Hydrothermal growth of double-layer TiO2 nanostructure film for quantum dot sensitized solar cells

A double-layer (DL) film with a TiO₂ nanosheet-layer on a layer of TiO₂ nanorod-array, was synthesized on a transparent conductive fluorine-doped tin oxide substrate by a two-step hydrothermal method. Starting from the precursors of NaSeSO₃, CdSO₄ and the complex of N(CH₂COOK)₃, CdSe quantum dots (QDs) were grown on the DL-TiO₂ substrate by chemical bath deposition method. The samples were characterized by X-ray diffraction, Scanning electron microscopy, Energy dispersion spectroscopy, and their optical scattering property was measured by light reflection spectrometry. Some CdSe QDs sensitized DL-TiO₂ films serve as the photoanodes, were assembled into solar cell devices and their photovoltaic performance were also characterized. The short circuit current and open-circuit voltage of the solar cells range from 0.75 to 4.05 mA/cm² and 0.20 − 0.42 V under the illumination of one sun (AM1.5, 100 mW/cm²), respectively. The photocurrent density of the DL-TiO₂ film is five times higher than that of a bare TiO₂ nanorod array photoelectrode cell.     

Preparation of TiO2 paste using poly(vinylpyrrolidone) for dye sensitized solar cells

The surface morphology of titanium oxide (TiO₂) films as a photoanode in dye sensitized solar cells plays a vital role in converting light to electricity. Therefore, TiO₂ films were prepared using TiO₂ paste with different compositions of poly(vinylpyrrolidone) (PVP) as a binder to optimize their physico-chemical properties. The paste was prepared with commercial TiO₂ powder mixed with acetylacetone, PVP, 4-octylphenol polyethoxylate, acetic acid and ethanol. The chemical composition remains the same for all pastes except PVP. The quantity of the PVP was optimized in such a way that it provides a thick film with a good network connection. The impact of the quantity of PVP in the TiO₂ paste was analyzed. The prepared TiO₂ film structure was characterized by X-ray diffraction. The surface morphology was analyzed by scanning electron microscopy. The electrochemical performance of the prepared TiO₂ as a photoanode was also investigated. Among the four different photoanodes, the cells fabricated with a TiO₂ film prepared with 0.4 g of PVP exhibited the highest power conversion efficiency of 6.77%, short-circuit photocurrent density and open circuit voltage of 12.38 mA/cm² and 0.77 V, respectively.     

Visible light degradation of Orange II using xCuyOz/TiO2 heterojunctions

Cu₂O/TiO₂, Cu/Cu₂O/TiO₂ and Cu/Cu₂O/CuO/TiO₂ heterojunctions were prepared and studied for their potential application as photocatalysts able to induce high performance under visible light. Orange II was used as a representative dye molecule. The effect of the amount and composition of the photosensitizers toward the activation of TiO₂ was studied. In each case, the global mechanism of Inter Particle Electrons Injection (IPEI) was discussed. The highest photocatalytic activity was observed for the system Cu/Cu₂O/CuO (MB2 catalyst) under visible light (t_1/2 = 24 min, k = 159.7 × 10⁻³ min⁻¹) and for the heterojunction cascade Cu/Cu₂O/CuO/TiO₂ (MB2 (50%)/TiO₂) under UV–vis light (t_1/2 = 4 min, k = 1342 × 10⁻³ min⁻¹). In the last case, the high performance was attributed firstly to the electromotive forces developed under this configuration in which CuO energy bands mediate the electrons transfer from Cu₂O to TiO₂. The formation of monobloc sensitizers also accounts for the decrease of the probability of the charges lost. It was demonstrated that “Cu₂O/CuO” governs the capability of the heterojunction cascade and Cu does not play a significant role regardless of the heterojunction cascade efficiency. The electrical energy consumption per order of magnitude for photocatalytic degradation of Orange II was investigated for some representative catalytic systems. Visible/MB2 and UV/vis MB2 (50%)/TiO₂ exhibited respectively 0.340 and 0.05 kWh m⁻³ demonstrating the high efficiency of the systems.     

