Surface plasmon polariton

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Surface plasmon polaritons (SPPs) are electromagnetic waves that travel along a metaldielectric or metal–air interface, practically in the infrared or visible-frequency. The term "surface plasmon polariton" explains that the wave involves both charge motion in the metal ("surface plasmon") and electromagnetic waves in the air or dielectric ("polariton").[1]

They are a type of surface wave, guided along the interface in much the same way that light can be guided by an optical fiber. SPPs are shorter in wavelength than the incident light (photons).[2] Hence, SPPs can have tighter spatial confinement and higher local field intensity.[2] Perpendicular to the interface, they have subwavelength-scale confinement. An SPP will propagate along the interface until its energy is lost either to absorption in the metal or scattering into other directions (such as into free space).

Application of SPPs enables subwavelength optics in microscopy and lithography beyond the diffraction limit. It also enables the first steady-state micro-mechanical measurement of a fundamental property of light itself: the momentum of a photon in a dielectric medium. Other applications are photonic data storage, light generation, and bio-photonics.[2][3][4][5]

Excitation

Figure 1: (a) Kretschmann and (b) Otto configuration of an Attenuated Total Reflection setup for coupling surface plasmons. In both cases, the surface plasmon propagates along the metal/dielectric interface
Figure 2: Grating Coupler for Surface Plasmons. The wave vector is increased by the spatial frequency

SPPs can be excited by both electrons and photons. Excitation by electrons is created by firing electrons into the bulk of a metal. As the electrons scatter, energy is transferred into the bulk plasma. The component of the scattering vector parallel to the surface results in the formation of a surface plasmon polariton.[6]

For a photon to excite an SPP, both must have the same frequency and momentum. However, for a given frequency, a free-space photon has more momentum than an SPP because the two have different dispersion relations (see below). This momentum mismatch is the reason that a free-space photon from air cannot couple directly to an SPP. For the same reason, an SPP on a smooth metal surface cannot emit energy as a free-space photon into the dielectric (if the dielectric is uniform). This incompatibility is analogous to the lack of transmission that occurs during total internal reflection.

Nevertheless, coupling of photons into SPPs can be achieved using a coupling medium such as a prism or grating to match the photon and SPP wave vectors (and thus match their momenta). A prism can be positioned against a thin metal film in the Kretschmann configuration or very close to a metal surface in the Otto configuration (Figure 1). A grating coupler matches the wave vectors by increasing the parallel wave vector component by an amount related to the grating period (Figure 2). This method, while less frequently utilized, is critical to the theoretical understanding of the effect of surface roughness. Moreover, simple isolated surface defects such as a groove, a slit or a corrugation on an otherwise planar surface provides a mechanism by which free-space radiation and SPs can exchange energy and hence couple.

Fields and dispersion relation

The properties of an SPP can be derived from Maxwell's equations. We use a coordinate system where the metal–dielectric interface is the ${\displaystyle z=0}$  plane, with the metal at ${\displaystyle z<0}$  and dielectric at ${\displaystyle z>0}$ . The electric and magnetic fields as a function of position ${\displaystyle (x,y,z)}$  and time t are as follows:[7][8]

${\displaystyle E_{x,n}(x,y,z,t)=E_{0}e^{ik_{x}x+ik_{z,n}|z|-i\omega t}}$
${\displaystyle E_{z,n}(x,y,z,t)=\pm E_{0}{\frac {k_{x}}{k_{z,n}}}e^{ik_{x}x+ik_{z,n}|z|-i\omega t}}$
${\displaystyle H_{y,n}(x,y,z,t)=H_{0}e^{ik_{x}x+ik_{z,n}|z|-i\omega t}}$

