30 October 2017 Surface-to-volume ratio controls the radiation of stratified plasmonic antennas
Author Affiliations +
J. of Nanophotonics, 11(4), 046006 (2017). doi:10.1117/1.JNP.11.046006
Abstract
Surface plasmons are excited at a metal/dielectric interface, through the coupling between conduction electrons and incident photons. The surface plasmon generation is therefore strongly determined by the accessibility of the surface to the incoming electromagnetic field. We demonstrate the role of this surface for plasmonic nanoantennas with identical volumes and resonant lengths. An antenna is stratified parallel to the plane of its main dipolar resonance axis and the influence of the number of layers and the spacing between them on the optical properties of the antenna are investigated experimentally. We show that increasing the number of layers and, hence, increasing the total accessible surface of the antenna, results in an enhanced scattering cross section and a redshift which indicates that lower energy photons are required to couple to the metal electrons. In particular, the far-field enhancement observed for double-layer nanostructures suggests that standard single-layer metal deposition can be easily and advantageously substituted with metal/dielectric/metal deposition to boost light scattered by a plasmonic antenna.
Abasahl, Santschi, and Martin: Surface-to-volume ratio controls the radiation of stratified plasmonic antennas

1.

Introduction

Plasmonic nanoantennas can localize light to a subdiffraction-limited spot12.3.4 and reradiate it into the far-field. In the so-called hot spot, the field intensity is enhanced by several orders of magnitude at the resonance wavelength.56.7.8 These fundamental properties stem from the localized surface plasmon resonances. Additional features can be enabled by engineering the shape of nanoantennas, such as the broadband response of bowtie antennas,9 the directionality of nano Yagi-Uda antennas,10 and the ultralocalized and enhanced near-fields of gap antennas.1112.13.14.15.16.17.18.19.20.21.22.23 Several elements determine the field enhancement of a nanoantenna: strong photon–electron coupling at the metal surface, capacitive coupling at the disruption of the induced current path in the gap or at the end of the structure, and coupling to the surrounding environment. Although at optical frequencies the lateral dimensions of a nanoantenna are much smaller than the bulk penetration depth, the electric current density is not distributed uniformly, but rather it is higher at the surface of the structure. An example of such an electric field distribution can be seen in Fig. 1(a) for a nanorod, where the inside of the structure is depleted from the field intensity, while the latter increases close to the surface. In this article, the effect of the strong photon–electron interaction at the surface of a nanoantenna is investigated for such a nanorod geometry, Fig. 1(a). Specifically, the overall surface of the nanoantenna is altered while maintaining the total metal volume. To this end, the nanorod antenna shown in Fig. 1(a) is stratified according to Figs. 1(b) and 1(c). The antenna is excited with the electric field polarized along the x-direction, so that the dielectric interlayers added by the stratification do not interrupt the current path of the main dipole resonance. Each nanoantenna shown in Fig. 1 has the same volume, but their surfaces—especially the segments carrying the maximum current associated with the dipole resonance—increase between (a–c). In this article, we will show both numerically and experimentally that the increase of surfaces that support the plasmonic current associated with a stratified nanoantenna has a strong influence on its radiation properties. The optical measurements are supported by a number of calculations based on the surface integral equation (SIE) method24 and the influence of the number of interlayers and their thicknesses is studied.

Fig. 1

(a–c) top: Schematic representation of simple dipole (a), and stratified antennas with (b) two and (c) three metallic layers. For all antennas, the length is 110 nm, the total Au thickness is 40 nm and the spacer material between the metallic layers is air. The propagation vector and the electric field polarization are along the z- and x-axes, respectively. (a–c) bottom: Calculated electric field intensity in the cross section at the half length for the three antennas at their corresponding resonance wavelengths. (d) Calculated induced volume current through the cross section at half length for the three antennas. Solid line: real part and dashed line: imaginary part.

