Magn. Magn. Mat. 320, 9195 (2008).CrossRefGoogle Scholar
Isai, K., Suwa, M., and Watarai, H., Analytical Sciences, 25, 13 (2009).CrossRefGoogle Scholar
de Montferrand, C, et al. ., Acta Biomaterialia, 9(4), 61506157 (2013).CrossRefGoogle Scholar
Kober, M., Moros, M., Grazu, V., de la Fuente, J. M., Luna, M., and Briones, F., Nanotechnology, 23, 155501 (2012).CrossRefGoogle Scholar
Smith, D. A., Barnakov, Y. A., Scott, B. L., White, S. A., and Stokes, K. L., J. Appl. Phys. 97, 10M504 (2005).CrossRefGoogle Scholar