where

• n indicates the material (1 for the metal at ${\displaystyle z<0}$  or 2 for the dielectric at ${\displaystyle z>0}$ );
• ω is the angular frequency of the waves;
• the ${\displaystyle \pm }$  is + for the metal, − for the dielectric.
• ${\displaystyle E_{x},E_{z}}$  are the x- and z-components of the electric field vector, ${\displaystyle H_{y}}$  is the y-component of the magnetic field vector, and the other components (${\displaystyle E_{y},H_{x},H_{z}}$ ) are zero. In other words, SPPs are always TM (transverse magnetic) waves.
• k is the wave vector; it is a complex vector, and in the case of a lossless SPP, it turns out that the x components are real and the z components are imaginary—the wave oscillates along the x direction and exponentially decays along the z direction. ${\displaystyle k_{x}}$  is always the same for both materials, but ${\displaystyle k_{z,1}}$  is generally different from ${\displaystyle k_{z,2}}$
• ${\displaystyle {\frac {H_{0}}{E_{0}}}=-{\frac {\varepsilon _{1}\omega }{k_{z,1}c}}}$ , where ${\displaystyle \varepsilon _{1}}$  is the permittivity of material 1 (the metal), and c is the speed of light in vacuum. As discussed below, this can also be written${\displaystyle {\frac {H_{0}}{E_{0}}}={\frac {\varepsilon _{2}\omega }{k_{z,2}c}}}$ .

A wave of this form satisfies Maxwell's equations only on condition that the following equations also hold:

${\displaystyle {\frac {k_{z1}}{\varepsilon _{1}}}+{\frac {k_{z2}}{\varepsilon _{2}}}=0}$

and

${\displaystyle k_{x}^{2}+k_{zn}^{2}=\varepsilon _{n}\left({\frac {\omega }{c}}\right)^{2}\qquad n=1,2}$

Solving these two equations, the dispersion relation for a wave propagating on the surface is

${\displaystyle k_{x}={\frac {\omega }{c}}\left({\frac {\varepsilon _{1}\varepsilon _{2}}{\varepsilon _{1}+\varepsilon _{2}}}\right)^{1/2}.}$

Figure 3: Dispersion curve for surface plasmon polaritons. At low k, the surface plasmon curve (red) approaches the photon curve (blue)

In the free electron model of an electron gas, which neglects attenuation, the metallic dielectric function is[9]

${\displaystyle \varepsilon (\omega )=1-{\frac {\omega _{P}^{2}}{\omega ^{2}}},}$

where the bulk plasma frequency in SI units is

${\displaystyle \omega _{P}={\sqrt {\frac {ne^{2}}{{\varepsilon _{0}}m^{*}}}}}$

where n is the electron density, e is the charge of the electron, m is the effective mass of the electron and ${\displaystyle {\varepsilon _{0}}}$  is the permittivity of free-space. The dispersion relation is plotted in Figure 3. At low k, the SPP behaves like a photon, but as k increases, the dispersion relation bends over and reaches an asymptotic limit called the "surface plasma frequency". Since the dispersion curve lies to the right of the light line, ω = kc, the SPP has a shorter wavelength than free-space radiation such that the out-of-plane component of the SPP wavevector is purely imaginary and exhibits evanescent decay. The surface plasma frequency is the asymptote of this curve, and is given by

${\displaystyle \omega _{SP}=\omega _{P}/{\sqrt {1+\varepsilon _{2}}}.}$

In the case of air, this result simplifies to

${\displaystyle \omega _{SP}=\omega _{P}/{\sqrt {2}}.}$

If we assume that ε2 is real and ε2 > 0, then it must be true that ε1 < 0, a condition which is satisfied in metals. Electromagnetic waves passing through a metal experience damping due to Ohmic losses and electron-core interactions. These effects show up in as an imaginary component of the dielectric function. The dielectric function of a metal is expressed ε1 = ε1′ + iε1″ where ε1′ and ε1″ are the real and imaginary parts of the dielectric function, respectively. Generally |ε1| >> ε1″ so the wavenumber can be expressed in terms of its real and imaginary components as[7]

${\displaystyle k_{x}=k_{x}'+ik_{x}''=\left[{\frac {\omega }{c}}\left({\frac {\varepsilon _{1}'\varepsilon _{2}}{\varepsilon _{1}'+\varepsilon _{2}}}\right)^{1/2}\right]+i\left[{\frac {\omega }{c}}\left({\frac {\varepsilon _{1}'\varepsilon _{2}}{\varepsilon _{1}'+\varepsilon _{2}}}\right)^{3/2}{\frac {\varepsilon _{1}''}{2(\varepsilon _{1}')^{2}}}\right].}$

The wave vector gives us insight into physically meaningful properties of the electromagnetic wave such as its spatial extent and coupling requirements for wave vector matching.

