Hostname: page-component-586b7cd67f-dsjbd Total loading time: 0 Render date: 2024-11-23T10:39:05.270Z Has data issue: false hasContentIssue false
  • English
  • Français

Electrical Control of LSPR from Gold Nanoparticles Using Electrochemical Oxidation

Published online by Cambridge University Press:  31 January 2011

Takashi Miyazaki ,
Rei Hasegawa ,
Hajime Yamaguchi ,
Hitoshi Nagato ,
Haruhi Oh-oka ,
Isao Amemiya  and
Shuichi Uchikoga
Takashi Miyazaki
Affiliation:
[email protected], Toshiba Corporation, Corporate Research & Development Center, Kawasaki, Japan
Rei Hasegawa
Affiliation:
[email protected], Toshiba Corporation, Corporate Research & Development Center, Kawasaki, Japan
Hajime Yamaguchi
Affiliation:
[email protected], Toshiba Corporation, Corporate Research & Development Center, Kawasaki, Japan
Hitoshi Nagato
Affiliation:
[email protected], Toshiba Corporation, Corporate Research & Development Center, Kawasaki, Japan
Haruhi Oh-oka
Affiliation:
[email protected], Toshiba Corporation, Corporate Research & Development Center, Kawasaki, Japan
Isao Amemiya
Affiliation:
[email protected], Toshiba Corporation, Corporate Research & Development Center, Kawasaki, Japan
Shuichi Uchikoga
Affiliation:
[email protected], Toshiba Corporation, Toshiba Research Europe Limited, Cambridge, United Kingdom
Get access

Abstract

Large shift of localized surface plasmon resonance (LSPR) spectrum of gold nanoparticles was attained by electrochemical oxidation of the nanoparticle surface. This oxidation occurred in a cell consisting of a pair of indium tin oxide (ITO) electrodes with water medium between the electrodes. On one side of the ITO electrode, the gold nanoparticles were adsorbed. The LSPR spectrum was moved consecutively to the red by increasing the applied positive voltage. By the application of 5 V to the cell, the spectrum shift as large as 55 nm was obtained. Though the spectrum shift has already been observed by changing liquid crystal (LC) orientation surrounding gold nanoparticles, the amount of the shift was not large (11 nm). That was because the variation of the effective refractive index of LC was rather small. Our large shift due to electrochemical oxidation resulted from the large refractive index of Au-O. The upper limit of the LSPR spectrum shift by our method is estimated to be 138 nm.

Keywords

Aunanostructureoptical
Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 1208: Symposium O – Excitons and Plasmon Resonances in Nanostructures II , 2009 , 1208-O10-04
Copyright
Copyright © Materials Research Society 2010

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 Miller, M. M.; Lazarides, A. A.; J. Opt. A: Pure Appl. Opt. 8, s239 (2006)Google Scholar
2 Link, S.; Mohamed, M. B.; El-Sayed, M. A.; J. Phys. Chem. B 103, 3073 (1999)Google Scholar
3 Sherry, L. J.; Jin, R.; Mirkin, C. A.; Schatz, G. C.; Duyne, R. P. V.; Nano Lett. 6, 2060 (2006)Google Scholar
4 Mock, J. J.; Smith, D. R.; Schultz, S.; Nano Lett. 3, 485 (2003)Google Scholar
5 Ni, W.; Chen, H.; Kou, X.; Yeung, M. H.; Wang, J.; J. Phys. Chem. C 112, 8105 (2008)Google Scholar
6 McFarland, A. D.; Van Duyne, R. P.; Nano Lett. 3, 1057 (2003)Google Scholar
7 Hanarp, P.; Kall, M.; Sutherland, D. S.; J. Phys. Chem. B 107, 5768 (2003)Google Scholar
8 Kossyrev, P. A.; Yin, A.; Cloutier, S. G.; Cardimona, D. A.; Huang, D.; Alsing, P. M.; Xu, J. M.; Nano Lett. 5, 1978 (2005)Google Scholar
9 Tsai, H. C.; Hu, E.; Perng, K.; Chen, M. K.; Wu, J. C.; Chang, Y. S.; Surf. Sci. Lett. 537, L447 (2003)Google Scholar
10 Curry, A., Nusz, G., Chilkoti, A., and Wax, A., Optics Express, 13, 2668 (2005)Google Scholar
11 Hofmann, S., Sanz, J.M.: Surf. Interface Anal., 15, 175 (1980)Google Scholar
12 Tanuma, S., Powell, C.J., Penn, D.R.: Surf. Interface Anal. 21, 165 (1994)Google Scholar