We prepared of electrodes that consist of TiO2 with addition of tin-doped indium oxide (ITO) or fluorine-doped tin oxide (FTO) nanoparticles and the application of such electrodes on dye-sensitized solar cell. As compared to TiO2 alone, the addition of ITO and FTO nanoparticles resulted in an efficiency improvement of ~20% up to ~54% for the TiO2-ITO and TiO2-FTO systems, respectively. This improvement was partly attributed to a slightly enhanced dye-adsorption behavior and a change in the TiO2 surface chemistry due to the presence of ITO or FTO nanoparticles.
KEYWORDS: Electrodes, Nanoparticles, Solar cells, Electron transport, Particles, Dye sensitized solar cells, Nanostructures, Scanning electron microscopy, Resistance, Nanorods
Dye-sensitized solar cells (DSSC) utilizing titania (TiO2) nanomaterials in conjunction with a light-absorbing dye have been extensively explored for the last few decades. Earlier efforts to surpass the 10% overall light conversion efficiency of these devices emphasized the synthesis of dyes with enhanced light-absorbing capabilities, but slow progress in the increase in efficiency has directed attention to the exploration into the modification of the TiO2 nanostructure. Up to this point, the most efficient electrodes in DSSC devices have consisted of 10 micron-thick mesoporous TiO2 film with an interconnected network of 15-20nm particles. This type of structure has shown to impart a large enough surface area for efficient light absorption and charge formation, but the random distribution of nanometer-sized particles is thought to be the limiting factor for enhanced electron transport, hindering further progress in achieving higher efficiencies. Our research utilizes TiO2 nanorods in an attempt to explore and compare the electron transport pathways associated with 1) a random distribution of nanoparticles and 2) a straightforward arrangement of nanorods within the TiO2 nanostructure. It is assumed that a more ordered structure of nanorods would minimize inefficient electron percolation pathways and improve ion diffusion at the TiO2-dye-electrolyte interface by eliminating the randomization of the particle network, by increasing contact points for good electrical connection, and by decreasing small necking points that have shown to develop between adjacently-bound particles in the current TiO2 nanoparticle structure after sintering. The current-voltage (I-V) behavior of three solar cell electrode structures consisting of (1) TiO2 nanoparticle film, (2) TiO2 nanoparticle-nanorod film, and (3) TiO2 nanorod film were compared and analyzed to determine whether the nanorod structure provided a more efficient pathway for effective electron conduction. SEM analysis was also done to examine the structural alignment and morphology of each TiO2 electrode.
Optically transparent superhydrophobic silica-based coatings were obtained by means of sol-gel processing and self-assembling. Superhydrophobicity was achieved through a combination of enhanced surface roughness by incorporating nanoclusters and modification of surface chemistry by self-assembly. The self-assembly monolayer (SAM) was prepared using the chemical coupling reaction between chlorosilyl groups and hydroxylated coating surface. The optical transparence of such hydrophobic coatings was found to be higher than 95%, which is attributed to the fact that the roughness scale is too small to scatter the visible light. The water contact angle was of approximately 150°.
Nanomaterials are advantageous for photoelectrochemical solar cell devices for high efficient conversion of light to electrical power due to its large surface area at which photoelectrochemical processes take place. One of the current solar cell systems utilizes dye-functionalized mesoporous titania films that consist of an interconnected network of nanometer-sized crystals. This type of structure imparts a large surface area for efficient dye adsorption and, thus, efficient electron-hole formation. This structure formed with connected nanoparticles possesses mesoscopic pores with an irregular and non-uniform pore structure. Such a structure imparts two problems: the transport of electrons through such a random structure, particularly through the necks between two particles, may become a limiting step, and the irregular mesoporous structure may not be ideal for dye assembly. In addition, a liquid electrolyte has to be used to accommodate such irregular mesoporous structures. In this paper, we propose to explore and present some preliminary results of ordered dye-functionalized titania nanostructures for potential enhancement of electron percolation pathways and light conversion. Such dye-sensitized, uniformly-sized, and unidirectionally-aligned titania nanorods and indium-tin-oxide nanorods coated with a titania layer have been synthesized and characterized for discussion.
Metal-insulator core-shell structures have been demonstrated to have interesting and tunable optical properties. Systems previously investigated include silica-capped gold particles and gold shells surrounding silica particles. However, many of the systems studied so far have been spherical (or zero-dimensional). Thus, it would be of interest to look at the synthesis and optical properties of one-dimensional (i.e., rod-like) nanostructures. In this paper, the authors present and discuss the formation and properties of silica and titania nanorods encapsulated with a thin gold shell. Nanorods of silica and titania ~10 μm in length and with diameters ~ 90-200 nm are made by combining sol-gel electrophoresis with a suitable template. After removing the template at high temperature, the surface of the rods is re-hydrolyzed by heating in water. 3-Aminopropyltrimethoxysilane is reacted with the surface hydroxyl groups, self-assembling amine functionality on the surface of the rods. These groups act as anchoring sites for the gold, which forms a thin shell around the oxide nanorod. UV-vis absorbance spectra of these samples are analyzed to determine the relationships between shell thickness, core size, core material and properties.
Dye-functionalized mesoporous silica has gained considerable attention for use in optical applications. Much interest into the tunable functionality of these small-scale optical materials has been the focus for possible use in lasers, light filters, sensors, solar cells, and photocatalysis. Extensive exploration into functionalizing mesoporous silica has been made using sol-gel methods for incorporating polymeric dyes within the pore channels of the silica network to modify optical properties. However, research so far has been focused on functionalization of mesoporous silica powders or films on dense substrates, limiting applications in practice because of the difficult accessibility of mesopores. In this paper, we studied the development of hierarchically-structured mesoporous silica with chromophore dye molecules covalently linked within the channel walls of pores for the selective adsorption and detection of specific ions and chemical compounds. Hierarchically-structured, unidirectionally-aligned mesoporous silica was synthesized within the pores of polycarbonate membranes by surfactant-assisted sol electrophoretic deposition. After the removal of surfactants from the mesopores, the inner surface of the mesopores was functionalized with silane-containing chromophore molecules through self-assembly. Full coverage of these dye molecules on the surface of the mesopores was anticipated due to the fact that these reactant chromophore molecules, in solution, migrate through the pores. The organic chromophore dye molecules, assembled onto the surface of the mesopores, would have the amino groups exposed to the surface. These groups would have the capability to selectively interact with ions or chemical compounds in solution, for instance lead ions in water. Hence, the absorption spectrum of the chromophore dye molecules attached to the mesopores of silica was altered after exposure to lead ions in solution. In addition, the ion concentration in solution also differed. Such functionalized, hierarchically-structured mesoporous silica would have applications such as membranes for removal of, and sensors for, detecting trace amounts of ions and chemical compounds in water and air.
Access to the requested content is limited to institutions that have purchased or subscribe to SPIE eBooks.
You are receiving this notice because your organization may not have SPIE eBooks access.*
*Shibboleth/Open Athens users─please
sign in
to access your institution's subscriptions.
To obtain this item, you may purchase the complete book in print or electronic format on
SPIE.org.
INSTITUTIONAL Select your institution to access the SPIE Digital Library.
PERSONAL Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.