Au-Loaded Titanium Dioxide Nanoparticles Synthesized by Modified Sol-Gel/Impregnation Methods and Their Application to Dye-Sensitized Solar Cells

Ninsonti, Hathaithip; Chomkitichai, Weerasak; Baba, Akira; Wetchakun, Natda; Kangwansupamonkon, Wiyong; Phanichphant, Sukon; Shinbo, Kazunari; Kato, Keizo; Kaneko, Futao

doi:https://doi.org/10.1155/2014/865423

International Journal of Photoenergy

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Materials, Designs, Fabrications, and Applications of Organic Electronic Devices

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Volume 2014 | Article ID 865423 | https://doi.org/10.1155/2014/865423

Au-Loaded Titanium Dioxide Nanoparticles Synthesized by Modified Sol-Gel/Impregnation Methods and Their Application to Dye-Sensitized Solar Cells

Hathaithip Ninsonti,^1,2Weerasak Chomkitichai,^2,3Akira Baba,²Natda Wetchakun,⁴Wiyong Kangwansupamonkon,⁵Sukon Phanichphant,⁶Kazunari Shinbo,²Keizo Kato,²and Futao Kaneko²

Academic Editor: K. R. Justin Thomas

Received03 Dec 2013

Accepted10 Mar 2014

Published07 Apr 2014

Abstract

Au-loaded TiO₂ nanoparticles were synthesized by the modified sol-gel method together with the impregnation method. Anatase phase of TiO₂ was obtained in all samples with an average particle size of 20 nm. For the enhancement of DSSCs, the dye-sensitized solar cells composed of the ITO/Au-loaded TiO₂/N-719/electrolyte/Pt were fabricated. Au-loaded TiO₂ films were deposited by using squeegee method. Finally, the fabricated cells were studied upon an irradiation of solar light to study the performance. The fabricated cell with up to 1.0 mol% Au-loaded TiO₂ could enhance the performance by localized surface plasmon effect and scattering property.

1. Introduction

Recently, an increase in energy demand has led to significant progress in environmental remediation and renewable energy technologies such as photocatalytic oxidation, adsorption/separation processing, solar cells, fuel cells, and biofuels. One of the various renewable energy options, solar cell, stands out as the most ultimately sustainable choice in terms of its availability and huge potential. The solar cell for renewable energy options is applied through catalyst materials. Titanium dioxide (TiO₂) is one of the most efficient materials for dye-sensitized solar cells (DSSCs) due to its chemical stability, nontoxicity, good electrical properties, and inexpensiveness [1–4]. The phase structure of TiO₂ exists in three polymorphs: anatase, rutile, and brookite. The anatase TiO₂ is used as dye-sensitized solar cells material because it has band gap energy of 3.2 eV of which the absorption thresholds correspond to 380 nm, suggesting that it is easy for photon-electron transfer under solar light irradiation [3]. At the present time many studies on dye-sensitized solar cells (DSSCs) have been reported due to their high efficiency property and low cost of materials [1–4].

In the active layer of DSSCs, a monolayer of organic dye molecules covered with covalent bond on anatase TiO₂ film is generally used [5]. When the metal nanoparticles are incorporated in TiO₂ film of DSSCs, localized surface plasmon or light scattering can enhance the electric field on the active dye layer which can increase the light absorption [6–8]. Moreover, metal nanoparticles can perform as an electron acceptor from the photo-excited semiconductors. Therefore, the electron transfer rate could be improved and the increase of photocurrent was obtained [6, 9]. Au has several advantages such as high conductivity and chemical and thermal stability [10]. For these reasons, Au nanoparticles were chosen to induce light scattering and localized surface plasmon excitation for the improvement of DSSCs performance.

There are many ways to synthesize TiO₂ such as precipitation method [11–13], solvothermal method [14–17], sol-gel method [18–22], spray pyrolysis [23–26], and microwave method [27–29]. Sol-gel process consists of 2 main reactions, hydrolysis and condensation [18–22, 30–33]. In our previous work, we reported the preparation of TiO₂ by the modified sol-gel method using cellophane membrane to decrease the diffusion rates of reactants in hydrolysis and condensation steps. This synthesis method had many advantages such as good reproducibility, good ability to obtain TiO₂ in nanosized scale, and good production for high purity products [30, 31].

