Surface plasma resonant effect of gold nanoparticles on the photoelectrodes of dye-sensitized solar cells
© Meen et al.; licensee Springer. 2013
Received: 9 July 2013
Accepted: 4 September 2013
Published: 30 October 2013
In this study, we prepared different shapes of gold nanoparticles by seed-mediated growth method and applied them on the photoelectrodes of dye-sensitized solar cells (DSSCs) to study the surface plasma resonant (SPR) effect of gold nanoparticles on the photoelectrodes of dye-sensitized solar cells. The analyses of field emission scanning electron microscopy show that the average diameter of the spherical gold nanoparticles is 45 nm, the average length and width of the short gold nanorods were 55 and 22 nm, respectively, and the average length and width of the long gold nanorods were 55 and 14 nm, respectively. The aspect ratio of the short and long gold nanorods was about 2.5 and 4, respectively. The results of ultraviolet–visible absorption spectra show that the absorption wavelength is about 540 nm for spherical gold nanoparticles, and the absorption of the gold nanorods reveals two peaks. One is about 510 to 520 nm, and the other is about 670 and 710 nm for the short and long gold nanorods, respectively. The best conversion efficiency of the dye-sensitized solar cells with spherical gold nanoparticles and short and long gold nanorods added in is 6.77%, 7.08%, and 7.29%, respectively, and is higher than that of the cells without gold nanoparticles, which is 6.21%. This result indicates that the effect of gold nanoparticles on the photoelectrodes can increase the conductivity and reduce the recombination of charges in the photoelectrodes, resulting in the increase of conversion efficiency for DSSCs. In addition, the long gold nanorods have stronger SPR effect than the spherical gold nanoparticles and short gold nanorods at long wavelength. This may be the reason for the higher conversion efficiency of DSSCs with long gold nanorods than those of the cells with spherical gold nanoparticles and short gold nanorods.
KeywordsGold nanoparticles Dye-sensitized solar cells Seed-mediated growth method
Recently, a new type of solar cell based on dye-sensitized nanocrystalline titanium dioxide has been developed by O'Regan and Grätzel. The most attractive features of this technology are reduced production costs and ease of manufacture. Dye-sensitized solar cells (DSSCs) based on nanocrystalline TiO2 electrodes are currently attracting widespread attention as a low-cost alternative to replace conventional inorganic photo voltaic devices[2–6]. The function of DSSCs is based upon the injection of electrons of photoexcited state of the sensitizer dye into the conduction band of the semiconductor. Constant researches attempt to achieve four goals: to promote the adsorption of dye, to harvest more solar light, to smoothen the progress of transport of photoexcited electrons, and to facilitate the diffusion of an electrolyte ion. A record of the cell convertible efficiency of 11% was achieved using N3 (RuL2(NCS)2, L = 2,2′-bipyridyl-4,4′-dicarboxylic acid) dye and the electrolyte containing guanidinium thiocyanate. Grätzel et al. used DSSCs sensitized by N3 dye using guanidinium thiocyanate as self-assembly-facilitating agent, leading to improvement in efficiency[8–11]. Some of the cheaper dyes have also been used as sensitizers to improve the absorption in the visible region[12–14]. Gold nanoparticles cannot only increase the conductivity, the different shapes will result to different intensities of the surface plasma resonance (SPR). Recent studies have shown that metal or metal ion-doped semiconductor composites exhibit shift in the Fermi level to more negative potentials. Such a shift in the Fermi level improves the energetics of the composite system and enhances the efficiency of interfacial charge-transfer process. In addition, Chou et al. prepared TiO2/nanometal composite particles by dry particle coating technique. This study shows that the power conversion efficiency η of the DSSCs with a film of TiO2/Au (or TiO2/Ag) on the working electrode always exceeds that of the conventional DSSCs due to the presence of the Schottky barrier. In this study, we prepared different shapes of gold nanoparticles by seed-mediated growth method to apply on the photoelectrodes of the DSSCs. The gold nanoparticles and DSSCs were investigated by field emission scanning electron microscopy (FE-SEM), ultraviolet–visible (UV–vis) absorption spectra, current–voltage characteristics, electrochemical impedance spectroscopy (EIS), and incident photon conversion efficiency (IPCE) analyses to study the SPR effect of the gold nanoparticles on the photoelectrodes of the dye-sensitized solar cells.
Hydrogen tetrachloroaurate(III) trihydrate (HAuCl4‧3H2O, 99.9%), hexadecyltrimethylammonium bromide (CTAB), silver nitrate (AgNO3, 99.8%), ascorbic acid (AA, 99.7%), sodium borohydride (NaBH4, 99.9%) were used as reactants. TiO2 powder and 4-tert-butylpyridine were used as preparation paste of the photoelectrodes. The deionized (DI) water that was used throughout the experiments was purified using a Milli-Q system (Millipore Co., Billerica, MA, USA). Glassware was cleaned by soaking it in aqua regia and then washing it with DI water.
