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Optics Express

Optics Express

  • Editor: C. Martijn de Sterke
  • Vol. 17, Iss. 14 — Jul. 6, 2009
  • pp: 12145–12154
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Sensitivity enhancement in grating coupled surface plasmon resonance by azimuthal control

F. Romanato, K. H. Lee, H. K. Kang, G. Ruffato, and C. C. Wong  »View Author Affiliations


Optics Express, Vol. 17, Issue 14, pp. 12145-12154 (2009)
http://dx.doi.org/10.1364/OE.17.012145


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Abstract

We present a method for improving the sensing capability of grating coupled surface plasmon resonance (GCSPR) sensors. The grating is rotated azimuthally (φ) until the excitation of double surface plasmon polaritions (SPPs) by a single wavelength is possible. Close to this condition, further tuning of the incident wavelength will merge the double SPPs into a multi-SPP resonance which is angularly broad but spectrally sharp. This is the condition where the momentum vector of the propagating SPP is perpendicular to the incident light momentum. We demonstrate this sensitivity enhancement on a Au grating surface using a dodecanethiol (C12) self-assembled monolayer (SAM). Using this method, a shift in resonance angle as large as 3° can be observed. The simulated sensitivity of this method shows that a sensitivity up to 800°/RIU is achievable, which is one order of magnitude greater than that in a conventional fixed grating (φ=0°) as well as the prism-coupled Kretschmann configuration.

© 2009 OSA

1. Introduction

Surface Plasmon Polaritons (SPP) are electromagnetic waves coupled with surface plasma charge oscillations that propagate along the metal/dielectric interface. Due to its non-radiative nature, SPP can be excited by an incident EM-wave illuminating the metal surface (Surface Plasmon Resonance - SPR) only in proper configurations such as prism-coupling and grating-coupling setup [1

1. H. Raether, “Surface Plasmons on Smooth and Rough Surfaces and on Gratings,” (Springer-Verlag, 1988).

]. The resonance condition is extremely sensitive to the changes in refractive index on the metal film within a thickness comparable to the vertical extinction length of SPP [2

2. L. S. Jung, C. T. Campbell, T. M. Chinowsky, M. N. Mar, and S. S. Yee, “Quantitative interpretation of the response of surface plasmon resonance sensors to adsorbed films,” Langmuir 14(19), 5636–5648 (1998). [CrossRef]

]. Due to these properties, SPR reveals itself as a useful instrument for the study of surface optical properties and it is a highly suitable candidate as a sensor for liquid or gas solutions [3

3. I. Lundstrom, “Real-time biospecific interaction analysis,” Biosens. Bioelectron. 9(9–10), 725–736 (1994). [CrossRef]

5

5. K. A. Peterlinz and R. Georgiadis, “In Situ Kinetics of Self-Assembly by Surface Plasmon Resonance Spectroscopy,” Langmuir 12(20), 4731–4740 (1996). [CrossRef]

] and surface chemistry [6

6. J. Homola, S. S. Yee, and G. Gauglitz, “Surface plasmon resonance sensors: review,” Sens. Actuators B Chem. 54(1–2), 3–15 (1999). [CrossRef]

].

Currently, several groups are using different SPR approaches to detect the change of refractive index [7

7. A. J. Haes and R. P. Van Duyne, “A unified view of propagating and localized surface plasmon resonance biosensors,” Anal. Bioanal. Chem. 379(7–8), 920–930 (2004).

10

10. C. Yu and J. Irudayaraj, “Multiplex biosensor using gold nanorods,” Anal. Chem. 79(2), 572–579 (2007). [CrossRef]

]. Sensors using prism-coupled SPR (PCSPR) with Kretschmann configuration [11

11. J. Melendez, R. Carr, D. U. Bartholomew, K. Kukanskis, J. Elkind, S. Yee, C. Furlong, and R. Woodbury, “A commercial solution for surface plasmon sensing,” Sens. Actuators B Chem. 35(1–3), 212–216 (1996). [CrossRef]

] typically show refractive index sensitivity for typical angular interrogation architecture that ranges between 50 and 150°/RIU [12

12. B. Liedberg, I. Lundstrom, and E. Stenberg, “Principle of biosensing with an extended coupling matrix and surface plasmon resonance,” Sens. Actuators B Chem. 11(1–3), 63–72 (1993). [CrossRef]

