Atomic layer deposition of SiO2 from Tris(dimethylamino)silane and ozone by using temperature-controlled water vapor treatment

Atomic layer deposition of SiO₂ from tris(dimethylamino)silane (TDMAS) and ozone as precursors on Si(100) surfaces at near-room temperatures was studied by infrared absorption spectroscopy with a multiple internal reflection geometry. TDMAS can be adsorbed at OH sites on hydroxylated Si surfaces at room temperature. Ozone oxidation of the TDMAS-treated Si surface is effective in removing hydroaminocarbon adsorbates introduced during TDMAS adsorption at room temperature. After oxidation by ozone, treatment with H₂O vapor at a substrate temperature of around 160 °C causes regeneration of OH sites for TDMAS adsorption. Cycles involving TDMAS adsorption and ozonization at room temperature followed by H₂O treatment at 160 °C permit the buildup of layers of SiO₂. The amount of residual hydroaminocarbon at the interface between the growing SiO₂ film and the substrate can be reduced with the ozone treated Si surface as a starting surface.     

Layer-by-layer assembly of poly (N-acryloyl-N'-propylpiperazine) and poly (acrylic acid): Effect of pH and temperature

Layer-by-layer assembly technique was applied to fabricate multilayer films of poly(N-acryloyl-N'-propylpiperazine) (PAcrNPP) and poly(acrylic acid). The film buildup was followed by Quartz Crystal Microbalance, and the effect of temperature and pH on the layer-by-layer assembly was investigated. Below the lower critical solution temperature of PAcrNPP, the adsorption amount increased with increase of temperature. As the pH of dipping solutions was systematically varied from 2.0 to 7.5, adsorption amount of polymers initially increased and then decreased. The relationship between adsorption amount and degree of ionization of polymers was discussed. When an eight-bilayer film was alternately exposed to HCl aqueous solution (pH = 3.5) and neutral water (pH = 6.5), the film showed pH-response, which could be the result of polymer rearrangement.     

A three-dimensional electrode for photoelectrochemical cell: TiO2 coated ITO mesoporous film

In this letter, TiO₂ coated ITO mesoporous film was prepared by dipping doctor-blade ITO mesoporous film in TiO₂ sol, followed by sintering at 500 °C for 30 min. The CdS quantum dots (QDs) were deposited on TiO₂ coated ITO mesoporous film using sequential chemical bath deposition (S-CBD) method to form a three-dimensional (3D) electrode. The photo-activity of ITO mesoporous film/TiO₂/CdS electrode was investigated by forming a photoelectrochemical cell, which indicated that the ITO mesoporous film/TiO₂/CdS electrode was efficient in photoelectrochemical cell as a working electrode. The 3D electrode showed lower performance than the conventional electrode of TiO₂ mesoporous film/CdS, and more works are needed to improve the performance of 3D electrode.     

Investigation of low resistance transparent MoO3/Ag/MoO3 multilayer and application as anode in organic solar cells

Depending on the resistivity and transmittance, transparent conductive oxides (TCO) are widely used in thin film optoelectronic devices. Thus doped In₂O₃ (ITO), ZnO, SnO₂ are commercially developed. However, the deposition process of these films need sputtering and/or heating cycle, which has negative effect on the performances of the organic devices due to the sputtering and heat damages. Therefore a thermally evaporable, low resistance, transparent electrode, deposited onto substrates room temperature, has to be developed to overcome these difficulties. For these reasons combination of dielectric materials and metal multilayer has been proposed to achieve high transparent conductive oxides. In this work the different structures probed were: MoO₃ (45 nm)/Ag (x nm)/MoO₃ (37.5 nm), with x = 5-15 nm. The measure of the electrical conductivity of the structures shows that there is a threshold value of the silver thickness: below 10 nm the films are semiconductor, from 10 nm and above the films are conductor. However, the transmittance of the structures decreases with the silver thickness, therefore the optimum Ag thickness is 10 nm. A structure MoO₃ (45 nm)/Ag (10 nm)/MoO₃ (37.5 nm) resulted with a resistivity of 8 × 10^− 5 Ω cm and a transmittance, at around 600 nm, of 80%. Such multilayer structure can be used as anode in organic solar cells according to the device anode/CuPc/C₆₀/Alq₃/Al. We have already shown that when the anode of the cells is an ITO film the introduction of a thin (3 nm) MoO₃ layer at the interface anode (ITO)/organic electron donor (CuPc) allows reducing the energy barrier due to the difference between the work function of ITO and the highest occupied molecular orbital of CuPc [1]. This property has been used in the present work to achieve a high hole transfer efficiency between the CuPc and the anode. For comparison MoO₃/Ag/MoO₃/CuPc/C₆₀/Alq₃/Al and ITO/MoO₃/CuPc/C₆₀/Alq3/Al solar cells have been deposited in the same run. These devices exhibit efficiency of the same order of magnitude.     

