Structure Of Films Research Articles

Metal-semiconductor-metal UVA photodetector based on TiO2 thin films synthesized via liquid phase deposition method

In this work, titanium dioxide (TiO2) thin film-based metal-semiconductor–metal (MSM) ultraviolet (UV) photodetectors (PDs) were fabricated on glass substrates via liquid phase deposition (LPD) technique at various deposition time in the range of 3–6 h. Varying deposition time significantly impacted the physical properties of the films. Increasing the deposition time revealed a mixture of clusters and hexagonal-like structures in film’s morphology. The energy band gap of the TiO2 films decreased from 3.30 to 3.09 eV upon increasing the deposition time. Photodetection characteristics were examined by exposing the MSM UV PD to 390 nm UV light with an intensity of 1.6 mW cm−2 and a bias voltage of 5 V. The fabricated PDs implied characteristics of I-V ohmic contact. The optimum photodetection characteristics were achieved for TiO2 film deposited at 6 h which exhibited 36.9 μA maximum photocurrent, 20080.3% sensitivity, 201.80 gain, 225 mA W−1 responsivity, 81.07% external quantum efficiency, 0.276 s response time, and 0.274 s recovery time. The photoelectric properties of the films were strongly affected by the increased grain size and improved crystallinity of the films due to the prolonged deposition time. The optimum film demonstrated its potential to be a promising candidate for UV PD applications.

Preparation and properties of fluorinated VAc-VeoVa10 latex emulsified with allyl nonyl phenoxy propyl alcohol polyoxyethylene ether ammonium sulphate

Purpose The traditional VeoVa10-VAc copolymer latex, which prepared via the emulsion polymerization of the mixed monomers of VAc and VeoVa10, has the poor water resistance and thermal stability because of the migration of the conventional emulsifier molecules and the low bond energy of C-C bond. The purpose of this work is that the fluorinated monomer is used to modify the latex. The film of the resultant latex has the C-F bond with high bond energy and low surface energy, which can effectively improve the heat resistance and water resistance of the resultant film. In addition, the reactive emulsifier is used to replace the conventional emulsifier. The drawbacks of the conventional emulsifier molecules migrate and desorb can be avoided when the polymer latex is stored, thereby also improving the water resistance. Design/methodology/approach The modified VAc-VeoVa10 latex has been successfully synthesized via the semi-continuous seeded emulsion polymerization, which VAc and VeoVa10 is used as the main monomers and HFMA was used as the functional monomer. KPS and reactive surfactants of SE-10 were used as the initiator and emulsifier, respectively. The structure of resultant latex film was characterized by Fourier transform infrared spectroscopy (FTIR). The latex films were tested by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and contact angle (CA). The particle size and its distribution of the latex were measured by the nano particle size analyzer. Findings The factors that had an influence on the properties of the latex and the film were investigated in detail. The stability of the resultant latex is good. The average particles of the latex and its distribution are small and uniform, respectively. In comparison with the conventional latex film, the thermal stability and hydrophobicity of the resultant latex film are improved obviously. Practical implications The resultant latex can be used in both the waterborne interior and exterior wall coatings, pickering stabilized waterborne polymer dispersions, polymer powders, environmentally friendly polymer-modified waterproof mortar and other fields, which can be satisfied with the high demand of thermal stability and hydrophobicity. Originality/value The modification of poly (VAc-VeoVa10) by reactive surfactant and fluorinated monomer is seldom reported. In this study, the fluorinated poly (VAC-VeoVa) latex is prepared via the reactive surfactants, which VAc and VeoVa10 is used as the main monomers and hexafluorobutyl methacrylate is used as the functional monomer. Potassium persulfate (KPS) and allyl nonyl phenoxy propyl alcohol polyoxyethylene ether ammonium sulfate are used as the initiator and emulsifier, respectively.