,13

13. R. Karlsson and R. Ståhlberg, “Surface plasmon resonance detection and multispot sensing for direct monitoring of interactions involving low-molecular-weight analytes and for determination of low affinities,” Anal. Biochem. 228(2), 274–280 (1995). [CrossRef]

], with higher sensitivity at shorter wavelengths [14

14. J. Homola, I. Koudela, and S. S. Yee, “Surface plasmon resonance sensor based on diffraction gratings and prism couplers: sensitivity comparison,” Sens. Actuator B 54(1–2), 16–24 (1999). [CrossRef]

]. However, PCSPR sensors suffer from cumbersome optical alignment [15

15. D. W. Unfricht, S. L. Colpitts, S. M. Fernandez, and M. A. Lynes, “Grating-coupled surface plasmon resonance: a cell and protein microarray platform,” Proteomics 5(17), 4432–4442 (2005). [CrossRef]

] and are not amenable to miniaturization and integration [16

16. X. D. Hoa, A. G. Kirk, and M. Tabrizian, “Towards integrated and sensitive surface plasmon resonance biosensors: a review of recent progress,” Biosens. Bioelectron. 23(2), 151–160 (2007). [CrossRef]

].

Another common way for SPR excitation is to use a metallic grating. Grating coupled SPR (GCSPR) sensors with either wavelength or angular interrogation have been demonstrated to have sensitivity 2–3 times lower than PCSPR [17

17. K. H. Yoon, M. L. Shuler, and S. J. Kim, “Design optimization of nano-grating surface plasmon resonance sensors,” Opt. Express 14(11), 4842–4849 (2006). [CrossRef]

,18

18. D. C. Cullen and C. R. Lowe, “A direct surface plasmon-polariton immunosensor: Preliminary investigation of the non-specific adsorption of serum components to the sensor interface,” Sens. Actuators B Chem. 1(1–6), 576–579 (1990). [CrossRef]

]. However, GCSPR has the intrinsic possibility to be used with different sensing architectures and interrogation systems. A parallel SPR angular detection was shown by Unfrict et al. to have the possibility for multi detection for proteomic multiarray. Homola’s group demonstrated an SPR biosensor with a refractive index sensitivity of 695 nm/RIU by using wavelength interrogation, exploiting the advantages of both long-range and short-range surface plasmons excited simultaneously on a diffraction grating [19

19. M. Vala, J. \, and J. Homola, “Diffraction grating-coupled surface plasmon resonance based on spectroscopy of long-range and short-range surface plasmons,” Proc. SPIE 6585, 658522 (2007). [CrossRef]

]. Most recently, Alleyne [20

20. C. J. Alleyne, A. G. Kirk, R. C. McPhedran, N. A. P. Nicorovici, and D. Maystre, “Enhanced SPR sensitivity using periodic metallic structures,” Opt. Express 15(13), 8163–8169 (2007). [CrossRef]

] has exploited the generation of an optical band gap in GCSPR by using prism-coupled to achieve sensitivity down to 680°/RIU by bandgap-assisted GCSPR. A miniaturized GCSPR sensor implemented with a CCD allowed detection sensitivity of 50°/RIU over 200 sensing parallel channels [21

21. J. M. Brockman and S. M. Fernandes, “Grating-coupled surface plasmon resonance for rapid, label-free, array based sensing,” Am. Lab. 33, 37–41 (2001).

23

23. J. Dostalek, J. Homola, and M. Miler, “Rich information format surface plasmon resonance biosensor based on array of diffraction gratings,” Sens. Actuators B Chem. 107(1), 154–161 (2005). [CrossRef]

].

2. Experimental

The 1D sinusoidal grating used in this study, with a period of 487 nm and amplitude of 25 nm, was generated by interference lithography (IL). The IL system was performed using Lloyd’s configuration [27

27. B. Thomas, O. Reilly, and I. H. I. Smith, “Linewidth uniformity in Lloyd’s mirror interference lithography systems,” J. Vac. Sci. Technol. B 26(6), 2131–2134 (2008).

] using a rotating sample holder stage with precision 0.01° in order to have a fine control of the periodicity over the sample. A 40 mW helium cadmium (HeCd) laser from KIMMON emitting a single TEM 00 mode at 325 nm/441.6 nm is used as the source. The resulting grating has an almost perfect sinusoidal profile with a local roughness of the order of 1 nm rms. Subsequently the grating was formed by thermally evaporating a gold (7nm)/silver (37nm) bi-metallic layer. Silver is preferred because it has a smaller extinction coefficient than gold and therefore suffers less loss during coupling (higher plasmonic coupling efficiency). However a very thin gold coating is used to protect silver from oxidation and provides an inert surface for bio functionalization.