Polythiophene thin films electrochemically deposited on sol-gel based TiO2 for photovoltaic applications

In this work, the influence of titanium dioxide (TiO₂) thin films on the efficiency of organic photovoltaic devices based on electrochemically synthesized polythiophene (PT) was investigated. TiO₂ films were produced by sol-gel methods with controlled thickness. The best TiO₂ annealing condition was determined through the investigation of the temperature influence on the electron charge mobility and resistivity in a range between 723 K and 923 K. The PT films were produced by chronoamperometric method in a 3-electrode cell under a controlled atmosphere. High quality PT films were produced onto 40 nm thick TiO₂ layer previously deposited onto fluorine doped tin oxide (FTO) substrate. The morphology of PT films grown on both substrates and its strong influence on the device performance and PT minimum thickness were also investigated. The maximum external quantum efficiency (IPCE) reached was 9% under monochromatic irradiation (λ = 610 nm; 1 W/m²) that is three orders of magnitude higher than that presented by PT-homolayer devices with similar PT thickness. In addition, the open-circuit voltage (V_oc) was about 700 mV and the short-circuit current density (J_sc) was 0.03 A/m² (λ = 610 nm; 7 W/m²). However, as for the PT-homolayer also the TiO₂/PT based devices are characterized by antibatic response when illuminated through FTO. Finally, the Fill Factor (FF) of these devices is low (25%), indicating that the series resistance (R_s), which is strongly dependent of the PT thickness, is too large. This large R_s value is compensated by TiO₂/PT interface morphology and by FTO/TiO₂ and TiO₂/PT interface phenomena producing preferential paths in which the internal electrical field is higher, improving the device efficiency.     

Electrical characterization of the polyaniline/p-silicon and polyaniline titanium dioxide tetradecyltrimethylammonium bromide /p-silicon heterojunctions

Au/PANI/p-Si/Al and Au/PANI TiO₂ TTAB/p-Si/Al heterojunctions have been fabricated by spin coating of soluble polyaniline (PANI) and PANI titanium dioxide (TiO₂) tetradecyltrimethylammonium bromide (TTAB) on the chemically cleaned p-Si substrates. The thicknesses of the polymeric films have been determined by a profilometer. The current-voltage (I-V) characteristics of the heterojunctions have been obtained in the temperature range of 98-258 K. These devices have showed the rectifying behavior such as diode. The I-V characteristics of the devices have been analyzed on the basis of the standard thermionic emission theory at low forward bias voltage regime. It has been shown that the values of ideality factor decrease while the values of barrier height increase with increasing temperature. This temperature dependence has been attributed to the presence of barrier inhomogeneities at the organic/inorganic semiconductor interface. Furthermore, analysis of the double logarithmic I-V plots at higher forward bias voltages at all temperatures indicates that transport through the organic thin film is explained by a space-charge-limited current process characterized by exponential distribution of traps within the band gap of the organic film. The total concentration of traps has been found to be 3.52 × 10¹⁴ cm^− 3 and 3.14 × 10¹⁵ cm^− 3 for PANI and PANI TiO₂ TTAB layer, respectively.     

Rapid thermal melted TiO2 nano-particles into ZnO nano-rod and its application for dye sensitized solar cells

TiO₂ nano-particles with an anchored ZnO nano-rod structure were synthesized using the hydrothermal method to grow ZnO nano-rods and coated TiO₂ nano-particles on ZnO nano-rods using the rapid thermal annealing method on ITO conducting glass pre-coated with nano porous TiO₂ film. The XRD study showed that there was little difference in crystal composition for various types of TiO₂ nano-particles anchored to ZnO nano-rods. The as-prepared architecture was characterized using field-emission scanning electron microscopy (FE-SEM). Films with TiO₂ nano-particles anchored to ZnO nano-rods were used as electrode materials to fabricate dye sensitized solar cells (DSSCs). The best solar energy conversion efficiency of 2.397% was obtained by modified electrode material, under AM 1.5 illumination, achieved up to J_sc = 15.382 mA/cm², V_oc = 0.479 V and fill factor = 32.8%.     

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.     

