Journal of Nanomaterials

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1D Nanomaterials 2011

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Volume 2012 |Article ID 843402 |

Hua Qi, O. J. Glembocki, S. M. Prokes, "Plasmonic Properties of Vertically Aligned Nanowire Arrays", Journal of Nanomaterials, vol. 2012, Article ID 843402, 7 pages, 2012.

Plasmonic Properties of Vertically Aligned Nanowire Arrays

Academic Editor: Steve Acquah
Received13 Jul 2011
Revised20 Sep 2011
Accepted04 Oct 2011
Published11 Jan 2012


Nanowires (NWs)/Ag sheath composites were produced to investigate plasmonic coupling between vertically aligned NWs for surface-enhanced Raman scattering (SERS) applications. In this investigation, two types of vertical NW arrays were studied; those of ZnO NWs grown on nanosphere lithography patterned sapphire substrate via vapor-liquid-solid (VLS) mechanism and Si NW arrays produced by wet chemical etching. Both types of vertical NW arrays were coated with a thin layer of silver by electroless silver plating for SERS enhancement studies. The experimental results show extremely strong SERS signals due to plasmonic coupling between the NWs, which was verified by COMSOL electric field simulations. We also compared the SERS enhancement intensity of aligned and random ZnO NWs, indicating that the aligned NWs show much stronger and repeatable SERS signal than those grown in nonaligned geometries.

1. Introduction

Nanostructures, especially nanowires (NWs), have inspired much interest due to their potential applications in electronics, photonics, and life science [15]. In particular, NWs used for surface-enhanced Raman scattering (SERS) are of significant interest since SERS spectra can provide trace level detection and a chemical fingerprint by which a molecule can be identified. Several NWs types have been used to investigate the SERS effect, including silver NWs [6, 7], gold NWs [8], semiconductor NWs [9], and dielectric NWs [1012]. It has been demonstrated that the geometry of the nanowires and the orientation of the molecules play an important role in the SERS process [1014]. However, most of the reported NW structures were randomly distributed on a surface, where the largest SERS enhancements noted were in the NW crossing [10] and between the NW and the substrate [14]. Since it has been shown experimentally that the largest enhancements were between two closely aligned parallel NWs [13], an obvious extension of this result is to investigate the SERS enhancements of a large number of aligned parallel NW arrays. Thus, in this work, we have investigated the effect of close parallel NW alignment on the SERS response and on the reproducibility of the SERS signal. In addition, we have also investigated the plasmonic properties of periodic and nonperiodic NW arrays.

Since the “hot spots” or regions of plasmon coupling are the region from which SERS would have the largest enhancement and closely aligned NW should experience coupling along the whole lengths of the wires, we have produced arrays of plasmonic nanowires to investigate this SERS effect. Here we used two types of vertical NWs, ZnO NWs, and Si NWs, respectively, to investigate SERS enhancement due to the plasmonic coupling between closely packed NWs. Many lithographic techniques have been used to fabricate ordered patterns on a surface, including photolithography, e-beam lithography [15, 16], ion beam lithography [17], X-ray lithography [18, 19], nanoimprint lithography [20, 21], and scanning probe lithography [22, 23]. However, all of these techniques are time consuming and costly. Here we employed the nanosphere lithography (NSL) approach [2426], which has the advantages of low cost and simplicity, to produce the hexagonal gold dot patterns on c-sapphire and to successfully grow vertically aligned ZnO nanowires by the well-known VLS process. In this way, the ZnO NWs can be arranged in a repeatable hexagonal pattern creating ordered and aligned NW arrays for surface-enhanced Raman scattering (SERS) applications. The closely packed vertical Si NWs were fabricated by wet chemical etching [27]. The Si NWs and ZnO NWs arrays were coated with a thin layer of Ag, using an electroless plating technique, and their plasmonic properties were investigated.

2. Experimental Details

A bare c-sapphire piece with the size of 1 × 1 cm−1 was cleaned in a piranha solution at 90°C for 30 min to produce a hydrophilic surface, rinsed by DI-H2O, and dried under a flow of nitrogen. Commercial silica nanospheres (NSs) slurry, with a diameter of 300 nm, was further diluted in a mixture of the surfactant Triton X-100 and methanol (1 : 400 by volume), with a dilution fraction of 1 : 3. NS lithography was performed on the sapphire surface by spin-coating the diluted silica nanosphere at a speed of 3600 rpm for 60 s. The sapphire surface, having a single layer of closely packed NS, was then covered by 10 nms of gold, using an FC-2000 Temescal e-beam metal evaporation system, at a rate of 0.5 Å/s. After the gold deposition, the NS were removed by sonicating in DI-H2O for 1-2 minutes. Well-ordered gold particles in hexagonal patterns were left on the sapphire surface, and they served as a catalyst during the vertical ZnO growth.