Reflectivity spectra were acquired using a J.A. Woollam Co. VASE instrument with an angular and wavelength spectroscopic resolution of 0.005° and 0.3 nm respectively. The measurements are collected before and after C12-SAM coating on Au grating in air environment. The sample is sitting on the center of rotation of the rotator, thus the location for data collection before and after coating with C12-SAM is not changed with azimuthal rotation.

Incoming light with a k⃗ph wave-vector forms an angle θ with the normal z-axis. Measurements are taken in a θ/2θ symmetric reflectivity configuration, with θ scanned from 15° to 80° with a step size of 0.5°, using a 75W Xe lamp, monochromatized between 590 nm and 800 nm in steps of 4 nm. In our experimental method, the scattering plane is fixed and the gratings are mounted on a sample holder that can be rotated azimuthally to define the φ angle. Grating orientations used in this experiment were 0° and 60°. The grating lattice period has been determined in 487.3 nm using asymmetric diffraction configuration.

3. Results

Fig. 1. Comparison of SPR spectrum between uncoated (solid line) and C12-coated (dashed line) Au grating. (a) Grating with φ=0° (conventional mounted grating), where different line colors correspond to different incident wavelengths; and (b) φ=60° (2 SPPs by single wavelength excitation condition), different colors of line represent difference incident wavelength.

4. Analysis and discussion

The analysis of the wave-vector components allows a description of double SPP excitation using the schematic shown in Fig. 2. The excitation of SPPs on a grating is achieved when the on-plane component of the incident light wave-vector and the diffracted SPP wave-vector ksp match the momentum conservation condition:

ksp=kph±mg
(1)

where kph=2πλ(sinθin,0),θin, θin is the angle of incidence, the crystal momentum is g=2πΛ(cosφ,sinφ) whose rotation is measured by φ, and Λ is the grating pitch. Only the first diffraction order (m=1) is used because in our case, g⃗ is always greater than kph. All quadrants of the circle can be explored for SPP excitation as long as Eq. (1) is satisfied. For symmetry reason, only ky positive half space is shown.

Fig. 2. Schematic represents wave-vectors combination. The large circle represents equimagnitude g⃗ vectors. The smaller black and green circles represent equi-magnitude vectors before, (k⃗spp1), and after (k⃗spp2), the surface functionalization with C12 SAM. The dashed lines represent a photon wave-vector and the dotted lines represent the SPP propagation direction, β. The letters A and B represent the g⃗ vector with azimuthal rotation φ=0° and φ=60° respectively. The capital letters with the primes represent the intersection of the photon wave-vector with the SPP semicircles.

sp vectors with equal

The largest circle in k -space represents equi-magnitude g⃗ vectors at different azimuthal orientation. The two smaller circles represent all possible k⃗sp vectors with equal magnitude respectively before and after C12 surface functionalization and whose modulus is given by

kSPP=kph=εMεDεM+εD=kphM
(2)

where εM and εD are the dielectric constants of the metal and the dielectric medium respectively. After the coating, the SPP modulus increases because of the small increase in εD due to the surface SAM functionalization with C12.

The dashed line at the tip of the circle of radius g⃗ represents the x component of the photon wave-vector kph, the only component that participates in SPP excitation. The line is scaled linearly in sinθin such that the full length of the line at the incident angle θin of 90° corresponds to the maximum value of kph..

The intersections of the kph dashed horizontal line with the smaller kspp circle determine the conditions for which Eq. (1) is satisfied and allows identification of both incident angle θin for SPP resonance excitation and SPP propagation direction, β. We consider first the case of the uncoated sample - the smallest of the semicircles. For example, point B on the g⃗ circle is identified by the azimuthal angle φ and allows the excitation of SPP at two possible conditions: B1 and B1, with β+ and β-, respectively. Within the double SPP range (point B), a small increment in wavelength makes the points B1 and B1 merge, to form a very broad resonance as shown by wavelength dependence of the reflectivity spectra (Fig. 1(b)). On the contrary, at φ=0° (point A) it is clear that the photon wave-vector can intersect the SPP circle only in the first quadrant but not the second, thus exciting only a single SPP for each wavelength (Fig. 1.).