Propagation length and skin depth

As an SPP propagates along the surface, it loses energy to the metal due to absorption. The intensity of the surface plasmon decays with the square of the electric field, so at a distance x, the intensity has decreased by a factor of ${\textstyle \exp\{-2k_{x}''x\}}$ . The propagation length is defined as the distance for the SPP intensity to decay by a factor of 1/e. This condition is satisfied at a length[10]

${\displaystyle L={\frac {1}{2k_{x}''}}.}$

Likewise, the electric field falls off evanescently perpendicular to the metal surface. At low frequencies, the SPP penetration depth into the metal is commonly approximated using the skin depth formula. In the dielectric, the field will fall off far more slowly. The decay lengths in the metal and dielectric medium can be expressed as[10]

${\displaystyle z_{i}={\frac {\lambda }{2\pi }}\left({\frac {|\varepsilon _{1}'|+\varepsilon _{2}}{\varepsilon _{i}^{2}}}\right)^{1/2}}$

where i indicates the medium of propagation. SPPs are very sensitive to slight perturbations within the skin depth and because of this, SPPs are often used to probe inhomogeneities of a surface.

Experimental applications

Nanofabricated systems that exploit SPPs demonstrate potential for designing and controlling the propagation of light in matter. In particular, SPPs can be used to channel light efficiently into nanometer scale volumes, leading to direct modification of resonate frequency dispersion properties (substantially shrinking the wavelength of light and the speed of light pulses for example), as well as field enhancements suitable for enabling strong interactions with nonlinear materials. The resulting enhanced sensitivity of light to external parameters (for example, an applied electric field or the dielectric constant of an adsorbed molecular layer) shows great promise for applications in sensing and switching.

Current research is focused on the design, fabrication, and experimental characterization of novel components for measurement and communications based on nanoscale plasmonic effects. These devices include ultra-compact plasmonic interferometers for applications such as biosensing, optical positioning and optical switching, as well as the individual building blocks (plasmon source, waveguide and detector) needed to integrate a high-bandwidth, infrared-frequency plasmonic communications link on a silicon chip.

In addition to building functional devices based on SPPs, it appears feasible to exploit the dispersion characteristics of SPPs traveling in confined metallo-dielectric spaces to create photonic materials with artificially tailored bulk optical characteristics, otherwise known as metamaterials.[5]

The excitation of SPPs is frequently used in an experimental technique known as surface plasmon resonance (SPR). In SPR, the maximum excitation of surface plasmons are detected by monitoring the reflected power from a prism coupler as a function of incident angle, wavelength or phase.[11] This technique can be used to observe nanometer changes in thickness, density fluctuations, or molecular adsorption.

Surface plasmon-based circuits, including both SPPs and localized plasmon resonances, have been proposed as a means of overcoming the size limitations of photonic circuits for use in high performance data processing nano devices.[12]

The ability to dynamically control the plasmonic properties of materials in these nano-devices is key to their development. A new approach that uses plasmon-plasmon interactions has been demonstrated recently. Here the bulk plasmon resonance is induced or suppressed to manipulate the propagation of light.[13] This approach has been shown to have a high potential for nanoscale light manipulation and the development of a fully CMOS- compatible electro-optical plasmonic modulator.