Using the sapphire substrate prepared above, the growth of the vertical ZnO NWs was carried out in a horizontal furnace via the vapor-liquid-solid (VLS) growth mechanism. The mixture powder of ZnO : C (1 : 1 by weight) used as the source was placed at one end of an alumina boat, and the substrate with the gold pattern was put directly above the material sources, face down. The furnace was heated to 900°C while flowing simultaneously a mixture of argon and oxygen gases in a ratio of 25 : 1 through the tube.

For the formation of the Si NW arrays, commercial p-type Si (100) wafer with narrow resistivity range of 6.3–7.0 Ω-cm was cleaned by piranha solution for 30 min at 90°C and then rinsed by DI water. Then 5% HF aqueous solution was used to remove the oxide layer for 2 min, which generated a fresh Si surface passivated with H-termination. The resulting clean Si wafer was put into a mixture of 4.8 M HF and 0.005 M AgNO3 solution for 1 min. Then the wafer with a layer of silver was taken out of the solution, rinsed with DI water, and immediately immersed into wet etching chemicals of 4.8 M HF and 0.4 M H2O2 in the dark. After 30 min, the wafer was taken out, rinsed with DI water, and immersed in dilute HNO3 (1 : 1 v/v) to dissolve the extra Ag catalyst. Finally the wafer was washed with 5% HF again to remove the oxide layer, cleaned with DI water, and dried under a flow of N2. All was carried out at room temperature.

An electroless silver plating approach was employed to produce ZnO or Si NWs core/Ag sheath composites for the SERS investigations. The detailed procedure has been well demonstrated in our previous report [11, 12]. Briefly silver mirror reaction was used to produce neutral Ag in solution, and the freshly formed Ag nanoparticles were simultaneously deposited on NW surface, coating the whole surface of the nanowires.

A LEO scanning electron microscope (SEM) with energy dispersive X-ray (EDX) was used to investigate the topographies of NS patterned surface, growth of the vertical ZnO NWs, etching of the Si NWs, and electroless silver plating of the vertical ZnO or Si NWs. The SERS measurements of ZnO NWs were carried out utilizing a well-known SERS molecule, benzene thiol (BT), and a confocal μ-Raman system which consisted of a Mitutoyo Microscope and an Ocean Optics QE65000 spectrometer equipped with a thermoelectrically cooled CCD. The 514.5 nm line of an Ar ion laser was used as the excitation source. The microscope utilized a 100x 0.7 NA objective for focusing the laser light and was coupled to the spectrometer through a fiber optic cable. The spectra were collected with low laser power of 0.75 mW at the sample. This was done to prevent desorption and damage to the SERS-active molecules, benzene thiol, and to prevent alterations to the Ag layer. The SERS behavior of Si NWs arrays was performed using a Delta Nu system which consists of an Olympus Microscope and a Raman spectrometer equipped with a thermoelectrically cooled CCD. The 785 nm line of Ti : Sapphire laser was used as the excitation source to detect the SERS strength dependence on a single NW/silver composite. The microscope utilized a 50x 0.75 NA objective for focusing the laser light. The spectra were collected with a laser power of 3 mW at the sample.

3. Results and Discussion

A single layer of closely packed silica nanospheres produced by self-assembly is shown in Figures 1(a) and 1(b). By this simple and high throughput way, the NS patterned area tens of microns in size can be easily produced. After the deposition of 10 nm of gold, the liftoff was performed in DI-H2O by sonicating. Hexagonal periodic Au particle arrays were obtained, as shown in Figure 1(c). When performing the sonicating lift-off process, 1-2 minutes was used. Longer sonication time usually led to the loss of the hexagonal gold patterns, while a shorter time resulted in incomplete liftoff of the nano-spheres from the substrate. Figure 1(d) shows an SEM image after the patterned sample was lifted off and annealed at 500°C for 10 min. The distance between two nearest nanoparticle centers is around 170 nm. Considering the 3D structure of the gold particles, the spacing may even be smaller, down to less than 100 nm, which provides one way to obtain ordered ZnO NW arrays for further plasmonic studies.