pH and iodide ion effect on corrosion inhibition of histidine self-assembled monolayer on copper

Self-assembled monolayer (SAM) of histidine (His) was prepared on copper surface at various pH values. The effect of KI additives on corrosion protection efficiency of His SAM was also studied. The protection abilities of these films against copper corrosion in 0.5 M HCl aqueous solution were investigated using electrochemical impedance spectroscopy and polarization techniques. The results show that the film formed on the electrode is more stable at pH = 10 than that at other pH values. When the iodide ions were added into the His self-assembly solution (pH = 10), protection efficiency was further improved. The inhibition mechanism has been discussed by quantum chemical calculations.     

Determination of selenium in natural waters by adsorptive differential pulse cathodic stripping voltammetry

In this work bovine albumin was used innovatively as a medium for adsorptive accumulation of Se–I₂ on thin mercury film electrode. Se–I₂ was formed by reaction between Se(IV) and iodide in HCl media. The adsorbed Se–I₂ was stripped in 0.05 M HCl by differential pulse cathodic potential scan. The proposed method was successfully applied to analysis of Se(IV) and Se(VI) in natural waters sampled from some lagoons south of Caspian Sea. The optimum reaction conditions and other analytical parameters and influence of cations and anions were studied. The detection limit was 0.37 ng mL⁻¹. The obtained results were compared with the results of DPCSV after electrochemical preconcentration, HG-AAS and ICP-AES.     

Fabrication of transparent conductive films with a sandwich structure composed of ITO/Cu/ITO

New transparent conductive films that had a sandwich structure composed of ITO/Cu/ITO multilayer films were prepared by a conventional RF and DC magnetron sputtering process on a polycarbonate substrate without intentional substrate heating. The thickness of each layer in the ITO/Cu/ITO films was kept constant at 50 nm/5 nm/45 nm. The optoelectrical and structural properties of the films were compared with conventional ITO single-layer films and ITO/Cu/ITO multilayered films. Although both films had identical thickness, 100 nm, the ITO/Cu/ITO films showed a lower resistivity, 3.5 × 10⁻⁴ Ω cm. In optical transmittance measurements, however, the ITO single-layer films showed a higher transmittance of 74% in the wavelength range of 300-800 nm. XRD spectra showed that both the ITO and ITO/Cu/ITO films were amorphous. The figure of merit, φ_TC, reached a maximum of 5.2 × 10⁻⁴ Ω⁻¹ for the ITO/Cu/ITO films, which was higher than the φ_TC of the ITO films (1.6 × 10⁻⁴ Ω⁻¹). The φ_TC results suggested that ITO/Cu/ITO films had better optoelectrical properties than conventional ITO single-layer films.     

Study of composition reproducibility of electrochemically co-deposited CuInSe2 films onto ITO

CuInSe₂ thin films were electrodeposited onto ITO substrates from aqueous solution containing 4.5 mM CuSO₄, 10 mM In₂(SO₄)₃ and 10 mM SeO₂ isopotentionally and by two-step deposition technique — changing the deposition potential during the deposition process step-wise: from lower to higher and vice versa in the potential range of − 0.6 to − 1.0 V (vs. Ag/AgCl). Solution pH was varied from 1.3 to 1.9 at temperatures 293 and 313 K to clarify the region for co-deposition of In-rich CuInSe₂ films on ITO with high composition reproducibility. Morphology and composition of CuInSe₂ layers depended not only on deposition temperature and potential, but also on the direction of potential change in the case of two-step process. The potential change from lower negative values to higher ones resulted in layers with low adhesivity. Alternatively, from higher potential to lower potential, the homogeneous, well-structured, adhesive and smooth layers were deposited. Modifying deposition periods in a two-step process, the chemical composition of films can be tailored. At pH < 1.9 reproducibility of the film's composition was low. ITO electrodes were found not to be stable at pH < 1.9.     