JNP_11_4_046006_f001.png

In the stratified antennas shown in Fig. 1, the dielectric spacing between each layer is small and, consequently, the phase difference for the currents flowing in the individual metal layers is negligible for the considered illumination wavelength. However, the total metal/dielectric interfaces for the surface current is increased in the stratified geometries, enhancing the coupling between electrons and photons at those interfaces. This can be seen in Fig. 1(d), where the current I through the cross section of the center for a single-layer, a double-layer, and a triple-layer antenna is calculated, by integrating the current density over the cross section surface S

(1)

I=SJ(r)·ds,
where J(r)=σE(r) is the volume current density, σ is the conductivity of the material, and E(r) is the electric field. According to these calculations, the current through the central cross section of the stratified antennas at their corresponding resonance is 12.5% stronger for the double-layer and 16% stronger for the triple-layer antenna as compared to a single-layer antenna. The electric field intensity distributions on the cross sections of the three different antennas [Figs. 1(a)1(c)] indicate that although the lateral dimensions of the antennas are much smaller than the wavelength and comparable to the penetration depth of the bulk material, the field is not uniform inside the structure and is more concentrated closer to the surface. This indicates that increasing the total surface of a nanoantenna with a given volume and a given resonance length can have a significant influence on its response.

Figure 2 shows the scattering cross sections for antennas with different numbers of horizontal cuts calculated with the SIE.24 In this figure, an antenna with length, width, and height of 110, 40, and 40 nm, respectively, is cut along its main axis into 2 to 10 pieces. The total height of the metallic parts is kept constant at 40 nm and the spacing between two neighboring parts is 10 nm and filled with air. In practice, the spacing will be filled with a dielectric but here we assume the spacers to be air in order to minimize the spectral shift of the dipole resonance caused by dielectrics.9 The bulk permittivity of gold has been employed for the metal in the calculations.25 There are two main trends in these spectra: first, an increase in the maximum of the scattering cross section and, second, the spectrum exhibits a redshift with the number of layers.

Fig. 2

Scattering cross section for nanoantenna with zero, 1, 2, 3, 4, and 10 cuts (corresponding respectively to 1, 2, 3, 4, and 11 layers). The spectra have been normalized with respect to the maximum of the spectrum of the single-layer structure. The spacer in each case is air with a thickness of 10 nm.

JNP_11_4_046006_f002.png

As mentioned, the number of layers increases the total surface of the metal, leading to a larger metal/dielectric interface. Consequently, the amount of electrons available for coupling with the photons is increased and the scattering cross section augments. Due to the rapid decay of the electromagnetic field in the metal, the electromagnetic field would be required to penetrate laterally into the spacer medium; hence, the smaller the interlayer the more difficult it is for the field to penetrate into the spacer. Figure 3 represents the scattering cross section spectra for a double-layer antenna with varying spacer thicknesses. According to this figure, the antenna with the largest spacer exhibits the largest scattering cross section. In order to minimize retardation effects, the spacer thickness is kept so small that the phase difference between the upper and the lower dipoles remains negligible and the metallic bars have almost in-phase resonances. For smaller spacers, the region between the upper and the lower layer screens the electromagnetic field and the response of the antenna converges to a conventional one-layer antenna. Let us emphasize that the variation of the scattering cross section for a two-layer antenna with different spacer thicknesses is not as pronounced as for a constant spacer with varying numbers of layers. The intensity of the electric near-field computed for antennas with one, two, and three layers is shown in Fig. 4. The calculations indicate that the maximum near-field intensity for the three cases is almost similar: introducing the interlayers does not produce new hot spots and the response of the structure remains dipolar.26

Fig. 3

Scattering cross section of the antennas with one and two layers. The spectra have been normalized with respect to the maximum of the spectrum of the monolayer structure. The SiO2 spacer thickness varies between 0 and 6 nm.

JNP_11_4_046006_f003.png

Fig. 4

Cross section of the antennas in Fig. 1 with the electric field intensity distribution at their resonance wavelength at y=0  nm.