The same understanding is applicable for light exciting SPP on the C12 coated sample. Due to larger kspp, different excitation condition is expected. The intersection points changes from B1 and B1 to B2 and B2 and from A 1 to A 2. The sensitivity of the GCSPP is higher at high azimuthal angles because the condition for double SPP excitation around the circumference of the kspp circle generates a shifts in k-space between points B1’ and B2’, which is much larger than that between points A1 and A2 provided by a single SPP excitation condition for φ=0°.

The estimated refractive index sensitivity, S, of this configuration can be defined as:

S=θn=θkphxkphxkSPPkSPPn
(3)

In order to calculate S, we assume the rippling amplitude, δ, of the grating is so shallow (δ/Λ=0.05 in our case) that the dispersion curve of SPP traveling at the metal-dielectric interface of a grating can be approximated by the case of a flat sample as described by Eq. (2). With Fig. 2 as a reference, the analytical expression for the sensitivity in angular interrogation can be found as:

S=1cosθr(Mn0)31Λ2+sin2θλ22cosϕsinθΛλcosϕΛsinθλ
(4)

where M is defined in Eq. (2), n 0 is the refractive index of the surrounding dielectric medium, λ is the incident wavelength and θr is the resonance angle that is equal to

θr=sin1(λΛcosϕM2(λΛ)2sin2ϕ)
(5)

The functional behavior of sensitivity for the first and second SPP dip is shown in Fig. 3 for a typical wavelength of λ=606 nm. Both the sensitivities diverge when φ approaches its critical value ϕMAX, i.e. the maximum ϕ angle that supports SPP resonances. In this configuration, incident photon momentum is tangential to the kspp circle and its length equals to the kx-component of the grating momentum in so that the denominator of the third term in Eq. (4) becomes null. Another condition for second dip sensitivity singularity is when the φ approaches critical azimuthal angle, φc, necessary to excite double SPP resonances, namely when the full length of the incident photon momentum is required to intersect the edge of the kspp circle. Since the incident angle θin=90°, cosθ in the denominator of the first term Eq. (4) approaches 0 and S diverges.

Fig. 3. Sensitivity, S as a function of grating azimuthal angle, φ for the two dips for the SPR sensor with angular interrogation. The right y-scale refers to sensitivity values normalized to the first dip sensitivity at φ=0 (Sr=S/S1(0)). In the subset figure, more detail is shown.

Although φ close to the critical values provides a great enhancement in S (up to 2400 °/RIU, 35 times higher than φ=0°), these configurations should be avoided because of experimental limits. For φφc, θr becomes large (θ>70°) and broad, becoming impossible to resolve the SPP minimum. In addition, when φφMAX, the two resonance dips merge into a single broad dip which makes the two minima indistinguishable. Thus only limited parts of the azimuthal angular range are suitable for enhancing sensitivity significantly. The best conditions correspond to the middle of the “U-shape” of second dip functional behavior (inset of Fig. 3) where the sensitivity ranges from 900 to 1100 °/RIU, about 15 times higher than φ=0° whose value is 67°/RIU. The sensitivity computed for the first SPP dip is smaller all over this range but it still provides values of the order of 500°/RIU.

The experimental determinations of the wavevector kph of the incoming light necessary for the SPP excitation have been successfully fitted with the help of Eq. (1), using as fitting parameters only the effective index of refraction and azimuthal angle. After surface functionalization we have determined a total increment in index of refraction equal to Δn=0.00357±0.00007 RIU. This is a value that agrees with the estimation of Δn=0.0038 RIU performed for effective refractive index change generated by a full surface coverage of closepacked self assembled C12 molecules, considering their length=1.488 nm and dielectric constant εC12=2.205. Also the theoretical sensitivity determination is in good agreement with the experimental determination obtained as a ratio between Δθ, the angular differences before and after C12 coating and the Δn determination as shown in Fig. 4(a). The average experimental sensitivity is of the order of 520°/RIU for the first dip and reaches maximum values of 857 °/RIU for the second dip.

