Printer Friendly

Fabrication and characteristics of macroporous Ti[O.sub.2] photocatalyst.

1. Introduction

For the environment protection purpose, the disposal of various toxic dyes from the textile industry has attracted extensive attention. Rhodamine B (RhB) is widely used as a colorant in textiles and food stuffs and is also a well-known water tracer fluorescent [1]. It is harmful to human beings and animals and causes irritation of the skin, eyes, and respiratory tract.

Owing to high photocatalytic efficiency, good oxidation capability, stable chemical reaction, low cost, and nontoxicity, titanium dioxide (Ti[O.sub.2]) has been applied widely in wastewater treatment [2-4], environment purification [5, 6], solar energy transfer [7, 8], chemical sensing [9, 10]. Recently, it was found that incorporation of well-defined porosity of Ti[O.sub.2] materials could greatly enhance the photoactivity in the area of environmental remediation and energy conversion [1113]. For a variety of practical applications, the fabrication of desired structure with network is important as well as control in grain size, crystallinity, and composition [14-16].

At present, porous Ti[O.sub.2], combining the outstanding properties of Ti[O.sub.2] with their porous structure, has gained great research interests, and various synthetic techniques had been developed. For example, Liu et al. prepared anatase Ti[O.sub.2] porous thin films by sol-gel method with CTAB surfactant as a pore-forming agent, and many factors were studied [17]. Bala et al. fabricated hollow spheres of anatase Ti[O.sub.2] by spherical CaC[O.sub.3] nanoparticles as a template and investigated the photocatalytic activity [18]. Zheng et al. synthesized rutile and anatase Ti[O.sub.2] mesoporous single crystals with diverse mophologies by silica-templated hydrothermal method [19]. Dong et al. prepared highly ordered transparent Ti[O.sub.2] macropore arrays via a glass-clamping method and investigated the potential application in degradation of organic dyes [20]. However, the general synthesis usually involved complicated multistep to obtain porous skeleton. Firstly, it is required to assemble spheres into colloidal crystals as templates, and then the precursor is filled into interstices among the crystals for several times [21-23]. Moreover, for an efficient photodegradation catalyst, the macroporous structure is essential due to the run-through-macropore network which maximizes the uptake and the diffusion of the organic molecules [24-26]. Additionally, the porous structures are propitious to enhance the light scattering and improve the utilization rate of irradiation light [27-29].

Herein, a simple method without assembly and filling steps was introduced in this work for the preparation of macroporous Ti[O.sub.2] through a sol-gel process using polystyrene spheres as sacrificial templates. Compared with the Ti[O.sub.2] materials synthesized in the absence of PS spherical template [30, 31], the macroporous Ti[O.sub.2] photocatalyst sintered at 500[degrees]C exhibits much higher activity on the degradation of RhB under the UV irradiation. The macroporous Ti[O.sub.2] material present great potential in the fields of environmental remediation and energy conversion and storage.

2. Experiment

2.1. Materials. Tetrabutyl titanate (Ti[(O[C.sub.4][H.sub.9]).sub.4]), sodium styrene sulfonate, sodium hydrogen carbonate, potassium persulfate, ethanol, Rhodamine B (RB), acetic acid, and nitric acid were all analytical grade and used without further purification. Styrene was washed by 5% NaOH solution several times to remove polymerization inhibitor. All of the reagents were purchased from Shanghai Chemical Reagent Ltd. Co.

2.2. Preparation of PS Microspheres. PS spheres were obtained by emulsion polymerization of styrene according to previous reports [32-34]. At first, 150g deionized water was poured into a 300 mL jacket reactor, which was kept at 85[degrees]C until the end of the reaction. Then, 0.08 g sodium styrene sulfonate as the emulsifier and 0.0633 g sodium hydrogen carbonate as the buffer were dissolved in the deionized water. Under constant stirring, 18.30 mL styrene monomer was added to this solution, accompanied with nitrogen protection. After 1h, 0.0833 g potassium persulfate as an initiator was introduced into the solution. After 18 h polymerization, the monodispersed PS spheres with the average diameter of 278 nm were obtained, and the standard deviation of spheres was less than 2.76%.