In this research, TiO₂ and Au-loaded TiO₂ nanoparticles were synthesized by the modified sol-gel method and coupling the modified sol-gel with impregnation methods, respectively. The as-prepared samples were characterized by X-ray diffractometry, scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray spectrophotometry, and Brunauer-Emmett-Teller techniques. The obtained particles were used to enhance DSSCs performance.

2. Experimental

2.1. Preparation of TiO₂ Nanoparticles

Titanium dioxide (TiO₂) nanoparticles were synthesized by the modified sol-gel method [30, 31]. Titanium tetraisopropoxide (Ti[OCH(CH₃)₂]₄ (TTIP), Aldrich, England), absolute ethanol (C₂H₅OH, Merck, Germany), and ammonia (NH₃, Merck, Germany) were used as the starting materials for synthesizing TiO₂ nanoparticles. Titanium tetraisopropoxide (20 mL) was dissolved in 250 mL absolute ethanol and mixed until a homogeneous solution was obtained. The mixture of TTIP and absolute ethanol was loaded into a cellophane membrane and suspended for 1 h in a clear solution containing 1 : 1 ratio of ethanol (95%) and deionized water and 7 mL of ammonia solution (25%) as shown in Figure 1. After the completion of the dialysis process, the suspension was centrifuged at 7500 rpm for 10 min, washed with deionized water, and then dried in an oven at 60°C for 24 h. The white powders were then calcined in a furnace at a temperature of 400°C for 3 h.

2.2. Preparation of Au-Loaded TiO₂ Nanoparticles

The nominal 0.50–3.0 mol% Au-loaded TiO₂ powders were prepared by the impregnation method. The appropriate amounts of gold (III) chloride hydrate ((H(AuCl₄)·H₂O, Electron Microscopy Science) solution were added in TiO₂ nanoparticles as described previously in Section 2.1. Then, the as-prepared samples were mixed until being homogeneous. Finally, the obtained powders were dried at 60°C for 24 h and calcined at 400°C for 3 h.

2.3. Characterization of TiO₂ and Au-Loaded TiO₂ Nanoparticles

The crystal structure and crystallinity of TiO₂ and Au-loaded TiO₂ nanoparticles were examined by X-ray diffractometry (JDX-3530, JEOL, Japan) using the Ni-filtered monochromatic with CuK_α radiation. The detection range was 15–75° with the step size of 0.10° (2θ°/s). Morphologies and particle sizes of TiO₂ and Au-loaded TiO₂ nanoparticles were investigated by scanning electron microscopy (SEM, JSM5410-LV, JEOL, Japan) and transmission electron microscopy (TEM, JEM-2010, JEOL, Japan). The chemical composition of TiO₂ and Au-loaded TiO₂ nanoparticles was examined by energy dispersive X-ray spectrophotometry (EDXS, ISIS300, Oxford, England). Specific surface area () of the samples was investigated by the Brunauer-Emmett-Teller (BET, Micromeritics Tristar 3000). An average particle diameter () of TiO₂ and Au-loaded TiO₂ nanoparticles was calculated using the following formula: = , where and are the weight densities of TiO₂ () and Au (), respectively.