The final error of the refractive index determination has been estimated on the basis of chi-square minimization based on a priori determination of the SPP angular position. The reflectivity minima of this preliminary data set have been determined with a typical uncertainty of ±0.07° deg. However the a posteriori determination of the SPP angular average deviation with respect to the dispersion curve best fit is much smaller, on the order of 0.015°, as can be confirmed by a simple graphical inspection. Taking into account this more realistic value for the final evaluation of the uncertainty, the value of δΔn is 7×10-5 RIU. However, because our experimental system has an instrumental resolution of 0.001°, we believe it will be possible to greatly decrease the present angular uncertainty by increasing the statistical signal-to-noise ratio and using appropriate algorithms for data analysis. We expect that experimental uncertainties of Δn on the order of ±5×10-7 RIU is achievable.

In order to better describe the detection improvement given by azimuthal rotation, we have also measured the typical figure of merit for angular and yield interrogation respectively defined as:

FOMang=SΔθFWHM=(θn)ΔθFWHM
(6)
FOMY=1Δn(YcoatYuncoated)Yuncoated
(7)

where S is the sensitivity given by Eq. (4), ΔθFWHM is the angular full width at half maximum of the reflectivity minima, whereas Ycoat and Yuncoat are the minimum yield of the reflectivity spectra collected before and after C12 functionalization at SPR resonances. Figure 4(b) shows the angular and yield FOM at zero and after the azimuthal rotation for all the reflectivity spectra. It clearly appears an enhancement of both the figures of merit after the azimuthal rotation that amounts up to a factor 4 and 10 for the angular and yield FOM respectively. This means that the distance between two dips, before and after the functionalization, scales with a factor greater than the enlargment of the reflectivity dip width. Moreover, it must be noticed that the reflectivity yield is even more sensitive than the angular position. It clearly appears from the reflectivity spectra of Fig. 1 that whereas the minimum yield between coated and uncoated are almost the same for zero azimuth, it changes dramatically after azimuthal rotation. Finally, we note that both the angular and the yield FOM have similar functional behavior: they increase approaching the condition of two dips merging when β +=β-=90°. This is due to the dynamical excitation of the plasmons with different directions. While in the case of the null azimuth the plasmon momentum is collinear with exciting light momentum before and after the C12 functionalization, in the case of the azimuthally rotated grating the plasmons that are excited before and after functionalization have different orientations (in Fig. 2 compare the β angles of B points against A points). A complete analysis comprising both angular and reflectivity yield however involves a full dynamical analysis which exceeds the scope of this preliminary work.

Fig. 4. (b) Figure of merit for angular (∙,▪) and yield (ο, ▫) interrogation of the SPR reflectivity minima. (a) Energy dispersion curve for the kph necessary for SPP excitation before (solid line) and after (dashed line) C12 SAM functionalization. The experimental data obtained by the reflectivity minima of Fig. 1 have been fitted using Eq. (1).

5. Conclusion

In summary, we have shown that an enhancement in sensitivity can be obtained in GCSPR when double SPPs are excited after azimuthal rotation of the grating. The difference between uncoated and C12 SAMs coated metallic gratings is easily detectable in the vicinity of the double SPP condition. The shift in resonance angle detected is as large as 3° which is one order of magnitude higher than conventional prism-based SPR. In addition, the calculated sensitivity of this method is greater than 800°/RIU, one order of magnitude higher than conventional mounted grating (φ=0°).

Acknowledgements

This work has been partially supported by project NanoSPARC: Nanostructures for surface plasmon amplification & radiation control (ARC 5/06) of Ministery of Education of Singapore and partially also from project Surface Plasmonics for enhanced Nano Detectors and Innovative Devices of CARIPARO Foundation.

References and links

1.

H. Raether, “Surface Plasmons on Smooth and Rough Surfaces and on Gratings,” (Springer-Verlag, 1988).

2.

L. S. Jung, C. T. Campbell, T. M. Chinowsky, M. N. Mar, and S. S. Yee, “Quantitative interpretation of the response of surface plasmon resonance sensors to adsorbed films,” Langmuir 14(19), 5636–5648 (1998). [CrossRef]

3.

I. Lundstrom, “Real-time biospecific interaction analysis,” Biosens. Bioelectron. 9(9–10), 725–736 (1994). [CrossRef]

4.

W. Lukosz, “Integrated-optical and surface-plasmon sensors for direct affinity sensing. Part II: Anisotropy of adsorbed or bound protein adlayers,” Biosens. Bioelectron. 12(3), 175–184 (1997). [CrossRef]

5.

K. A. Peterlinz and R. Georgiadis, “In Situ Kinetics of Self-Assembly by Surface Plasmon Resonance Spectroscopy,” Langmuir 12(20), 4731–4740 (1996). [CrossRef]

6.