Characterization of TiO2 thin films prepared by electrolytic deposition for lithium ion battery anodes

The electrolytic deposition of TiO₂ thin films on platinum for lithium batteries is carried out in TiCl₄ alcoholic solution and the films are subsequently annealed. The as-prepared films are amorphous TiO(OH)₂·H₂O, transformed into anatase TiO₂ at 350 °C, and then gradually into rutile TiO₂ at 500 °C. Cyclic voltammograms show oxidation and reduction peaks at 2.20 and 1.61 V, respectively, corresponding to charge and discharge plateaus at 1.98 and 1.75 V vs. Li⁺/Li. The specific capacity decreases with increasing current density for film of 128-nm thickness in the initial discharge. It is observed that the diffusion flux of Li⁺ insertion/extraction into/from TiO₂ controls the reaction rate at higher current densities. Consequently, at low film thickness, high discharge capacity (per weight) is found for the initial cycle at a current density of 10 μA cm^− 2. However, the capacity of prepared films in various thicknesses approach 103 ± 5 mAh g^− 1 after 50 cycles, since the formation of cracks for thicker films offers shorter diffusion paths for Li⁺. In addition, TiO₂ films show electrochromic properties during lithiation and delithiation.     

Fabrication of dye sensitized solar cell using TiO2 coated carbon nanotubes

We fabricated a dye sensitized solar cells (DSCs) using TiO₂ coated multi-wall carbon nanotubes (TiO₂-CNTs). Carbon nanotubes (CNTs) have excellent electrical conductivity and good chemical stability. We introduced CNTs in DSCs to improve solar cell performance through reduction of series resistance. TiO₂-CNTs were obtained by Sol-Gel method. Compared with a conventional TiO₂ cell, the TiO₂-CNTs content (0.1 wt.%) cell showed ∼ 50% increase in conversion efficiency, which is attributed to the increase in short circuit current density (J_sc). The enhancement in J_sc occurs due to improvement in interconnectivity between the TiO₂ particles and the TiO₂-CNTs in the porous TiO₂ film.     

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.     

Preparation and characterization of nanostructured NiO/MnO2 composite electrode for electrochemical supercapacitors

Nanostructured nickel-manganese oxides composite was prepared by the sol-gel and the chemistry deposition combination new route. The surface morphology and structure of the composite were characterized by scanning electron microscope and X-ray diffraction. The as-synthesized NiO/MnO₂ samples exhibit higher surface area of 130-190 m² g⁻¹. Cyclic voltammetry and galvanostatic charge/discharge measurements were applied to investigate the electrochemical performance of the composite electrodes with different ratios of NiO/MnO₂. When the mass ratio of MnO₂ and NiO in composite material is 80:20, the specific capacitance value of NiO/MnO₂ calculated from the cyclic voltammetry curves is 453 F g⁻¹, for pure NiO and MnO₂ are 209, 330 F g⁻¹ in 6 mol L⁻¹ KOH electrolyte and at scan rate of 10 mV s⁻¹, respectively. The specific capacitance of NiO/MnO₂ electrode is much larger than that of each pristine component. Moreover, the composite electrodes showed high power density and stable electrochemical properties.     

Microstructure and photocatalytic activity of mesoporous TiO2 film coated on an aluminum foam

A TiO₂ film was synthesized via a surfactant assisted sol-gel process and dip-coated on the surface of an open-celled aluminum foam. The film shows a typical mesoporous structure composed of anatase crystalline grains with the average size of 10 nm, and has the thickness of about 3.5 μm as well as the BET surface area of 78.1 m²/g. It exhibits high photocatalytic efficiency toward the decomposition of formaldehyde at continuous flow mode. The relatively small grain size of TiO₂ and relatively thick mesoporous structure, which is favorable for high photochemical activity and the mass transfer of the reactants, should be responsible for the properties.     

