Emission studies on photonic crystals fabricated using dyed polystyrene colloids Rajesh V. Nair, R. Vijaya, Keiji Kuroda, and Kazuaki Sakoda Citation: J. Appl. Phys. 102, 123106 (2007); doi: 10.1063/1.2825636 View online: http://dx.doi.org/10.1063/1.2825636 View Table of Contents: http://jap.aip.org/resource/1/JAPIAU/v102/i12 Published by the American Institute of Physics. Related Articles Magnetophotonic crystal comprising electro-optical layer for controlling helicity of light J. Appl. Phys. 111, 07A913 (2012) Multimodal strong coupling of photonic crystal cavities of dissimilar size Appl. Phys. Lett. 100, 081107 (2012) Highly modified spontaneous emissions in YVO4:Eu3+ inverse opal and refractive index sensing application Appl. Phys. Lett. 100, 081104 (2012) High quality factor two dimensional GaN photonic crystal cavity membranes grown on silicon substrate Appl. Phys. Lett. 100, 071103 (2012) Extraction of optical Bloch modes in a photonic-crystal waveguide J. Appl. Phys. 111, 033108 (2012) Additional information on J. Appl. Phys. Journal Homepage: http://jap.aip.org/ Journal Information: http://jap.aip.org/about/about_the_journal Top downloads: http://jap.aip.org/features/most_downloaded Information for Authors: http://jap.aip.org/authors Downloaded 24 Feb 2012 to 59.162.23.76. Redistribution subject to AIP license or copyright; see http://jap.aip.org/about/rights_and_permissions JOURNAL OF APPLIED PHYSICS 102, 123106 共2007兲 Emission studies on photonic crystals fabricated using dyed polystyrene colloids Rajesh V. Nair and R. Vijayaa兲 Department of Physics, Indian Institute of Technology Bombay, Powai, Mumbai 400076, India Keiji Kuroda Quantum Dot Research Center, National Institute for Materials Science, Tsukuba, Japan Kazuaki Sakoda Quantum Dot Research Center, National Institute for Materials Science, Tsukuba, Japan and Graduate School of Pure and Applied Sciences, University of Tsukuba, Tsukuba, Japan 共Received 22 September 2007; accepted 24 October 2007; published online 21 December 2007兲 Three dimensionally ordered photonic crystals are fabricated with rhodamine B dyed polystyrene colloidal spheres using the inward growing self-assembling method in less than 3 h. This avoids the difficulties due to infiltration of active materials into passive photonic crystals. The superior optical quality of the photonic crystals fabricated using this method results in high reflectance values even at large angles of incidence. The study of emission characteristics on these functionalized photonic crystals shows a clear trend dependent on the angle of emission, wavelength, and the angle-resolved transmittance. The dip observed in the emission spectrum clearly matches the photonic stop band position at different angles of observation. The emission spectrum measured at different angles was found to follow a simple functional form related to the intrinsic emission of the dye and the stop band effect due to the photonic crystal environment. © 2007 American Institute of Physics. 关DOI: 10.1063/1.2825636兴 I. INTRODUCTION Photonic crystals are artificial structures with a periodic variation of refractive index and are useful for controlling, manipulating, and localizing the propagation of light.1–3 In order to explore the utility of photonic crystals for applications in low-threshold laser design, specially functionalized photonic crystals with active media are required. The active media used for emission studies with photonic crystals should have a narrow emission linewidth, large quantum efficiency for emission, and be easy to infiltrate into the photonic crystals without disturbing the ordering in the initial photonic crystal template. Important light sources that have been used for emission studies are lanthanides or rare-earth atoms, organic dyes, and quantum dots. All these active media can be infiltrated into the photonic crystals using different techniques.4–6 The emission spectra of lanthanides have characteristic sets of sharp peaks.7 Since the linewidth of their emission spectrum is small, the effect of the photonic stop band will be felt more strongly, but the quantum efficiency of lanthanides is very low. In contrast, organic dyes have broad emission spectra.8 They also have high quantum efficiency and are strongly dependent on chemical interactions and environment. The main drawback of dyes as emission probes in photonic crystals is the process of photobleaching, which limits their usage with time. The inhibition of spontaneous emission from an organic dye infiltrated in a photonic crystal was studied in Refs. 9 and 10. Modified spontaneous emission has been observed a兲 Author to whom correspondence should be addressed. Electronic mail: [email protected]. 