Exploring proton doping in poly-3-methylpyrrole by infrared spectroscopy

Structural changes induced by electrochemical redox processes or by pH variations on conducting poly-3-methylpyrrole, electrochemically synthesized in NaClO₄ acetonitrile solution, have been studied by infrared spectroscopy. With this aim infrared spectra of perchlorate doped poly-3-methylpyrrole films at different oxidation states as well as after immersion in acid (pH = 1) and basic (pH = 12.6) aqueous solutions have been analysed. The existence of proton-doping mechanism in this polymer has been confirmed from the comparative study of spectra of oxidized/reduced and acid/basic treated polymer.     

Voltammetric detection of bisphenol a by a chitosan-graphene composite modified carbon ionic liquid electrode

In this paper 1-ethyl-3-methylimidazolium tetrafluoroborate based carbon ionic liquid electrode (CILE) was fabricated and further modified with chitosan (CTS) and graphene (GR) composite film. The fabricated CTS-GR/CILE was further used for the investigation on the electrochemical behavior of bisphenol A (BPA) by cyclic voltammetry and differential pulse voltammetry. A well-defined anodic peak appeared at 0.436 V in 0.1 mol/L pH 8.0 Britton-Robinson buffer solution, which was attributed to the electrooxidation of BPA on the modified electrode. The electrochemical parameters of BPA on the modified electrode were calculated with the results of the charge transfer coefficient (α) as 0.662 and the apparent heterogeneous electron transfer rate constant (k_s) as 1.36 s^− 1. Under the optimal conditions, a linear relationship between the oxidation peak current of BPA and its concentration can be obtained in the range from 0.1 μmol/L to 800.0 μmol/L with the limit of detection as 2.64 × 10^− 8 mol/L (3σ). The CTS-GR/CILE was applied to the detection of BPA content in plastic products with satisfactory results.     

Electrochemical and thermodynamic studies to evaluate inhibition effect of 2-[(4-phenoxy-phenylimino)methyl]-phenol in 1 M HCl on mild steel

Inhibition of the corrosion of mild steel in 1.0 M HCl solution by a Schiff base compound named 2-[(4-phenoxy-phenylimino)methyl]-phenol (APS) was investigated at different temperatures (25–55 °C) using electrochemical measurements. The inhibition efficiency increased as APS concentration and temperature increased. It was found that adsorption for APS on mild steel complies with the Langmuir adsorption isotherm in all studied temperature. Thermodynamic parameters (ΔG_ads, ΔH_ads and ΔS_ads) for APS adsorption on mild steel were found out and discussed at each temperature. Time dependency of mild steel in 1.0 M HCl solution in the absence and presence of APS was also studied. The surface morphology of mild steel was examined via SEM analysis.     

Radiochemical and Raman spectroscopy study of the nature of adsorbed layers on a silver electrode

The structure of the layers formed on a silver electrode by the adsorption of pyridine, Cl^?, CN^? and SO₄^2? is discussed. A comparison of the amount of the species adsorbed with their Raman spectra shows that there is no simple relation between the species concentration and the enhancement of the Raman intensity. Furthermore, the inhomogeneity of the layers is shown by Raman microscopy observations. These results lead us to propose the formation of a new species stabilized in the colloidal silver layer. The Raman enhancement could be explained by the existence of a resonance effect.     