For the vertical ZnO nanowire growth, the well-known vapor-liquid-solid (VLS) growth mechanism was used. Due to the need to form a eutectic with the Au dots for NW growth, high selectivity of the growth resulted, and well-ordered ZnO NW arrays were obtained, as shown in Figure 2(a). Since the NW growth rate depends on the size of the initial Au catalyst, some differences in the NW total lengths were noted. However, the hexagonal patterns are quite recognizable. To produce the patterned nanowire arrays required, we optimized the growth time to 10 minutes in order to control the nanowire growth length, as shown in Figure 2(a). In the case of longer NWs, the detailed information is discussed in what follows. In addition, the distance between the gold catalyst can be controlled by varying the size of the nanospheres, which provides a way to control the spacing between the vertical NWs. A representative image of the vertical ZnO NW covered with a thin layer of silver using the electroless plating approach is shown in Figure 2(b), by which the roughness of the silver-coated NW surface is visible.

Representative surface-enhanced Raman scattering (SERS) spectra of three regions are shown in Figure 2(c), including a well-ordered NWs area, random NWs area, and no NWs area. Figure 2(d) is a corresponding optical microscope image, showing the different areas. The major Raman peaks at 1002, 1071, and 1576 cm−1 can, respectively, be assigned to symmetric ring breathing, in plane C–H bending and in plane C–C stretching of the phenyl ring from the active molecules, benzene thiol (BT), which are in good agreement with those reported previously [2833]. It is obvious that the strongest SERS signal is obtained on the well-ordered vertical NWs arrays area, while no enhancement is received on the area without NWs, further confirming the important effect of dielectric ZnO NW on SERS mechanism, as reported previously [10]. The intensity of the 1567 cm−1 SERS band on the patterned vertical NW area is about 4 times stronger than those of the random NW area. This observation can be attributed to the reproducibility of the well-patterned NWs, while the NWs on the random area are stochastic. It has been demonstrated that the randomly distributed dielectric NW core/Ag sheath composite lying on the surface can also produce notable SERS signal due to the interactions between silver-silver particles and silver-NW substrate [11, 12]. In addition, there may be plasmonic coupling in the well-ordered area because of the close distance between the adjacent aligned NWs. Since this effect increases with the number of aligned NWs, this may also be contributing to the enhanced SERS measured. It is well known that the SERS effect relies on enhanced electric fields that are created because of light-induced plasmons in the silver nanoparticles. As reported earlier [11], the plasmons in closely spaced metal nanostructures are coupled to form regions of very high field, further enhancing the SERS response.

The strongest SERS enhancement displayed above was obtained using the short vertical ZnO NWs with the length of less than 700 nm. In fact, we also investigated the SERS behavior on the well-ordered and patterned sample with longer NWs. Several-microns-long vertical ZnO NWs of patterned area and unpatterned area are, respectively, shown in Figures 3(a) and 3(b). As shown in Figure 3(c), the SERS intensity is moderately greater in the aligned case than in the nonaligned case. Figure 3(d) is an optical microscope image of the measured surface area with ordered or random ZnO NWs. It is well known that SERS signals depend on density, size, morphology, and thickness of the coated material. However, in the case of closely packed and vertically aligned random NWs, the silver particle coverage is gradually decreasing as a function of depth, from the NWs top to the bottom, which can be attributed to the well-known capillary effect since we introduced solutions to perform the electroless silver plating. This defect of the silver particles coverage on NWs could affect the strength of SERS due to lack of “hot spots.” In fact, the NW density of unpatterned area is greater than in the patterned case. This is logical, since in the unpatterned area, a continuous Au film is used as a catalyst, and thus, in the VLS growth, a large number of catalyst islands form to grow NWs. In the patterned area, however, only a very small fraction of the substrate is covered in Au islands, since most of the area is taken up by the nanospheres, which of course get removed prior to growth, leaving only the small triangular regions of Au, as shown in Figure 1(c). Since, as noted above, it is harder to get a high coverage of the silver particles along the whole length of the NW in closely spaced random NW arrays due to the capillary effect, one might expect a reduction in the SERS response, although a higher totally NW density is present. In the case of the patterned area, the NWs result in better Ag coverage due to the lower NW density and thus a more open structure. It is also noted that increasing the plating time or concentration of the plating solution does not help to improve the silver plating of closely packed NWs and usually results in NW breakage or a pileup of silver nanostructures on the tip of the NWs, blocking the way to further silver plating of the NWs parting depth.