0021-8979/2007/102共12兲/123106/5/$23.00 for inverse photonic crystal made of TiO2 infiltrated with organic dye.11,12 The directional dependence of spontaneous emission has been analyzed quantitatively for a gravity sedimented polystyrene 共PS兲 photonic crystal doped with an organic dye and for quantum dot infiltrated titania inverse photonic crystals.13 In that work, the so-called “escape function” was proposed, and this function was found to follow the non-Lambertian distribution for the photonic crystals and the Lambertian distribution function for a random media. Directional fluorescence spectra of the laser dye in opal and inverse opal have been analyzed in Ref. 14 in the first and second order photonic stop band, and an enhancement of emission in the blue side of the spectrum for a given direction of emission was reported. In all these earlier works, photonic crystals are fabricated using the gravity sedimentation method followed by the infiltration of the active species 共dyes兲 using chemical routes. During the infiltration of these materials, the initial photonic crystal template may get disturbed by the solvent used or result in incomplete infiltration, thus decreasing the efficiency of controlled emission. Therefore, it will be better if these active species are attached to the building blocks using chemical methods before the fabrication of photonic crystals thus avoiding spatial diffusion during emission studies.10 Then, using these modified building blocks of submicron spheres, high-quality three dimensionally ordered 共functionalized兲 photonic crystals can be fabricated, and the effect of the photonic stop band on the emission of active species can be probed. In Ref. 7, the dye is homogeneously distributed in a layer inside the sphere, and the photonic crystals are fabricated using these spheres by the gravitational sedimentation method. Photoluminescence modification has also been observed recently for a 102, 123106-1 © 2007 American Institute of Physics Downloaded 24 Feb 2012 to 59.162.23.76. Redistribution subject to AIP license or copyright; see http://jap.aip.org/about/rights_and_permissions 123106-2 Nair et al. J. Appl. Phys. 102, 123106 共2007兲 FIG. 1. 共Color online兲 共a兲 SEM image for a photonic crystal made using PSRhB colloidal spheres of diameter 302 nm 共scale bar is 2 m兲. 共b兲 AFM image of the photonic crystal shows the 共111兲 plane of the fcc lattice 共scan area 1 m ⫻ 1 m兲. 共c兲 CLSM image of the photonic crystal shows the size of the domains 共scale bar is 20 m兲. photonic crystal fabricated using these fluorescent microspheres.15 It may be noted that gravitational self-assembly16 suffers from the disadvantage of a large number of unwanted and uncontrolled defects in the fabricated crystals and requires more time for the growth of crystals. We have used dyed PS spheres 共Micro Particles, Germany兲 as the building blocks for the fabrication of photonic crystals. The dye selected was rhodamine-B, which has a broad emission spectrum in the visible region. The dye is homogeneously distributed throughout the interior of the sphere with a concentration of approximately 0.09 wt. %. Since the dye is entrapped inside the sphere, its photostability can be greatly modified as compared with dyes infiltrated through solution chemistry,17 and hence this limitation is overcome. This is very important for designing lasers using the photonic band gap concept. The quality of the fabricated photonic crystal is ascertained through standard structural and optical characterizations. The dyed photonic crystal sample is excited with a frequency-doubled Nd: YAG laser, and the emission characteristics due to the photonic crystal environment are measured at different angles. The focus of this paper is mainly on the use of dye-polymer colloids as the building blocks avoiding the infiltration process for the active species, adopting a recently reported method