Modeling the influence of technological parameters of the magnetron sputtering process using the Caroline D12C system on the proportion of nanocrystallites in the structure of thin silicon films

Modeling the influence of technological parameters of the magnetron sputtering process using the Caroline D12C system on the proportion of nanocrystallites in the structure of thin silicon films

Impact of Silver Incorporation and Flash-Lamp-Annealing on the Photocatalytic Response of Sputtered ZnO Films

Thin films of silver-doped zinc oxide (SZO) were deposited at room temperature using a DC reactive magnetron co-sputtering technique using two independent Zn and Ag targets. The crystallographic structure, chemical composition and surface morphology of SZO films with different silver concentrations were correlated with the photocatalytic (PC) properties. The crystallization of the SZO films was made using millisecond range flash-lamp-annealing (FLA) treatments. FLA induces significant structural ordering of the wurtzite structure and an in-depth redistribution of silver, resulting in the formation of silver agglomerates. The wurtzite ZnO structure is observed for silver contents below 10 at.% where Ag is partially incorporated into the oxide matrix, inducing a decrease in the optical band-gap. Regardless of the silver content, all the as-grown SZO films do not exhibit any significant PC activity. The best PC response is achieved for samples with a relatively low Ag content (2–5 at.%) after FLA treatment. The enhanced PC activity of SZO upon FLA can be attributed to structural ordering and the effective band-gap narrowing through the combination of silver doping and the plasmonic effect caused by the formation of Ag clusters.

Features of the structure and resistive switching of titanium oxide films on Y-cut piezoelectric substrate of a LiNbO3 crystal

The difference in the structure of titanium oxide thin films deposited on fused silica substrates and the Y-cut of a lithium niobate crystal is demonstrated. In both cases, the film is amorphous; however, an insignificant amount of rutile crystallites is observed in the film formed on the Y-cut of the lithium niobate crystal. It is shown that the electrical characteristics of the films depend not only on the material of the substrate, but, in the case of the lithium niobate substrate, also on the direction of an electric field. This is caused by the deformation of the substrate due to the inverse piezoelectric effect.

Flexible Near‐Infrared Organic Photodetectors With Ultralow Dark Current by Layer‐by‐Layer Blade Coating

AbstractNear‐infrared organic photodetector (NIR OPD) is promising for emerging wearable biosensing applications. However, their practical application is hindered by the high dark currents of devices that limit the detection of faint light. In this work, highly sensitive flexible NIR OPDs are presented with ultralow dark currents, fabricated using a layer‐by‐layer blade coating (LBL‐BC) technique. In the active layer, a fully fused‐ring molecule FM2, featuring a fixed molecular skeleton, is employed as an electron acceptor to reduce the trap density. The LBL‐BC method enhances the film order and phase purity of the active layer, significantly reduces the trap density of states, and optimizes the vertical phase separation structure of the thin film, thereby preventing reverse charge injection. As a result, a highly sensitive flexible NIR OPD is developed exhibiting an ultralow dark current density of 4.83 × 10−9 A cm−2 at −0.3 V bias and an extremely low noise current density of 7.65 × 10−15 A Hz−1/2 at 10 Hz, comparable to commercial silicon photodiodes. Furthermore, this flexible device is successfully applied for real‐time monitoring of human heartbeat rate, oxygen saturation, and motion recognition. These findings advance the development of highly sensitive NIR OPDs and their application in wearable biosensing technologies.

Angle-dependent ion-beam etching of RuAl thin films for structuring GHz-frequency electronics