Synthesis of gold nanoparticles
We used seed-mediated growth method to prepare the gold nanoparticles. This method involves two main steps: (1) preparation of seed solution, where the gold seed solution was prepared by first combining (5 mL, 0.5 mM) and CTAB (5 mL, 0.2 M), followed by the addition of freshly made NaBH4 (0.6 mL, 0.01 M) under vigorous stirring. Then, the mixture was left undisturbed, aged for 2 h at 25°C for further use. (2) The other is the preparation of a growth solution that consists of HAuCl4‧3H2O (5 mL, 1 mM), 0.2 mL AgNO3 (spherical and short and long rods are 0.01 and 0.04 M, respectively), and CTAB (5 mL, 0.2 M). AA (70 μL, 0.0788 M) was then added and followed by brief stirring (approximately 1 min). Finally, the spherical gold nanoparticles were synthesized, every 10 s, a drop for the short gold nanorods (aspect ratio of about 2.5), and every 1 min, a drop for the long gold nanorods (aspect ratio of about 4). Lastly, 25 μL of the seed solution was added to the growth solution. The mixture was allowed to react at 30°C. Centrifugation of the gold nanoparticles was carried out at 4,000 rpm for 20 min, and the supernatant was removed and then suspended with the same volume of deionized water. This process was repeated three times.
Assembling the DSSC
We used the scraper method to prepare the photoelectrode on fluorine-doped tin oxide glass substrate. The TiO2 coatings were prepared from commercial TiO2 particles (P25). The compositions of the TiO2 paste were TiO2, 4-tert-butylpyridine, and deionized water. The concentration of the TiO2 paste was 10 wt.%. The concentration of the gold nanoparticles added in the TiO2 paste is about 1.5 wt.%. With the addition of gold nanoparticles, the TiO2 film was scraped to the desired thickness on the substrate by scratching. After drying, we pressed the TiO2 film by suitable pressure and annealed it at 450°C for 30 min to complete the photoelectrode. The size of the TiO2 film electrodes used was 0.25 cm2 (0.5 cm × 0.5 cm). Finally, we kept the photoelectrode immersed in a mixture containing a 3 × 10-4 M solution of N3 dye and ethyl alcohol at 45°C for 1.5 h in the oven. The electrode was assembled into a sandwich-type open cell using platinum plate as a counter electrode.
The surface morphology of the samples was observed using FE-SEM. The ultraviolet–visible absorption spectra of the samples were observed using a UV–vis spectrophotometer. The current–voltage characteristics and EIS of the samples were measured using Keithley 2400 source meter (Keithley Instruments Inc., Cleveland, OH, USA) and were determined under simulated sunlight with white light intensity, PL = 100 mW/cm2. In the IPCE measurement, a xenon lamp (Oriel (Newport Corporation, Jiangsu, China), model 66150, 75 W) was used as the light source, and a chopper and lock-in amplifier were used for phase-sensitive detection.
Results and discussion
The parameters of current–voltage characteristics for DSSCs without and with different shapes of gold nanoparticles
Nanorod (AR 2.5)
Nanorod (AR 4.0)
Characteristic parameters of the DSSCs without and with gold nanoparticles
Nanorod (AR 2.5)
Nanorod (AR 4.0)
In this study, we prepared different shapes of gold nanoparticles by the seed-mediated growth method to apply on the photoelectrodes of dye-sensitized solar cells. The diameter of the spherical gold nanoparticles is 45 nm, the length and width of the short gold nanorods are 55 and 22 nm, respectively, and the length and width of the long gold nanorods are 55 and 14 nm, respectively. The absorption spectrum of the TiO2 film with gold nanoparticles added is better than that of the film without gold nanoparticles, and the film with gold nanorods has stronger SPR intensity than that with spherical gold nanoparticles at long wavelength. This SPR effect results in higher conversion efficiency of the dye-sensitized solar cells with long gold nanorods those with spherical gold nanoparticles and short gold nanorods.
Dye-sensitized solar cells
Electrochemical impedance spectroscopy
Field emission scanning electron microscopy
Incident photon conversion efficiency
Ultraviolet-visible absorption spectra.
This research is supported by the National Science Council, Republic of China, under contract nos. NSC 101-2221-E-150-041 and NSC 100-2221-E-150-058.
