Film Substrate Research Articles

Enhanced adhesion strength of copper deposited epoxy composite films for chip substrates by tuning copper oxide and internal stress

Copper oxides and internal stress have an obvious influence on adhesion strength of copper deposited polymer composites. However, the effect of the evolution behavior of copper oxides and internal stress on adhesion force of chip substrates is no clear and rare far. Herein, the copper deposited epoxy-phenolic/silica composite film with different desmear time was fabricated by using wet chemistry and electrochemistry methods. The chemical structure, surface roughness, morphology, surface chemical state, crystal structure and adhesion strength of copper and epoxy resin substrate were characterized by scanning electron microscope (SEM), interference microscope, X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR). The adhesion strength of samples is increased from 3 N/cm to 4.7 N/cm. The effect of the evolution behavior of copper oxides and internal stress on adhesion strength of copper deposited epoxy resin composite films at the interfaces was systematically investigated, the mechanisms and reason of increasing adhesion strength and interfacial adhesion failure for copper deposited epoxy resin composite substrates were revealed. This work will provide a guidance in theory and experiment to enhance interfacial adhesion force of epoxy resin composite films for advanced substrate in the future.

Construction of superhydrophobic PDMS@PS-SiO2 films with self-cleaning properties via a simple template approach for efficient water harvesting

Superhydrophobic materials have a wide range of applications in the fields of anticorrosion, anti-dust, anti-ice and anti-fouling due to their self-cleaning, anti-wetting and anti-bacterial properties. However, there are problems in the preparation process, such as cumbersome processes, inconsistent properties of the prepared hydrophobic surfaces, and environmental pollution by fluoropolymers. Therefore, it is especially critical to develop a simple method to prepare green and efficient superhydrophobic surfaces. Here, a simple template method is used to prepare superhydrophobic surfaces. The Polystyrene (PS) honeycomb patterned film was used as a template, and the microstructure inside the pores of the PS film was changed by filling silica particles inside the template. Reproduction of the surface microstructure of PS films using polydimethylsiloxane (PDMS). The shape and size of the template structure are adjusted to regulate the surface microstructure, which in turn achieves the control of the overall hydrophobicity. The transition from PDMS hydrophobicity to superhydrophobicity was achieved by changing the structure of the PS film surface. The PDMS@PS-SiO2 film achieved a water contact angle of 153°, an increase of 48° compared to the original film. Tested at different temperatures and pH, PDMS@PS-SiO2 film has good stability performance. Immersing the film in pollutants still maintains its own cleaning properties and is not easily contaminated for long-term use. The morphology of the film surface was observed using electron microscopy to demonstrate the successful preparation of the film as well as to explore the reason for the variation of the hydrophobic performance. In addition, using PDMS@PS-SiO2 film as the substrate of the hydrophobic film, the bionic water-collecting film was prepared with a water-collecting performance of 20.12 ± 0.15 mg min−1 cm−2. The reuse of mist was achieved. This method provides a new idea for the preparation of superhydrophobic surfaces and solving the problem of water shortage.

Magnetooptical gyrotropic effects in nanosized BiYIG films and diamagnetic YAG substrates

Magneto-optical gyrotropic Faraday and Kerr effects are studied in the BiY2Fe5O12 films with thicknesses ranging from 16 to 55 nm, in the wavelength range of 295 nm < λ < 830 nm (4.2–1.5 eV), and under magnetic fields of up to 1.2 T. It is shown that films produced by ac magnetron sputtering on the single-crystalline diamagnetic yttrium aluminum garnet substrates Y3Al5O12 (001) exhibit high structural and magneto-optical quality. The Verdet constant for diamagnetic Y3Al5O12 is determined, and the magnitude of the Kerr effect is estimated for the polished substrate. It is shown experimentally that for a substrate with diffusely reflective backside, the Kerr effect is about zero, except in the high-energy region. For all BiY2Fe5O12 films investigated, in the saturating magnetic fields of approximately 0.16–0.2 T, the value of specific Faraday rotation reaches 20 deg/μm (200 000 deg/cm), while the value of the Kerr effect reaches approximately 20 min (5.8 mrad). The critical thickness of the film–substrate interface was estimated, highlighting variations in the Kerr effect spectra associated with a decrease in the Bi content in thin films with the thicknesses of below 27 nm.

Role of sputtered atom and ion energy distribution in films deposited by physical vapor deposition: A molecular dynamics approach

We present a comparative molecular dynamics simulation study of copper film growth between various physical vapor deposition (PVD) techniques: a constant energy neutral beam, thermal evaporation, dc magnetron sputtering, high-power impulse magnetron sputtering (HiPIMS), and bipolar HiPIMS. Experimentally determined energy distribution functions were utilized to model the deposition processes. Our results indicate significant differences in the film quality, growth rate, and substrate erosion. Bipolar HiPIMS shows the potential for an improved film structure under certain conditions, albeit with increased substrate erosion. Bipolar HiPIMS (+180 V and 10% Cu+ ions) exhibited the best film properties in terms of crystallinity and atomic stress among the PVD processes investigated.

