Structure Of Films Research Articles

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.

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.

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.

The key role in the structure and properties of a novel CrNiTiMo high-entropy alloys films prepared by magnetron sputtering:bias voltage

In this study, CrNiTiMo high-entropy alloys films were prepared on 304 stainless steel and silicon wafer substrates by direct current magnetron sputtering and the effects of bias voltages (0 to −200 V) on microstructure, chemical composition, hardness and corrosion resistance were investigated. The results showed that the surface of the CrNiTiMo HEAs films exhibited equiaxed nanoparticles and are composed of uniformly distributed Cr, Ni, Ti, and Mo elements. Meanwhile, the films developed a columnar structure and formed a biphasic structure with body-centered cubic solid solution and amorphous phases. The roughness decreased and then increased with increasing bias voltage, and the film deposited at −50 V had the lowest roughness (1.02 ± 01 nm), which also had a maximum hardness of approximately 9.52 ± 0.2 GPa and a maximum elastic modulus of approximately 187 ± 6 GPa. In addition, all films showed better corrosion resistance compared to 304 stainless steel substrates at 3.5 wt% NaCl solution. The corrosion current density (icorr) of the films decreased and then increased with increasing bias voltages and reached the lowest icorr of about 2.49×10-8A/cm2, indicating that the films deposited at a bias voltage of −50 V had the best corrosion resistance. These was attributed to the formation of the passivation films mainly composed of TiO2 and Cr2O3 and the improvement of the surface quality of the film as well as the refinement of the columnar structure and particles.

Effects of thermal and laser annealing on the structure of Ge2Sb2Te5 thin films

In this study, we used Raman spectroscopy to compare the local structure of Ge2Sb2Te5 (GST) thin films with thicknesses of 90 nm and 271 nm that were crystallized through thermal annealing and laser radiation (laser annealing) during the recording of Raman spectra in situ. We found that for all crystallized films, the position of the main peaks in the Raman spectra was almost the same, and their structure corresponded to a hexagonal close packed state. It is noteworthy that the full width at half maximum (FWHM) of the main peaks varies considerably depending on the crystallization method used.

Cyclic hot corrosion behavior and mechanism of GH4738 superalloy in mixed molten salt

The research on the hot corrosion resistance of nickel-based superalloys is critical to determining and enhancing their service life. Therefore, this study investigates the cyclic hot corrosion behavior of GH4738 alloy coated with a mixed salt (75 wt.% Na2SO4+25 wt.% NaCl) at 750 °C and 800 °C. X-ray diffractometer (XRD), scanning electron microscope (SEM), energy dispersive spectrometer (EDS), and transmission electron microscope (TEM) are used to analyze the phase compositions and film structures of the corrosion products, as well as to explore the corrosion mechanism. The results show that a thicker oxide layer is formed at higher temperatures, indicating poorer hot corrosion resistance at elevated temperatures. The corrosion products form at both temperatures to show a distinct layered structure, the outer layer is mainly composed of Cr2O3 and a small amount of TiO2, while the inner layer consists of Al2O3, CrS, and TiS. In addition, it is found that the corrosion mechanism of O, S, and Cl elements in the corrosion process is synergistic and accompanied by alkaline melting.

Influence of the Acetylene Flow Rate and Process Pressure on the Carbon Deposition Behavior by Thermal Chemical Vapor Deposition Process

We used the chemical vapor deposition process to deposit carbon film at a high temperature (900 °C). The carbon films were deposited on AISI 1006 foils using an acetylene gas. We analyzed the carbon film deposited on the surface using Raman spectroscopy, scanning electron microscopy, and high-resolution transmission electron microscopy to define changes in the bonding structure of the carbon film. The results of Raman spectroscopy and high-resolution transmission electron microscopy revealed that as the acetylene flow rate increased, the shape of the deposited carbon film changed from graphene to graphite. In addition, in order to compare the quality of the carbon film in terms of mechanical and electrical properties, carbon films treated under various conditions were closely analyzed using nano-indenter and a sheet resistance meter. Therefore, the optimal condition (1 Torr-50 sccm) was selected in which graphene was uniformly deposited and had the lowest electrical resistance (500 Ω/sq) and highest hardness (12 GPa).