of photonic crystal fabrication resulting in samples of superior optical quality, clear observance of selective suppression in the angle-resolved emission, and the analysis of the experimental results through a model related to the angle-dependent transmittance leading to a simple functional form for the emission. II. FABRICATION OF DYED PHOTONIC CRYSTALS One of the most celebrated methods of fabrication of three dimensionally ordered photonic crystals in the visible region is the self-assembling route using colloidal suspensions of submicron size spheres made of organic or inorganic materials. A modified form of gravitational self-assembly, which is based on the capillary force to organize the colloids, gives samples of very high optical quality but requires more time and is limited by the diameter of the spheres.18 In contrast to the common self-assembly methods for the fabrication of photonic crystals, we have used the recently reported inward growing self-assembling method19 for fabricating the photonic crystals using dyed PS spheres, which has yielded high-quality photonic crystals in less than 3 h. The building blocks used were rhodamine-B dyed PS 共PS-RhB兲 spheres with a mean diameter of 302 nm with a polydispersity index of 0.17. First, a substrate 共glass兲 with a dimension of 2.5 cm⫻ 2.5 cm was treated with chromic acid overnight, washed with deionized water and ethanol, and dried in an oven. The colloidal solution of known concentration and volume is dropped on the substrate and spread uniformly using a 1 ml syringe pipette and left to dry in the ambient atmosphere. After 1 min, depending on the sphere diameter, beautiful colors start appearing, and these colors move toward the center of the film as growth takes place. The crystallization is completed within 3 h for these samples. All the prepared samples are heated at 75 ° C 共below the glass transition temperature of polymers兲 for 2 h after the growth to remove any solvent used in the fabrication from the pores and also to enhance the mechanical stability of the samples. The success of this method depends highly on the concentration, the volume of the solution used 共0.05–0.1 ml兲, the temperature, and any type of air flow in the fabrication room. The air flow can force the crystallization toward a particular direction instead of toward the center of the substrate. Under optimized conditions, a uniform film forms on the entire substrate with a central void of millimeter size. III. RESULTS AND DISCUSSION A. Structural characterization The structural characterization of the photonic crystals is carried out using a scanning electron microscope 共SEM兲 and an atomic force microscope 共AFM兲. The domain sizes are mapped using a confocal laser scanning microscope 共CLSM兲. The samples analyzed in a SEM are coated with a thin layer of gold to avoid any charging effect during the experiment, and AFM images are taken in tapping mode. The microscope images are taken in the reflection mode. Figure 1 shows the SEM, AFM, and CLSM images of the photonic crystals fabricated using the PS-RhB spheres having a mean diameter of 302 nm. The hexagonal ordering in Figs. 1共a兲 and 1共b兲 confirms the 共111兲 plane of the face-centered-cubic 共fcc兲 lattice parallel to the substrate.20 It has been observed previously that the absolute value of the zeta potential of dyed colloidal suspension decreases as compared to a nondyed colloidal suspension, and this will affect the stability of the colloids.21 In spite of this aspect, the present method produces photonic crystals with good structural quality. The microscope image 关Fig. 1共c兲兴 shows the domains separated by grain boundaries, and the uniform color for every domain Downloaded 24 Feb 2012 to 59.162.23.76. Redistribution subject to AIP license or copyright; see http://jap.aip.org/about/rights_and_permissions 123106-3 Nair et al. FIG. 2. Absorption spectra for PS-RhB colloidal suspension 共line 1兲 and for bare PS 共nondyed兲 colloidal suspension 共line 2兲. The peak shown using an arrow indicates the absorption due to the dye, which is absent for the bare colloidal suspension. The fluorescence spectrum for the PS-RhB colloidal suspension 共line 3, dashed-dotted line兲 shows the emission peak at 580 nm 共marked with a vertical line兲 when excited at 532 nm. is an indication that each of the