Plasmon-mediated resonance energy transfer by metallic nanorods
© Yu et al.; licensee Springer. 2013
Received: 10 April 2013
Accepted: 22 April 2013
Published: 3 May 2013
We investigate the enhancement of the resonance energy transfer rate between donor and acceptor associated by the surface plasmons of the Ag nanorods on a SiO2 substrate. Our results for a single nanorod with different cross sections reveal that the cylinder nanorod has the strongest ability to enhance the resonance energy transfer rate. Moreover, for donor and acceptor with nonparallel polarization directions, we propose simple V-shaped nanorod structures which lead to the remarkable resonance energy transfer enhancement that is ten times larger than that by the single nanorod structure. We demonstrate that these structures have good robustness and controllability. Our work provides a way to improve the resonance energy transfer efficiency in integrated photonic devices.
78.67.Qa, 73.20.Mf, 42.50.Ex
KeywordsResonance energy transfer Silver nanorods Surface plasmons
Resonance energy transfer (RET) between nanosystems is extensively researched in nanophotonics, which has various important applications ranging from biological detections and chemical sensors to quantum information science [1–11]. RET may proceed in different transfer distances: the Dexter process  based on wave function overlap transfers within the range of about 1 nm, and the Forster process  caused by the near-field resonant dipole-dipole interaction transfers usually within the range of 10 nm. The efficient transfer energy distance is still very short. It is thus important to enhance the efficiency of RET in a long distance.
The RET rate by the dipole-dipole interactions can be greatly manipulated by the electromagnetic environment; many different kinds of electromagnetic environments have been used to enhance the resonant dipole-dipole interaction strength and the efficiency of the RET, such as optical cavities [2, 14–17], optical lens or fiber [18, 19], and metamaterials [20, 21]. In the last decades, it has been demonstrated that surface plasmon supported by metal nanostructures is a powerful tool to enhance the efficiency of RET. Since Andrew et al.  demonstrated long-distance plasmon-mediated RET using Ag films, a great deal of efforts have been devoted to investigate plasmon-mediated RET using nanoparticles [22–25], plasmonic waveguides [9, 11, 26], single nanowires [27–30], and nanorod or nanowire arrays [10, 19, 31]. Most of the previous works focus on the case of the donor and acceptor having parallel transition dipole moments. However, in practical devices, it is extremely difficult to satisfy the parallel condition between the dipole moments of the donor and acceptor, and when the donor and acceptor have nonparallel dipole moments, the RET rate may decrease evidently. It is thus important to design nanostructures to achieve big RET enhancement for donor and acceptor with nonparallel dipole moments.
In this paper, we investigate the enhancement of the RET rate between donor and acceptor associated by surface plasmons of Ag nanorods on a SiO2 substrate. Firstly, we consider single nanorods with different cross sections, and the results reveal that the cylinder nanorod has the strongest ability to enhance the RET rate. We also find that the enhancement of RET rate in the single nanorod structure decreases when the donor and acceptor have nonparallel dipole moment directions. We then propose simple V-shaped nanorod structures for a donor-acceptor pair with nonparallel dipole moments. We find that these structures can lead to a remarkable resonance energy transfer enhancement ten times larger than that by the single nanorod structure. We demonstrate that the enhancing effect by these structures can be controlled by the nanorod length of the branch in the V-shaped structure and that these structures are robust regardless of the shape and material of the corner part. This controllability and robustness are also preserved for donor-dipole pair with asymmetric configuration. Therefore, these structures can be applied in integrated photonic devices.
where n A and n D are the unit vectors along the directions of the dipole moments of the acceptor and donor, respectively, ω is the transition frequency, G(r A , r D , ω) is the dyadic Green's function , E D (r A , ω) is the electric field at the position of the acceptor induced by the donor dipole in the presence of the plasmonic structures, while Gvac(r A , r D , ω) and ED,vac(r A , ω) correspond to the case in vacuum but without the plasmonic structures.