J. Homola, S. S. Yee, and G. Gauglitz, “Surface plasmon resonance sensors: review,” Sens. Actuators B Chem. 54(1–2), 3–15 (1999). [CrossRef]

7.

A. J. Haes and R. P. Van Duyne, “A unified view of propagating and localized surface plasmon resonance biosensors,” Anal. Bioanal. Chem. 379(7–8), 920–930 (2004).

8.

K. A. Willets and R. P. Van Duyne, “Localized surface plasmon resonance spectroscopy and sensing,” Annu. Rev. Phys. Chem. 58(1), 267–297 (2007). [CrossRef]

9.

J. Perez-Juste, I. Pastoriza-Santos, L. M. Liz-Marzan, and P. Mulvaney, “Gold nanorod: systhesis, characterization and application,” Coord. Chem. Rev. 249(17–18), 1870–1901 (2005). [CrossRef]

10.

C. Yu and J. Irudayaraj, “Multiplex biosensor using gold nanorods,” Anal. Chem. 79(2), 572–579 (2007). [CrossRef]

11.

J. Melendez, R. Carr, D. U. Bartholomew, K. Kukanskis, J. Elkind, S. Yee, C. Furlong, and R. Woodbury, “A commercial solution for surface plasmon sensing,” Sens. Actuators B Chem. 35(1–3), 212–216 (1996). [CrossRef]

12.

B. Liedberg, I. Lundstrom, and E. Stenberg, “Principle of biosensing with an extended coupling matrix and surface plasmon resonance,” Sens. Actuators B Chem. 11(1–3), 63–72 (1993). [CrossRef]

13.

R. Karlsson and R. Ståhlberg, “Surface plasmon resonance detection and multispot sensing for direct monitoring of interactions involving low-molecular-weight analytes and for determination of low affinities,” Anal. Biochem. 228(2), 274–280 (1995). [CrossRef]

14.

J. Homola, I. Koudela, and S. S. Yee, “Surface plasmon resonance sensor based on diffraction gratings and prism couplers: sensitivity comparison,” Sens. Actuator B 54(1–2), 16–24 (1999). [CrossRef]

15.

D. W. Unfricht, S. L. Colpitts, S. M. Fernandez, and M. A. Lynes, “Grating-coupled surface plasmon resonance: a cell and protein microarray platform,” Proteomics 5(17), 4432–4442 (2005). [CrossRef]

16.

X. D. Hoa, A. G. Kirk, and M. Tabrizian, “Towards integrated and sensitive surface plasmon resonance biosensors: a review of recent progress,” Biosens. Bioelectron. 23(2), 151–160 (2007). [CrossRef]

17.

K. H. Yoon, M. L. Shuler, and S. J. Kim, “Design optimization of nano-grating surface plasmon resonance sensors,” Opt. Express 14(11), 4842–4849 (2006). [CrossRef]

18.

D. C. Cullen and C. R. Lowe, “A direct surface plasmon-polariton immunosensor: Preliminary investigation of the non-specific adsorption of serum components to the sensor interface,” Sens. Actuators B Chem. 1(1–6), 576–579 (1990). [CrossRef]

19.

M. Vala, J. \, and J. Homola, “Diffraction grating-coupled surface plasmon resonance based on spectroscopy of long-range and short-range surface plasmons,” Proc. SPIE 6585, 658522 (2007). [CrossRef]

20.

C. J. Alleyne, A. G. Kirk, R. C. McPhedran, N. A. P. Nicorovici, and D. Maystre, “Enhanced SPR sensitivity using periodic metallic structures,” Opt. Express 15(13), 8163–8169 (2007). [CrossRef]

21.

J. M. Brockman and S. M. Fernandes, “Grating-coupled surface plasmon resonance for rapid, label-free, array based sensing,” Am. Lab. 33, 37–41 (2001).

22.

R. Baggio, G. J. Carven, A. Chiulli, M. Palmer, L. J. Stern, and J. E. Arenas, “Induced fit of an epitope peptide to a monoclonal antibody probed with a novel parallel surface plasmon resonance assay,” J. Biol. Chem. 280(6), 4188–4194 (2005).

23.

J. Dostalek, J. Homola, and M. Miler, “Rich information format surface plasmon resonance biosensor based on array of diffraction gratings,” Sens. Actuators B Chem. 107(1), 154–161 (2005). [CrossRef]

24.