2.4. Fabrication of DSSCs

DSSCs were fabricated by TiO₂ and Au-loaded TiO₂ nanoparticles for comparison of the efficiency performance. ITO glass substrate with a sheet resistance of 10 Ω/sq was used as an anode. Dish washing liquid solution, water, distilled water, and DI water were used for cleaning of ITO substrate. After cleaning process, squeegee technique was used to deposit TiO₂ or Au-loaded TiO₂ layers as follows: TiO₂ or Au-loaded TiO₂ nanoparticles were dispersed in ethanol with the concentration of 2, 3, 4, or 5 M in order to optimize the appropriate thickness. Then, TiO₂ or Au-loaded TiO₂ pastes were coated on ITO substrates by squeegee technique. TiO₂ or Au-loaded TiO₂ films were then calcined at 450°C for 90 min. To prevent the corrosion of Au particles by iodine electrolyte, Au-loaded TiO₂ films were immersed in 0.001 M 1-octadecanethiol (CH₃(CH₂)₁₇SH, Aldrich, England) for 15 h after calcination step. N-719 (di-tetrabutylammonium cis-bis (isothiocyanato) bis(2,2′-bipyridyl-4,4′-dicarboxylato) ruthenium (II), Sigma-Aldrich) was used as a photosensitized dye. TiO₂ or Au-loaded TiO₂ films were immersed in 0.5 mM N-719 dye for 12 h. DSSCs were fabricated as shown in Figure 2. 0.1 M LiI, 0.05 M I₂, 0.6 M tBP, and 0.5 M tetrabutylammonium iodide in acetonitrile were used as electrolyte (for the optimization of the appropriate thickness, only 0.1 M LiI and 0.05 M I₂ in acetonitrile were used as electrolyte). Pt film prepared by vacuum evaporation technique was used as the cathode.

2.5. Characterization of the Fabricated DSSCs

The absorption of TiO₂ and Au-loaded TiO₂ films was observed by UV-vis spectroscopy technique (UV-vis spectrometer, V-650, JASCO). Photovoltaic properties were studied by irradiating a solar simulator (HAL-C100, 100 W compact xenon light source, ASAHI SPECTRA) to the fabricated DSSCs.

3. Results and Discussion

3.1. Synthesis and Characterization of Au-Loaded TiO₂ Nanoparticles

In this research, the TiO₂ and Au-loaded TiO₂ nanoparticles were prepared by the modified sol-gel method and the modified sol-gel method together with the impregnation method, respectively. The preparation of the TiO₂ was followed from our previously reported research [30, 31]. The sol-gel method consists of hydrolysis and condensation of titanium alkoxides, Ti (OR)_n, to form oxopolymers, which are converted to an oxide complex as equation mentioned in our previous report [30].

The rates of hydrolysis and condensation are important factors that might affect characteristic of Au-loaded TiO₂. Smaller particle sizes were obtained from hydrolysis and condensation rates which are controlled by basic solution [34–37]. Consequently, cellophane membrane was used to control the hydrolysis and condensation rates in the reaction to acquire the nanosized particles [30, 31]. Moreover, TiO₂ loading with Au was produced by the impregnation method which is a very simple technique and does not require expensive equipment. The homogeneous powders of TiO₂ show white color, while increase of Au ions changed the color to grayish purple.

The structure confirmation of TiO₂ and Au-loaded TiO₂ nanoparticles was obtained by comparison with the Joint Committee on Powder Diffraction Standards (JCPDS) Card Files numbers 21-1272 and 04-0784. Figure 3 shows the XRD patterns of the TiO₂ and 1.0 mol% Au-loaded TiO₂ nanoparticles. The results of the TiO₂ and 1.0 mol% Au-loaded TiO₂ nanoparticles confirmed anatase structures according to JCPDS file number 21-1272 [30, 31]. The Au-loading might not affect the phase of TiO₂ nanoparticles. The diffraction peaks of Au were found on Au-loaded TiO₂ nanoparticles at 2θ value of 38.2°and 44.4° according to JCPDS file number 04-0784. The high intensity value of the XRD peaks shows that all of the samples have well crystalline structure and the broad peaks at 2θ value of 25.2° show that the particles have a small average crystallite size.

The specific surface area () of the TiO₂ and Au-loaded TiO₂ nanoparticles was found to be in the range of 69–109 m²g⁻¹ with the particle diameter in the range of 14–21 nm, corresponding well with the XRD results. It was reported that high surface area of TiO₂ active layer has many advantages such as large amount of dye adsorption, high light-harvesting efficiency, rapid electron transport, and low electron recombination [38–40]. Therefore, high photoefficiency could be expected.