CMOS compatible electro-optic plasmonic modulators will be key components in chip-scale photonic circuits.[14]

In surface second harmonic generation, the second harmonic signal is proportional to the square of the electric field. The electric field is stronger at the interface because of the surface plasmon resulting in a non-linear optical effect. This larger signal is often exploited to produce a stronger second harmonic signal.[15]

The wavelength and intensity of the plasmon-related absorption and emission peaks are affected by molecular adsorption that can be used in molecular sensors. For example, a fully operational prototype device detecting casein in milk has been fabricated. The device is based on monitoring changes in plasmon-related absorption of light by a gold layer.[16]

Materials used

Surface plasmon polaritons can only exist at the interface between a positive-permittivity material and a negative-permittivity material.[17] The positive-permittivity material, often called the dielectric material, can be any transparent material such as air or (for visible light) glass. The negative-permittivity material, often called the plasmonic material,[18] may be a metal or other material. It is more critical, as it tends to have a large effect on the wavelength, absorption length, and other properties of the SPP. Some plasmonic materials are discussed next.

Metals

For visible and near-infrared light, the only plasmonic materials are metals, due to their abundance of free electrons,[18] which leads to a high plasma frequency. (Materials have negative real permittivity only below their plasma frequency.)

Unfortunately, metals suffer from ohmic losses that can degrade the performance of plasmonic devices. The need for lower loss has fueled research aimed at developing new materials for plasmonics[18][19][20] and optimizing the deposition conditions of existing materials.[21] Both the loss and polarizability of a material affect its optical performance. The quality factor ${\displaystyle Q_{SPP}}$  for a SPP is defined as ${\displaystyle {\frac {\varepsilon '^{2}}{\varepsilon ''}}}$ .[20] The table below shows the quality factors and SPP propagation lengths for four common plasmonic metals; Al, Ag, Au and Cu deposited by thermal evaporation under optimized conditions.[21] The quality factors and SPP propagation lengths were calculated using the optical data from the Al, Ag, Au and Cu films.

Wavelength Regime Metal ${\displaystyle Q_{SPP}(\times 10^{-3})}$  ${\displaystyle L_{SPP}(\mu m)}$
Ultraviolet (280 nm) Al 0.07 2.5
Visible (650 nm) Ag 1.2 84
Cu 0.42 24
Au 0.4 20
Near-Infrared (1000 nm) Ag 2.2 340
Cu 1.1 190
Au 1.1 190
Telecom (1550 nm) Ag 5 1200
Cu 3.4 820
Au 3.2 730

Silver exhibits the lowest losses of current materials in both the visible, near-infrared (NIR) and telecom wavelengths.[21] Gold and copper perform equally well in the visible and NIR with copper having a slight advantage at telecom wavelengths. Gold has the advantage over both silver and copper of being chemically stable in natural environments making it well suited for plasmonic biosensors.[22] However, an interband transition at ~470 nm greatly increases the losses in gold at wavelengths below 600 nm.[23] Aluminum is the best plasmonic material in the ultraviolet regime (< 330 nm) and is also CMOS compatible along with copper.

Other materials

The fewer electrons a material has, the lower (i.e. longer-wavelength) its plasma frequency becomes. Therefore, at infrared and longer wavelengths, various other plasmonic materials also exist besides metals.[18] These include transparent conducting oxides, which have typical plasma frequency in the NIR-SWIR infrared range.[24] At longer wavelengths, semiconductors may also be plasmonic.

Some materials have negative permittivity at certain infrared wavelengths related to phonons rather than plasmons (so-called reststrahlen bands). The resulting waves have the same optical properties as surface plasmon polaritons, but are called by a different term, surface phonon polaritons.

Effects of roughness

In order to understand the effect of roughness on SPPs, it is beneficial to first understand how a SPP is coupled by a grating Figure2. When a photon is incident on a surface, the wave vector of the photon in the dielectric material is smaller than that of the SPP. In order for the photon to couple into a SPP, the wave vector must increase by ${\displaystyle \Delta k=k_{SP}-k_{x,{\text{photon}}}}$ . The grating harmonics of a periodic grating provide additional momentum parallel to the supporting interface to match the terms.