Abstract The ruthenium aluminide (RuAl) alloy is a promising electrode material for wireless surface acoustic wave sensors working under harsh conditions at high temperatures. However, during the structuring of RuAl thin films using ion-beam etching, etched material can redeposit at the edges of the electrodes and form objects, so-called fences, on top of the structured features. These decrease the high-temperature stability and lead to an undesired alteration of the sensor performance. In this work, the angle-dependent ion-beam etching of RuAl thin-films was investigated to inhibit the formation of such fence structures. The etch rate was determined as a function of the etching angle between ion-beam and sample surface in a range between 90° and 40°.
Furthermore, finger structures with pitches below 500 nm, which are required for devices working in the intended GHz regime, were patterned to study the influence of the etching angle on the profile of the RuAl electrode fingers using transmission electron microscopy and energy-dispersive X-ray spectroscopy. The results show that an etching angle of 50° results in the highest etch rate. For etching angles of 50° and below, the width of the fences is reduced below 10 nm, so they break off during standard resist removal procedures. Such low etching angles lead to shadowed areas on the side of structured features, in which unetched material remains. However, this material can be removed by using a two-step etching process combining a 50° step with a 90° step. This process is capable of structuring fence-free trapezoidal-shaped electrode finger profiles. Therefore, the developed process is well suited for the fabrication of high-temperature GHz-frequency RuAl electrodes.

Selectable growth and electronic structures of two-dimensional layered InSe and In2Se3 films

Selectable growth and electronic structures of two-dimensional layered InSe and In2Se3 films

Transmission anomalies in 2D photonic crystals from the checkerboard family: from broken to hidden symmetries and plasmon “spoofing”

In a field representation, the main symmetry of the electromagnetic response of complementary metal film structures is described by the Babinet principle, which is expected to be strictly obeyed by structures in vanishingly thin films of a perfect electric conductor. On the other hand, a softer version of this based on transmittance, the transmittance Babinet principle (TBP), is not so restrictive. The goal of this work is to study how severely this broken symmetry affects the optical response of such structures. We consider two geometrically distinct series of planar complementary structures from the checkerboard family: regular and bowtie. The self-complementary structure of these series is known to be very singular and breaks even the rigorous Babinet principle. Here, we study complete simulated transmittance spectral maps (T-Maps), which accumulate the whole spectral response of an entire series of structures in a single plot. The ab initio simulated T-Maps of these 2D photonic crystals were simulated for linearly polarized waves propagating perpendicular to these planar structures, made in a vanishingly thin film of a perfect electric conductor. While we confirm the expected long wavelength validity of the TBP, we show that in the frequency range where diffraction effects dominate, the standard derivation of the TBP no longer applies, and with the help of our T-Maps, we demonstrate a total collapse of the TBP in the structures considered. We show that this broken symmetry practically eliminates all but one transmission band on the hole side of the T-Maps and that the remaining strong band is a “spoof” plasmon, free of multiple frequency replicas, an important feature for optical filter applications. In addition, by symmetry arguments and simulations, we discovered that the T-Maps for bowtie and doubled-period regular structures are identical. We discuss how this hidden symmetry can benefit various applications by providing a convenient scaling, whereby simplified structures can deliver a tailored response.

Thermal stress concentration points and stress mutations in nano-multilayer film structures

Abstract In the multilayer film-substrate system, the buckling, delamination and cracking of the film caused by the thermal stress concentration point and the stress mutation are the main factors leading to the failure of the corresponding device function. In this paper, we studied the multilayer film system composed of the substrate and the three-layer film. The thermal stress distribution inside the structure was calculated by the finite element method (FEM). It was observed that there was a large thermal stress difference between the layers. This is mainly due to the mismatch of thermal expansion coefficient (CTE) between materials. Different materials have different degrees of change with the external environment temperature, and the layers are squeezed. In particular, there are obvious thermal stress concentration points at the corners of the base layer and the transition layer, which is due to the sudden change of the shape at the geometric section of the structure, resulting in a sudden increase in local stress. In order to solve this problem, we have chamfered the substrate and added an intermediate layer between the substrate and the transition layer to analyze whether the difference between the thermal stress concentration point and the thermal stress can be reduced or eliminated, and the service life of the multilayer structure can be extended. The conclusion shows that chamfering and increasing the intermediate layer can reduce the stress mutation and weaken the thermal stress concentration point, which can effectively improve the interlayer bonding strength.