Structural Properties of Cs<sup>1+</sup> Doped H<sub>3</sub>PMo<sub>12</sub>O<sub>40</sub> Nanocrystalline Polyoxometalate Thin Films

The microwave assisted chemical bath deposition (MA-CBD) technique were used to deposite nanocrystalline thin films of polyoxometalates like phosphomolybdic acid (PMA) (H3PMo12O40) and Cesium (Cs+) doped phosphomolybdic acid (Cs-PMA) (Cs3-PMo12O40). Thermo gravimetric and Differential thermal analysis (TGDTA), Fourier transform infrared spectroscopy (FTIR), Energy dispersive X-ray analysis (EDAX), X-ray diffractometry (XRD) and Scanning electron microscopy (SEM) tools are used for the thermal, structural, morphological and compositional analysis of microwave treated H3PMo12O40 and Cs3- PMo12O40 thin films. The completion of decomposition process at 600 oC of Cs3-PMo12O40 compound is confirmed from TGDTA analysis. The polycrystalline spinel cubic crystal structure of H3PMo12O40 and Cs3-PMo12O40 thin films were confirmed from X-ray diffractometer. The crystallite size of H3PMo12O40 and Cs3-PMo12O40 compound found to be in the range of 50 - 53 nm. The formation of H3PMo12O40 and Cs3-PMo12O40 materials were confirmed from the presence of main four absorption peaks observed in the range from 800 cm-1 to 1100 cm-1. The SEM microphotographs analysis identify the microwave assisted H3PMo12O40 and Cs3-PMo12O40 films have spherical shaped porous nanocrystalline morphology. The grain size of H3PMo12O40 and Cs3-PMo12O40 synthesized material found to be in the range of 10 - 12 A˚ The stoichiometric preparation of H3PMo12O40 and Cs3-PMo12O40 thin films with presence of P, Mo, O and Cs peaks of metal ions is observed from EDAX spectra.

Topochemical Polymerization at Diacetylene Metal-Organic Framework Thin Films for Tuning Nonlinear Optics.

Developing the topochemical polymerization of metal-organic frameworks (MOFs) is of pronounced significance for expanding their functionalities but is still a challenge on third-order nonlinear optics (NLO). Here, we report diacetylene MOF (CAS-1-3) films prepared using a stepwise deposition method and film structural transformation approach, featuring dynamic structural diversity. The MOF structures were determined by the three-dimensional electron diffraction (3D ED) method from nanocrystals collected from the films, which provides a reliable strategy for determining the precise structure of unknown MOF films. We demonstrate the well-aligned diacetylene groups in the MOFs can promote topological polymerization to produce a highly conjugated system under thermal stimulation. As a result, the three MOF films have distinct NLO properties: the CAS-1 film exhibits saturable absorption (SA) while CAS-2 and CAS-3 films exhibit reverse saturable absorption (RSA). Interestingly, due to the topochemical polymerization of the MOF films, a transition from SA to RSA response was observed with increasing temperatures, and the optical limiting effect was significantly enhanced (∼46 times). This study provides a new strategy for preparing NLO materials and thermally regulation of nonlinear optics.

Comparative analysis of structural characteristics and thermal insulation properties of ZrO2 thin films deposited via chemical and physical vapor phase processes

ZrO2 is a flagship material for the development of efficient thermal barrier coatings not only for aerospace applications but also on steel molds for plastic injection, especially to produce high quality miniaturized parts of low environmental impacts. In the present study, ZrO2 thin films of thicknesses ranging between 4 and 40 μm were deposited on steel substrates by two key gas phase technologies, magnetron sputtering (PVD) and direct liquid injection metal organic CVD (DLI-MOCVD). The film morphology, structure and chemical composition were comparatively investigated and correlated to their heat transfer properties. All films were nearly stoichiometric and presented a columnar structure mainly formed of the monoclinic crystalline phase. The magnetron sputtering coatings were denser and smoother than the CVD ones, for which highly porous tree-like microstructures were observed without degradation of their mechanical properties. All films exhibited efficient thermal insulation properties, the thickest 40 µm magnetron sputtering coating displaying the most significant reduction in heat transfer. The CVD films provided the highest thermal gradient decrease across their thickness, probably thanks to their higher porosity associated to a multi-angle tree-like columnar structure, both acting as scattering zones of phonons involved in heat flow diffusion. By controlling the local deposition conditions influencing the nucleation and growth mechanisms, the film porous microstructure can thus be tuned to optimize the coating thermal properties.

Research on Chinese Hero Films from the Perspective of Film Narratology

From the perspective of film narratology, a comparative analysis of Chinese hero films reveals how many films use narrative techniques to construct heroic phenomena. Based on Chinese history, mythology, legends, or modern backgrounds, they shape heroic images with national characteristics and the spirit of the times, better disseminate culture and inherit spirit, and play a positive role in shaping national identity and cultural confidence. Based on this, this article mainly focuses on the research content of Chinese hero films from the perspective of film narratology, briefly describing the historical development, narrative structure, narrative themes and symbols of Chinese hero films, and comparing and analyzing the narrative structures, themes and techniques in different hero films, in order to provide corresponding reference for relevant personnel.

