Enhancing efficiency of dye-sensitized solar cells by combining use of TiO2 nanotubes and nanoparticles

Titanium dioxide nanotubes (TiNTs) were fabricated from commercial P25 TiO₂ powders via alkali hydrothermal transformation. Dye-sensitized solar cells (DSCs) were constructed by application of TiNTs and P25 nanoparticles with various weight percentages. The influence of the TiNT concentration on the performance of DSCs was investigated systematically. The electrochemical impedance spectroscopy (EIS) technique was employed to quantify the recombination resistance, electron lifetime and time constant in DSCs both under illumination and in the dark. The DSC based on TiNT/P25 hybrids showed a better photovoltaic performance than the cell purely made of TiO₂ nanoparticles. The open-voltage (V_oc), fill factor (FF) and efficiency (η) continuously increased with the TiO₂ nanotube concentration from 0 to 50 wt%, which was correlated with the suppression of the electron recombination as found out from EIS studies. Respectable photovoltaic performance of ca. 7.41% under the light intensity of 100 mW cm⁻² (AM 1.5G) was achieved for DSCs using 90 wt% TiO₂ nanotubes incorporated in TiO₂ electrodes.     

Surface treatment of TiO2 films for dye-sensitized solar cells using atmospheric-pressure non-equilibrium DC pulse discharge plasma jet

In this paper, we report the utilization of the DC pulse discharge plasma jet technique as a means for the preparation of titanium oxide (TiO₂) films on fluorine dope tin oxide (FTO) coated glass substrates used for dye-sensitized solar cells (DSCs). The TiO₂ film made on these experimental bases exhibited the BET specific surface area of 95 m²/g, the pore volume of 0.3 cm²/g and the TEM particle size of ∼25 nm. The DSCs made by the TiO₂ film exhibited an energy conversion efficiency of 5.7% at 100 mW/cm² light intensity. Consequently, we believe that the optimization between the specific surface area and photocurrent density of TiO₂ film was achieved by the plasma surface treatment which also contributed to the improvement of energy conversion efficiency of DSCs.     

Photoactivity of anatase–rutile TiO2 nanotubes formed by anodization method

Titania (TiO₂) nanotubes were prepared by anodizing titanium (Ti) foils in an electrochemical bath consisting of 1 M glycerol with 0.5 wt.% NH₄F.The pH of the bath was kept constant at 6 and the anodization voltage was varied from 5 V, 20 V to 30 V. It is found that the morphology of the anodized titanium is a function of anodization voltage with pits-like oxide formed for the sample made at 5 V and samples made at 20 V and 30 V consisted of well-aligned nanotubes growing perpendicularly on the titanium foil. However, the nanotubes formed on the samples made at 30 V were not uniform in terms of the nanotubes' diameter and wall thickness. Regardless of the anodization voltage, as anodised samples were amorphous. The crystal structure evolution was studied as a function of annealing temperatures and was characterised by X-ray diffraction and Raman spectroscopy analyses. Crystallization of the nanotubes to anatase phase occurred at 400 °C while rutile formation occurred at 700 °C. Disintegration of the nanotube arrays was observed at 600 °C and the structure completely vanished at 700 °C. TiO₂ nanotube annealed at 400 °C and containing 100% anatase revealed the highest photocatalytic activity for the degradation of methyl orange. Consequently, these results indicate that diameter, wall thickness, crystal structure and degree of crystallinity of the TiO₂ nanotube arrays are the important factors influencing the efficiency of the photocatalytic activity.     

Carbon nanotube-induced preparation of vanadium oxide nanorods: Application as a catalyst for the partial oxidation of n-butane

A vanadium oxide-carbon nanotube composite was prepared by solution-based hydrolysis of NH₄VO₃ in the presence of carbon nanotubes. The carbon nanotubes induce the nucleation of the 1D vanadium oxide nanostructures, with the nuclei growing into long freestanding nanorods. The vanadium oxide nanorods with the lengths up to 20 μm and the widths of 5-15 nm exhibit a well-ordered crystalline structure. Catalytic tests show that the composite with nanostructured vanadium oxide is active for the partial oxidation of n-butane to maleic anhydride at 300 °C.     

