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Journal of Nanomaterials
Volume 2012 (2012), Article ID 762510, 6 pages
Highly Ordered Macropore Arrays as Transparent Photocatalysts
Wuhan National Laboratory for Optoelectronics and College of Optoelectronic Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074, China
Received 29 February 2012; Accepted 20 March 2012
Academic Editor: Jiaguo Yu
Copyright © 2012 Yuan Dong 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.
Highly ordered transparent TiO2 macropore arrays were synthesized via a simple glass-clamping method at room temperature. The as-synthesized TiO2 macropore arrays show high transmittance in the visible light region and can be used as transparent photocatalysts for degradation of organic dyes.
Transparent devices have received considerable attentions in recent years due to their potential applications in fields where traditional silicon-based technique could not approach, such as transparent displays, transparent transistors, solar cells, transparent supercapacitors, and ultraviolet (UV) detectors [1–5]. TiO2, as one of the most important wide bandgap semiconductors, has been studied to be used as transparent device because of its outstanding physical and chemical properties. For example, TiO2 transparent thin films would make great impact in fields like photoelectrodes , antireflection films , self-clean glass , and nonlinear optical devices .
Two-dimensional (2D) ordered arrays are of great significance in many research areas of modern science and technology, with the applications including optical and optoelectronic devices , dye-sensitized solar cells , surface-enhanced Raman spectroscopy , catalysis , and sensors [13, 14]. Recently, 2D TiO2 ordered arrays, combining the outstanding properties of TiO2 with their 2D ordered assembling, have gained great research interests, and many kinds of methods have been developed to synthesize 2D TiO2 ordered arrays. For example, Wang et al. described an atomic layer deposition (ALD) method to fabricate TiO2 ordered nanobowl arrays, which can be used to separate monosized submicron spheres . Yang et al. reported an rf-sputtering method to synthesize ordered hollow TiO2 hemisphere films , and described their applications in dye-sensitized solar cells (DSSCs) as high-efficiency photoelectrodes. Kannaiyan et al. developed a method to fabricate 2D hybrid CdS/TiO2 composite nanodot arrays  and studied the photocatalytic properties of the hybrid thin film. However, complicated procedures or expensive equipments are usually required, and it is still quite desired to develop simple method to synthesize 2D TiO2 ordered arrays. On the other hand, it would be more desired to make the 2D TiO2 ordered arrays transparent to fit special applications in transparent electronics.
In this paper, we developed a simple and low-cost glass-clamping method to synthesize highly ordered TiO2 macropore arrays by using hexagonally arranged PS sphere monolayer as the sacrificial mask. As-synthesized highly ordered TiO2 macropore arrays showed high transmittance as approximately 92% in the visible light region and can be used as interesting transparent photocatalysts for the degradation of polluted organic dyes.
Monodispersed polystyrene (PS) spheres were first synthesized via the emulsifier-free method developed by Holland et al. . The corresponding SEM images of the as-obtained PS can be seen in Figure S1 (see Supplementary Material available online at http://dx.doi.org/10.1155/2012/762510). The second step is to assemble a PS monolayer on a cleaned glass substrate. During this step, a piece of glass substrate was used, which was precleaned by boiling in piranha solution (H2SO4 : H2O2 = 7 : 3 v/v). After being cleaned, the glass substrate was put in the bottom of a Petri dish (), which was filled with deionised water until the level of the water equals to the upper surface of the glass substrate. Then, 15 μL monodispersed PS spheres suspensions (wt 5%; water : ethanol = 1 : 1) were dropped onto the glass, which were found to rapidly spread and form a PS spheres monolayer on the glass substrate (Scheme 1(a)).
After putting another piece of the precleaned glass substrate on the surface of the PS spheres monolayer, a syringe was utilized to drain the Petri dish, resulting in the formation of dried PS spheres monolayer between the two pieces of glass substrates (Scheme 1(b)). To get highly ordered TiO2 macropore arrays, a drop of tetra-n-butyl-titanate (TBT) solution was then dripped from the edge of the PS spheres monolayer as shown. Stored in air for several days, the TBT solution slowly spread and filled the cavities of the PS spheres monolayer, where it homogeneously hydrolyzed and formed into amorphous Ti(OH)4 (Scheme 1(c)). After completely hydrolyzed, the upper glass substrate was peeled off, and the bottom glass substrate with Ti(OH)4/PS spheres was annealed at 450°C for 5 hours, resulted in the formation of the final highly ordered TiO2 macropore arrays.
3. Results and Discussion
After annealing, the product was first characterized by using X-ray diffraction (XRD) to get information about its composition. Figure S2 is the corresponding XRD pattern of the product, which can be easily indexed to crystalline TiO2 with the anatase phase (JCPDS Card, number 89-4203). No peaks from other impurities were detected, indicating the formation of pure TiO2 product.
The PS spheres used in the work have diameters of about 500 nm (Figure S1). Figure 1(a) is a typical SEM image of the as-synthesized PS spheres monolayer, which is found to be hexagonal arranged on the glass substrate on a large scale. The inset fast Fourier transform (FFT) pattern of the PS monolayer shows regularly arranged spots, confirming its uniform hexagonal arrangement. By using the PS spheres monolayer as the templates, highly ordered TiO2 macropore arrays were obtained on a large scale, as can be seen from Figure 1(b). The SEM image in Figure 1(c) also reveals that the TiO2 product consists of highly ordered TiO2 hemispheres with diameters of around 500 nm, similar to the PS spheres. The thickness of the TiO2 hemisphere is around 30 nm (Figure 1(d)). Confined by the PS spheres monolayer templates, all the TiO2 hemispheres arranged hexagonally on the substrate, forming into the final TiO2 macropore arrays. The FFT pattern inset in Figure 1(b) confirms its regular hexagonal arrangement.