${\displaystyle k_{SPP}=k_{x,{\text{photon}}}\pm n\ k_{\text{grating}}={\frac {\omega }{c}}\sin {\theta _{0}}\pm n{\frac {2\pi }{a}},}$

where ${\displaystyle k_{\text{grating}}}$  is the wave vector of the grating, ${\displaystyle \theta _{0}}$  is the angle of incidence of the incoming photon, a is the grating period, and n is an integer.

Rough surfaces can be thought of as the superposition of many gratings of different periodicities. Kretschmann proposed[25] that a statistical correlation function be defined for a rough surface

${\displaystyle G(x,y)={\frac {1}{A}}\int _{A}z(x',y')\ z(x'-x,y'-y)\,dx'\,dy',}$

where ${\displaystyle z(x,y)}$  is the height above the mean surface height at the position ${\displaystyle (x,y)}$ , and ${\displaystyle A}$  is the area of integration. Assuming that the statistical correlation function is Gaussian of the form

${\displaystyle G(x,y)=\delta ^{2}\exp \left(-{\frac {r^{2}}{\sigma ^{2}}}\right)}$

where ${\displaystyle \delta }$  is the root mean square height, ${\displaystyle r}$  is the distance from the point ${\displaystyle (x,y)}$ , and ${\displaystyle \sigma }$  is the correlation length, then the Fourier transform of the correlation function is

${\displaystyle |s(k_{\text{surf}})|^{2}={\frac {1}{4\pi }}\sigma ^{2}\delta ^{2}\exp \left(-{\frac {\sigma ^{2}k_{\text{surf}}^{2}}{4}}\right)}$

where ${\displaystyle s}$  is a measure of the amount of each spatial frequency ${\displaystyle k_{\text{surf}}}$  which help couple photons into a surface plasmon.

If the surface only has one Fourier component of roughness (i.e. the surface profile is sinusoidal), then the ${\displaystyle s}$  is discrete and exists only at ${\displaystyle k={\frac {2\pi }{a}}}$ , resulting in a single narrow set of angles for coupling. If the surface contains many Fourier components, then coupling becomes possible at multiple angles. For a random surface, ${\displaystyle s}$  becomes continuous and the range of coupling angles broadens.

As stated earlier, SPPs are non-radiative. When a SPP travels along a rough surface, it usually becomes radiative due to scattering. The Surface Scattering Theory of light suggests that the scattered intensity ${\displaystyle dI}$  per solid angle ${\displaystyle d\Omega }$  per incident intensity ${\displaystyle I_{0}}$  is[26]

${\displaystyle {\frac {dI}{d\Omega \ I_{0}}}={\frac {4{\sqrt {\varepsilon _{0}}}}{\cos {\theta _{0}}}}{\frac {\pi ^{4}}{\lambda ^{4}}}|t_{012}^{p}|^{2}\ |W|^{2}|s(k_{\text{surf}})|^{2}}$

where ${\displaystyle |W|^{2}}$  is the radiation pattern from a single dipole at the metal/dielectric interface. If surface plasmons are excited in the Kretschmann geometry and the scattered light is observed in the plane of incidence (Fig. 4), then the dipole function becomes

${\displaystyle |W|^{2}=A(\theta ,|\varepsilon _{1}|)\ \sin ^{2}{\psi }\ [(1+\sin ^{2}\theta /|\varepsilon _{1}|)^{1/2}-\sin {\theta }]^{2}}$

with

${\displaystyle A(\theta ,|\varepsilon _{1}|)={\frac {|\varepsilon _{1}|+1}{|\varepsilon _{1}|-1}}{\frac {4}{1+\tan {\theta }/|\varepsilon _{1}|}}}$

where ${\displaystyle \psi }$  is the polarization angle and ${\displaystyle \theta }$  is the angle from the z-axis in the xz-plane. Two important consequences come out of these equations. The first is that if ${\displaystyle \psi =0}$  (s-polarization), then ${\displaystyle |W|^{2}=0}$  and the scattered light ${\displaystyle {\frac {dI}{d\Omega \ I_{0}}}=0}$ . Secondly, the scattered light has a measurable profile which is readily correlated to the roughness. This topic is treated in greater detail in reference.[26]