2.3. Preparation of Ti[O.sub.2] Sol. With the Ti[(O[C.sub.4][H.sub.9]).sub.4] as precursor, ethanol as solvent and glacial acetic acid as inhibitor, Ti[O.sub.2] sol was synthesized by sol-gel method according to references elsewhere [35, 36]. The procedure can be divided into three steps. At first, solution A was prepared by mixing 3 mL deionized water and 16 mL absolute ethyl alcohol. And then solution B was obtained by adding 10 mL Ti[(O[C.sub.4][H.sub.9]).sub.4] and 2 mL glacial acetic acid into 32 mL ethanol slowly with the rapid stirring. At last, solution A was dripped slowly into solution B under rapid stirring. The homogeneous and transparent solution of Ti[O.sub.2] sol was thus obtained.

2.4. Preparation of Macroporous Ti[O.sub.2]. In a typical synthesis of macroporous Ti[O.sub.2], 11 mL PS spheres suspension with the concentration of 5.88 wt% was added slowly into 10 mL as-prepared Ti[O.sub.2] sol. The intimate mixture was obtained by stirring and ultrasonication. Then, the mixture was placed in an oven at 70[degrees]C for 12 h and then Ti[O.sub.2]/PS sphere composites were obtained. To prepare macroporous Ti[O.sub.2], the as-obtained composites were sintered in muffle furnace at 500[degrees]C for 2h in air. The ultima product was denoted as m-Ti[O.sub.2]. For contrast, the synthesis of Ti[O.sub.2] nanoparticles was the similar to the preparation of macroporous Ti[O.sub.2] without adding the PS spheres, which was labeled as r-Ti[O.sub.2].

2.5. Characterization. Field emission scanning electron microscopy (FE-SEM) was carried out on FEI Sirion-200 and transmission electron microscopy TEM was taken on JEOL JEM-2100. The XRD patterns of the synthesized samples were obtained by a Bruker-AXS D8 Advance diffractometer with CuK[alpha] radiation ([lambda] = 0.15418 nm). To determine the proper sintering temperature and analyze the weight content of PS spheres in the Ti[O.sub.2]/PS composites, both the as-prepared PS spheres and Ti[O.sub.2]/PS composites were investigated by thermogravimetry and derivative thermogravimetry (TG-DTG), which was operated at a program-controlled temperature elevation rate of 10[degrees]C/min in the air. [N.sub.2] adsorption-desorption isotherms were measured on a Quantachrome NOVA 2000e sorption analyzer at liquid nitrogen temperature (77 K). The samples were degassed at 120[degrees]C overnight prior to the measurement. The surface areas were calculated by the multipoint Brunauer-Emmett-Teller (BET) method.

2.6. Photocatalytic Experiment. The photocatalytic activity tests of the synthesized Ti[O.sub.2] were performed by the degradation of Rhodamine B (RhB) under UV light irradiation under ambient conditions. The experiment was performed in a water-jacket reactor operated at 20[degrees]C. The light source was a 450 W high-pressure mercury lamp (Foshan Electrical and Lighting Co. Ltd.) with a strong peak centered at 362 nm. The distance between the sample and the lamp was about 10 cm. In a typical process, 0.1 g of the obtained product was placed into 100 mL of RhB aqueous solution (2 x [10.sup.-5] mol/L) under magnetic stirring. 5 mL of the mixture was collected at a given time interval of 15 min and was then centrifuged to discard any sediment. Then the concentration of RhB was determined on a TU-1810 UV-vis spectrophotometer at [[lambda].sub.max] = 553 nm [37, 38]. The decomposition efficiency of RhB was calculated by the following formula:

Decomposition efficiency = [A.sub.0] - [A.sub.t] / [A.sub.0] x 100%, (1)

where [A.sub.0] and [A.sub.t] represent the absorbance of the RhB solution before irradiation and the absorbance at time t, respectively.