It is hard to investigate the detailed morphology of the nanostructures at high-resolution SEM due to the charging issue of sapphire substrate, on which vertical ZnO nanowires were usually grown. Thus, we employed semiconductor Si NWs, which was produced by chemical wet etching and has similar vertically aligned nanostructures to ZnO NWs. A typical side view SEM image of Si NWs is shown in Figure 4(a), indicating that the NWs are uniform with a high density and close spacing. The lengths of the NWs are close to 30 μm. As shown in Figure 4(b), the vertical Si NWs were covered by a thin layer of silver nanoparticles by electroless plating as described above. The SERS measurements at different spots were performed. As shown in Figure 4(c), the SERS intensity is very uniform across Si NWs array sample, demonstrating that the wet chemical etching and electroless plating results in repeatable and uniform plasmonic NW large area arrays. The lines for the SERS-active molecules, BT, are very similar to those reported previously [2833]. When the SERS intensity of the Si NW arrays was compared to the ZnO NW arrays using the 514 nm laser line, an order of magnitude greater signal was noted for the Si NWs. This is most likely to a much higher density of wires, which are also more closely spaced, leading to greater plasmon coupling.

Vertical NWs with smaller separation distance can result in the formation of hot spots corresponding to very intense electric field. Kottmann and Martin [34] have shown that coupled parallel metallic wires lead to a significantly enhanced coupled plasmon resonance in the overall structure. Finite element COMSOL simulation of the NW array plasmonic properties is shown in Figure 5. As can be seen in Figure 5(a), parallel and closely packed NWs/Ag composites induced high electric field along the whole length of the nanowires, which result in the very large enhancement of the observed SERS signals. Figure 5(b) is a side view of the parallel NW/Ag composites, clearly demonstrating the strong plasmonic coupling between the NW/Ag composites. Furthermore, on average, the strong plasmonic coupling is not dramatically influenced by small variations in the nanowire diameters. Figure 5(c) shows the influence of a 10% increase in the thickness of the central nanowire. The local fields around the nanowire are reduced leading to a factor of 4 decrease in the very local SERS enhancement. However, note that areas that are only several nanowires away from our defect show virtually no change in the SERS enhancement. In fact as shown in Figure 5(d), the line of nanowires that are two rows above the defect are not impacted by the defect at all. Thus, the plasmonic fields behave similarly to semiconductor bands that have local densities of states from impurities that are isolated from the semiconductor conduction or valence bands. This analogy further suggests that even in the “amorphous” case, which is random distributions of aligned nanowires, there should still be a high SERS uniformity across the array, as shown in Figure 4.

4. Conclusion

We have successfully produced ordered, parallel ZnO and Si nanowire arrays on c-sapphire and Si substrates, respectively. The area of periodic ZnO NWs exhibits 4 times stronger SERS signal than those of random ZnO NWs, demonstrating the feasibility of using metal/dielectric nanowire periodic arrays to enhance the SERS signal. The wet chemically etched Si NWs were also studied, demonstrating the strong plasmonic coupling between the parallel NWs/Ag composites. These results are in good agreement with our COMSOL simulations of the closely packed vertical NWs/Ag composites. Since large SERS enhancements and SERS uniformity and repeatability are important issues, this study provides potential for the development of reliable, remotely deployable, and more sensitive optically based sensors.


We are thankful for the support of the Office of Naval Research (ONR), the American Society for Engineering Education program, the National Basic Research Program (2011CB933101) and Nanoscience Institute at Naval Research Lab (NRL).