References

1. ^ S.Zeng; Baillargeat, Dominique; Ho, Ho-Pui; Yong, Ken-Tye; et al. (2014). "Nanomaterials enhanced surface plasmon resonance for biological and chemical sensing applications" (PDF). Chemical Society Reviews. 43 (10): 3426–3452. doi:10.1039/C3CS60479A. PMID 24549396.
2. ^ a b c NIST researchers, Nanofabrication Research Group (2009-08-20). "Three-Dimensional Plasmonic Metamaterials". National Institute of Science and Technology. Retrieved 2011-02-15.
3. ^ Yarris, Lynn (2009-08-20). "GRIN Plasmonics…" (Online news release). U.S. Department of Energy National Laboratory Operated by the University of California. Retrieved 2011-02-15.
4. ^ Barnes, William L.; Dereux, Alain; Ebbesen, Thomas W. (2003). "Surface plasmon subwavelength optics". Nature. 424 (6950): 824–30. Bibcode:2003Natur.424..824B. doi:10.1038/nature01937. PMID 12917696.
5. ^ a b NIST researchers, Nanofabrication Research Group. "Nanoplasmonics" (Online). National Institute of Science and Technology. Retrieved 2011-02-15.
6. ^ Zeng, Shuwen; Yu, Xia; Law, Wing-Cheung; Zhang, Yating; Hu, Rui; Dinh, Xuan-Quyen; Ho, Ho-Pui; Yong, Ken-Tye (2013). "Size dependence of Au NP-enhanced surface plasmon resonance based on differential phase measurement". Sensors and Actuators B: Chemical. 176: 1128–1133. doi:10.1016/j.snb.2012.09.073.
7. ^ a b Raether, Heinz (1988). Surface Plasmons on Smooth and Rough Surfaces and on Gratings. Springer Tracts in Modern Physics 111. New York: Springer-Verlag. ISBN 978-3540173632.
8. ^ Cottam, Michael G. (1989). Introduction to Surface and Superlattice Excitations. New York: Cambridge University Press. ISBN 978-0750305884.
9. ^ Kittel, Charles (1996). Introduction to Solid State Physics (8th ed.). Hoboken, NJ: John Wiley & Sons. ISBN 978-0-471-41526-8.
10. ^ a b Homola, Jirí (2006). Surface Plasmon Resonance Based Sensors. Springer Series on Chemical Sensors and Biosensors, 4. Berlin: Springer-Verlag. ISBN 978-3-540-33918-2.
11. ^ Vo-Dinh, Tuan (2017). "Chapter 13 - Biomolecule Sensing Using Surface Plasmon Resonance". Nanotechnology in Biology and Medicine Methods, Devices, and Applications, Second Edition. United States: CRC Press. pp. 259–288. ISBN 978-1439893784.
12. ^ Ozbay, E. (2006). "Plasmonics: Merging Photonics and Electronics at Nanoscale Dimensions". Science. 311 (5758): 189–93. Bibcode:2006Sci...311..189O. doi:10.1126/science.1114849. hdl:11693/38263. PMID 16410515.
13. ^ Akimov, Yu A; Chu, H S (2012). "Plasmon–plasmon interaction: Controlling light at nanoscale". Nanotechnology. 23 (44): 444004. doi:10.1088/0957-4484/23/44/444004. PMID 23080049.
14. ^ Wenshan Cai; Justin S. White & Mark L. Brongersma (2009). "Compact, High-Speed and Power-Efficient Electrooptic Plasmonic Modulators". Nano Letters. 9 (12): 4403–11. Bibcode:2009NanoL...9.4403C. doi:10.1021/nl902701b. PMID 19827771.