Formation of titanium oxide nanotubes using chemical treatments and their characteristic properties

Needle-shaped titanium oxide crystals with a diameter of 8 nm were obtained when titania nanopowders were treated chemically with NaOH aqueous solution and subsequently with HCl aqueous solution under various conditions (e.g., at 110 °C for 20 h). Transmission electron microscopy showed that the needle-shaped products have a tube structure with an inner diameter of approximately 5 nm and an outer diameter of approximately 8 nm. TiO₂ nanotubes with a large specific surface area of ≈ 400 m²/g are expected to have great potentials for use as high-performance photocatalysts or adsorbents. The amount of residual Na⁺ ions in the nanotubes can be controlled by HCl treatment, resulting in the formation of Na-Ti-O titanate nanotubes. The titania and titanate nanotubes can also be modified during the treatment. When calcium acetate solution was used for the treatment, a new type of bioactive nanotube was prepared. An apatite layer was formed on a compact composed of the nanotubes within 1 day of soaking in simulated body fluid. An animal test using rats showed that new-bone-tissue formation around the nanotube compact started 3 days after implantation. When oxoacid solutions, such as perchloric acid, phosphoric acid or sulfuric acid, were used in the treatment, new types of nanotube showing proton conduction were prepared; one of the nanotube compacts showed a high electrical conductivity of 8 × 10^− 2 S/cm at 150 °C. These nanotubes are expected to have applications in the fields of medicine and energy generation, as well as photocatalytic applications.     

Hydrothermal synthesis, characterization, photocatalytic activity and dye-sensitized solar cell performance of mesoporous anatase TiO2 nanopowders

Mesoporous anatase TiO₂ nanopowder was synthesized by hydrothermal method at 130 °C for 12 h. The samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), selected-area electron diffraction (SAED), HRTEM, and Brunauer-Emmett-Teller (BET) surface area. The as-synthesized sample with narrow pore size distribution had average pore diameter about 3-4 nm. The specific BET surface area of the as-synthesized sample was about 193 m²/g. Mesoporous anatase TiO₂ nanopowders (prepared by this study) showed higher photocatalytic activity than the nanorods TiO₂, nanofibers TiO₂ mesoporous TiO₂, and commercial TiO₂ nanoparticles (P-25, JRC-01, and JRC-03). The solar energy conversion efficiency (η) of the cell using the mesoporous anatase TiO₂ was about 6.30% with the short-circuit current density (Jsc) of 13.28 mA/cm², the open-circuit voltage (Voc) of 0.702 V and the fill factor (ff) of 0.676; while η of the cell using P-25 reached 5.82% with Jsc of 12.74 mA/cm², Voc of 0.704 V and ff of 0.649.     

Transformation of microporous titanium glycolate nanorods into mesoporous anatase titania nanorods by hot water treatment

High surface area titanium glycolate microporous multi-faceted nanorods were synthesized from the reaction of titanium alkoxides (Ti(OEt)₄, Ti(O ⁱ Pr)₄, or Ti(O ⁿ Bu)₄) with ethylene glycol, using a sol–gel reflux method. The specific surface area of the as-synthesized titanium glycolate nanorods obtained from Ti(OEt)₄ is ~480 m²/g. A hot water treatment at 90 °C for 1 h transformed the titanium glycolate microporous nanorods into mesoporous anatase TiO₂ nanorods. The shape of the nanorods was conserved after hot water treatment and the microporous to mesoporous transformation took place without significant change in the surface area (477 m²/g). Micro Raman spectroscopy, scanning electron microscopy, transmission electron microscopy, X-ray diffraction, solid state NMR, and nitrogen adsorption/desorption were used to characterize the samples. As a demonstration of potential applications, the thus formed mesoporous anatase TiO₂ nanorods were tested for their photocatalytic efficiency in the degradation of crystal violet, and a photodegradation mechanism is proposed.     

Annealing study of titanium oxide nanotube arrays

Titanium dioxide nanotube arrays fabricated by anodization of titanium foil and annealed at different temperatures were studied using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and positron annihilation spectroscopy (PAS). The crystallization process and morphological changes of the nanotubes have been discussed. It was found that anatase (1 0 1) only appeared on the walls of the nanotubes. The atomic concentration of fluoride and the ratio of Ti/O decreased when the annealing temperature increased. Vacancy type defects were found to diffuse toward the surface when the samples were annealed at 200 °C and 400 °C and healing of vacancies occurred at 600 °C. In addition, fluoride may form some complexes with vacancies on the surface hence lowering the value of S parameter.     