Optical properties of TiO2 thin films deposited on polycarbonate by ion beam assisted evaporation

TiO₂ thin films were deposited on polycarbonate (PC) substrate by ion beam assisted evaporation. The grain size increased with the ion anode voltage and film thickness. The TiO₂ thin films had an amorphous structure. Moiré deflectometry was used to measure the nonlinear refractive indices of TiO₂ thin films on PC substrates. The nonlinear refractive index was measured to be of the order of 10^− 8 cm² W^− 1 and a change in refractive index was of the order of 10^− 5. Dense TiO₂ films exhibited high linear refractive indices, red-shift of the optical absorbance, and absorbance in the near-IR region.     

The effect of Li intercalation on different sized TiO2 nanoparticles and the performance of dye-sensitized solar cells

The effect of Li⁺ insertion into different sized TiO₂ nanoparticles and their influences on the photoconversion efficiency of dye-sensitized solar cells (DSSC) were investigated. TiO₂ nanoparticles with different particle sizes (22 nm, 14 nm and 6 nm) doped with Li⁺ were employed to form thin film electrodes and their properties were characterized by X-ray diffraction (XRD) and electrochemical impedance spectroscopy analysis. XRD evidenced the presence of anatase as the main phase. From the XRD analysis, it was observed that the Li⁺ ions could be inserted into both the surface and bulk of the TiO₂ nanoparticles. In the larger particle size, the Li⁺ ions are inserted into the bulk anatase where as Li⁺ ions bounded on the TiO₂ surface for the smaller crystallite size. The photovoltaic properties were measured by a current-voltage meter under AM1.5 simulated light radiation. It exhibited that the overall photoconversion efficiency of DSSC was decreased in the larger particles while it was enhanced in the smaller nanoparticles when Li⁺ was doped into the TiO₂ nanoparticles. A nearly 40% decrease in the efficiency (η) of DSSC was observed upon intercalation of Li⁺ ions into 22 nm sized TiO₂ nanoparticles (P25). The 14 nm sized TiO₂ nanoparticles (P90) showed slightly less efficiency (η) upon Li⁺ doping than that of the undoped sample. However, the smallest sized TiO₂ nanoparticles (6 nm) showed higher efficiency than that of the undoped one. This phenomenon is explained based on electron trapping and charge recombination due to lithium doping.     

Influence of calcination ambient and film thickness on the optical and structural properties of sol-gel TiO2 thin films

Influence of both calcination ambient and film thickness on the optical and structural properties of sol-gel derived TiO₂ thin films have been studied. X-ray diffraction results show that prepared films are in an anatase form of TiO₂. Films calcined in argon or in low vacuum (∼2 × 10⁻¹ mbar) are found to be smaller in crystallite size, more transparent at low wavelength region of ∼300-450 nm, denser, have higher refractive index and band gap energy compared to air-calcined films. Scanning electron microscopic study reveals that surfaces of TiO₂ films calcined in argon or in low vacuum are formed by densely packed nano-sized particulates. Presence of voids and signs of agglomeration can be seen clearly in the surface microstructure of air-calcined films. In the thickness range ∼200-300 nm, band gap energy and crystallite size of TiO₂ films remain practically unaffected with film thickness but refractive index of thinner film is found to be marginally higher than that of thicker film. In this work, it has been shown that apart from temperature and soaking time, partial pressure of oxygen of the ambient is also an important parameter by which crystallite size, microstructure and optical properties of the TiO₂ films may be tailored during calcination period.     

Structure induced optical properties of anodized TiO2 nanotubes

TiO₂ nanotubes were synthesized by means of anodization and investigated for their structure dependent optical properties. The anodization was conducted at operating voltages between 5 and 30 V for 3 h in a neutral, organic electrolyte consisting of 0.3 wt% NH₄F + 2 wt% H₂O + ethylene glycol and the resulting nanotubes were annealed at 450 °C for 2 h in air at atmospheric pressure. It is shown that an increase in the applied anodization voltage yielded an increase in the wall thickness, diameter and length of the nanotubes and that these varying morphologies have a direct influence on the crystallite size of the nanotubes during annealing. Photoluminescence spectra indicated that the optical bandgap of the TiO₂ nanotube film decreased with the increase in the anodization voltage, whereas supplementary Raman spectra showed a decrease in the confinement of the optical phonon modes as the crystallite sizes increased, in coherence with the phonon confinement model. These results present significant insights into the size-dependent properties of these novel nanostructured forms of TiO₂ and play an important role in their implementation in photovoltaic devices, such as the dye-sensitized solar cell.     

