Hostname: page-component-78c5997874-g7gxr Total loading time: 0 Render date: 2024-11-18T18:52:46.922Z Has data issue: false hasContentIssue false

Effective Medium Theory of DNA-linked Gold Nanoparticle Aggregates:Effect of Aggregate Shape

Published online by Cambridge University Press:  17 March 2011

Anne A. Lazarides
Affiliation:
Department of Chemistry, Northwestern UniversityEvanston, IL 60208-3113
K. Lance Kelly
Affiliation:
Department of Chemistry, Northwestern UniversityEvanston, IL 60208-3113
George C. Schatz
Affiliation:
Department of Chemistry, Northwestern UniversityEvanston, IL 60208-3113
Get access

Abstract

We present a dynamical effective medium theory (EMT) of the dielectric properties of nanoparticle aggregates formed from DNA-linked gold nanoparticles. Experimental measurements show that such aggregateshave reduced UV extinction and plasmon bands that are considerably red-shifted and broadened relative to the plasmon absorption feature observed in spectra of dispersed colloid. The EMT, which can be used to reproduce the observed spectral changes, is tested by comparing aggregate spectra calculated using the EMT dielectric function with spectra from explicit coupled particle calculations, and good agreement is found. The EMT dielectric function is used as well in discrete dipole calculations to calculate extinction spectra for a variety of aggregate shapes not amenable to analytic solution, and the sensitivity of the spectra to aggregate shape is examined. We find that the spectra are only weakly sensitive to aggregate shape, and conclude that, when calculating extinction of the DNA-linked aggregates for comparison with experiment, spherical shapes can be assumed.

Type
Research Article
Copyright
Copyright © Materials Research Society 2001

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

1. Mucic, R. C., Storhoff, J. J., Letsinger, R. L. and Mirkin, C. A., Nature 382, 607 (1996).Google Scholar
2. Elghanian, R., Storhoff, J. J., Mucic, R. C., Letsinger, R. L., and Mirkin, C. A., Science 277, 1078 (1997).Google Scholar
3. Storhoff, J. J., Elghanian, R., Mucic, R. C., Mirkin, C. A., and Letsinger, R. L., J. Am. Chem.Soc. 120, 1959 (1998).Google Scholar
4. Storhoff, J. J., Lazarides, A. A., Mirkin, C. A., Letsinger, R. L., Mucic, R. C. and Schatz, G. C., J.Am. Chem. Soc. 122, 4640(2000).Google Scholar
5. Lazarides, A. A. and Schatz, G. C., J. Phys. Chem. 104, 460–7 (2000).Google Scholar
6. Lazarides, A. A. and Schatz, G. C., J. Chem. Phys. 112, 2987 (2000).Google Scholar
7. Lazarides, A. A. and Schatz, G. C., J. Chem. Phys., to be submitted.Google Scholar
8. Lazarides, A. A., Kelly, K. L., Jensen, T. R., and Schatz, G. C., Theochem, 529, 59 (2000).Google Scholar
9. Draine, B. T., Flatau, P. J.. J. Opt. Soc. Am. A. 11 1491 (1994); B.T. Draine, J. J. Goodman. Astrophys. J. 405, 685 (1993); Program DDSCAT, by B. T. Draine, P. J. Flatau. University of California, SanDiego, Scripps Institute of Oceanography, 8605 La Jolla Dr., La Jolla, CA 92093.Google Scholar
10. Yang, W. H., Schatz, G. C. and Duyne, R. P. Van, J. Chem. Phys. 103, 869 (1995); T. Jensen, L. Kelly, A. Lazarides and G. C. Schatz, J. Cluster Science 10, 295 (1999).Google Scholar