Synthesis of highly-active single-crystalline TiO2 nanorods and its application in environmental photocatalysis

Highly-active anatase TiO₂ nanorods have been successfully synthesized via a simple two-step method, hydrothermal treatment of anatase/rutile titanium dioxide nanoparticle powder in a composite-hydroxide eutectic system of 1:1 M KOH/NaOH, followed by acid post-treatment. The morphology and crystalline structure of the obtained nanorods were characterized using XRD, TEM, SEM/EDX and BET surface area analyzer. The obtained TiO₂ nanorods have a good crystallinity and a size distribution (about 4-16 nm); with the dimensions of 200-300 nm length and of 30-50 nm diameter. Compared with its precursor anatase/rutile TiO₂ nanoparticles and the titanate nanotubes, the pure anatase TiO₂ nanorods have a large specific surface area with a mesoporous structure. The photocatalytic performance of the prepared nanorods was tested in the degradation of the commercial Cibacrown Red (FN-R) textile dye, under UV irradiation. Single-crystalline anatase TiO₂ nanorods are more efficient for the dye removal.     

Sputter deposition and surface treatment of TiO2 films for dye-sensitized solar cells using reactive RF plasma

Sputter deposition followed by surface treatment was studied using reactive RF plasma as a method for preparing titanium oxide (TiO₂) films on indium tin oxide (ITO) coated glass substrate for dye-sensitized solar cells (DSCs). Anatase structure TiO₂ films deposited by reactive RF magnetron sputtering under the conditions of Ar/O₂(5%) mixtures, RF power of 600 W and substrate temperature of 400 °C were surface-treated by inductive coupled plasma (ICP) with Ar/O₂ mixtures at substrate temperature of 400 °C, and thus the films were applied to the DSCs. The TiO₂ films made on these experimental bases exhibited the BET specific surface area of 95 m²/g, the pore volume of 0.3 cm²/g and the TEM particle size of ∼ 25 nm. The DSCs made of this TiO₂ material exhibited an energy conversion efficiency of about 2.25% at 100 mW/cm² light intensity.     

Mass production of multi-wall carbon nanotubes by metal dusting process with high yield

Carbon nanotube materials were synthesized over Fe-Ni nanoparticles generated during disintegration of the surface of alloy 304L under metal dusting environment. The metal dusting condition was simulated and optimized through exposing stainless steel samples during long term repetitive thermal cycling in CO/H₂ = 1/1, total gas flow rate 100 cm³/min, at 620 °C for 300 h. After reaction, surface morphology of the samples and also carbonaceous deposition which had grown on sample surfaces were examined by stereoscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Results revealed that multi-wall carbon nanotubes could be formed over nanocatalyst generated on the alloy surface by exploiting metal dusting process. By optimization of reaction parameters the yields of carbon nanotube materials obtained were 700-1000%. Also it has been shown herein that the amount of carbon nanotube materials remarkably increases when the reaction time is extended up to 300 h, indicating a possibility of the mass production by this easy method.     

Electrochemical characteristics of nanotubes formed on Ti-Nb alloys

Titanium and Ti alloys have been used extensively as bone-implant materials due to their high strength-to-weight ratio, good biocompatibility and excellent corrosion resistance. In this work, we have investigated the effects of the β-stabilizing element Nb on the morphology of nanotubes formed on Ti-xNb alloys using 1.0 M H₃PO₄ electrolyte containing 0.8 wt.% NaF and various electrochemical methods. Oxide layers consisting of highly ordered nanotubes with a wide range of diameters (approximately 55-220 nm) and lengths (approximately 730 nm-2 μm) can be formed on alloys in the Ti-xNb system as a function of Nb content. The nanotubes formed on the Ti-Nb alloy surface were transformed from the anatase to rutile structure of titanium oxide. The titanium oxide nanotube surface was observed to have lower corrosion resistance in 0.9% NaCl solution compared to titanium oxides surfaces on Ti-xNb alloys without the nanotube morphology.     