3. Results and Discussion

3.1. Material Characterization. TG-DTG curves of both PS spheres and the Ti[O.sub.2]/PS composites are shown in Figure 1. For PS spheres, three weight loss stages, below 300, 300-400, and 400-500[degrees]C, can be observed. The PS spheres undergo endothermic desorption of physically adsorbed water and residual solvent at low temperature below 300[degrees]C. The major weight loss of about 90% between 300 and 400[degrees]C can be assigned to the thermal decomposition of the polystyrene, which was decomposed from long chain to shorter chain and then depolymerized into volatile monomers with low molecular weight. While, the third stage in the range of 400-500[degrees]C can be attributed to the combustion of the residual coke. With respect to the Ti[O.sub.2]/PS nanocomposite, it is found that PS spheres can be completely removed at 500[degrees]C (Figure 1(b)). Thus, 500[degrees]C was selected as the calcination temperature to prepare the macroporous Ti[O.sub.2] photocatalyst. The weight content of Ti[O.sub.2] in the Ti[O.sub.2]/PS nanocomposite is calculated to be 43.2%.

XRD are employed to characterize the crystallite structure of the synthesized Ti[O.sub.2] catalysts. It can be seen from Figure 2(a) that the diffraction peaks of Ti[O.sub.2] after being calcinated at 450[degrees]C can be indexed to anatase phase Ti[O.sub.2] (JCPDS NO. 21-1272) and rutile phase Ti[O.sub.2] (JCPDS NO. 21-1276), indicating that the sample calcined at 450[degrees]C is composed of bicrystalline phase. When the calcination temperature was increased to 500[degrees]C, all diffraction peaks can be indexed to pure anatase phase (JCPDS NO. 21-1272), and no characteristic peaks of other impurities can be detected. Thus, 500[degrees]C is a proper sintering temperature to prepare anatase phase macroporous Ti[O.sub.2], which is in accordance with the TG-DTG analysis (Figure 1). The sharp diffraction peaks in Figure 2(b) illustrate the well crystallization of m-Ti[O.sub.2] after the heat treatment. The crystallite size (D) was calculated to be about 10 nm according to the Scherrer formula D = K[lambda]/[beta] cos[theta] [39], where K is a constant (shape factor, about 0.9), [lambda] is the X-ray wavelength (0.15418 nm), [beta] is the full-width at half-maximum, and d is the diffraction angle. The values of [beta] and [theta] were taken from Ti[O.sub.2] (101) diffraction line.

TEM images of the PS spheres and m-Ti[O.sub.2] are given in Figure 3. Figure 3(a) shows the TEM image of the PS spheres. The size of the PS spheres is about 278 nm, and the standard deviation of monodispersed spheres is less than 2.76%. This indicates that the PS spheres are suitable to be employed as macroporous templates. As shown in Figure 3(b), the PS spheres are wrapped by Ti[O.sub.2] nanoparticles before being sintered. Figure 3(c) shows the low-magnification TEM image of macroporous Ti[O.sub.2] sintered at 500[degrees]C in air, from which macropores can be clearly seen, suggesting that PS spheres have been completely removed after calcination at 500[degrees]C in air. And the SEM image (Figure 3(e)) also demonstrates well-defined macroporous structure. The size of the hollow spheres is about 240 nm, which is smaller than the size of original PS spheres template, suggesting the significant shrinkage after the PS removal via calcination. Additionally, Figure 3(c) also illustrates that run-through-macropore network structure was formed. And the SEM images in Figure 3(e) further confirm that the macropores left by the templates are interconnective with neighboring hollow spheres. High-resolution TEM image (Figure 3(d)) displays that the crystalline size of Ti[O.sub.2] nanoparticles is about 10 nm, which is in good agreement with the XRD analysis.