Low-indium content bilayer transparent conducting oxide thin films as effective anodes in organic photovoltaic cells

Bilayer In-doped CdO/Sn-doped In₂O₃ (CIO/ITO) transparent conducting oxide (TCO) thin films were prepared by depositing thin ITO films by ion-assisted deposition on CIO films grown by metal-organic chemical vapor deposition. The optical, electrical, and microstructural properties of these bilayer TCO films were investigated in detail. A low sheet resistance of ~ 4.9 Ω/□ is achieved for the CIO/ITO (170/40 nm) bilayers without annealing. With a significantly lower In content (20 vs. ~ 93 at.%) and a much higher conductivity (> 12,000 vs. 3000-5000 S/cm) than commercial ITO, these bilayer films were investigated as anodes in bulk-heterojunction organic photovoltaic (OPV) devices having a poly(2-methoxy-5-(3,7-dimethyloctyloxy)-1,4-phenylenevinylene) + [6,6]-phenyl C₆₁ butyric acid methyl ester active layer. Device performance metrics in every way comparable to those of devices fabricated on commercial ITO are achieved, demonstrating that CIO/ITO bilayers are promising low-In content, highly conductive and transparent electrode candidates for OPV cells.     

Adsorption of vitamin E on mesoporous titania nanocrystals

Tri-block nonionic surfactant and titanium chloride were used as starting materials for the synthesis of mesoporous titania nanocrystallite powders. The main objective of the present study was to examine the synthesis of mesoporous titania nanocrystals and the adsorption of vitamin E on those nanocrystals using X-ray diffraction (XRD), transmission electron microscopy, and nitrogen adsorption and desorption isotherms. When the calcination temperature was increased to 300 °C, the reflection peaks in the XRD pattern indicated the presence of an anatase phase. The crystallinity of the nanocrystallites increased from 80% to 98.6% with increasing calcination temperature from 465 °C to 500 °C. The N₂ adsorption data and XRD data taken after vitamin E adsorption revealed that the vitamin E molecules were adsorbed in the mesopores of the titania nanocrystals.     

Surface potential measurement of organic photo-diode consisting of fullerene/copper phthalocyanine double layered device

We investigated the surface potential built across the electrode/fullerene (C₆₀) or copper phthalocyanine (CuPc) interface and C₆₀/CuPc interface as a function of the thickness of the semiconductor film in the dark condition and under illumination. The surface potential of C₆₀ on Au, Al and Mg changes negatively with the increment of film thickness and it saturates at − 0.25, − 1.0 and − 1.5 V within 20 nm. The Fermi level alignment at C₆₀/electrode interface is established within ∼ 20 nm from electrode, and very high electric field exists due to the displacement of negative electronic charges from electrode into C₆₀. On the other hand, the surface potential of CuPc on ITO changes to + 0.1 V, and the work functions of C₆₀ and CuPc were estimated as 5.0 eV and 4.7 eV. C₆₀ film also accepts electrons from CuPc at hetero-junction interface, and the Fermi-level alignment was again obtained at C₆₀/CuPc interface under illumination. The built-in potential of ca. 0.3 V formed at C₆₀/CuPc interface was considered as the origin of the reduction of open-circuit voltage in ITO/CuPc/C₆₀/Au device compared with the optimum value of 0.6 V. On the other hand, the very high electric field formed at C₆₀/Mg contact improved the photovoltaic properties.     

Electrodeposition of SmS optical thin films on ITO glass substrate

SmS optical thin films were deposited on the surface of ITO glass with an electrodeposition method using aqueous solution containing SmCl₃·6H₂O and Na₂S₂O₃·5H₂O. The phase composition was analyzed by X-ray diffraction (XRD) and microstructure of the film was characterized by atomic force microscope (AFM). It is showed that SmS thin film could be obtained in the solution with n(Sm)/n(S) = 1:4, pH = 4.0 and annealing in Ar atmosphere at 200 °C for 0.5 h. The as-prepared thin films on the ITO glass exhibit a dense microstructure. The band gap of the thin film has been found to be 3.6 eV.     

Investigation of inhibition effect of rhodanine-N-acetic acid on mild steel corrosion in HCl solution

Corrosion inhibition effect of rhodanine-N-acetic acid (R-NA) on mild steel (MS) corrosion in 0.1 M HCl solution was investigated. For this purpose, potentiodynamic polarization, electrochemical impedance spectroscopy (EIS), linear polarization resistance (LPR) as well as hydrogen gas evolution (VH₂−t) and the change of open circuit potential as a function of immersion time (E_ocp − t) were used. The MS surfaces exposed to 0.1 M HCl solution in the absence and presence of inhibitor were examined by scanning electron microscopy (SEM). The thermodynamic parameters of adsorption were calculated and discussed. In order to gain more information about the adsorption mechanism, the EIS technique was used to evaluate the potential of zero charge (PZC) and a mechanism of adsorption process was proposed. It was found that, R-NA is a good corrosion inhibitor for the MS corrosion in 0.1 M HCl solution. The inhibition efficiency increased with increasing inhibitor concentration and reached 98% at 1.0 × 10⁻² M R-NA. The high inhibition efficiency was related to adsorption of R-NA on steel surface. Surface SEM images showed a good surface coverage of inhibitor on the metal surface.     