  1. Y. Sun and J. A. Rogers, “Fabricating semiconductor nano/microwires and transfer printing ordered arrays of them onto plastic substrates,” Nano Letters, vol. 4, no. 10, pp. 1953–1959, 2004. View at: Publisher Site | Google Scholar
  2. T. Mårtensson, C. P. T. Svensson, B. A. Wacaser et al., “Epitaxial III-V nanowires on silicon,” Nano Letters, vol. 4, no. 10, pp. 1987–1990, 2004. View at: Publisher Site | Google Scholar
  3. P. Mohan, J. Motohisa, and T. Fukui, “Controlled growth of highly uniform, axial/radial direction-defined, individually addressable InP nanowire arrays,” Nanotechnology, vol. 16, no. 12, pp. 2903–2907, 2005. View at: Publisher Site | Google Scholar
  4. S. D. Hersee, X. Sun, and X. Wang, “The controlled growth of GaN nanowires,” Nano Letters, vol. 6, no. 8, pp. 1808–1811, 2006. View at: Publisher Site | Google Scholar
  5. M. T. Björk, C. Thelander, A. E. Hansen et al., “Few-electron quantum dots in nanowires,” Nano Letters, vol. 4, no. 9, pp. 1621–1625, 2004. View at: Publisher Site | Google Scholar
  6. R. Gunawidjaja, S. Peleshanko, H. Ko, and V. V. Tsukruk, “Bimetallic nanocobs: decorating silver nanowires with gold nanoparticles,” Advanced Materials, vol. 20, no. 8, pp. 1544–1549, 2008. View at: Publisher Site | Google Scholar
  7. S. J. Seung, J. M. Baik, and M. Moskovits, “Polarization-dependent surface-enhanced raman scattering from a silver-nanoparticle-decorated single silver nanowire,” Nano Letters, vol. 8, no. 10, pp. 3244–3247, 2008. View at: Publisher Site | Google Scholar
  8. H. Wei, F. Hao, Y. Huang, W. Wang, P. Nordlander, and H. Xu, “Polarization dependence of surface-enhanced Raman scattering in gold nanoparticle-nanowire systems,” Nano Letters, vol. 8, no. 8, pp. 2497–2502, 2008. View at: Publisher Site | Google Scholar
  9. C. Fang, A. Agarwal, E. Widjaja et al., “Metallization of silicon nanowires and SERS response from a single metallized nanowire,” Chemistry of Materials, vol. 21, no. 15, pp. 3542–3548, 2009. View at: Publisher Site | Google Scholar
  10. S. M. Prokes, O. J. Glembocki, R. W. Rendell, and M. G. Ancona, “Enhanced plasmon coupling in crossed dielectric/metal nanowire composite geometries and applications to surface-enhanced Raman spectroscopy,” Applied Physics Letters, vol. 90, no. 9, Article ID 093105, 2007. View at: Publisher Site | Google Scholar
  11. H. Qi, D. Alexson, O. Glembocki, and S. M. Prokes, “Plasmonic coupling on dielectric nanowire core-metal sheath composites,” Nanotechnology, vol. 21, no. 8, Article ID 085705, 2010. View at: Publisher Site | Google Scholar
  12. H. Qi, D. Alexson, O. Glembocki, and S. M. Prokes, “The effect of size and size distribution on the oxidation kinetics and plasmonics of nanoscale Ag particles,” Nanotechnology, vol. 21, no. 21, Article ID 215706, 2010. View at: Publisher Site | Google Scholar
  13. S. M. Prokes, D. A. Alexson, O. J. Glembocki, H. D. Park, and R. W. Rendell, “Effect of crossing geometry on the plasmonic behavior of dielectric core/metal sheath nanowires,” Applied Physics Letters, vol. 94, no. 9, Article ID 093105, 2009. View at: Publisher Site | Google Scholar
  14. O. J. Glembocki, R. W. Rendell, S. M. Prokes, D. A. Alexson, A. Fu, and M. A. Mastro, “Dielectric-Substrate interactions with metal/dielectric nanowires composites in surface-enhanced Raman spectroscopy,” Physical Reviews B, vol. 80, no. 1, 2009. View at: Google Scholar
  15. R. R. W. Pease, “Nanolithography and its prospects as a manufacturing technology,” Journal of Vacuum Science & Technology B, vol. 10, no. 1, pp. 278–285, 1992. View at: Google Scholar
  16. M. A. McCord, “Electron beam lithography for 0.13 μm manufacturing,” Journal of Vacuum Science and Technology B, vol. 15, no. 6, pp. 2125–2129, 1997. View at: Google Scholar
  17. J. Melngailis, A. A. Mondelli, I. L. Berry, and R. Mohondro, “A review of ion projection lithography,” Journal of Vacuum Science and Technology B, vol. 16, no. 3, pp. 927–957, 1998. View at: Google Scholar
  18. H. I. Smith and M. L. Schattenburg, “X-ray lithography, from 500 to 30 nm: X-ray nanolithography,” IBM Journal of Research and Development, vol. 37, no. 3, pp. 319–329, 1993. View at: Google Scholar