Preparation and Keep-Refreshing Effect of Chitosan/Sea Buckthorn Polysaccharide Composite Film on the Preservation of Yellow Cherry Tomatoes.

In this study, sea buckthorn polysaccharides (SBP) were added as functional substances to chitosan (CS), and chitosan/sea buckthorn polysaccharide (SCS) composite films were prepared using the casting method. The effects of SBP addition on the optical properties, physical properties, mechanical properties, structure, antioxidant activity, and antibacterial activity of the SCS composite films were studied, and the prepared SCS composite films were used to preserve yellow cherry tomatoes. The results showed that SCS composite films exhibited good UV resistance, water solubility, and antioxidant activity, but its apparent structure, hydrophobicity, and mechanical properties needed further improvement. Meanwhile, SBP has inhibitory effects on all 8 experimental strains. In addition, the SCS composite film with the addition of 200 mg/L SBP could reduce the weight loss rate of yellow cherry tomatoes, maintain hardness, delay the decrease of total soluble solids, titratable acid, and Vitamin C content, and inhibit the accumulation of malondialdehyde. SCS composite films are beneficial for enhancing the quality of yellow cherry tomatoes during storage, and their application in fruit and vegetable preservation has development prospects.

Structural transition in the single layer growth of diindenoperylene on silica.

When forming a film on a substrate, rod shaped organic molecules can order in lying-down or standing-up phases. We have studied the growth of diindenoperylene films on amorphous silicon dioxide by means of molecular dynamics simulations and analyzed the film structure. The vapor deposition process was emulated by depositing single molecules at a fixed rate on the substrate. At 400K, we observed a transition from disordered lying-down to standing-up molecules, which agrees well with experimental observations. This transition, which depends sensitively on the kinetic parameters, requires both a sufficiently high thermal energy to overcome the energy barrier and a sufficiently large cluster size. Our results indicate that a higher degree of initial disorder in the lying-down phase results in a larger probability for the system to undergo the transition to the standing-up phase.

Ta5+-substitution effects on crystal structure and ferroelectric property in HfO2-based films

To investigate the Ta5+-substitution effects on crystal structure and ferroelectric property in HfO2-based films, Ta x Hf1−x O2+δ films with various film thicknesses and Ta content were prepared. The ferroelectric orthorhombic phase was formed in a wide film thickness range of 20–100 nm while in a narrow composition range of x = 0.10–0.14. These thickness-insensitive and composition-sensitive characteristics of Ta5+-substituted HfO2 film are similar to Y3+ rather than Zr4+. The X-ray photoelectron spectroscopy measurement suggests that the ionic state of Ta is not reduced and Ta x Hf1−x O2+δ film has an excess oxygen state. The excess oxygen may consist of a combination of oxygen vacancies and more interstitial oxygens. These defects facilitate the formation of the ferroelectric phasebut also decrease the breakdown voltage and increase the leakage current in Ta5+-substituted HfO2 films. On the other hand, the generation of excess oxygen indicates the possibility of controlling oxygen vacancies which deteriorate fatigue and retention properties.

Assessing the Fatigue Stress Behavior of Starch Biodegradable Films with Nanoclay Using Accelerated Survival Test Methods

A destructive degradation model was applied on films made from different concentrations of starch, glycerol and nanoclay using various elongation levels as a stress variable at different stress times and stretch cycles. The log tensile quotient (logarithm of the tensile strength to the corresponding break cycle) was recorded as the response variable. The log tensile quotient increased, and the log exact break time decreased, as the elongation level increased. The treatment containing the highest starch and nanoclay and lowest glycerol content proved to be the most resistant to stress conditions and the most versatile in relation to the varying log tensile quotients, while the treatments containing the lowest nanoclay and highest glycerol contents, regardless of the starch concentration, manifested the lowest log tensile quotient at higher levels of log exact break time. According to multiple regression findings, the break cycle governed mostly the stress conditions in the degradation model, followed by the sample ID and the log exact break time. The term log tensile quotient, attempted for the first time on data concerning biodegradable films enhanced with nanoclay, seems very promising for deeper research due to its ability to retrieve predictive information from survival equations and to discriminate the difference between film structures.