Construction of a MoOx/MoS2 Heterojunction via the Surface Sulfurization of the Oxide and Its Photocurrent-Switching Characteristics in the Range of the Broadband Light Spectrum.

In order to utilize the longer wavelength light, the surface sulfurization of MoO3 was carried out. The photocurrent responses to typical 650, 808, 980, and 1064 nm light sources with Au gap electrodes were investigated. The results showed that the surface S-O exchange of MoO3 improved the interfacial charge transfer in the range of the broadband light spectrum. The S and O can be exchanged on the surface of MoO3 nanosheets under the hydrothermal condition, leading to the formation of a surface MoOx/MoS2 heterojunction. The interfacial interaction between the MoO3 nanosheets and MoS2 easily generated free electrons and holes, and it effectively avoided the recombination of photogenerated carriers. Meanwhile, the surface S-doping of MoO3 also resulted in the generation of an oxygen vacancy and sulfur vacancy on MoO3-xS2-y. The plasmonic characteristics of MoO3-x contributed to the enhancement of the interfacial charge transfer by photoexcitation. Otherwise, even with zero bias applied, a good photoelectric signal was still obtained with polyimide film substrates and carbon electrodes. This indicates that the formation of the heterojunction generates a strong built-in electric field that drives the photogenerated carrier transport, which can be self-powered. This study provides a simple and low-cost method for the surface functionalization of some metal oxides with a wide bandgap.

Conventional epitaxy of NiO thin films on muscovite mica and c-Al2O3 substrates

Fiber-textured and epitaxial NiO thin films were deposited on Si(100), c-Al2O3, and muscovite mica(001) substrates using reactive magnetron sputtering at substrate temperatures of 300°C and 400°C, to investigate the effect of film thickness and substrate temperature on epitaxial growth of NiO films. The as-deposited films exhibited a face-centered cubic structure with a larger lattice constant, attributed to strain induced during the sputtering process. With an increase in substrate temperature to 400°C, the d-spacing decreased due to strain release, approaching the NiO bulk value for the thickest film. The NiO film grown on Si(100) displayed fiber texture. On c-plane sapphire, NiO thin films exhibited twin domains and three-fold symmetry, consistent with expected crystallographic orientation relationship for NaCl-structured materials on sapphire:(111)NiO∥(0001)Al2O3and[01¯1]NiO∥[1¯010]Al2O3, [011¯]NiO∥[101¯0]Al2O3. On muscovite mica(001) substrates, the observed epitaxial shows that the mechanism is conventional epitaxy, rather than van der Waals epitaxy, consistent with the epitaxial growth of the non-layered non-van-der-Waals compound NiO. The epitaxial relationship was identified as of (111)NiO∥(001)Mica and [01¯1]NiO∥[010]Mica, [011¯]NiO∥[01¯0]Mica.

Optimization of electrochromic Mo doping WO3 films: A study on dual-phase stacked structures for energy-efficient smart windows

Amorphous tungsten trioxide (a-WO3) films were prepared on ITO conductive glass via electrodeposition and subsequently crystallized to obtain crystalline WO3 (c-WO3) films by heating a-WO3. A dual-phase stacked WO3 film was fabricated by covering Mo-a-WO3 film onto c-WO3/ITO substrate using electrodeposition and thermal-assisted electrodeposition methods, respectively. Optimization of electrochromic performance was achieved by varying Mo doping levels (0∼5 atom%). Results demonstrate that appropriate Mo doping (3 atom%) enhances the electrochromic properties of a-WO3 films. Mo doping introduced structural distortions that reduced energy barriers and enhanced ion mobility, leading to improved electrochemical and electrochromic properties. The intermediate c-WO3 layer improves adhesion between a-WO3 top film and ITO glass substrate, while the porous structure of a-WO3 layer increases the number of active sites for electrochromic reactions. Mo3-a-WO3/c-WO3 dual-phase stacked film with doping 3 atom% Mo shows an optical modulation range of 83.4 % at 633 nm, a coloration efficiency of 74.3 cm2/C, rapid response time (bleaching/coloration: 3.4 s/6.1 s), and 86.6 % retention of its maximum current density after 2000 cycles, respectively. The high oxidation ion diffusion coefficient (3.53 × 10−10 cm2/s) and reduction diffusion coefficient (1.55 × 10−10 cm2/s) were also observed. This dual-phase stacked film shows significant improvements in electrochromic performance due to the synergistic effects between the dual phases and Mo-doping. Electrochromic device (ECD) assembled with Mo3-a-WO3/c-WO3 dual-phase films as the working electrode, ITO glass as the counter electrode, and 1 mol/L LiClO4/PC solution as the electrolyte exhibited an optical modulation range of 74.2 % and response time (bleaching/ coloring) of 6.8 s/3.7 s. These findings confirm that ECD with Mo-a-WO3/c-WO3 dual-phase films offer excellent electrochromic performance.