Sol-gel derived cerium-oxide-silicon-oxide nanocomposite for cypermethrin detection

Cerium oxide (CeO₂) nanoparticles have been self-assembled onto sol-gel derived silicon-oxide (SiO₂) film fabricated onto indium tin oxide (ITO) coated glass plate. These SiO₂-CeO₂ nanocomposite films have been used to immobilize the double stranded calf thymus deoxy ribose nucleic acid (dsCT-DNA) by physical adsorption to detect cypermethrin (CM). Both CeO₂-SiO₂/ITO electrode and dsCT-DNA/CeO₂-SiO₂/ITO bioelectrodes have been characterized using Fourier transform infrared (FTIR) spectroscopy, scanning electron microsopy (SEM) and differential pulse voltammetry (DPV) to confirm the formation of CeO₂-SiO₂ nanocomposite and binding of dsCT-DNA with CeO₂-SiO₂ nanocomposite. Electrochemical response studies of dsCT-DNA/CeO₂-SiO₂/ITO bioelectrode carried out as a function of CM concentration using DPV technique exhibit detection limit up to 0.0025 ppm with response time of 30 s.     

Size and morphology controlled synthesis of gold nanoparticles in green solvent: Effect of reducing agents

The effect of reducing agents on the synthesis of Au(0) metallic nanoparticles (Au NPs) prepared in green solvent medium of β-d-glucose-water dispersions has been reported first. The different equivalent amounts of NaBH₄ and pH values adjusted by NaOH were tested for the reduction of Au salt (HAuCl₄·3H₂O (hydrogen tetrachloroaurate (III) trihydrate) to obtain Au NPs. The type and the amount of reducing agent and the pH of the solution affected the size and morphology of the NPs. Addition of 4 equivalents of NaBH₄ produced homogeneously dispersed 5.3 nm (σ = 0.7) diameter particles. Excess addition of NaBH₄ caused the NPs to settle down as the precipitate forming mesh or wire structure. When salt was reduced by the addition of NaOH (pH = 8.0) the particles were larger (14.2 nm) and less homogeneous (σ = 2.8). At pH = 12.2 the NPs settled at the bottom of the vial when preparation was left overnight. The wire and mesh like structures were obtained at higher pH = 12.2.     

Organic photovoltaic cells fabricated on a SnOx/Ag/SnOx multilayer transparent conducting electrode

Transparent conducting multilayer structured electrode of a few nm Ag layer embedded in tin oxide thin film SnO_x/Ag/SnO_x was fabricated on a glass by RF magnetron sputtering at room temperature. The multilayer of the SnO_x(40 nm)/Ag(11 nm)/SnO_x(40 nm) electrode shows the maximum optical transmittance of 87.3% at 550 nm and a quite low electrical resistivity of 6.5 × 10^− 5 Ω cm, and the corresponding figure of merit (T¹⁰/R_S) is equivalent to 3.6 × 10^− 2 Ω^− 1. A normal organic photovoltaic (OPV) structure of poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate)/polythiophene:phenyl-C60-butyric acid methyl ester/Al was fabricated on glass/SnO_x/Ag/SnO_x to examine the compatibility of OPV as a transparent conducting electrode. Measured characteristic values of open circuit voltage of 0.62 V, saturation current of 8.11 mA/cm² and fill factor of 0.54 are analogous to 0.63 V, 8.37 mA/cm² and 0.58 of OPV on commercial glass/indium tin oxide (ITO) respectively. A resultant power conversion efficiency of 2.7% is also very comparable with the 3.09% of the same OPV structure on the commercial ITO glass as a reference, and which reveals that SnO_x/Ag/SnO_x can be appropriate to OPV solar cells as a sound transparent conducting electrode.