[N.sub.2] adsorption-desorption measurements were performed to investigate the textural properties of the macroporous Ti[O.sub.2]. The [N.sub.2] adsorption-desorption isotherms of r-Ti[O.sub.2] and m-Ti[O.sub.2] are shown in Figure 4. One can see that the isotherm of the r-Ti[O.sub.2] is of typical type IV, characteristic of mesoporous materials, according to IUPAC classification. The adsorbed nitrogen volume for m-Ti[O.sub.2] becomes steep in the P/[P.sub.0] range of 0.8-1.0, which indicates the presence of large macropores. Based on the Brunauer-Emmett-Teller (BET) equation, the specific surface areas of r-Ti[O.sub.2] and m-Ti[O.sub.2] were evaluated to be about 91.2 and 87.8 [m.sup.2]/g, respectively.

3.2. Photocatalytic Activity Test. The photocatalytic activities of the prepared Ti[O.sub.2] samples were examined through the photodegradation of RhB under UV light irradiation. The degradation efficiency was illustrated by the change of the RhB concentration during the photodegradation process and the results were shown in Figure 5. The photocatalytic results reveal that the photocatalytic activity of the macroporous Ti[O.sub.2] was significantly improved as compared to that of the traditional Ti[O.sub.2] nanoparticles. For the macroporous Ti[O.sub.2], 92.63% of the RhB was decomposed after 2h irradiation. However, as to the r-Ti[O.sub.2] sample, the degradation percentage is only 81.66%. Here, the macroporous structure is believed to facilitate the transportation of reactant molecules and products through the interior space due to the run-through-macropore networks [40-43] and to favor the harvesting of exciting light due to enlarged surface area and multiple scattering within the porous framework [43, 44]. So the enhanced photoactivity of m-Ti[O.sub.2] could be achieved.

4. Conclusions

In summary, macroporous Ti[O.sub.2] photocatalyst was successfully synthesized via a simple sol-gel method using polystyrene spheres as sacrificial templates. The prepared macroporous Ti[O.sub.2] exhibited higher photocatalytic activity than the Ti[O.sub.2] sample through a template-free approach in catalyzing the degradation of RhB under UV light illumination. And the superior photocatalytic performance can be related to the run-through-macropore network structure. Considering the facile preparation and high photocatalytic activity, the macroporous Ti[O.sub.2] materials display a good potential in the fields of environmental remediation and energy conversion and storage.

Conflict of Interests

The authors have no conflict of interests in relation to the instrumental companies directly or indirectly.


This work was supported by the National Natural Science Foundation of China (U1361119, 51174077), Specialized Research Fund for the Doctoral Program of Higher Education (20124116120002), the Education Department Key Programs for Science and Technology Research of He'nan Province (13A430336, 2011A480003).


[1] S. D. Richardson, C. S. Willson, and K. A. Rusch, "Use of rhodamine water tracer in the marshland upwelling system," Ground Water, vol. 42, no. 5, pp. 678-688, 2004.

[2] J. Ryu and W. Choi, "Substrate-specific photocatalytic activities of Ti[O.sub.2] and multiactivity test for water treatment application," Environmental Science and Technology, vol. 42, no. 1, pp. 294-300, 2008.

[3] H. Cui, H. Liu, J. Shi, and C. Wang, "Function of Ti[O.sub.2] lattice defects towards photocatalytic process: view of electronic driven force," International Journal of Photoenergy, vol. 2013, Article ID 364802, 16 pages, 2013.

[4] P Chou, S. Matsui, K. Misaki, and T. Matsuda, "OH radical formation at distinct faces of rutile Ti[O.sub.2] crystal in the procedure of photoelectrochemical water oxidation," The Journal of Physical Chemistry C, vol. 117, no. 45, pp. 23832-23839, 2013.

[5] R. Daghrir, P. Drogui, and D. Robert, "Modified Ti[O.sub.2] for environmental photocatalytic applications: a review," Industrial & Engineering Chemistry Research, vol. 52, no. 10, pp. 3581-3599, 2013.

[6] H. Huang, H. Huang, P. Hu, X. Ye, and D. Y. C. Leung, "Removal of formaldehyde using highly active Pt/Ti[O.sub.2] catalysts without irradiation," International Journal of Photoenergy, vol. 2013, Article ID 350570, 6 pages, 2013.