JNP_11_4_046006_f004.png

The redshift of the dipole resonance with increasing numbers of layers is another feature visible in Fig. 2. In order to push further our understanding of the redshift with increasing numbers of layers, the optical response of the antenna can be mimicked by a combination of lumped circuit elements according to the method provided in Ref. 27. A layer of the antenna is represented by two parallel inductive and capacitive branches. As shown in Fig. 5(a), the inductive branch comprises an inductivity L in series with a resistor Rant representing the current path and its associated loss due to the finite metal conductivity. The capacitive branch is composed of a capacitor C in parallel with a resistor Rrad representing the fringe field and radiative loss, respectively. The capacitance of the antenna is related to the charge accumulation at both ends of the structure, while the inductance is closely connected to the current flow between both ends. The circuit element values used for this study are as follows: C=47  aF, L=2.3  fH, Rrad=59.02  Ω, and Rant=0.847  Ω.27 By bringing two antenna layers close to each other, to a distance where phase retardation between the two dipoles is negligible, the dipoles start to interact through the mutual coupling M between the inductors and the coupling capacitors Ccp, as shown in Fig. 5(b). The capacitor Ccp accounts for the pole-to-pole charge interaction and phase retardation and is—under the assumptions made previously—much larger than the dipole capacitor C. If the interparticle distance tends to zero, the capacitance Ccp goes to infinity, which corresponds to a short cut circuit. Therefore, the circuit can be simplified to four parallel branches: two capacitances C and two inductances LM. As M>0, the resonance frequency shifts from almost 1/LC to higher values 1/(LM)C, corresponding to stronger coupling for small spacers. In Fig. 5(c), the full circuit response of the system with respect to the change in relative mutual inductance is shown. In this case, the capacitances Ccp and the loss elements are considered. Increasing the thickness of the interlayer and, equivalently, decreasing the relative mutual inductance, enhances the radiation and redshifts the resonance.

Fig. 5

Lumped circuit model for (a) a single-layer antenna and (b) a two-layer antenna. (c) Response of the circuit in (b) when changing the amplitude of the mutual inductance M.

JNP_11_4_046006_f005.png

In order to provide experimental evidences for the predicted enhancement, arrays of gold nanodisks with diameters of 100, 140, 150, 160, and 170 nm and a pitch of 300 nm were fabricated on a glass substrate using standard electron beam lithography following evaporations and lift-off. The SEM image of a double-layer antenna is shown in Fig. 6(c). For the single-layer antennas, a 1-nm Cr adhesion layer and 40-nm Au were subsequently evaporated. For the double-layer antennas, a bilayer of Cr (1 nm)/Au (20 nm) and a 15-nm spacer of SiO2 and again a bilayer of Cr (1 nm)/Au (20 nm) were evaporated. Optical measurements were performed in transmission with a low numerical aperture 10× objective. Different antenna arrays with the same area were measured and normalized to the direct transmission through the glass substrate without any structure. Figure 6(a) shows extinction (1-transmission)28 measurements and corresponding SIE periodic calculations29 for the five arrays of single-layer, respectively double-layer disks in blue, respectively green. According to these results, the fabricated structures have lower and broader extinction in comparison with the calculations; most likely caused by nanofabrication imperfections and the discrepancy between the permittivity used for the calculation and that of the effectively fabricated antennas.30 However, an enhancement of the extinction, together with a redshift, is clearly visible in that figure when comparing double-layer antennas with single-layer ones [Fig. 6(b)]. In addition, the enhancement is more pronounced for smaller structures and decreases from 28% for 110 nm disks down to 5% for 170 nm disks for the measurements and from 10% to 1.5% for the calculations. This can be attributed to the ratio of the region with penetrated field into the interlayer area to the total increased surface, which decreases for larger structures. Surprisingly, the enhancement observed in the experiment is slightly higher than the enhancement calculated using SIE. This may be related to the inhomogeneity of the evaporation which can cause the formation of many hot spots that can boost the dipolar emission. In that case, the enhancement can be higher for the double-layer antenna since the number of hot spots is larger and the inhomogeneity caused by surface roughness is more pronounced for a 20-nm layer of gold than for a 40-nm layer. In addition, the bulk permittivity of gold used for the calculations might not perfectly match that of fabricated nanostructures. Let us finally mention for the experiments that the thickness of the dielectric layer cannot be excessively thick since an increase of the structure aspect ratio produces pyramidal structures because of the clogging of the lift-off mask during deposition.31