The calculations of the electric field induced by the dipole are performed by the finite element method with the commercial COMSOL Multiphysics software. All metal structures in this paper are set to be silver; the electric permittivity of silver is gathered by fitting the experimental data of Johnson and Christy with piecewise cubic interpolation . All nanostructures are set on a semi-infinite SiO2 substrate with the refractive index of 1.456, and the surrounding medium is air.
Results and discussion
resulting in the same nETR shown in Figure 2c. While for the case of θ D = 60° and θ A = 60°, it can be seen that the nETR decreases evidently, the resonance wavelength is about 1,157 nm, and the maximum enhancement is reduced to about 7,500. The above results demonstrate that, in order to produce high RET enhancement in the single nanorod structure, the direction of the donor or acceptor dipole should be along the principle axis of the nanorod, otherwise the enhancement decreases evidently.
We then consider the structure with gap widths g = 10 nm for further optimization. To this end, we study a similar structure with different corner parts. The schematic picture of the structure with a cylinder-shaped corner part is shown in Figure 3b. The gap between each nanorod and the corner part was kept at g = 10 nm; the radius of the cylinder corner part is thus . The nETR spectra for these two V-shaped structures are displayed in Figure 4b. Compared with the structure with a sharp corner part, the nETR spectrum for the structure with a cylinder corner part has a lower maximum enhancement of about 76,200, while the resonance wavelength is almost unchanged. This indicates that as the gap widths are unchanged, the choice of the corner part shape has no important influence on the RET-enhancing ability of the V-shaped structures, which means that these structures have good fault tolerance in manufactory.
Even though the enhancing ability of the V-shaped structures is not influenced crucially by the shape of the corner part, the condition g = 10 nm here still requires the sophisticated control of the fabrication technology. In order to further reduce the difficulties in the fabrication process, we choose the V-shaped structure with a cylinder-shaped corner part shown in Figure 3b and consider reducing the radius of the corner so that the gap widths can be larger. The nETR spectra for different radii with are displayed in Figure 4c, in which the center of the cylinder is unchanged. Compared with the case of radius r0, it can be seen that for the case of radius r0/2, the peak wavelength of the spectrum is blueshifted to 1,182 nm, and the maximum enhancement increases to about 82,100, while if the radius is further reduced to r0/4, the nETR spectrum does not show evident change any more. This indicates that when the radius of the cylinder corner part is less than r0/2, its influence to the nETR spectrum may be negligible.
On the other hand, we may also change the material properties of the cylinder corner part. The nETR spectra for different materials of the cylinder corner part are displayed in Figure 4d. Here the radius is set to corresponding to the gap widths of g = 10 nm. The cases of material refraction index n = 1.5 and n = 3.4 are displayed together with the case of silver cylinder. We can see that when the material of the cylinder corner is changed, the resonance wavelength and the maximum enhancement in the nETR spectra both vary slightly.
The above results imply that the role of the corner part of V-shaped structures in nETR is minor. Based on this, we may remove the corner part so that the V-shaped structure consists of two nanorod branches only, as shown in Figure 3c. The nETR spectrum in this structure is also displayed in Figure 4d with n = 1; we can see that the resonance wavelength is 1,177 nm with a maximum enhancement of nearly 84,000. This resonance wavelength is very close to that in the case of single nanorod structure, while the maximum enhancement is ten times higher than the latter. Compared with other V-shaped structures having corner parts, this simple structure is thus more suitable to be applied in practical experiment and applications in integrated photonic devices.
In summary, we have investigated the enhancement of the RET rate between donor and acceptor associated by the surface plasmons of the Ag nanorods on a SiO2 substrate. For donor-acceptor pair with parallel dipole moment directions, we have considered single nanorod with different cross sections, and the results revealed that the cylinder nanorod has the strongest ability to enhance the RET rate. We also found that the enhancement of RET rate in the single nanorod structure decreases for donor-acceptor pairs with nonparallel dipole moment directions. We then proposed simple V-shaped nanorod structures for nonparallel donor-acceptor pair. We demonstrate that the enhancement effect in these structures can be controlled by the nanorod length of the branch in the V-shaped structure. Our initial design of the V-shaped structure contains a corner part to improve the coupling between two nanorod branches, while we then find that the enhancement ability of the V-shaped structures is robust regardless of the shape and material of the corner part. Therefore, we may remove the corner part, and the V-shaped structure with two nanorod branches can lead to the remarkable RET rate enhancement that is ten times larger than that by the single nanorod. We also demonstrate that the controllability and robustness of these V-shaped structures are preserved for donor-acceptor pair with asymmetric configuration. Our work provides guidance on the application of simple nanorod structures to improve RET efficiency in integrated photonic devices.