D. Y. Kim, “Effect of the azimuthal orientation on the performance of grating-coupled surface-plasmon resonance biosensors,” Appl. Opt. 44(16), 3218–3223 (2005). [CrossRef]

25.

F. Romanato, K. H. Lee, H. K. Kang, C. C. Wong, Y. Zong, and W. Knoll, “Azimuthal dispersion and energy mode condensation of grating-coupled surface plasmon polaritons,” Phys. Rev. B 77(24), 245435–245441 (2008). [CrossRef]

26.

C. D. Bain, E. B. Troughton, Yu.-T. Tao, J. Evall, G. M. Whitesides, and R. G. Nuzzo, “Formation of monolayer films by the spontaneous assembly organic thiols from solution onto gold,” J. Am. Chem. Soc. 111(1), 321–335 (1989). [CrossRef]

27.

B. Thomas, O. Reilly, and I. H. I. Smith, “Linewidth uniformity in Lloyd’s mirror interference lithography systems,” J. Vac. Sci. Technol. B 26(6), 2131–2134 (2008).

28.

F. Schreiber, “Structure and growth of self-assembling monolayers,” Prog. Surf. Sci. 65(5–8), 151–257 (2000). [CrossRef]

29.

X. F. Ang, F. Y. Li, W. L. Tan, Z. Chen, C. C. Wong, and J. Wei, “Self-assembled monolayer for reduced temperature direct metal thermocompression bonding,” Appl. Phys. Lett. 91(6), 061913 (2007). [CrossRef]

OCIS Codes
(240.6680) Optics at surfaces : Surface plasmons
(280.4788) Remote sensing and sensors : Optical sensing and sensors

ToC Category:
Optics at Surfaces

History
Original Manuscript: May 4, 2009
Revised Manuscript: June 15, 2009
Manuscript Accepted: June 15, 2009
Published: July 2, 2009

Citation
F. Romanato, K. H. Lee, H. K. Kang, G. Ruffato, and C. C. Wong, "Sensitivity enhancement in grating coupled surface plasmon resonance by azimuthal control," Opt. Express 17, 12145-12154 (2009)
http://www.opticsinfobase.org/oe/abstract.cfm?URI=oe-17-14-12145


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References

  1. H. Raether, “Surface Plasmons on Smooth and Rough Surfaces and on Gratings,” (Springer-Verlag, 1988).
  2. L. S. Jung, C. T. Campbell, T. M. Chinowsky, M. N. Mar, and S. S. Yee, “Quantitative interpretation of the response of surface plasmon resonance sensors to adsorbed films,” Langmuir 14(19), 5636–5648 (1998). [CrossRef]
  3. I. Lundstrom, “Real-time biospecific interaction analysis,” Biosens. Bioelectron. 9(9-10), 725–736 (1994). [CrossRef]
  4. W. Lukosz, “Integrated-optical and surface-plasmon sensors for direct affinity sensing. Part II: Anisotropy of adsorbed or bound protein adlayers,” Biosens. Bioelectron. 12(3), 175–184 (1997). [CrossRef]
  5. K. A. Peterlinz and R. Georgiadis, “In Situ Kinetics of Self-Assembly by Surface Plasmon Resonance Spectroscopy,” Langmuir 12(20), 4731–4740 (1996). [CrossRef]
  6. J. Homola, S. S. Yee, and G. Gauglitz, “Surface plasmon resonance sensors: review,” Sens. Actuators B Chem. 54(1-2), 3–15 (1999). [CrossRef]
  7. A. J. Haes and R. P. Van Duyne, “A unified view of propagating and localized surface plasmon resonance biosensors,” Anal. Bioanal. Chem. 379(7-8), 920–930 (2004).
  8. K. A. Willets and R. P. Van Duyne, “Localized surface plasmon resonance spectroscopy and sensing,” Annu. Rev. Phys. Chem. 58(1), 267–297 (2007). [CrossRef]
  9. J. Perez-Juste, I. Pastoriza-Santos, L. M. Liz-Marzan, and P. Mulvaney, “Gold nanorod: systhesis, characterization and application,” Coord. Chem. Rev. 249(17-18), 1870–1901 (2005). [CrossRef]
  10. C. Yu and J. Irudayaraj, “Multiplex biosensor using gold nanorods,” Anal. Chem. 79(2), 572–579 (2007). [CrossRef]
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