Fig. 6

(a) Measured extinction spectra (solid lines) and periodic SIE calculations (dashed lines) for the arrays of gold single- (blue) and double-layer (green) disks with the diameters of 110, 140, 150, 160, and 170 nm. The thickness of the single-layer disks as well as the total metal thickness for double-layer disks is 40 nm and the thickness of the intermediate SiO2 spacer is 15 nm. Each array has a period of 300 nm and is realized with electron beam lithography, evaporation, and lift-off. (b) Extinction enhancement percentage for different disk diameters. Green and orange bars represent the calculated and measured enhancement, respectively. (c) SEM image of an array of double-layer nanodisks. (d) SEM image of a double-layer disk. The white color bar corresponds to 40 nm.

JNP_11_4_046006_f006.png

2.

Conclusion

In this study, we have investigated the effect of increasing the total metal/dielectric interface for nanoantennas with a fixed metal volume and a constant length. It has been shown that, although the cross section of the antennas is much smaller than the working wavelength, the interaction between the incoming photons and the metal/dielectric interface of the antenna plays a significant role for the optical response of the antenna. Based on this fact, nanoantennas with a larger number of horizontal cuts (i.e., more number of layers) have shown higher scattering cross sections. By increasing the number of interlayers, the scattering cross section increases. In addition, the penetration of the field into an interlayer with a higher thickness is easier and therefore, the photon–electron interaction for the added surfaces is higher. The far-field enhancement obtained for double-layer structures suggests that in practice, standard single layer deposition can be easily substituted by metal/dielectric/metal deposition, where the thickness of the dielectric is 10±5  nm. This approach lends itself to the fabrication of composite plasmonic nanostructures that combine metals and dielectric materials, including semiconductors.32

Acknowledgments

It is a pleasure to acknowledge stimulating discussions with Dr T. V. Raziman. Funding from the European Research Council (ERC-2015-AdG-695206 Nanofactory) is gratefully acknowledged. The authors declare no competing financial interests.

References

1. T. Klar et al., “Surface-plasmon resonances in single metallic nanoparticles,” Phys. Rev. Lett. 80(19), 4249–4252 (1998).PRLTAO0031-9007 http://dx.doi.org/10.1103/PhysRevLett.80.4249 Google Scholar

2. J. P. Kottmann and O. J. F. Martin, “Plasmon resonant coupling in metallic nanowires,” Opt. Express 8, 655–663 (2001).OPEXFF1094-4087 http://dx.doi.org/10.1364/OE.8.000655 Google Scholar

3. P. Muhlschlegel et al., “Resonant optical antennas,” Science 308(5728), 1607–1609 (2005).SCIEAS0036-8075 http://dx.doi.org/10.1126/science.1111886 Google Scholar

4. K. M. Mayer and J. H. Hafner, “Localized surface plasmon resonance sensors,” Chem. Rev. 111(6), 3828–3857 (2011).CHREAY0009-2665 http://dx.doi.org/10.1021/cr100313v Google Scholar

5. S. A. Maier, “Plasmonic field enhancement and SERS in the effective mode volume picture,” Opt. Express 14(5), 1957–1964 (2006).OPEXFF1094-4087 http://dx.doi.org/10.1364/OE.14.001957 Google Scholar

6. A. V. Zayats and I. Smolyaninov, “Near-field photonics: surface plasmon polaritons and localized surface plasmons,” J. Opt. A: Pure Appl. Opt. 5(4), S16–S50 (2003). http://dx.doi.org/10.1088/1464-4258/5/4/353 Google Scholar