15. ^ V. K. Valev (2012). "Characterization of Nanostructured Plasmonic Surfaces with Second Harmonic Generation". Langmuir. 28 (44): 15454–15471. doi:10.1021/la302485c. PMID 22889193.
16. ^ Minh Hiep, Ha; Endo, Tatsuro; Kerman, Kagan; Chikae, Miyuki; Kim, Do-Kyun; Yamamura, Shohei; Takamura, Yuzuru; Tamiya, Eiichi (2007). "A localized surface plasmon resonance based immunosensor for the detection of casein in milk" (free download pdf). Science and Technology of Advanced Materials. 8 (4): 331. Bibcode:2007STAdM...8..331M. doi:10.1016/j.stam.2006.12.010.
17. ^ Pochi Yeh (3 March 2005). Optical Waves in Layered Media. Wiley. ISBN 978-0-471-73192-4.
18. ^ a b c d West, P.R.; Ishii, S.; Naik, G.V.; Emani, N.K.; Shalaev, V.M.; Boltasseva, A. (2010). "Searching for better plasmonic materials". Laser & Photonics Reviews. 4 (6): 795–808. arXiv:0911.2737. Bibcode:2010LPRv....4..795W. doi:10.1002/lpor.200900055. ISSN 1863-8880.
19. ^ Boltasseva, A.; Atwater, H. A. (2011). "Low-Loss Plasmonic Metamaterials". Science. 331 (6015): 290–291. Bibcode:2011Sci...331..290B. doi:10.1126/science.1198258. ISSN 0036-8075. PMID 21252335.
20. ^ a b Blaber, M G; Arnold, M D; Ford, M J (2010). "A review of the optical properties of alloys and intermetallics for plasmonics". Journal of Physics: Condensed Matter. 22 (14): 143201. arXiv:1001.4867. Bibcode:2010JPCM...22n3201B. doi:10.1088/0953-8984/22/14/143201. ISSN 0953-8984. PMID 21389523.
21. ^ a b c McPeak, Kevin M.; Jayanti, Sriharsha V.; Kress, Stephan J. P.; Meyer, Stefan; Iotti, Stelio; Rossinelli, Aurelio; Norris, David J. (2015). "Plasmonic Films Can Easily Be Better: Rules and Recipes". ACS Photonics. 2 (3): 326–333. doi:10.1021/ph5004237. ISSN 2330-4022. PMC 4416469. PMID 25950012.
22. ^ Homola, Jir (2003). "Present and future of surface plasmon resonance biosensors". Analytical and Bioanalytical Chemistry. 377 (3): 528–539. doi:10.1007/s00216-003-2101-0. ISSN 1618-2642. PMID 12879189.
23. ^ Etchegoin, P. G.; Le Ru, E. C.; Meyer, M. (2006). "An analytic model for the optical properties of gold". The Journal of Chemical Physics. 125 (16): 164705. Bibcode:2006JChPh.125p4705E. doi:10.1063/1.2360270. ISSN 0021-9606. PMID 17092118.
24. ^ Dominici, L; Michelotti, F; Brown, TM; et al. (2009). "Plasmon polaritons in the near infrared on fluorine doped tin oxide films". Optics Express. 17 (12): 10155–67. Bibcode:2009OExpr..1710155D. doi:10.1364/OE.17.010155. PMID 19506669.
25. ^ Kretschmann, E. (April 1974). "Die Bestimmung der Oberflächenrauhigkeit dünner Schichten durch Messung der Winkelabhängigkeit der Streustrahlung von Oberflächenplasmaschwingungen". Optics Communications (in German). 10 (4): 353–356. Bibcode:1974OptCo..10..353K. doi:10.1016/0030-4018(74)90362-9.
26. ^ a b Kretschmann, E. (1972). "The angular dependence and the polarisation of light emitted by surface plasmons on metals due to roughness". Optics Communications. 5 (5): 331–336. Bibcode:1972OptCo...5..331K. doi:10.1016/0030-4018(72)90026-0.