domains has the same orientation. The SEM, AFM, and CLSM images confirm that good quality photonic crystals can be prepared from dyed PS spheres using this method. B. Optical characterization The absorption and fluorescence spectrum for the dyed colloidal suspension was measured using an absorption spectrophotometer and a spectroflurometer. The results are shown in Fig. 2. The absorption spectrum for the PS-RhB colloidal suspension is shown as line 1. A small peak appears around 560 nm 共shown using a downward arrow on line 1兲 for the PS-RhB colloidal suspension corresponding to the absorption of the dye, and it is absent in the case of a bare PS colloidal suspension whose absorption spectrum is shown as line 2. In both of these cases, the absorption increases toward the ultraviolet region due to the absorption of PS. Line 3 shows the fluorescence spectrum for PS-RhB colloidal suspension at an excitation wavelength of 532 nm 共dasheddotted line兲. The emission wavelength is centered at 580 nm J. Appl. Phys. 102, 123106 共2007兲 shown using a vertical line. The absorption and fluorescence spectra of the dyed colloidal suspension give the excitation and the expected peak emission wavelength of the dyed colloids required for the laser-induced emission studies on the photonic crystals prepared from them 共to be discussed in the next section兲. The reflection/transmission measurements are routinely used for probing the photonic stop band characteristics of photonic crystals. A Perkin-Elmer Lambda 950 spectrophotometer with a halogen lamp as the source, having beam dimensions of 12.5 mm⫻ 5 mm for unpolarized light, is used for measuring the photonic stop band. Figure 3共a兲 shows the transmittance measured from the 共111兲 plane of a bare PS photonic crystal 共dashed-dotted line兲 and a PS-RhB photonic crystal as well as the reflectance spectra of a PSRhB photonic crystal 共black line兲. It is clear that the high reflection wavelength region is accompanied by a wellresolved minimum in transmission for PS-RhB photonic crystal. The reflection peak is slightly shifted to the shorter wavelength region as compared with the transmission minimum in the PS-RhB photonic crystal. This is because the reflection spectrum is measured at 8°, while the transmission spectrum is measured at normal incidence. The reflection spectrum for a nondyed PS photonic crystal also shows reflectance values as high as 50%, and the photonic stop band position is centered at 611 nm 共not shown here兲. The dip in transmission spectrum at 560 nm, shown using a downward arrow in Fig. 3共a兲, is due to the absorption of RhB dye as expected from the absorption measurement on the colloidal suspension. This dip is absent in the transmission spectrum of the nondyed PS photonic crystal. The photonic stop band is centered at 609 nm with a peak reflectance of 60% for the PS-RhB photonic crystal with a gap size 共⌬ / 兲 of 8%. The thickness of the photonic crystal, and hence the number of layers, can be estimated22 from the Fabry-Pérot oscillations on either side of the stop band as 4.84 m 共the number of layers is 20兲 for the PS-RhB photonic crystal. The photonic band structure calculation for the PS photonic crystal23 shows that the first order photonic stop band should center at 0.6 a / , where a is the fcc lattice constant, and is the free space wavelength. From our measurements, FIG. 3. 共Color online兲 共a兲 The reflection 共black line兲 and transmission 共blue line兲 spectra for a photonic crystal fabricated using PS-RhB colloids having a diameter of 302 nm show the photonic stop band at 609 nm. The dashed-dotted line is the transmission spectrum for the photonic crystal made from nondyed PS spheres having a sphere diameter of 280 nm. 