Anodic TiO2 nanotubes from stirred baths: hydroxyapatite growth & osteoblast responses

Self-organized porous nano-tubular TiO₂ was anodically formed on titanium from electrolyte containing 1 M Na₂SO₄ and 0.5 wt.% NaF. The oxidation was carried out for 2 h at 20 V and the electrolytes were stirred using (i) magnetic pellet and (ii) ultrasonic waves. The nanotubes have single-pore diameter of 50–90 nm under the magnetic pellet stirring and 75–110 nm under the ultrasonic agitation. The coatings were amorphous in this condition. Amorphous coatings cannot nucleate apatite easily and require crystallization heat-treatments for inducting apatite. The current nanotubes were heated for 2 h at 500 °C. This treatment converted them to crystalline mixed anatase and rutile. These heat-treated coatings were then immersed in simulated body fluid (SBF) for 5, 168 and 504 h to nucleate apatite. Apatite produced on ultrasonically obtained nanotube contained finer crystals.     

Nanostructured surface changes of Ti-35Ta-xZr alloys with changes in anodization factors

The purpose of this study was to investigate the changes of the nanostructured surface of Ti-35Ta-xZr alloys for dental application resulting from changes in anodization factors. TiO₂ nanotubes were formed on Ti-35Ta-xZr alloys by anodization in H₃PO₄-containing NaF solutions. Anodization was carried out using a scanning potentiostat. Microstructures of the alloys were examined by optical microscopy (OM), field emission scanning electron microscopy (FE-SEM) and x-ray diffraction (XRD). Microstructures of the Ti-35Ta-xZr alloys were changed from α" phase to β phase, and morphologies changed from a needle-like to an equiaxed structure, with increasing Zr content. As the Zr content increased from 3 to 7 to 15 wt.%, the average thickness of the TiO₂ nanotubes increased from 4.5 μm to 6.1 μm to 9.0 μm. When the anodizing potential was increased from 3 V to 10 V, the thickness of the nanotube layers increased from about 0.5 μm to 9.5 μm. As the anodization time increased from 30 min to 180 min at 10 V, the nanotube thickness increased from 4 μm to 9.5 μm. The amorphous oxide phase in the nanotubes transformed to anatase and rutile phases of TiO₂ by heat treatment above 300 °C.     

Pore size control and electrochemical capacitor behavior of chemically activated polyacrylonitrile – Carbon nanotube composite films

Activated polyacrylonitrile (PAN)/carbon nanotube (CNT) composite film based electrodes have been prepared by chemical activation with potassium hydroxide for electrochemical capacitors. This paper analyses the following aspects of specific capacitance, pore size distribution and surface area: influence of activation temperature, molarity of activating agent, composition of PAN/carbon nanotube precursor films and electrolytes. A maximum value of specific capacitance of ∼302 Fg⁻¹ was achieved for the samples activated at 800 °C. Energy density for PAN/CNT 80/20 sample when tested with ionic liquid/organic electrolyte system was as high as ∼22 W h kg⁻¹. Pore size control predominantly below 5 nm was observed in these activated PAN samples. Data analysis showed that micropores make a significant contribution to the capacitance performance of these materials in both 6 M KOH as well as in BMIMBF₄/acetonitrile electrolytes.     

Transparent conductive titanium-doped indium oxide films prepared by a magnetic null discharge sputter source

Titanium-doped indium oxide (ITiO) films were prepared on soda-lime glass substrate using a magnetic null discharge (MND) sputter source. The ITiO thin films containing 10 wt.% Ti showed the minimum resistivity of ρ = 5.5 × 10⁻³ Ω cm. The optical transmittance increases from 70% at 450 nm to 80% at 700 nm in visible spectrum. Photoelectron peaks for In 3d, Ti 2p, O 1s and C 1s were detected for the ITiO film in the binding energy range of 0-1100 eV. The surface roughness of the sample showed a change from 10 nm to 50 nm. The ITiO film used for TCO layer of DSCs exhibited an energy conversion efficiency of about 3.8% at light intensity of 100 mW/cm².     