YCY and JML are PhD students at Sun Yat-sen University. CJJ and XHW are professors of Sun Yat-sen University.
Normalized energy transfer rate
Resonance energy transfer.
This work was financially supported by the National Basic Research Program of China (2010CB923200), the National Natural Science Foundation of China (grant U0934002), and the Ministry of Education of China (grant V200801).
- Barnes WL, Andrew P: Quantum optics: energy transfer under control. Nature 1999, 400: 505–506.View Article
- Andrew P, Barnes WL: Förster energy transfer in an optical microcavity. Science 2000, 290: 785–788. 10.1126/science.290.5492.785View Article
- Jares-Erijman EA, Jovin TM: FRET imaging. Nat Biotech 2003, 21: 1387–1395. 10.1038/nbt896View Article
- Lovett BW, Reina JH, Nazir A, Briggs GAD: Optical schemes for quantum computation in quantum dot molecules. Phys Rev B 2003, 68: 205319.View Article
- Andrew P, Barnes WL: Energy transfer across a metal film mediated by surface plasmon polaritons. Science 2004, 306: 1002–1005. 10.1126/science.1102992View Article
- Li Z, Hao F, Huang Y, Fang Y, Nordlander P, Xu H: Directional light emission from propagating surface plasmons of silver nanowires. Nano Lett 2009, 9: 4383–4386. 10.1021/nl902651eView Article
- Rolon JE, Ulloa SE: Förster energy-transfer signatures in optically driven quantum dot molecules. Phys Rev B 2009, 79: 245309.View Article
- Yao P, Hughes S: Macroscopic entanglement and violation of Bell's inequalities between two spatially separated quantum dots in a planar photonic crystal system. Opt Express 2009, 17: 11505–11514. 10.1364/OE.17.011505View Article
- Martín-Cano D, Martín-Moreno L, García-Vidal FJ, Moreno E: Resonance energy transfer and superradiance mediated by plasmonic nanowaveguides. Nano Lett 2010, 10: 3129–3134. 10.1021/nl101876fView Article
- Zhou Z-K, Li M, Yang Z-J, Peng X-N, Su X-R, Zhang Z-S, Li J-B, Kim N-C, Yu X-F, Zhou L, Hao Z-H, Wang Q-Q: Plasmon-mediated radiative energy transfer across a silver nanowire array via resonant transmission and subwavelength imaging. ACS Nano 2010, 4: 5003–5010. 10.1021/nn100578bView Article
- Gonzalez-Tudela A, Martin-Cano D, Moreno E, Martin-Moreno L, Tejedor C, Garcia-Vidal FJ: Entanglement of two qubits mediated by one-dimensional plasmonic waveguides. Phys Rev Lett 2011, 106: 020501.View Article
- Dexter DL: A theory of sensitized luminescence in solids. J Chem Phys 1953, 21: 836–850. 10.1063/1.1699044View Article
- Förster T: Intermolecular energy migration and fluorescence. Ann Phys 1948, 2: 55–75.View Article
- Goldstein EV, Meystre P: Dipole-dipole interaction in optical cavities. Phys Rev A 1997, 56: 5135–5146. 10.1103/PhysRevA.56.5135View Article
- Hopmeier M, Guss W, Deussen M, Göbel EO, Mahrt RF: Enhanced dipole-dipole interaction in a polymer microcavity. Phys Rev Lett 1999, 82: 4118. 10.1103/PhysRevLett.82.4118View Article
- Gallardo E, Martínez LJ, Nowak AK, Sarkar D, van der Meulen HP, Calleja JM, Tejedor C, Prieto I, Granados D, Taboada AG, García JM, Postigo PA: Optical coupling of two distant InAs/GaAs quantum dots by a photonic-crystal microcavity. Phys Rev B 2010, 81: 193301.View Article