Morphologies, particle sizes, and element chemical compositions were investigated by scanning electron microscopy (SEM) as shown in Figure 4(a). The SEM result shows the rough morphology and the presence of agglomerated nanoparticles with an average diameter of 50–100 nm. From the EDS spectra as shown in Figure 4(e), the chemical compositions of 1.0 mol% Au-loaded TiO₂ showed the characteristic X-ray energy level of titanium, oxygen. The characteristic peaks of Au were observed to confirm the presence of Au corresponding to the XRD results. Furthermore, element composition of Au-loaded TiO₂ was investigated by EDS mapping mode. Figures 4(b), 4(c), and 4(d) show element composition of Ti, O, and Au in 1.0 mol% Au-loaded TiO₂ nanoparticles. The presence of Au in the sample was confirmed. Further analysis for the accurate sizes and morphology of the nanoparticles was carried out by TEM observation. The average particle diameter of TiO₂ and Au-loaded TiO₂ nanoparticles was in the range of 15–20 nm as shown in Figure 5.

(a)

(b)

(c)

(d)

(e)

3.2. Characterization and Optimization of Au-Loaded TiO₂ Films

Figure 6 shows the UV-vis absorption spectra of TiO₂ and 0.50–3.0 mol% Au-loaded TiO₂ films deposited on ITO substrate. A broad peak of Au appeared in the wavelength of 530–580 nm and increased intensity with increasing the Au loading amount on the TiO₂ nanoparticles. This result indicated that the localized surface plasmon resonance could be excited on Au-loaded TiO₂ nanoparticles [41]. As mentioned in the previously reported research by many groups, the film thickness is one of the most important factor effects on the performance of DSSCs [42, 43]. The film thickness was optimized by varying the concentration of 3.0 mol% Au-loaded TiO₂ paste in the squeegee process. The thickness of 3.0% Au-loaded TiO₂ films was increased with increasing the concentration of Au-loaded TiO₂ paste, as shown in Figure 7(a). Figure 7(b) shows the effect of 3.0% Au-loaded TiO₂ film thickness on short-circuit photocurrent properties of DSSCs. It was found that the short-circuit photocurrent increased with increasing film thickness up to 8 μm (Figure 7(c)). However, the photocurrent decreased with the film thickness more than 8 μm.

(a)

(b)

(c)

3.3. Photovoltaic Properties of the Fabricated DSSCs Using TiO₂ and Au-Loaded TiO₂ Nanoparticles

Photovoltaic properties of the fabricated DSSCs using TiO₂ and different nominal 0.50–3.0 mol% of Au-loaded TiO₂ nanoparticles were studied to compare the enhancement of photovoltaic performance of DSSCs. Figure 8 shows current density versus voltage curves of fabricated DSSCs using TiO₂ and 0.50–3.0 mol% Au-loaded TiO₂ nanoparticles. Photovoltaic performances were calculated from these curves as shown in Table 1. The open circuit voltage () is almost constant value with Au-loading amount. This indicates that the Au-loading to TiO₂ does not affect the Fermi level because the is originated from the energy difference between Fermi level of TiO₂ layer and the oxidation/reduction potential of the electrolyte [44]. The results show that the short-circuit current densities of the fabricated DSSCs with TiO₂, 0.50, 1.0, 2.0, and 3.0 mol% Au-loaded TiO₂ nanoparticles were 10.04, 12.48, 13.06, 8.27, and 7.02 mA/cm², corresponding to the efficiency of 4.34, 5.40, 5.52, 4.13, and 3.33%, respectively. These results confirmed that Au-loading could enhance the performances of DSSCs with the loading amount up to 1.0 mol%. However, the short-circuit current density and the efficiency of the fabricated DSSCs were decreased upon the increasing amount of 2.0 mol% Au loading. These effects might be possibly due to the fact that the active site was shielded by the large amount of Au loading or rougher morphology of the Au-loaded TiO₂ layers.