Optimization of Post-Annealing Temperature of RF Magnetron-Sputtered ZnO Thin Films for Enhancing Performances of UV Photodetectors

In this study, we examined the surface morphology and crystal structure of RF-sputtered ZnO thin films that were annealed at various temperatures. Also, we fabricated UV photodetectors with an Au-ZnO-ITO sandwich structure, utilizing the thin films annealed at 600 °C. The surface roughness of the film initially increases and then decreases as the annealing temperature rises, and the crystalline quality improves with an increase in the annealing temperature. Due to the Schottky heterojunction formed by the Au-semi contact, the fabricated UV photodetector exhibits a responsivity of 7.91 mA W−1 under 405 nm UV light. And the device demonstrates high response stability and rapid response sensitivity, with a swift rise time of 80 ms at a light intensity of 2.56 mW cm−2.

Strategies for the incorporation of organosolv lignin in hydroxypropyl methylcellulose-based films: A comparative study

Organosolv lignin extracted from vine pruning residues was added to hydroxypropyl methylcellulose (HPMC)-based films using three strategies: i) lignin incorporated into the film (lignin-based film), ii) lignin nanoparticles (LNPs) incorporated into the film (LNPs-based film), and iii) lignin coated on HPMC films' surface (lignin-coated film). The films obtained by solvent casting were evaluated in terms of morphology, water barrier and mechanical properties, and antioxidant capacity. Results showed that LNPs incorporation did not affect the films´ water vapour permeability (WVP). Nonetheless, the lignin-based and lignin-coated films improved the water barrier properties of HPMC-based films, achieving a 31.5 and 36 % reduction of WVP, respectively. The morphological evaluation, performed by scanning electron microscopy, revealed films' morphology changes with the lignin incorporation, which was more evident in the lignin-based films. Fourier transform infrared spectroscopy (FTIR) showed minor changes in the film's structure using the different lignin incorporation methods. The mechanical properties were improved, including a significant increase in the tensile strength in the lignin-based and lignin-coated films. All films showed high radical scavenging activity (RSA) after 24 h, with a gradual increase in the lignin-coated films throughout time. The lignin-coated films showed to be the most promising incorporation strategy to improve the HPMC-based film's properties.

Preparation and characterization of high-stability gel foam for fracture plugging in reservoirs

A high-stability gel foam is successfully prepared by forming a gel structure in the liquid film using polymer and crosslinker. The foaming properties, gel characteristics, foam stability, and microstructure of the high-stability gel foam are systematically studied. Although increasing the viscosity of the liquid film reduces the foam volume, it significantly enhances the foam stability. Considering the foaming properties, gel characteristics, and economic benefits, the optimal formulation of the gel foam system is determined to be 0.8% surfactant, 0.3% hydroxypropyl guar gum (HPG), and 0.2% organic titanium crosslinker (ATC). Microstructural analysis revealed that, compared to water-based and polymer foams, gel foam has smaller bubble sizes, lower drainage rates, and slower coarsening rates. This improvement is mainly attributed to the increased viscosity and thickness of the liquid film after gel and the formation of a three-dimensional network structure. Water loss rate experiment shows that the foam stability is stronger when the liquid film has certain viscosity and elasticity to resist external disturbances. However, higher viscosity and film strength do not necessarily result in better foam stability. The final water loss rate of the gel foam after being placed at 100 °C for 10 h is 74.45%, much lower than that of other higher-strength gel foams (greater than 99%). Fracture plugging experiments demonstrated that the plugging rate of gel foam is high (80%), whereas water-based foam achieved only 37.5%. The gel foam can effectively plug fractures and expand the swept volume, showing great potential for improving oil reservoir recovery.