- Huang Y-G, Chen G, Jin C-J, Liu WM, Wang X-H: Dipole-dipole interaction in a photonic crystal nanocavity. Phys Rev A 2012, 85: 053827.View Article
- Le Kien F, Gupta SD, Nayak KP, Hakuta K: Nanofiber-mediated radiative transfer between two distant atoms. Phys Rev A 2005, 72: 063815.View Article
- Rist S, Eschner J, Hennrich M, Morigi G: Photon-mediated interaction between two distant atoms. Phys Rev A 2008, 78: 013808.View Article
- Yang Y, Xu J, Chen H, Zhu S-Y: Long-lived entanglement between two distant atoms via left-handed materials. Phys Rev A 2010, 82: 030304.View Article
- Xu J, Al-Amri M, Yang Y, Zhu S-Y, Zubairy MS: Entanglement generation between two atoms via surface modes. Phys Rev A 2011, 84: 032334.View Article
- Zhang J, Fu Y, Lakowicz JR: Enhanced Förster resonance energy transfer (FRET) on a single metal particle. J Phys Chem C 2006, 111: 50–56.View Article
- Xie HY, Chung HY, Leung PT, Tsai DP: Plasmonic enhancement of Förster energy transfer between two molecules in the vicinity of a metallic nanoparticle: nonlocal optical effects. Phys Rev B 2009, 80: 155448.View Article
- Chung H, Leung P, Tsai D: Enhanced intermolecular energy transfer in the vicinity of a plasmonic nanorice. Plasmonics 2010, 5: 363–368. 10.1007/s11468-010-9151-xView Article
- Zhao L, Ming T, Shao L, Chen H, Wang J: Plasmon-controlled Förster resonance energy transfer. J Phys Chem C 2012, 116: 8287–8296. 10.1021/jp300916aView Article
- Martín-Cano D, González-Tudela A, Martín-Moreno L, García-Vidal FJ, Tejedor C, Moreno E: Dissipation-driven generation of two-qubit entanglement mediated by plasmonic waveguides. Phys Rev B 2011, 84: 235306.View Article
- Chen W, Chen G-Y, Chen Y-N: Coherent transport of nanowire surface plasmons coupled to quantum dots. Opt Express 2010, 18: 10360–10368. 10.1364/OE.18.010360View Article
- Cheng M-T, Luo Y-Q, Song Y-Y, Zhao G-X: Plasmonic waveguides mediated energy transfer between two distant quantum dots. J Mod Opt 2010, 57: 2177–2181. 10.1080/09500340.2010.532573View Article
- Chen G-Y, Lambert N, Chou C-H, Chen Y-N, Nori F: Surface plasmons in a metal nanowire coupled to colloidal quantum dots: scattering properties and quantum entanglement. Phys Rev B 2011, 84: 045310.View Article
- Chen W, Chen G-Y, Chen Y-N: Controlling Fano resonance of nanowire surface plasmons. Opt Lett 2011, 36: 3602–3604. 10.1364/OL.36.003602View Article
- Ono A, Kato J-I, Kawata S: Subwavelength optical imaging through a metallic nanorod array. Phys Rev Lett 2005, 95: 267407.View Article
- Novotny L, Hecht B: Principles of Nano-Optics. Cambridge: Cambridge University Press; 2006.View Article
- Dung HT, Knöll L, Welsch D-G: Intermolecular energy transfer in the presence of dispersing and absorbing media. Phys Rev A 2002, 65: 043813.View Article
- Tai CT: Dyadic Green Functions in Electromagnetic Theory. New York: IEEE; 1993.
- Johnson PB, Christy RW: Optical constants of the noble metals. Phys Rev B 1972, 6: 4370–4379. 10.1103/PhysRevB.6.4370View Article
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