4. Conclusion

In this research, the Au-loaded TiO₂ nanoparticles were successfully synthesized by the modified sol-gel method together with the impregnation method. Anatase phase of TiO₂ was obtained in all samples with an average particle size of 20 nm. The DSSC was improved by an effect of the Au-loaded titanium dioxide (Au-loaded TiO₂). For the enhancement of DSSCs, the fabricated cell with up to 1.0 mol% Au-loaded TiO₂ could enhance the performance by localized surface plasmon effect and scattering property.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

This research was supported by a Grant-in-Aid for Young Scientists (B) (23760010) and Grant-in-Aid for Scientific Research (C) (25390051) from the Japan Society for the Promotion of Science (JSPS), the Thailand Research Fund, The Royal Golden Jubilee Ph.D. Program (PHD/0358/2551), the National Science and Technology Department Agency (NSTDA), Thailand Graduate Institute of Science and Technology (TGIST: TG-55-10-52-051 M), the National Nanotechnology Center (NANOTEC), NSTDA, Ministry of Science and Technology, through its program of Center of Excellence Network, Thailand, and the Department of Chemistry, Faculty of Science, Chiang Mai University, Chiang Mai, Thailand. Sukon Phanichphant wishes to thank the National Research University Project under Thailand’s Office of the Higher Education Commission for financial support.