Ion beam modification of TiO2 films prepared by Cat-CVD for solar cell

The effects of nitrogen ion bombardment on TiO₂ films prepared by the Cat-CVD method have been studied to improve the optical and electrical properties of the material for use in Si thin film solar cells. The refractive index n and the dark conductivity of the TiO₂ film increased with irradiation time. The refractive index n of the TiO₂ film was changed from 2.1 to 2.4 and the electrical conductivity was improved from 3.4 × 10^− 2 to 1.2 × 10^− 1 S/cm by the irradiation. These results are due to the formation of Ti-N bonds and oxygen vacancies in the film.     

Preparation and characterization of regioregular poly(3-octylthiophene-2,5-diyl)/copper indium disenillide/titania heterojunction polymer solar cells

By optimizing the P3OT/CISe ratio, TiO₂ content in the P3OT/CISe active layer, annealing temperature and time, this study investigated hybrid Al/Ca/P3OT:CISe:TiO₂/PEDOT:PSS/ITO thin film solar cells with improved efficiency. Due to an increase in charge-carrier transport and a decrease of electron-hole recombination, it is possible to increase the efficiency of hybrid solar cells by adding TiO₂ nanoparticles to the P3OT:CISe active film. Also, performance enhancement of the solar cells can occur with an increase of CISe content in P3OT as well as the addition of a PEDOT:PSS layer to the cell structure. The optimum TiO₂ content in P3OT:CISe layer is 15 wt.%. The optimum annealing temperature and time are 125 °C and 30 min, respectively. The formation of large CISe and TiO₂ aggregates that reduce charge mobility may cause the decrease of efficiency. The rough surface may effectively reduce the charge-transport distance and provide nanoscale phase separation that further enhances internal light scattering and light absorption. The best results for the open circuit voltages (V_oc), short-circuit current density (J_sc), fill factor (FF), and efficiency (η_e) of Al/Ca/POCT15/PEDOT:PSS/ITO hybrid solar cells obtained at optimized conditions were V_oc = 0.49, J_sc = 3.20, FF = 42.96, and η_e = 0.674, respectively.     

Fabrication of TiO2 nanotube film by well-aligned ZnO nanorod array film and sol-gel process

High density TiO₂ nanotube film with hexagonal shape and narrow size distribution was fabricated by templating ZnO nanorod array film and sol-gel process. Well-aligned ZnO nanorod array films obtained by aqueous solution method were used as template to synthesize ZnO/TiO₂ core-shell structure through sol-gel process. Subsequently, TiO₂ nanotube array films survived by removing the ZnO nanorod cores using wet-chemical etching. Polycrystalline anatase TiO₂ nanotube films were ∼ 1.5 μm long and ∼ 100 nm in inter diameter with a wall thickness of ∼ 10 nm.     

Interfacial characteristics and dielectric properties of Ba0.65Sr0.35TiO3 thin films

Ba_0.65Sr_0.35TiO₃ (BST) thin films were deposited on Pt/Ti/SiO₂/Si substrates by radio frequency magnetron sputtering technique. X-ray photoelectron spectroscopy (XPS) depth profiling data show that each element component of the BST film possesses a uniform distribution from the outermost surface to subsurface, but obvious Ti-rich is present to BST/Pt interface because Ti⁴⁺ cations are partially reduced to form amorphous oxides such as TiO_x (x < 2). Based on the measurement of XPS valence band spectrum, an energy band diagram in the vicinity of BST/Pt interface is proposed. Dielectric property measurements at 1 MHz reveal that dielectric constant and loss tangent are 323 and 0.0095 with no bias, while 260 and 0.0284 with direct current bias of 25 V; furthermore, tunability and figure of merit are calculated to be 19.51% and 20.54, respectively. The leakage current density through the BST film is about 8.96 × 10^− 7 A/cm² at 1.23 V and lower than 5.66 × 10^− 6 A/cm² at 2.05 V as well as breakdown strength is above 3.01 × 10⁵ V/cm.