[7] R. Giovannetti, M. Zannotti, L. Alibabaeu, and S. Ferraro, "Equilibrium and kinetic aspects in the sensitization of monolayer transparent Ti[O.sub.2] thin films with porphyrin dyes for DSSC applications," International Journal of Photoenergy, vol. 2014, Article ID 834269, 9 pages, 2014.

[8] B. Wang and L. L. Kerr, "Stability of CdS-coated Ti[O.sub.2] solar cells," Journal of Solid State Electrochemistry, vol. 16, no. 3, pp. 1091-1097, 2012.

[9] S. Phanichphant, C. Liewhiran, K. Wetchakun, A. Wisitsoraat, and A. Tuantranont, "Flame-made Nb-doped Ti[O.sub.2] ethanol and acetone sensors," Sensors, vol. 11, no. 1, pp. 472-484, 2011.

[10] L.-C. Jiang and W.-D. Zhang, "Electrodeposition of Ti[O.sub.2] nanoparticles on multiwalled carbon nanotube arrays for hydrogen peroxide sensing," Electroanalysis, vol. 21, no. 8, pp. 988-993, 2009.

[11] V. Tajer-Kajinebaf, H. Sarpoolaky, and T. Mohammadi, "Synthesis of nanostructured anatase mesoporous membranes with photocatalytic and separation capabilities for water ultrafiltration process," International Journal of Photoenergy, vol. 2013, Article ID 509023, 11 pages, 2013.

[12] C. S. Guo, M. Ge, L. Liu, G. Gao, Y. Feng, and Y. Wang, "Directed synthesis of mesoporous Ti[O.sub.2] microspheres: catalysts and their photocatalysis for bisphenol A degradation," Environmental Science and Technology, vol. 44, no. 1, pp. 419-425, 2010.

[13] Y.-C. Park, Y.-J. Chang, B.-G. Kum et al., "Size-tunable mesoporous spherical Ti[O.sub.2] as a scattering overlayer in high-performance dye-sensitized solar cells," Journal of Materials Chemistry, vol. 21, no. 26, pp. 9582-9586, 2011.

[14] C. J. W. Ng, H. Gao, and T. T. Yang Tan, "Atomic layer deposition of Ti[O.sub.2] nanostructures for self-cleaning applications," Nanotechnology, vol. 19, no. 44, Article ID 445604, 2008.

[15] Z. Bian, J. Zhu, F. Cao, Y. Huo, Y. Lu, and H. Li, "Solvothermal synthesis of well-defined Ti[O.sub.2] mesoporous nanotubes with enhanced photocatalytic activity," Chemical Communications, vol. 46, no. 44, pp. 8451-8453, 2010.

[16] H. Z. Zhang, F. Dong, S. N. Zhai, X. J. Kang, and S. M. Fang, "Preparation of ordered Ti[O.sub.2] macroporous membrane using PBMA colloid crystal as template," Advanced Materials Research, vol. 399-401, pp. 677-682, 2012.

[17] G. Q. Liu, Z. G. Jin, X. X. Liu, T. Wang, and Z. F. Liu, "Anatase Ti[O.sub.2] porous thin films prepared by sol-gel method using CTAB surfactant," Journal of Sol-Gel Science and Technology, vol. 41, no. 1, pp. 49-55, 2007

[18] H. Bala, Y. Yu, and Y. Zhang, "Synthesis and photocatalytic oxidation properties of titania hollow spheres," Materials Letters, vol. 62, no. 14, pp. 2070-2073, 2008.

[19] X. Zheng, Q. Kuang, K. Yan, Y. Qiu, J. Qiu, and S. Yang, "Mesoporous Ti[O.sub.2] single crystals: facile shape-, size-, and phase-controlled growth and efficient photocatalytic performance," ACS Applied Materials & Interfaces, vol. 5, no. 21, pp. 11249-11257, 2013.

[20] Y. Dong, J. Chao, Z. Xie, X. Xu, Z. Wang, and D. Chen, "Highly ordered Ti[O.sub.2] macropore arrays as trandparent photocatalysts," Journal of Nanomaterials, vol. 2012, Article ID 762510, 6 pages, 2012.