References

A. Fujishima, T. N. Rao, and D. A. Tryk, “Titanium dioxide photocatalysis,” Journal of Photochemistry and Photobiology C, vol. 1, no. 1, pp. 1–21, 2000.
View at: Google Scholar
K. Pirkanniemi and M. Sillanpää, “Heterogeneous water phase catalysis as an environmental application: a review,” Chemosphere, vol. 48, no. 10, pp. 1047–1060, 2002.
View at: Publisher Site | Google Scholar
Y. Hu, H.-L. Tsai, and C.-L. Huang, “Effect of brookite phase on the anatase-rutile transition in titania nanoparticles,” Journal of the European Ceramic Society, vol. 23, no. 5, pp. 691–696, 2003.
View at: Publisher Site | Google Scholar
V. Samuel, R. Pasricha, and V. Ravi, “Synthesis of nanocrystalline rutile,” Ceramics International, vol. 31, no. 4, pp. 555–557, 2005.
View at: Publisher Site | Google Scholar
O. Carp, C. L. Huisman, and A. Reller, “Photoinduced reactivity of titanium dioxide,” Progress in Solid State Chemistry, vol. 32, no. 1-2, pp. 33–177, 2004.
View at: Publisher Site | Google Scholar
K. G. Deepa, P. Lekha, and S. Sindhu, “Efficiency enhancement in DSSC using metal nanoparticles: A Size Dependent Study,” Solar Energy, vol. 86, no. 1, pp. 326–330, 2012.
View at: Publisher Site | Google Scholar
H. A. Atwater and A. Polman, “Plasmonics for improved photovoltaic devices,” Nature Materials, vol. 9, no. 3, pp. 205–213, 2010.
View at: Publisher Site | Google Scholar
V. E. Ferry, J. N. Munday, and H. A. Atwater, “Design considerations for plasmonic photovoltaics,” Advanced Materials, vol. 22, no. 43, pp. 4794–4808, 2010.
View at: Publisher Site | Google Scholar
S. Muduli, O. Game, V. Dhas et al., “TiO₂-Au plasmonic nanocomposite for enhanced dye-sensitized solar cell (DSSC) performance,” Solar Energy, vol. 86, no. 5, pp. 1428–1434, 2012.
View at: Publisher Site | Google Scholar
G. Sahu, S. W. Gordon, and M. A. Tarr, “Synthesis and application of core-shell Au-TiO₂ nanowire photoanode materials for dye sensitized solar cells,” RSC Advances, vol. 2, no. 2, pp. 573–582, 2012.
View at: Publisher Site | Google Scholar
J. H. Lee and Y. S. Yang, “Effect of HCl concentration and reaction time on the change in the crystalline state of TiO₂ prepared from aqueous TiCl₄ solution by precipitation,” Journal of the European Ceramic Society, vol. 25, no. 16, pp. 3573–3578, 2005.
View at: Publisher Site | Google Scholar
A. Sandoval, A. Aguilar, C. Louis, A. Traverse, and R. Zanella, “Bimetallic Au-Ag/TiO₂ catalyst prepared by deposition- precipitation: high activity and stability in CO oxidation,” Journal of Catalysis, vol. 281, no. 1, pp. 40–49, 2011.
View at: Publisher Site | Google Scholar
H. Wang, P. Liu, X. Cheng, A. Shui, and L. Zeng, “Effect of surfactants on synthesis of TiO₂ nano-particles by homogeneous precipitation method,” Powder Technology, vol. 188, no. 1, pp. 52–54, 2008.
View at: Publisher Site | Google Scholar
S. S. Kalanur, S. H. Lee, Y. J. Hwang, and O. S. Joo, “Enhanced photoanode properties of CdS nanoparticle sensitized TiO₂ nanotube arrays by solvothermal synthesis,” Journal of Photochemistry and Photobiology A: Chemistry, vol. 259, pp. 1–9, 2013.
View at: Google Scholar
M. Kang, S.-Y. Lee, C.-H. Chung et al., “Characterization of a TiO₂ photocatalyst synthesized by the solvothermal method and its catalytic performance for CHCl₃ decomposition,” Journal of Photochemistry and Photobiology A: Chemistry, vol. 144, no. 2-3, pp. 185–191, 2001.
View at: Google Scholar
Y. Lee, J. Chae, and M. Kang, “Comparison of the photovoltaic efficiency on DSSC for nanometer sized TiO₂ using a conventional sol-gel and solvothermal methods,” Journal of Industrial and Engineering Chemistry, vol. 16, no. 4, pp. 609–614, 2010.
View at: Publisher Site | Google Scholar
Y. Zhang, H. Zheng, G. Liu, and V. Battaglia, “Synthesis and electrochemical studies of a layered spheric TiO₂ through low temperature solvothermal method,” Electrochimica Acta, vol. 54, no. 16, pp. 4079–4083, 2009.
View at: Publisher Site | Google Scholar
D. Crişan, N. Drǎgan, M. Rǎileanu et al., “Structural study of sol-gel Au/TiO₂ films from nanopowders,” Applied Surface Science, vol. 257, no. 9, pp. 4227–4231, 2011.
View at: Publisher Site | Google Scholar
J. N. Hart, D. Menzies, Y.-B. Cheng, G. P. Simon, and L. Spiccia, “TiO₂ sol-gel blocking layers for dye-sensitized solar cells,” Comptes Rendus Chimie, vol. 9, no. 5-6, pp. 622–626, 2006.
View at: Publisher Site | Google Scholar
M. Hočevar, U. O. Krašovec, M. Bokalič et al., “Sol-gel based TiO₂ paste applied in screen-printed dye-sensitized solar cells and modules,” Journal of Industrial and Engineering Chemistry, vol. 19, no. 5, pp. 1464–1469, 2013.
View at: Google Scholar
C. M. Malengreaux, A. Timmermans, S. L. Pirard et al., “Optimized deposition of TiO₂ thin films produced by a non-aqueous sol-gel method and quantification of their photocatalytic activity,” Chemical Engineering Journal, vol. 195-196, pp. 347–358, 2012.
View at: Google Scholar
S. Šegota, L. Ćurković, D. Ljubas, V. Svetličić, I. F. Houra, and N. Tomašić, “Synthesis, characterization and photocatalytic properties of sol-gel TiO₂ films,” Ceramics International, vol. 37, no. 4, pp. 1153–1160, 2011.
View at: Google Scholar
H. M. N. Bandara, R. M. G. Rajapakse, K. Murakami, G. R. R. A. Kumara, and G. Anuradha Sepalage, “Dye-sensitized solar cell based on optically transparent TiO₂ nanocrystalline electrode prepared by atomized spray pyrolysis technique,” Electrochimica Acta, vol. 56, no. 25, pp. 9159–9161, 2011.