共b兲 Photonic stop band at angles of incidence of 8° 共at the extreme right兲, 15°, 30°, 35°, 45°, and 60° 共at the extreme left兲 for PS-RhB photonic crystal. The photonic stop band shifts steadily toward shorter wavelengths with an increase in the angle of incidence, as shown by the arrow. Downloaded 24 Feb 2012 to 59.162.23.76. Redistribution subject to AIP license or copyright; see http://jap.aip.org/about/rights_and_permissions 123106-4 Nair et al. FIG. 4. Schematic of the experimental arrangement used in the emission studies the first order stop band position is obtained at 0.65 a / in the nondyed PS photonic crystal, and at 0.7 a / for the dyed PS photonic crystal. This implies a slight shift to the highfrequency region for the dyed PS when compared with the bare PS, due to the change in the dielectric constant of the polymer after the dye is incorporated in it. We have done the angle-resolved reflection spectroscopy using unpolarized light to map the photonic stop band at different angles of incidence. This study will enable us to ensure that the stop band position overlaps with the emission profile of the dye in the experiment described in the next section. The results of angle-resolved reflectance measurements are shown in Fig. 3共b兲. With an increase in the angle of incidence 共兲, the photonic stop band shifts toward the shorter wavelength region as governed by the modified Bragg’s law.6 The angle-resolved reflection spectra recorded at different angles from 8° to 45° show that the full width at half maximum and the peak reflectance remain constant. This is a direct indication of the superior quality of the photonic crystals fabricated using this self-assembling method. At an angle of incidence of 60° 关shown in Fig. 3共b兲, extreme left兴 the peak reflectance reduces, and the shape of the spectrum changes drastically. This is due to multiple Bragg diffractions involving many crystal planes at higher angles of incidence.24 It may be seen that, in the case of 60° incidence, a photonic stop band is not present in the emission wavelength range of 550–650 nm of the RhB dye. C. Emission studies with functionalized photonic crystals For the clear features of the photonic crystal environment to emerge in the emission studies, the excitation wave- J. Appl. Phys. 102, 123106 共2007兲 length should be outside of the photonic stop band, while the emission wavelength should be within the stop band. Hence the excitation wavelength is chosen to be 532 nm, which is outside the stop band of the photonic crystal, in order to penetrate well into the crystal and interact with the dye. By varying the angle of incidence, as shown earlier in Fig. 3共b兲, it has been possible to shift the photonic stop band wavelength across the peak emission wavelength of 580 nm for this dye. Figure 4 illustrates our experimental setup for the study of the emission characteristics of the functionalized photonic crystals. The second harmonic 共532 nm兲 of a quasicontinuous-wave Nd: YAG laser 共SOLAR TII: LF2210兲 was used for excitation. The pulse duration and repetition rate of the laser were approximately 30 ns and 4 kHz, respectively. The laser beam with a diameter of 4 mm at the exit mirror and a power of 5 mW was focused on the sample with a lens of focal length 400 mm, so as to result in a spot size of 50 m. The emission from the dyed photonic crystal was collected at several angles 共at a distance of 100 mm from the sample surface兲 and detected by a spectrometer 共Ocean Optics, USB4000兲. This angle-resolved emission has been recorded by moving the detector at different angles 共兲 with respect to the direction of the incident excitation beam. The sample position and the excitation beam direction 关normal to the 共111兲 plane兴 were kept fixed. The advantage of this setup is that the same position of the sample is probed throughout the measurements with the probed sample volume being a constant. This enables a direct comparison between the emission spectra measured at different angles of the detector position. In Fig. 5共a兲, the emission spectra obtained at five different angles 共 = 4°, 15°, 30°, 45°, and 60°兲 of the detector are shown by solid lines. The effect of the dark current of the detector has been subtracted. We can see that the emission profile changes when the detection angle is varied. Reflectance data R共兲 measured at = 8°, 15°, 30°, and 45° in the same sample are also plotted by dotted lines 共here, the reflectance at 8° is plotted with the emission at 4°兲. It should be noted that the positions of the reflectance peaks coincide with those of the dips in the emission, indicating that the emission spectra are affected by the presence of the band gap. At an angle of incidence of 4° and 15°, the dip in emission spectrum is at the red end of the spectrum where the photonic stop band is present for those incident angles. At FIG. 5. 