Facile synthesis of solution-disposable carbon nanotube-TiO2 hybrids in organic media

Oleic acid-capped TiO₂ nanoparticles (NPs) were directly grown on untreated multiwalled carbon nanotubes (MWCNTs) from a stable titanium carboxylate complex through a solvothermal aminolysis process in organic media. The shape of the TiO₂ NPs loaded on the MWCNTs can be controlled from nanodots (∼ 3 nm in diameter) to nanorods (∼ 5 nm in diameter, 30-40 nm in length) by changing solvent components and by Co²⁺ doping. The resulting hybrids can be well dispersed in apolar organic solvents, which may provide possibilities for manipulating them in solutions for widespread applications.     

Fabrication of TiO2 nanotube arrays by electrochemical anodization in an NH4F/H3PO4 electrolyte

Highly ordered TiO₂ nanotube arrays were fabricated by electrochemical anodization of titanium in an NH₄F/H₃PO₄ electrolyte. A TiO₂ crystal phase was identified by X-ray diffraction, and the morphology, length and pore diameter of the TiO₂ nanotube arrays were determined by field-emission scanning electron microscopy (FE-SEM). The anodization parameters including the rate of magnetic stirring, F⁻ concentration, calcination temperature, anodization voltage and anodization time were investigated in detail. The results show that the as-prepared TiO₂ nanotube arrays possessed good uniformity, a well-aligned morphology with a length of 750 nm and an average pore diameter of 62 nm at a 150 rpm rate of magnetic stirring for 120 min at 20 V in an electrolyte mixture of 0.2 M H₃PO₄ and 0.3 M NH₄F with a 500 °C calcination to obtain 100% anatase phase. The adsorption of N-719 dye at different tube lengths was determined by UV-vis analysis and found to increase with increasing tube length. We also discuss the formation mechanism of the TiO₂ nanotube arrays. The findings indicate that the formation of the TiO₂ nanotube arrays proceeds by the combined action of the electrochemical etching and chemical dissolution.     

Structural and mechanical properties of titanium oxide thin films for biomedical application

Titanium oxide thin films were deposited by radiofrequency reactive sputtering in Ar-O₂ atmosphere on silicon (100) wafers and titanium alloy plates (Ti-6Al-4V). Thin films structural characterization was carried out by grazing incidence X-ray diffraction, atomic force microscopy, scanning and transmission electron microscopies. Chemical composition was checked by X-ray wavelength dispersive spectroscopy. Mechanical assessment was achieved by nano-indentation and nano-scratch measurements. The films deposited on silicon substrates are over-stoechiometric in oxygen, with an oxygen to titanium ratio of about 2.2. The growth of anatase and rutile phases was promoted by ranging the total and oxygen partial pressures between 0.17-1.47 Pa and 35-85%. The growth rate of films, determined by grazing incidence X-ray reflectivity, was ranging from 35 to 55 nm/h. The rutile single-phased films possess a hardness of about 2.5 times higher and a lower friction coefficient than the anatase films. The films which contain anatase possess a high surface root-mean-square roughness and a reduced elastic modulus of around 120 GPa close to reduced elastic moduli of hydroxyapatite bioceramic and titanium alloy. So the anatase film could be the best candidate as a titanium oxide intermediate layer between hydroxyapatite and titanium alloy in the field of biomedical implants.     

Synthesis of carbon nanotubes at low temperature by filament assisted atmospheric CVD and their field emission characteristics

Multiwalled carbon nanotubes (MWNTs) were synthesized using a hot filament assisted chemical vapor deposition (CVD) at the atmospheric pressure at a substrate temperature of 550 °C. The size of nanotubes was controlled by changing the size of catalyst particles. The structure and composition of these nanotubes were investigated using scanning electron microscopy, transmission electron microscopy, and Raman spectroscopy. The electron field emission current of MWNTs was also measured. It was found that the nanotubes with smaller the diameter had higher the emission current levels though synthesis conditions except catalyst particles were the same. These as-grown MWNTs had emission current densities of 6.5 mA/cm² and 2.5 mA/cm² at 1 V/μm for 5-8 nm and 20 nm size carbon nanotube samples, respectively. The results indicated that the MWNTs synthesized had low emission threshold voltages and high emission current levels that are favorable properties for field emission-based display device applications.