In-plane hard magnetic BaFe12O19 thin films grown on a-plane Al2O3 112¯0 substrates

Ferrimagnetic barium hexaferrite (BaFe12O19) thin films of varying thicknesses were grown on a-plane Al2O3 112̅0 substrates at elevated temperatures using pulsed laser deposition. X-ray diffraction measurements, Raman spectroscopy, and atomic force microscopy analyses were used to investigate the BaFe12O19 film growth and structure. The results indicate that the formation of an α-Fe2O3 ‘bridge layer’ promotes the growth of a BaFe12O19 phase showing an in-plane uniaxial magnetic anisotropy with an easy-axis of magnetization along the [ 0001 ] hexagonal c-axis direction. The crystallographic relationship between the existing phases is given by BaFe12O19 101̅0 //α-Fe2O3 112̅0 //Al2O3 112̅0. As the thickness increases, the fraction of the BaFe12O19 phase increases further. This is accompanied by a change in grain morphology turning from a columnar to a more elongated shape, where the short axis of the BaFe12O19 grains points along the [ 0001 ] easy axis direction.

Semiconductive Tendency of the Passive Film Formed on Super Austenitic Stainless Steel SR-50A in Acidic or Alkaline Chloride Solutions

Stainless steel is widely used in various industrial fields due to its excellent corrosion resistance and mechanical properties. The key to this corrosion resistance is the thin passive film that naturally forms on the metal surface. Passive films are characterized by oxide film theory and adsorption theory, each uniquely explaining the structure and mechanism of the protective film on the metal surface. Research on the semiconductive properties of passive films on stainless steel offers diverse viewpoints, classifying theories into the point defect model and the bipolar fixed charge-induced passivity. Specific changes in passive film attributes that lead to degradation, however, are not fully understood. In this study, we analyzed the inner and outer layers of the passive film on super austenitic stainless steel SR-50A under various conditions in acidic and alkaline chloride environments. The interpretations of these results were based on the point defect model and the bipolar model for the passivation mechanism, and correlations between p-type and n-type semiconductor properties and passivation behavior were examined. The surface of the stainless steel forms a passive film comprising two layers with p-type and n-type semiconductive properties, independent of the pH of the solutions. The corrosion resistance increases as the p-type and n-type semiconductive tendencies become more balanced, consequently enhancing the properties of the passive film.

The pH-dependent properties of cuprous oxide thin films prepared by electrochemical deposition for liquid petroleum gas sensing

Efficient liquid petroleum gas sensing was investigated by modulating the pH level (8, 9, 10, 11, and 12) of electrochemically deposited nanostructured cuprous oxide thin films in a lactate bath. The synthesized films were characterized by surface contact angle, XRD, SEM, UV–Vis absorption, Mott-Schottky, and AC impedance spectroscopy measurements. These displayed a unique initial increment or decrease followed by a persistent decrement or increment at pH 9–10. This turning pH point exhibited the least wetting polycrystalline Cu2O growth with the smallest crystallite size of ∼ 45 nm, the highest dislocation density of ∼50 µm−2, and a strain of 0.03 according to X-ray diffraction. SEM micrographs identified ∼ 1 µm-sized, closely structured grains with trigonal-prismatic shapes. The Mott-Schottky plots drawn from C-V measurements revealed a significant dependence of flat band potential and free carrier density on the deposition bath pH level. Cu2O films deposited using the lactate bath changed the conductivity at pH 9 from n-type to p-type when increasing the pH value. With the conductivity transition, films prepared at pH 9 displayed a relatively high direct band gap energy of 2.28 eV. Liquid petroleum gas (LPG) sensing at 70 °C demonstrated the most substantial gas response of 11.5 % at pH 10 Cu2O films. Cu2O thin films deposited at pH 9 emerged as the most stable and reproducible p-Cu2O LPG sensor, with response and recovery times ranging from 20 to 25 seconds. Remarkable changes in the film structures and morphologies were revealed with pH values above 9 after the gas exposure. The grain shape and distribution of pH 9 remained unchanged, assuring the stability of the sensing platform.

Biodegradable active composite film based on pea protein isolate, sage seed gum, and cumin essential oil: Fabrication and characterization

The present study perused the physicochemical, mechanical, thermal, barrier, and optical properties of pea protein isolate (PPI)-Sage seed gum (SG) (3:1, 1:1, and 1:3) composite films incorporated with cuminum essential oil (CEO, 0, 1, and 2 %). Results indicated that the thickness, contact angle (CA), yellowness index (a*), total color differences (∆E), and opacity (OP) significantly enhanced with increasing PPI portion and CEO concentration (p < 0.05), as well as heterogeneous and inconsistent structure were increased in film surface due to protein agglomeration and oil droplets. However, the moisture content (MC), water solubility (WS), and swelling ratio (SR) decreased. Results also indicated that the antioxidant property significantly increased (P < 0.05) following the increase in CEO concentration. The highest tensile strength (TS) and elastic modulus (EM) and the least elongation at break (EAB) in PPI 3-SG 1–0 % were estimated. The potential antimicrobial property of CEO containing film was confirmed, and the maximum inhibition zone for E.coli, S.aureus, C.albicans, and A.niger were measured in film containing 2 % CEO. The barrier properties of the film against water and oxygen (WVP, OXP) diminished with increases the SG ratios, due to the hydrophilic nature of SG. The FTIR analysis identified the functional groups in film components and the interaction between film components. The DSC thermogram indicated the thermal stability of films and the highest decomposition temperature in PPI 3-SG 1–2 % film. XRD revealed a semi-crystalline structure of biopolymer active films. With the increase of SG portion and CEO concentration, the crystallinity of the films was enhanced. Results also indicated that prepared films were more than 90 % biodegradable.