- O'Regan B, Grätzel M: A low-cost, high-efficiency solar cell based on dye-sensitized colloidal TiO2 films. Nature 1991, 353: 737–740.View ArticleGoogle Scholar
- McFarland EW, Tang K: A photovoltaic device structure based on internal electron emission. Nature 2003, 421: 616–618.View ArticleGoogle Scholar
- Wei BY, Lin HM, Kao CC, Li AK: Effect of calcination on photocatalytic activity of TiO2 nanopowders. Mater Sci Eng 2003, 35(1):64–69.Google Scholar
- Li Y, Hagen J, Schaffrath W, Otschik P, Haarer D: Titanium dioxide films for photovoltaic cells derived from a sol–gel process. Sol Energ Mat Sol C 1999, 56: 167–174.View ArticleGoogle Scholar
- Tachibana Y, Hara K, Takano S, Sayama K, Arakawa H: Investigations on anodic photocurrent loss processes in dye sensitized cells: comparison between nanocrystalline SnO2 and TiO2 films. Chem Phys Lett 2002, 364: 297–302.View ArticleGoogle Scholar
- O'Regan B, Schwartz DT, Zakeeruddin SM, Grätzel M: Electrodeposited nanocomposite n-p heterojunctions for solid-state dye-sensitized photovoltaics. Adv Mater 2000, 12: 1263–1267.View ArticleGoogle Scholar
- Grätzel M: Conversion of sunlight to electric power by nanocrystalline dye-sensitized solar cells. J Photoch Photobio A 2004, 164: 3–14.View ArticleGoogle Scholar
- Kuang D, Klein C, Snaith HJ, Baker RH, Zakeeruddin SM, Grätzel M: A new ion-coordinating ruthenium sensitizer for mesoscopic dye-sensitized solar cells. Inorg Chim Acta 2008, 361: 699–706.View ArticleGoogle Scholar
- Mende LS, Grätzel M: TiO2 pore-filling and its effect on the efficiency of solid-state dye-sensitized solar cells. Thin Solid Films 2006, 500: 296–301.View ArticleGoogle Scholar
- Nazeeruddin MK, Klein C, Liska P, Grätzel M: Synthesis of novel ruthenium sensitizers and their application in dye-sensitized solar cells. Coord Chem Rev 2005, 249: 1460–1467.View ArticleGoogle Scholar
- Ito S, Murakami TN, Comte P, Liska P, Grätzel C, Nazeeruddin MK, Grätzel M: Fabrication of thin film dye sensitized solar cells with solar to electric power conversion efficiency over 10%. Thin Solid Films 2008, 516: 4613–4619.View ArticleGoogle Scholar
- Kay A, Grätzel M: Artificial photosynthesis: 1. Photosensitization of TiO2 solar cells with chlorophyll derivatives and related natural porphyrins. J Phys Chem 1993, 97: 6272–6277.View ArticleGoogle Scholar
- Kay A, Humphry-Baker R, Grätzel M: Artificial photosynthesis. 2. Investigations on the mechanism of photosensitization of nanocrystalline TiO2 solar cells by chlorophyll derivatives. J Phys Chem 1994, 98: 952–959.View ArticleGoogle Scholar
- Cherepy NJ, Smestad GP, Grätzel M, Zhang JZ: Ultra fast electron injection: implications for a photoelectrochemical cell utilizing an anthocyanin dye-sensitized TiO2 nanocrystalline electrode. J Phys Chem B 1997, 101: 9342–9351.View ArticleGoogle Scholar
- Mock JJ, Barbic M, Smith DR, Schultz DA, Schultz S: Shape effects in plasmon resonance of individual colloidal silver nanoparticles. J Chem Phys 2002, 116: 6755–6759.View ArticleGoogle Scholar
- Subramanian V, Wolf EE, Kamat PV: Catalysis with TiO2/gold nanocomposites. Effect of metal particle size on the Fermi level equilibration. J Am Chem Soc 2004, 126: 4943–4950.View ArticleGoogle Scholar
- Chou CS, Yang RY, Yeh CK, Lin YJ: Preparation of TiO2/nano-metal composite particles and their applications in dye-sensitized solar cells. Powder Technol 2009, 194: 95–105.View ArticleGoogle Scholar
- Kern R, Sastrawan R, Ferber J, Stangl R, Luther J: Modeling and interpretation of electrical impedance spectra of dye solar cells operated under open-circuit conditions. Electrochim Acta 2002, 47: 4213–4225.View ArticleGoogle Scholar
- Han L, Koide N, Chiba Y, Islam A, Mitate T: Modeling of an equivalent circuit for dye-sensitized solar cells: improvement of efficiency of dye-sensitized solar cells by reducing internal resistance. Comptes Rendus Chimie 2006, 9: 645–651.View ArticleGoogle Scholar
- Adachi M, Sakamoto M, Jiu J, Ogata Y, Isoda S: Electron transport in dye-sensitized solar cells using electrochemical impedance spectroscopy. J Phys Chem 2006, 110: 13872–13880.View ArticleGoogle Scholar
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