View at: Publisher Site | Google Scholar
C. Jiang, W. L. Koh, M. Y. Leung, W. Hong, Y. Li, and J. Zhang, “Influences of alcoholic solvents on spray pyrolysis deposition of TiO₂ blocking layer films for solid-state dye-sensitized solar cells,” Journal of Solid State Chemistry, vol. 198, pp. 197–202, 2013.
View at: Google Scholar
C. Jiang, M. Y. Leung, W. L. Koh, and Y. Li, “Influences of deposition and post-annealing temperatures on properties of TiO₂ blocking layer prepared by spray pyrolysis for solid-state dye-sensitized solar cells,” Thin Solid Films, vol. 519, no. 22, pp. 7850–7854, 2011.
View at: Publisher Site | Google Scholar
M. Okuya, K. Nakade, and S. Kaneko, “Porous TiO₂ thin films synthesized by a spray pyrolysis deposition (SPD) technique and their application to dye-sensitized solar cells,” Solar Energy Materials and Solar Cells, vol. 70, no. 4, pp. 425–435, 2002.
View at: Publisher Site | Google Scholar
J. N. Hart, R. Cervini, Y.-B. Cheng, G. P. Simon, and L. Spiccia, “Formation of anatase TiO₂ by microwave processing,” Solar Energy Materials and Solar Cells, vol. 84, no. 1–4, pp. 135–143, 2004.
View at: Publisher Site | Google Scholar
J. N. Hart, D. Menzies, Y.-B. Cheng, G. P. Simon, and L. Spiccia, “A comparison of microwave and conventional heat treatments of nanocrystalline TiO₂,” Solar Energy Materials and Solar Cells, vol. 91, no. 1, pp. 6–16, 2007.
View at: Publisher Site | Google Scholar
S. Uchida, M. Tomiha, N. Masaki, A. Miyazawa, and H. Takizawa, “Preparation of TiO₂ nanocrystalline electrode for dye-sensitized solar cells by 28 GHz microwave irradiation,” Solar Energy Materials and Solar Cells, vol. 81, no. 1, pp. 135–139, 2004.
View at: Publisher Site | Google Scholar
N. Wetchakun, B. Incessungvorn, K. Wetchakun, and S. Phanichphant, “Influence of calcination temperature on anatase to rutile phase transformation in TiO₂ nanoparticles synthesized by the modified sol-gel method,” Materials Letters, vol. 82, pp. 195–198, 2012.
View at: Google Scholar
N. Wetchakun and S. Phanichphant, “Effect of temperature on the degree of anatase-rutile transformation in titanium dioxide nanoparticles synthesized by the modified sol-gel method,” Current Applied Physics, vol. 8, no. 3-4, pp. 343–346, 2008.
View at: Publisher Site | Google Scholar
C. Suresh, V. Biju, P. Mukundan, and K. G. K. Warrier, “Anatase to rutile transformation in sol-gel titania by modification of precursor,” Polyhedron, vol. 17, no. 18, pp. 3131–3135, 1998.
View at: Google Scholar
Q. Zhang, L. Gao, and J. Guo, “Effect of hydrolysis conditions on morphology and crystallization of nanosized TiO₂ powder,” Journal of the European Ceramic Society, vol. 20, no. 12, pp. 2153–2158, 2000.
View at: Publisher Site | Google Scholar
T. Sugimoto and X. Zhou, “Synthesis of uniform anatase TiO₂ nanoparticles by the gel-sol method. 2. Adsorption of OH- ions to Ti(OH)₄ gel and TiO₂ particles,” Journal of Colloid and Interface Science, vol. 252, no. 2, pp. 347–353, 2002.
View at: Publisher Site | Google Scholar
D. Bahnemann, “Photocatalytic water treatment: solar energy applications,” Solar Energy, vol. 77, no. 5, pp. 445–459, 2004.
View at: Publisher Site | Google Scholar
M. Harada, T. Sasaki, Y. Ebina, and M. Watanabe, “Preparation and characterizations of Fe- or Ni-substituted titania nanosheets as photocatalysts,” Journal of Photochemistry and Photobiology A: Chemistry, vol. 148, no. 1–3, pp. 273–276, 2002.
View at: Publisher Site | Google Scholar
M. Romero, J. Blanco, B. Sánchez et al., “Solar photocatalytic degradation of water and air pollutants: challenges and perspectives,” Solar Energy, vol. 66, no. 2, pp. 169–182, 1999.
View at: Google Scholar
M. Pan, N. Huang, X. Zhao, J. Fu, and X. Zhong, “Enhanced efficiency of dye-sensitized solar cell by high surface area anatase-TiO₂-modified P25 paste,” Journal of Nanomaterials, vol. 2013, pp. 1–6, 2013.
View at: Google Scholar
G. Dai, L. Zhao, S. Wang et al., “Double-layer composite film based on sponge-like TiO₂ and P25 as photoelectrode for enhanced efficiency in dye-sensitized solar cells,” Journal of Alloys and Compounds, vol. 539, pp. 264–270, 2012.
View at: Google Scholar
V. Dhas, S. Muduli, S. Agarkar et al., “Enhanced DSSC performance with high surface area thin anatase TiO₂ nanoleaves,” Solar Energy, vol. 85, no. 6, pp. 1213–1219, 2011.
View at: Publisher Site | Google Scholar
I.-K. Ding, J. Zhu, W. Cai et al., “Plasmonic Dye-sensitized solar cells,” Advanced Energy Materials, vol. 1, no. 1, pp. 52–57, 2011.
View at: Publisher Site | Google Scholar
C.-Y. Huang, Y.-C. Hsu, J.-G. Chen, V. Suryanarayanan, K.-M. Lee, and K.-C. Ho, “The effects of hydrothermal temperature and thickness of TiO₂ film on the performance of a dye-sensitized solar cell,” Solar Energy Materials and Solar Cells, vol. 90, no. 15, pp. 2391–2397, 2006.
View at: Publisher Site | Google Scholar
M. C. Kao, H. Z. Chen, S. L. Young, C. Y. Kung, and C. C. Lin, “The effects of the thickness of TiO₂ films on the performance of dye-sensitized solar cells,” Thin Solid Films, vol. 517, no. 17, pp. 5096–5099, 2009.
View at: Publisher Site | Google Scholar
M. Ghaffari, M. B. Cosar, H. I. Yavuz, M. Ozenbas, and A. K. Okyay, “Effect of Au nano-particles on TiO₂ nanorod electrode in dye-sensitized solar cells,” Electrochimica Acta, vol. 76, pp. 446–452, 2012.
View at: Google Scholar