7. A. V. Zayats, I. Smolyaninov and A. A. Maradudin, “Nano-optics of surface plasmon polaritons,” Phys. Rep. 408(3–4), 131–314 (2005).PRPLCM0370-1573 http://dx.doi.org/10.1016/j.physrep.2004.11.001 Google Scholar

8. A. M. Kern and O. J. F. Martin, “Excitation and reemission of molecules near realistic plasmonic nanostructures,” Nano Lett. 11(2), 482–487 (2011).NALEFD1530-6984 http://dx.doi.org/10.1021/nl1032588 Google Scholar

9. H. Fischer and O. J. F. Martin, “Engineering the optical response of plasmonic nanoantennas,” Opt. Express 16(12), 9144–9154 (2008).OPEXFF1094-4087 http://dx.doi.org/10.1364/OE.16.009144 Google Scholar

10. A. G. Curto et al., “Unidirectional emission of a quantum dot coupled to a nanoantenna,” Science 329(5994), 930–933 (2010).SCIEAS0036-8075 http://dx.doi.org/10.1126/science.1191922 Google Scholar

11. C. Girard et al., “Importance of confined fields in near-field optical imaging of subwavelength objects,” Phys. Rev. B 50, 14467–14473 (1994).PRBMDO1098-0121 http://dx.doi.org/10.1103/PhysRevB.50.14467 Google Scholar

12. H. Xu and M. Kall, “Polarization-dependent surface-enhanced Raman spectroscopy of isolated silver nanoaggregates,” ChemPhysChem 4(9), 1001–1005 (2003).CPCHFT1439-4235 http://dx.doi.org/10.1002/cphc.v4:9 Google Scholar

13. P. J. Schuck et al., “Improving the mismatch between light and nanoscale objects with gold bowtie nanoantennas,” Phys. Rev. Lett. 94(1), 017402 (2005).PRLTAO0031-9007 http://dx.doi.org/10.1103/PhysRevLett.94.017402 Google Scholar

14. P. Olk et al., “Two particle enhanced nano Raman microscopy and spectroscopy,” Nano Lett. 7(6), 1736–1740 (2007).NALEFD1530-6984 http://dx.doi.org/10.1021/nl070727m Google Scholar

15. K. D. Alexander et al., “A high-throughput method for controlled hot-spot fabrication in SERS-active gold nanoparticle dimer arrays,” J. Raman Spectrosc. 40(12), 2171–2175 (2009).JRSPAF0377-0486 http://dx.doi.org/10.1002/jrs.v40:12 Google Scholar

16. W. H. Zhang et al., “Mode-selective surface-enhanced Raman spectroscopy using nanofabricated plasmonic dipole antennas,” J. Phys. Chem. C 113(33), 14672–14675 (2009). http://dx.doi.org/10.1021/jp9042304 Google Scholar

17. W. Y. Li et al., “Dimers of silver nanospheres: facile synthesis and their use as hot spots for surface-enhanced Raman scattering,” Nano Lett. 9(1), 485–490 (2009).NALEFD1530-6984 http://dx.doi.org/10.1021/nl803621x Google Scholar

18. N. A. Hatab et al., “Free-standing optical gold bowtie nanoantenna with variable gap size for enhanced Raman spectroscopy,” Nano Lett. 10(12), 4952–4955 (2010).NALEFD1530-6984 http://dx.doi.org/10.1021/nl102963g Google Scholar

19. D. K. Lim et al., “Nanogap-engineerable Raman-active nanodumbbells for single-molecule detection,” Nat. Mater. 9(1), 60–67 (2010).NMAACR1476-1122 http://dx.doi.org/10.1038/nmat2596 Google Scholar

20. M. Rycenga et al., “Understanding the SERS effects of single silver nanoparticles and their dimers, one at a time,” J. Phys. Chem. Lett. 1(4), 696–703 (2010).JPCLCD1948-7185 http://dx.doi.org/10.1021/jz900286a Google Scholar

