Polarization Anisotropy of Multiple Localized Plasmon Resonance Modes in Noble Metal Nanocrescents
Source abstract
Abstract
Multiple localized surface plasmon resonance (LSPR) modes induced in gold and silver nanocrescents exhibit anisotropic behavior with respect to polarization of incident light. Extinction spectroscopy with polarization control was used to characterize the optical properties of asymmetric nanocrescents with diameters ranging from 100 to 500 nm. The analysis shows that selective induction of distinct dipole and quadrupole LSPR modes can be accomplished through polarization of incident light. Finite-difference time-domain calculations of the LSPR responses of the nanocrescent corroborate the polarization-dependent optical behavior. Simulations reveal optical near field enhancements with unique spatial patterns associated with the individual resonance modes depending on the polarization and wavelength of incident light. Quantitative analysis of the anisotropic LSPR behavior supports the potential for controlling the near field through selective induction of specific resonance modes with particular near field distributions.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Gold and Silver Nanoparticles Synthesis and Applications · Plasmonic and Surface Plasmon Research · Protein Interaction Studies and Fluorescence Analysis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, University of Utah, 315 South 1400 East, RM 2020, Salt Lake City, Utah 84112, United States
Department of Electrical and Computer Engineering, University of Utah, 50 Central Campus Drive, RM 3280, Salt Lake City, Utah 84112, United States
References (29)
Show source-provided references
1. Alvarez-Puebla R. · J. Phys. Chem. Lett. · 2010 · 1 · 242810.1021/jz100820m ↗
2. Banik M. · J. Phys. Chem. C · 2012 · 116 · 1041510.1021/jp302013k ↗
3. Berweger S. · J. Phys. Chem. Lett. · 2010 · 1 · 342710.1021/jz101289z ↗
4. Dey S. · J. Chem. Phys. · 2013 · 138 · 15420210.1063/1.4800965 ↗
5. Barrow S. J. · Nano Lett. · 2011 · 11 · 418010.1021/nl202080a ↗
6. Jana N. R. · J. Phys. Chem. B · 2001 · 105 · 406510.1021/jp0107964 ↗
7. Jana N. R. · Chem. Commun. · 2001 · 7 · 61710.1039/b100521i ↗
8. Im S. H. · Angew. Chem., Int. Ed. · 2005 · 44 · 215410.1002/anie.200462208 ↗
9. Deeb C. · J. Phys. Chem. C · 2012 · 116 · 2437410.1021/jp304647e ↗
10. Hanarp P. · J. Phys. Chem. B · 2003 · 107 · 576810.1021/jp027562k ↗
11. Aizpurua J. · Phys. Rev. Lett. · 2003 · 90 · 05740110.1103/PhysRevLett.90.057401 ↗
12. Larsson E. M. · Nano Lett. · 2007 · 7 · 125610.1021/nl0701612 ↗
13. Hulteen J. C. · J. Phys. Chem. B · 1999 · 103 · 385410.1021/jp9904771 ↗
14. Haes A. J. · J. Phys. Chem. B · 2005 · 109 · 1115810.1021/jp051178g ↗
15. Hao F. · Nano Lett. · 2007 · 7 · 72910.1021/nl062969c ↗
16. Li M. · Nanotechnology · 2012 · 23 · 11550110.1088/0957-4484/23/11/115501 ↗
17. Bochenkov V. E. · Nano Lett. · 2013 · 13 · 121610.1021/nl304675w ↗
18. McLellan J. M. · Nano Lett. · 2007 · 7 · 101310.1021/nl070157q ↗
19. Tao A. R. · J. Phys. Rev. B · 2005 · 109 · 15687
20. Zhao Y.-P. · J. Phys. Chem. B · 2006 · 110 · 315310.1021/jp057406o ↗
21. Koen K. A. · J. Phys. Chem. C · 2012 · 116 · 1619810.1021/jp301878e ↗
22. Ambjörnsson T. · Phys. Rev. B · 2006 · 73 · 08541210.1103/PhysRevB.73.085412 ↗
23. Yoshida K. · Phys. Rev. B · 2010 · 81 · 11540610.1103/PhysRevB.81.115406 ↗
24. Bukasov R. · ACS Nano · 2010 · 4 · 663910.1021/nn101994t ↗
25. Zhang Y. · Opt. Exp. · 2012 · 20 · 292410.1364/OE.20.002924 ↗
26. Shumaker-Parry J. S. · Adv. Mater. · 2005 · 17 · 213110.1002/adma.200500063 ↗
27. Bukasov R. · Nano Lett. · 2007 · 7 · 111310.1021/nl062317o ↗
28. Wang G. · J. Am. Chem. Soc. · 2010 · 132 · 1641710.1021/ja106506k ↗
29. Ha J. W. · Chem. Commun. · 2011 · 47 · 774310.1039/c1cc11679g ↗