[21] P. Jiang, J. Cizeron, J. F. Bertone, and V L. Colvin, "Preparation of macroporous metal films from colloidal crystals," Journal of the American Chemical Society, vol. 121, no. 34, pp. 7957-7958, 1999.

[22] M. Sadakane, T. Horiuchi, N. Kato, C. Takahashi, and W. Ueda, "Facile preparation of three-dimensionally ordered macroporous alumina, iron oxide, chromium oxide, manganese oxide, and their mixed-metal oxides with high porosity," Chemistry of Materials, vol. 19, no. 23, pp. 5779-5785, 2007

[23] M. Davis, D. A. Ramirez, and L. J. Hope-Weeks, "Formation of three-dimensional ordered hierarchically porous metal oxides via a hybridized epoxide assisted/colloidal crystal templating approach," Applied Materials & Interfaces, vol. 5, no. 16, pp. 7786-7792, 2013.

[24] T. Kimura, N. Miyamoto, X. Meng, T. Ohji, and K. Kato, "Rapid fabrication of mesoporous titania films with controlled macroporosity to improve photocatalytic property," Chemistry, vol. 4, no. 9, pp. 1486-1493, 2009.

[25] X.-Y. Li, L.-H. Chen, Y. Li et al., "Self-generated hierarchically porous titania with high surface area: photocatalytic activity enhancement by macrochannel structure," Journal of Colloid and Interface Science, vol. 368, no. 1, pp. 128-138, 2012.

[26] R.-F. Zhang, J. Ye, and N.-B. Long, "Large-sized Ti[O.sub.2]/Si[O.sub.2] macroporous materials for photodegradation of organic compounds in water and air," Advanced Materials Research, vol. 306307, pp. 1157-1161, 2011.

[27] L. Szymanski, P. Surolia, O. Byrne, K. R. Thampi, and C. Stubenrauch, "Porous "sponge-like" anatase Ti[O.sub.2] via polymer templates: synthesis, characterization, and performance as a light-scattering material," Colloid and Polymer Science, vol. 291, no. 4, pp. 805-815, 2013.

[28] F. Z. Huang, D. H. Chen, X. L. Zhang, R. A. Caruso, and Y.-B. Cheng, "Dual-function scattering layer of submicrometer-sized mesoporous Ti[O.sub.2] beads for high-efficiency dyesensitized solar cells," Advanced Functional Materials, vol. 20, no. 8, pp. 1301-1305, 2010.

[29] T. Yan, L. Li, G. Li, Y. Wang, W. Hu, and X. Guan, "Porous Sn[In.sub.4][S.sub.8] microspheres in a new polymorph that promotes dyes degradation under visible light irradiation," Journal of Hazardous Materials, vol. 186, no. 1, pp. 272-279, 2011.

[30] G. Cappelletti, "Ti[O.sub.2] nanoparticles: traditional and novel synthetic methods for photocatalytic paint formulations," in Nanoparticles: Properties, CLassification Characterization and Fabrication, S.L, pp. 213-254, Nova Science Publishers, 2010.

[31] S. Yurdakal, B. S. Tek, O. Alagoz et al., "Photocatalytic selective oxidation of 5-(Hydroxymethyl)-2-furaldehyde to 2,5-Furandicarbaldehyde in water by using anatase, rutile, and brookite Ti[O.sub.2] nanoparticles," Sustainable Chemistry & Engineering, vol. 1, no. 5, pp. 456-461, 2013.

[32] Q. Zhou, P. Dong, G.-Y. Yi, L.-X. Liu, and B.-Y. Cheng, "Preparation of Ti[O.sub.2] inverse opal via a modified filling process," Chinese Physics Letters, vol. 22, no. 5, pp. 1155-1158, 2005.

[33] X.-D. Wang, P. Dong, and G.-Y. Yi, "Evaporation self-assembly method to fabricate high-quality polystyrene microsphere colloid crystal," Acta Physica Sinica, vol. 55, no. 4, pp. 2092-2098, 2006.