21. K. D. Osberg et al., “Dispersible surface-enhanced Raman scattering nanosheets,” Adv. Mater. 24(45), 6065–6070 (2012).ADVMEW0935-9648 http://dx.doi.org/10.1002/adma.v24.45 Google Scholar

22. J. B. Herzog et al., “Dark plasmons in hot spot generation and polarization in interelectrode nanoscale junctions,” Nano Lett. 13, 1359–1364 (2013).NALEFD1530-6984 http://dx.doi.org/10.1021/nl400363d Google Scholar

23. L. Tong, H. Xu and M. Kall, “Nanogaps for sers applications,” MRS Bull. 39, 163–168 (2014).MRSBEA0883-7694 http://dx.doi.org/10.1557/mrs.2014.2 Google Scholar

24. A. M. Kern and O. J. F. Martin, “Surface integral formulation for 3D simulations of plasmonic and high permittivity nanostructures,” J. Opt. Soc. Am. A 26(4), 732–740 (2009).JOAOD60740-3232 http://dx.doi.org/10.1364/JOSAA.26.000732 Google Scholar

25. P. B. Christy and R. W. Johnson, “Optical constants of transition metals: Ti, V, Cr, Mn, Fe, Co, Ni, and Pd,” Phys. Rev. B 9(12), 15 (1974). http://dx.doi.org/10.1103/PhysRevB.9.5056 Google Scholar

26. J. P. Kottmann et al., “Field polarization and polarization charge distributions in plasmon resonant nanoparticles,” New J. Phys. 2, 27 (2000).NJOPFM1367-2630 http://dx.doi.org/10.1088/1367-2630/2/1/327 Google Scholar

27. B. Abasahl, C. Santschi and O. J. F. Martin, “Quantitative extraction of equivalent lumped circuit elements for complex plasmonic nanostructures,” ACS Photonics 1, 403–407 (2014). http://dx.doi.org/10.1021/ph400101w Google Scholar

28. C. F. Bohren and D. R. Huffman, Absorption and Scattering of Light by Small Particles, John Wiley & Sons, New York (1983). Google Scholar

29. B. Gallinet, A. M. Kern and O. J. F. Martin, “Accurate and versatile modeling of electromagnetic scattering on periodic nanostructures with a surface integral approach,” J. Opt. Soc. Am. A 27, 2261–2271 (2010).JOAOD60740-3232 http://dx.doi.org/10.1364/JOSAA.27.002261 Google Scholar

30. W. Haiss et al., “Determination of size and concentration of gold nanoparticles from UV-vis spectra,” Anal. Chem. 79(11), 4215–4221 (2007).ANCHAM0003-2700 http://dx.doi.org/10.1021/ac0702084 Google Scholar

31. Y. Ekinci et al., “Electric and magnetic resonances in arrays of coupled gold nanoparticle in-tandem pairs,” Opt. Express 16, 13287–13295 (2008).OPEXFF1094-4087 http://dx.doi.org/10.1364/OE.16.013287 Google Scholar

32. H. Wei and H. Xu, “Plasmonics in composite nanostructures,” Mater. Today 17(8), 372–380 (2014).MATOBY1369-7021 http://dx.doi.org/10.1016/j.mattod.2014.05.012 Google Scholar

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Banafsheh Abasahl, Christian Santschi, Olivier J. F. Martin, "Surface-to-volume ratio controls the radiation of stratified plasmonic antennas," Journal of Nanophotonics 11(4), 046006 (30 October 2017). http://dx.doi.org/10.1117/1.JNP.11.046006 Submission: Received 23 August 2017; Accepted 27 September 2017
Submission: Received 23 August 2017; Accepted 27 September 2017
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KEYWORDS
Antennas

Metals

Nanoantennas

Plasmonics

Scattering

Control systems

Dielectrics

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