Study of endogenous chloride ion content on the behavior of steel bar depassivation in sea sand concrete

In this study, we investigated the chloride concentration in sea sand that induces corrosion in steel bars, as well as the corrosion mechanisms of steel bar within sea sand concrete. Different analytical techniques indicated that the chloride concentration for steel bar corrosion in sea sand concrete was 0.03% (when the water-binder ratio was in the range of 0.4∼0.6). First, the calcium silicate in sea sand concrete reacted with Fe3+ to reduce the compactness of the oxide layer and increase the corrosion risk of steel bars. Second, as the water-binder ratio and chloride concentration gradually increased, the loose structure of the passive film increased, and the relatively dense structure decreased, which made it easier for chloride ions to penetrate the outer layer of the passive film to erode the steel matrix. Besides, the reaction of chloride ions with C3A to form Friedel's salt optimized the pore structure and reduced the content of free chloride ions. However, the adverse effect of chloride ions on the passive film of steel bars exceeded the beneficial impact of porosity reduction. These findings allow us to better apply sea sand to improve the sustainable development of environment.

SYNTHESIS of P(N-ISOPROPYL ACRYLAMIDE - HYDROXYPROPYL METHACRYLATE) THERMO RESPONSIVE COPOLYMER FILMs BY INITIATED CHEMICAL VAPOR DEPOSITION METHOD

This study illustrates the deposition of thermo responsive p(N-isopropyl acrylamide-hydroxypropyl methacrylate) p(NIPAAm-HPMA) copolymer thin films by initiated chemical vapor deposition (iCVD) method using tert-butyl peroxide (TBPO) as the initiator. Copolymers were deposited at three different HPMA flow rates and the effects of NIPAAm/HPMA flow rate ratio on the deposition rate, structure and responsive properties of the as-deposited films were investigated. The highest deposition rate of 50 nm/min was observed for the copolymer deposited using lowest NIPAAm/HPMA monomer ratio studied. The deposition rate showed a significant increase with decreasing NIPAAm/HPMA flow ratio. Results of FTIR and XPS spectroscopy analyses revealed a significant preservation of structural retention in iCVD p(NIPAAm-HPMA) thermo-responsive films. Lower critical solution temperatures (LCST) of p(NIPAAm-HPMA) films were determined by carrying out a temperature-dependent contact angle analysis. Accordingly, it was shown that LCST was varied between 19 and 23 oC, which was observed to be dependent on the NIPAAm/HPMA monomer ratio. That LCST range is considerably below the literature- reported values for pNIPAAM, which makes the as-deposited copolymer suitable for applications that require thermos-responsive properties at lower temperatures.

Coral-inspired fabrication of Ag-Cu2O-zwitterionic polymers-phosphor films with day and night antifouling properties

Inspired by the antifouling process observed in fluorescent corals, this study introduces a novel functional antifouling film consisting of Ag-Cu2O nanocomposites, zwitterionic polymers, and a phosphor substrate. Zwitterionic polymers serve as a dispersive medium for Ag-Cu2O nanocomposites, enabling a uniform coating and optimal structural through spin-coating. During daylight hours, visible light irradiation excites Ag-Cu2O nanocomposites to produce reactive oxygen species (ROS), which cooperates with the hydration layer, exhibit a high-level antifouling effect. Notably, the unique structural coating can emit a weak coral-like fluorescence at night, sustaining ROS release and further enhancing antifouling performance. The assembly structure of the composite film was studied by scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS) and water contact angle (WCA), while its antifouling performance was evaluated through antibacterial tests and a 30-day light-dark cycle anti-algae attachment experiment. The distinct nighttime antifouling capability contributes to 97.30 % anti-algae settled rate over a 30-day diurnal cycle. Moreover, we also investigated the effect of phosphor color on the composite film's antifouling properties. The blue phosphor group exhibited greater antifouling performance than the green or transparent phosphor group. The composite film created with multiple synergistic mechanisms exhibited auspicious antifouling performance. Further improvement and development of this composite film could unlock even greater potential for its antifouling properties.