Near- and Far-Field Properties of Plasmonic Oligomers under Radially and Azimuthally Polarized Light Excitation
Source abstract
Abstract
We present a comprehensive experimental and theoretical study on the near- and far-field properties of plasmonic oligomers using radially and azimuthally polarized excitation. These unconventional polarization states are perfectly matched to the high spatial symmetry of the oligomers and thus allow for the excitation of some of the highly symmetric eigenmodes of the structures, which cannot be excited by linearly polarized light. In particular, we study hexamer and heptamer structures and strikingly find very similar optical responses, as well as the absence of a Fano resonance. Furthermore, we investigate the near-field distributions of the oligomers using near-field scanning optical microscopy (NSOM). We observe significantly enhanced near-fields, which arise from efficient excitation of the highly symmetric eigenmodes by the radially and azimuthally polarized light fields. Our study opens up possibilities for tailored light-matter interaction, combining the design freedom of complex plasmonic structures with the remarkable properties of radially and azimuthally polarized light fields.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Plasmonic and Surface Plasmon Research · Near-Field Optical Microscopy · Orbital Angular Momentum in Optics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Applied Physics, Hebrew University of Jerusalem, Jerusalem, 91904, Israel
4th Physics Institute and Research Center SCoPE, University of Stuttgart, Pfaffenwaldring 57, D-70569 Stuttgart, Germany
Max Planck Institute for Solid State Research, Heisenbergstrasse 1, D-70569 Stuttgart, Germany
References (26)
Show source-provided references
1. Stockman M. I. · Opt. Express · 2011 · 19 · 2202910.1364/OE.19.022029 ↗
2. Halas N. J. · Chem. Rev. · 2011 · 111 · 391310.1021/cr200061k ↗
3. Luk’yanchuk B. · Nat. Mater. · 2010 · 9 · 70710.1038/nmat2810 ↗
4. Mirin N. A. · J. Phys. Chem. A · 2009 · 113 · 402810.1021/jp810411q ↗
5. Fan J. A. · Science · 2010 · 328 · 113510.1126/science.1187949 ↗
6. Hentschel M. · Nano Lett. · 2010 · 10 · 272110.1021/nl101938p ↗
7. Lassiter J. B. · Nano Lett. · 2010 · 10 · 318410.1021/nl102108u ↗
8. Frimmer M. · Phys. Rev. Lett. · 2012 · 108 · 07740410.1103/PhysRevLett.108.077404 ↗
9. Rahmani M. · Nano Lett. · 2012 · 12 · 210110.1021/nl3003683 ↗
10. Lassiter J. B. · Nano Lett. · 2012 · 12 · 105810.1021/nl204303d ↗
11. Ogüt B. · Nano Lett. · 2012 · 12 · 523910.1021/nl302418n ↗
12. Zhan Q. · Adv. Opt. Photonics · 2009 · 1 · 110.1364/AOP.1.000001 ↗
13. Youngworth K. · Opt. Express · 2000 · 7 · 7710.1364/OE.7.000077 ↗
14. Dorn R. · Phys. Rev. Lett. · 2003 · 91 · 23390110.1103/PhysRevLett.91.233901 ↗
15. Lerman G. M. · Opt. Express · 2008 · 16 · 456710.1364/OE.16.004567 ↗
16. Chen W. · Opt. Lett. · 2009 · 34 · 72210.1364/OL.34.000722 ↗
17. Lerman G. M. · Nano Lett. · 2009 · 9 · 213910.1021/nl900694r ↗
18. Brandl D. W. · J. Phys. Chem. B · 2006 · 110 · 1230210.1021/jp0613485 ↗
19. Bao K. · Appl. Phys. A: Mater. Sci. Process. · 2010 · 100 · 33310.1007/s00339-010-5861-3 ↗
20. Jäger S. · Nano Lett. · 2013 · 13 · 356610.1021/nl401173g ↗
21. Hentschel M. · Beilstein J. Nanotechnol. · 2013 · 4 · 5710.3762/bjnano.4.6 ↗
22. Sancho-Parramon J. · ACS Nano · 2012 · 6 · 841510.1021/nn303243p ↗
23. Gomez D. E. · Nano Lett. · 2013 · 13 · 372210.1021/nl401656e ↗
24. Oskooi A. F. · Comput. Phys. Commun. · 2010 · 181 · 68710.1016/j.cpc.2009.11.008 ↗
25. Lassiter J. B. · Nano Lett. · 2008 · 8 · 121210.1021/nl080271o ↗
26. Hentschel M. · ACS Nano · 2011 · 5 · 204210.1021/nn103172t ↗