共Color online兲 共a兲 Experimentally measured emission intensity 共solid line兲 and percentage of reflection 共dotted line兲 as a function of wavelength, at incident angles of 4°, 15°, 30°, 45°, and 60°. 共b兲 Detection angle dependence of emission obtained from the model. Downloaded 24 Feb 2012 to 59.162.23.76. Redistribution subject to AIP license or copyright; see http://jap.aip.org/about/rights_and_permissions 123106-5 J. Appl. Phys. 102, 123106 共2007兲 Nair et al. the incident angle of 30°, the dip in emission shifts toward the blue side of the spectrum where the photonic stop band is present, while the emission spectrum has recovered in the red part. This clearly shows that the dip observed is due to the photonic band gap effect, and the light emitted from the photonic crystals has a directional nature. In order to explain the detection angle dependence of the emission, we apply two assumptions: 共a兲 The emission at 60° shows an intrinsic profile without being affected by the photonic band gap because the band gap moves to a wavelength range much lower than the emission wavelength and 共b兲 transmittance T共兲 can be obtained simply as 1 − R共兲. In Fig. 5共b兲, the function F共兲 given by F共兲 = k1 + k2 ⫻ F60共兲 ⫻ 共1 − R共兲兲 共1兲 is plotted for = 4°, 15°, 30°, and 45°. Here, k1 and k2 are free parameters that describe the background signal, and the intensity of the dye emission. F60共兲 is the emission profile at 60°. It can be seen that the detection angle dependence of the emission is well reproduced by Eq. 共1兲, which is a product of the intrinsic emission with the angle-resolved transmittance. Since the active species are uniformly present even in the depth of the photonic crystal sample, the transmittance is a better parameter for this fit rather than the reflectance. It may be emphasized that the angle is used with the same meaning in the emission and transmittance data since the light in the emission band originates inside the crystal and gets measured by the detector placed at an angle to the incident beam direction, which is normal to the sample surface. The unintended defects in the self-assembled photonic crystals can cause random scattering of the light emitted by the functionalized building blocks. However, the directional property of the photonic crystal environment is strong enough in the samples studied here enabling a significant modification in the angle-resolved emission. The thicknesses of the photonic crystals in this case are significantly lower than those obtained by the sedimentation method. This is an advantage leading to lesser scattering events during the passage of the emitted light through the crystal. IV. CONCLUSIONS Good-quality photonic crystals are fabricated using the inward growing self-assembling method from PS-RhB spheres in a short time span of less than 3 h. The optical characterization results show a first order photonic stop band with a peak reflectance of more than 50%. With a laser excitation at 532 nm, which is in the absorption band of this dye, the emission characteristics were measured at different angles with respect to the direction of excitation. The emission profile could be analyzed from the measured angle dependence of the reflectance of these samples and was found to follow a simple functional form, which is a product of the intrinsic emission with the angle-resolved transmittance. ACKNOWLEDGMENTS RVN and RV thank the Department of Science and Technology and the University Grants Commission, Government of India, for financial support and are grateful for the use of the characterization facilities at the MEMS Department and the FIST-IRCC central facility at the Department of Physics, IIT Bombay. RVN and RV also thank Professor S. S. Major at the Physics Department of IIT Bombay for the use of the spectrophotometer. S. John, Phys. Rev. Lett. 58, 2486 共1987兲. E. Yablonovitch, Phys. Rev. Lett. 58, 2059 共1987兲. 3 K. Sakoda, Optical Properties of Photonic Crystals 共Springer, Heidelberg, 2001兲. 4 Y. A. Vlasov, N. Yao, and D. J. Norris, Adv. Math. 11, 165 共1999兲. 5 M. Megens and J.E. G. J. Wijnhoven, A. Lagendijk, and W. L. Vos, Phys. Rev. A 59, 4727 共1999兲. 6 R. V. Nair and R. Vijaya, J. Phys. D 40, 990 共2007兲. 7 B. Henderson and G. F. Imbush, Optical Spectroscopy of Inorganic Solids 共Clarendon Press, Oxford, 1989兲. 8 J. R. 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