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International Journal of Photoenergy

Materials, Designs, Fabrications, and Applications of Organic Electronic Devices

Au-Loaded Titanium Dioxide Nanoparticles Synthesized by Modified Sol-Gel/Impregnation Methods and Their Application to Dye-Sensitized Solar Cells

Abstract

1. Introduction

2. Experimental

2.1. Preparation of TiO2 Nanoparticles

2.2. Preparation of Au-Loaded TiO2 Nanoparticles

2.3. Characterization of TiO2 and Au-Loaded TiO2 Nanoparticles

2.4. Fabrication of DSSCs

2.5. Characterization of the Fabricated DSSCs

3. Results and Discussion

3.1. Synthesis and Characterization of Au-Loaded TiO2 Nanoparticles

3.2. Characterization and Optimization of Au-Loaded TiO2 Films

3.3. Photovoltaic Properties of the Fabricated DSSCs Using TiO2 and Au-Loaded TiO2 Nanoparticles

4. Conclusion

Conflict of Interests

Acknowledgments

References

Copyright

2.1. Preparation of TiO₂ Nanoparticles

2.2. Preparation of Au-Loaded TiO₂ Nanoparticles

2.3. Characterization of TiO₂ and Au-Loaded TiO₂ Nanoparticles

3.1. Synthesis and Characterization of Au-Loaded TiO₂ Nanoparticles

3.2. Characterization and Optimization of Au-Loaded TiO₂ Films

3.3. Photovoltaic Properties of the Fabricated DSSCs Using TiO₂ and Au-Loaded TiO₂ Nanoparticles