Due to the regular macropore structures of the TiO2 product, it is interesting to find that the TiO2 film on glass substrate exhibited different colours upon different tilts to the illuminated solar light. Figures 1(e) and 1(f) are the photographs of the TiO2 film to solar light with the tilt angles of around 20° and 30°, respectively. Under such angles, the film exhibited sky-blue and light green colors, respectively. This phenomenon can be well explained by the grating model suggested by Billon et al. , which indicates that highly ordered hexagonal pattern would behave as gratings. Thus, the structures would obey the Grating equation: where is the diffraction order, is the wavelength, is the distance between centres of two adjacent hemispheres, is the incident angle, and can be considered as the observation angle. In this case, if we keep, , and as constants, then when the observation angle is changed, we can observe that the colour perception of the surface will be changed. Such highly angular dependence character demonstrates that the synthesized TiO2 arrays film from the simple glass-clamping method has very good uniformity and regularity.
Due to the superior uniformity, regularity, and homogeneous thickness of the TiO2 ordered arrays, the TiO2 films synthesized by the glass-clamping method show very good transparency in the visible light region. Figure 2 is the transmittance spectrum of the 2D TiO2 ordered arrays on glass substrate, while a cleaned glass was also used to check as baseline during the testing. For comparison, the transmittance spectrum of a clean glass substrate was also depicted in Figure 2. From the spectrum, we can easily find out that the 2D TiO2 ordered arrays have great transparency, with a transmittance value of approximately 92% (transmittance value was measured on a Shimadzu UV-2550 spectrophotometer, Japan). Insets in Figure 2 are the digital photographs of the TiO2/glass substrate as well as the bare glass, where the under image (the image corresponds to the symbol of our lab) can be easily seen through the substrates. No obvious difference was found between the two substrates, indicating the excellent transparency of the TiO2 product.
In comparison to other semiconductor photocatalysts, TiO2 is a suitable material described as high-performance photocatalysts because of its biological and chemical inertness, cost-effectiveness, environmental friendliness, availability, and long-term stability against photo- and chemical-corrosion [19–21]. With regular shapes and excellent optical transparency, the as-obtained highly ordered TiO2 macropore arrays may be used as interesting transparent photocatalyst to fit some special applications. Photocatalytic properties of the highly ordered TiO2 macropore arrays were studied by photodegradation of organic dyes, such as methylene blue (MB), methyl orange (MO), and rhodamine B (RhB). All the organic dyes were dissolved in water with ratio of 15 μL : 15 mL. The TiO2 product was first immersed in the organic dye solution for 60 minutes to reach an adsorption equilibrium, before being irradiated by 365 nm UV light (50 mW/cm2). After every 30 minutes of UV light exposure, 400 μL of the testing organic dyes solution was subjected to UV-spectrophotometer. The concentration of organic dye solution was determined by the peak values from the UV-Vis absorption spectrum.
Figures 3(a), 3(b), and 3(c) show the spectra changes of main peaks originated from MB (664 nm), MO (554 nm), and RhB (460 nm) with the irradiation time, respectively. Under UV light illumination, the peaks of three organic dyes obviously decrease revealing good photocatalytic properties of the fabricated TiO2/glass. Furthermore, to quantify photocatalytic abilities of the as-synthesized TiO2/glass, the changes of the organic dye concentrations with reaction time were recorded and shown in Figure 3(d). Clearly, TiO2/glass showed not only higher adsorption ability but also higher photodecomposition ability to MB solution than to other dyes solutions at room temperature. During the dark reaction, about 20% of MB dyes were adsorbed. And about 93.6% of MB dyes were decomposed after 3 h irradiated by UV light. While for MO and RhB dyes, the adsorption effects in the presence of TiO2/glass were poor, and the concentrations of MO and RhB solutions decreased to 87.2% and 82.3% under exposure to UV light for 3 h, respectively, which were lower than that of MB solution.
As described above, the current glass-clamping method shows great superiority in fabricating transparent 2D ordered arrays on glass substrate. We found that such a simple method may also be extended to other substrates. As an example, we successfully synthesized 2D TiO2 ordered arrays on aluminium substrate, as can be seen in Figure S3.
In conclusion, we have developed a simple glass-clamping method to fabricate 2D TiO2 ordered arrays on a large scale by using hexagonally arranged PS monolayer as the sacrificial mask. The as-obtained 2D TiO2 ordered arrays show great uniformity and regularity with an excellent transparency of about 92%. The as-obtained 2D TiO2 ordered arrays were used as high performance transparent photocatalysts for the photodegradation of organic dyes, such as MB, MO, and RhB. Considering the high transmittance, the 2D TiO2 arrays might be utilized as self-cleaning glass, transparent optoelectronic devices, and other applications. Moreover, we have applied this simple method on the fabrication of 2D TiO2 ordered arrays on other substrates, which widely expands its potential applications.
This work was supported by the National Natural Science Foundation (21001046), the 973 Projects of China (2011CB933300), the Natural Science Foundation of Hu bei Province (2011CDB035), the Research Fund for the Doctoral Program of Higher Education (20100142120053), the Graduate Innovation Fund of Graduate Practice Base of Innovation and Enterprise (no. HF-09-20-2011-230), and the Director Fund of WNLO. The authors thank the Analytical and Testing Center of HUST for the sample characterizations.
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