Structural, electronic, and optical properties of Zn-doped V2O5 thin films

V2O5 shows a diverse range of applications due to its remarkable electronic and optical properties. This research is designed to tune the electronic and optical properties of V2O5 through modification in the energy band profile by varying Zn doping concentration. Density functional theory (DFT) calculations were used to investigate the Density of States (DOS) spectra for pure V2O5, exhibiting the prominent contribution of V-d and O-p orbitals, representing the p-d hybridized orbitals along with additional Zn-d orbital contribution in Zn-doped compositions. The effects of doping on the structural, morphological, elemental, and optical properties of the developed thin films were investigated employing x-ray diffraction (XRD), scanning electron microscope (SEM), x-ray dispersive spectroscopy (EDX), and spectroscopic ellipsometry (SE), respectively. x-ray diffraction analysis revealed the orthorhombic crystal structure in thin films. Surface morphology depicts the uniformly distributed compact rod-like features. The experimentally calculated band gap was found to decrease with Zn doping from 2.77 eV for pure V2O5 to 2.45 eV for maximum doping content. A significant variation is recorded in optical parameters like the increase in absorption coefficient and optical conductivity, which makes these more favorable for optoelectronic devices, particularly focusing on photovoltaics.

Reduction of a two-dimensional crystalline MoO3 monolayer

The atomic structure of MoOx films formed upon a gradual thermal reduction of an ordered MoO3 monolayer on the Pd(100) substrate was explored via surface science characterization techniques and density functional theory (DFT) calculations. Two main reduction stages were identified. First, the initial oxygen excess was gradually eliminated by altering the domain boundary length, orientation, and atomic structure. The films nevertheless remained O-rich, with numerous terminal oxygen atoms (formation of MoO groups), and an elevated work function. Second, multiple ordered O-lean phases were formed, characterized by either very few or no terminal oxygen atoms, and a much smaller surface work function. According to calculations, the positive charging of the Pd substrate stabilizes the oxygen excess during the first stage, but during the second reduction stage, the substrate becomes negatively charged, stabilizing enhanced cation oxidation states. On their basis, the mechanisms underlying the oxygen release from the initial c(2 × 2) domains were disclosed. The experiments showed that the film reduction is perfectly reversible, which highlights the very promising properties of the MoO3/Pd system for heterogeneous catalysis.

The effect of charge screening for cationic surfactants on the rigidity of interfacial nanoparticle assemblies

HypothesisFunctionalizing colloidal particles with oppositely charged surfactants is crucial for stabilizing emulsions, foams, all-liquid structures, and bijels. However, surfactants can reduce the attachment energy, the driving force for colloidal self-assembly at interfaces. An open question remains on how the inherent interfacial activity of cationic surfactants influences the interfacial rigidity of particle-laden interfaces. We hypothesize that charge screening among cationic surfactants regulates the rigidity of oil/water interfaces by reducing the attachment energy of nanoparticles. ExperimentsWe investigate the interfacial rigidity of cetyltrimethylammonium bromide (CTAB) functionalized silica nanoparticles (Ludox® TMA) by analyzing the shape deformation of 1,4-butanediol diacrylate (BDA) droplets under varying salt and alcohol concentrations. The nanoparticle packing density is assessed using scanning electron microscopy. Attachment energy is characterized through interfacial tension measurements, three-phase contact angle analysis, and CTAB adsorption studies. We also examine the effects of interfacial rigidities on the structure of bijel films formed via roll-to-roll solvent transfer-induced phase separation (R2R-STrIPS) using confocal laser scanning microscopy. FindingsIncreasing salt and alcohol concentrations decrease the interfacial rigidity of CTAB-functionalized nanoparticle films by reducing the interfacial tension. The contact angle has a minor influence on the rigidity. These results indicate that CTAB charge screening weakens the nanoparticle attachment energy to the interface. Controlling the rigidity enables the mass production of bijel sheets with consistent flatness, which is crucial for their potential applications in catalysis, energy storage, tissue engineering, and filtration membranes.