  19. J. P. Silverman, “X-ray lithography: status, challenges, and outlook for 0.13 μm,” Journal of Vacuum Science and Technology B, vol. 15, no. 6, pp. 2117–2124, 1997. View at: Google Scholar
  20. Y. S. Kim, K. Lee, J. S. Lee, G. Y. Jung, and W. B. Kim, “Nanoimprint lithography patterns with a vertically aligned nanoscale tubular carbon structure,” Nanotechnology, vol. 19, no. 36, Article ID 365305, 2008. View at: Publisher Site | Google Scholar
  21. I. W. Moran, A. L. Briseno, S. Loser, and K. R. Carter, “Device fabrication by easy soft imprint nano-lithography,” Chemistry Letters, vol. 20, no. 14, pp. 4595–4601, 2008. View at: Publisher Site | Google Scholar
  22. S. Manne, P. K. Hansma, J. Massie, V. B. Elings, and A. A. Gewirth, “Atomic-resolution electrochemistry with the atomic force microscope: copper deposition on gold,” Science, vol. 251, no. 4990, pp. 183–186, 1991. View at: Google Scholar
  23. W. T. Müller, D. L. Klein, T. Lee, J. Clarke, P. L. McEuen, and P. G. Schultz, “A Strategy for the chemical synthesis of nanostructures,” Science, vol. 268, no. 5208, pp. 272–273, 1995. View at: Google Scholar
  24. G. H. Chan, J. Zhao, E. M. Hicks, G. C. Schatz, and R. P. Van Duyne, “Plasmonic properties of copper nanoparticles fabricated by nanosphere lithography,” Nano Letters, vol. 7, no. 7, pp. 1947–1952, 2007. View at: Publisher Site | Google Scholar
  25. C. L. Haynes and R. P. Van Duyne, “Nanosphere lithography: a versatile nanofabrication tool for studies of size-dependent nanoparticle optics,” Journal of Physical Chemistry B, vol. 105, no. 24, pp. 5599–5611, 2001. View at: Publisher Site | Google Scholar
  26. J. C. Hulteen, D. A. Treichel, M. T. Smith, M. L. Duval, T. R. Jensen, and R. P. Van Duyne, “Nanosphere lithography: size-tunable silver nanoparticle and surface cluster arrays,” Journal of Physical Chemistry B, vol. 103, no. 19, pp. 3854–3863, 1999. View at: Publisher Site | Google Scholar
  27. M. L. Zhang, K. Q. Peng, X. Fan et al., “Preparation of large-area uniform silicon nanowires arrays through metal-assisted chemical etching,” Journal of Physical Chemistry C, vol. 112, no. 12, pp. 4444–4450, 2008. View at: Publisher Site | Google Scholar
  28. C. Jiang, W. Y. Lio, and V. V. Tsukruk, “Surface enhanced raman scattering monitoring of chain alignment in freely suspended nanomembranes,” Physical Review Letters, vol. 95, no. 11, Article ID 115503, pp. 1–4, 2005. View at: Publisher Site | Google Scholar
  29. J. Ding, V. I. Birss, and G. Liu, “Formation and properties of polystyrene-block-poly(2-cinnamoylethyl methacrylate) brushes studied by surface-enhanced raman scattering and transmission electron microscopy,” Macromolecules, vol. 30, no. 5, pp. 1442–1448, 1997. View at: Google Scholar
  30. W. M. Sears, J. L. Hunt, and J. R. Stevens, “Raman scattering from polymerizing styrene. I. Vibrational mode analysis,” The Journal of Chemical Physics, vol. 75, no. 4, pp. 1589–1598, 1981. View at: Google Scholar
  31. V. Zucolotto, M. Ferreira, M. Cordeiro et al., “Unusual interactions binding iron tetrasulfonated phthalocyanine and poly(allylamine hydrochloride) in layer-by-layer films,” Journal of Physical Chemistry B, vol. 107, no. 16, pp. 3733–3737, 2003. View at: Publisher Site | Google Scholar
  32. R. Aroca and A. Thedchanamoorthy, “Vibrational studies of molecular organization in evaporated phthalocyanine thin solid films,” Chemistry of Materials, vol. 7, no. 1, pp. 69–74, 1995. View at: Google Scholar
  33. M. Lütt, M. R. Fitzsimmons, and D. Li, “X-ray reflectivity study of self-assembled thin films of macrocycles and macromolecules,” Journal of Physical Chemistry B, vol. 102, no. 2, pp. 400–405, 1998. View at: Google Scholar
  34. J. P. Kottmann and O. J. F. Martin, “Plasmon resonant coupling in metallic nanowires,” Optics Express, vol. 8, no. 12, pp. 655–663, 2001. View at: Google Scholar

Copyright © 2012 Hua Qi et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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