[34] X.-D. Wang, G.-Y. Yi, and Y. Liu, "Preparation of [Al.sub.2][O.sub.3] catalytic material with run-through-macropore network structure," Chemical Journal of Chinese Universities, vol. 30, no. 2, pp. 349-354, 2009.

[35] C. Wang, Z.-X. Deng, G. Zhang, S. Fan, and Y. Li, "Synthesis of nanocrystalline Ti[O.sub.2] in alcohols," Powder Technology, vol. 125, no. 1, pp. 39-44, 2002.

[36] Y. Li, T. J. White, and S. H. Lim, "Low-temperature synthesis and microstructural control of titania nano-particles," Journal of Solid State Chemistry, vol. 177, no. 4-5, pp. 1372-1381, 2004.

[37] E. T. Soares, M. A. Lansarin, and C. C. Moro, "A study of process variables for the photocatalytic degradation of rhodamine B," Brazilian Journal of Chemical Engineering, vol. 24, no. 1, pp. 29-36, 2007

[38] K. Byrappa, A. K. Subramani, S. Ananda, K. M. Lokanatha Rai, R. Dinesh, and M. Yoshimura, "Photocatalytic degradation of rhodamine B dye using hydrothermally synthesized ZnO," Bulletin of Materials Science, vol. 29, no. 5, pp. 433-438, 2006.

[39] H. P. Klong and L. E. Alexander, X-Ray Diffraction Procedures for Crystalline and Amorphous Solids, Wiley, New York, NY, USA, 1954.

[40] Z.-Y. Yuan and B.-L. Su, "Insights into hierarchically mesomacroporous structured materials," Journal of Materials Chemistry, vol. 16, no. 7, pp. 663-677, 2006.

[41] C. M. A. Parlett, K. Wilson, and A. F. Lee, "Hierarchical porous materials: catalytic applications," Chemical Society Reviews, vol. 42, pp. 3876-3893, 2013.

[42] J. G. Yu, S. W. Liu, and H. G. Yu, "Microstructures and photoactivity of mesoporous anatase hollow microspheres fabricated by fluoride-mediated self-transformation," Journal of Catalysis, vol. 249, no. 1, pp. 59-66, 2007

[43] G. Kaune, M. Memesa, R. Meier et al., "Hierarchically structured titania films prepared by polymer/colloidal templating," ACS Applied Materials and Interfaces, vol. 1, no. 12, pp. 2862-2869, 2009.

[44] X. C. Wang, J. C. Yu, C. Ho, Y. D. Hou, and X. Z. Fu, "Photocatalytic activity of a hierarchically macro/mesoporous titania," Langmuir, vol. 21, no. 6, pp. 2552-2559, 2005.

Guiyun Yi, (1) BaolinXing, (1) Jianbo Jia, (1) Liwei Zhao, (2) Yuanfeng Wu, (1) Huihui Zeng, (1) and Lunjian Chen (1)

(1) School of Materials Science and Engineering, Henan Polytechnic University, Jiaozuo, Henan 454000, China

(2) Petroleum Engineering Research Institute of Dagang Oilfield, Tianjin 300270, China

Correspondence should be addressed to Guiyun Yi; and Lunjian Chen;

Received 5 February 2014; Accepted 26 February 2014; Published 20 March 2014

Academic Editor: Jianliang Cao
COPYRIGHT 2014 Hindawi Limited
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2014 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Title Annotation:Research Article
Author:Yi, Guiyun; Xing, Baolin; Jia, Jianbo; Zhao, Liwei; Wu, Yuanfeng; Zeng, Huihui; Chen, Lunjian
Publication:International Journal of Photoenergy
Date:Jan 1, 2014
Previous Article:Photoirradiation caused controllable wettability switching of sputtered highly aligned c-axis-oriented zinc oxide columnar films.
Next Article:Stability of high band gap P3HT: PCBM organic solar cells using Ti[O.sub.x] interfacial layer.

Terms of use | Privacy policy | Copyright © 2019 Farlex, Inc. | Feedback | For webmasters