Integrating Metal–Organic Frameworks and Polyamide 12 for Advanced Hydrogen Storage Through Powder Bed Fusion

This paper introduces a pioneering approach that combines ex situ synthesis with advanced manufacturing to develop ZIF-67-PA12 Nylon composites with mixed-matrix membranes (MMMs), with the goal of enhancing hydrogen storage systems. One method involves producing MOF-PA12 composite powders through an in situ process, which is then commonly used as a base powder for powder bed fusion (PBF) to fabricate various structures. However, developing the in situ MOF-PA12 matrix presents challenges, including limited spreadability and processability at higher MOF contents, as well as reduced porosity due to pore blockage by polymers, ultimately diminishing hydrogen storage capacity. To overcome these issues, PBF is employed to form PA12 powder into films, followed by the ex situ direct synthesis of ZIF-67 onto these substrates at loadings exceeding those typically used in conventional MMM composites. In this study, ZIF-67 mass loadings ranging from 2 to 30 wt.% were synthesized on both PA12 powder and printed film substrates, with loadings on printed PA12 films extended up to 60 wt.%. ZIF-67-PA12-60(f) demonstrated a hydrogen capacity of 0.56 wt.% and achieved 1.53 wt.% for ZIF-67-PA12-30(p); in comparison, PA12 exhibited a capacity of 0.38 wt.%. This was undertaken to explore a range of ZIF-67 Metal–organic frameworks (MOFs) to assess their impact on the properties of the composite, particularly for hydrogen storage applications. Our results demonstrate that ex situ-synthesized ZIF-67-PA12 composite MMMs, which can be used as a final product for direct application and do not require the use of in situ pre-synthesized powder for the PBF process, not only retain significant hydrogen storage capacities, but also offer advantages in terms of repeatability, cost-efficiency, and ease of production. These findings highlight the potential of this innovative composite material as a practical and efficient solution for hydrogen storage, paving the way for advancements in energy storage technologies.

Controlling Crystal Orientation in Films of Conjugated Polymers by Tuning the Surface Energy.

It has been a long-term goal to understand the molecular orientation in films of conjugated polymers, which is crucial to their efficient exploitation. Here, we show that the surface energies determine the crystal orientation in films of model conjugated polymers, substituted polythiophenes crystallized on substrates. We systematically increase the surface energy of edge-on crystals formed at the vacuum interface by attaching polar groups to the ends of the polymer side chains. This suppresses crystallization at the vacuum interface, resulting in a uniform face-on crystal orientation induced by the graphene substrate in polythiophene films as thick as 200 nm, which is relevant for devices. Surprisingly, face-on crystal orientation is attained in the modified polythiophenes crystallized even on amorphous surfaces. Furthermore, for the samples with still competing interfacial interactions, the crystal orientation can be switched in the same sample, depending on the crystallization conditions. Thus, we report a fundamental understanding and control of the equilibrium crystal orientation in films of conjugated polymers.

Programmable and flexible wood-based origami electronics

Natural polymer substrates are gaining attention as substitutes for plastic substrates in electronics, aiming to combine high performance, intricate shape deformation, and environmental sustainability. Herein, natural wood veneer is converted into a transparent wood film (TWF) substrate. The combination of 3D printing and origami technique is established to create programmable wood-based origami electronics, which exhibit superior flexibility with high tensile strength (393 MPa) due to the highly aligned cellulose fibers and the formation of numerous intermolecular hydrogen bonds between them. Moreover, the flexible TWF electronics exhibit editable multiplexed configurations and maintain stable conductivity. This is attributed to the strong adhesion between the cellulose-based ink and TWF substrate by non-covalent bonds. Benefiting from its anisotropic structure, the programmability of TWF electronics is achieved through sequentially folding into predesigned shapes. This design not only promotes environmental sustainability but also introduces its customizable shapes with potential applications in sensors, microfluidics, and wearable electronics.

Superconducting (Ba,K)Fe2As2 epitaxial films on single and bicrystal SrTiO3 substrates

The realization of single crystal and bicrystal films of superconducting materials is of great interest because they allow the investigation of the intragrain performance as well as the understanding of potential limitations in the grain boundary transparency. For many years, the realization of a high-quality (Ba,K)Fe2As2 film has been challenging. Here, the realization of (Ba,K)Fe2As2 epitaxial thin films on single crystal SrTiO3(001) and [001]-tilt-type SrTiO3 bicrystal substrates with high superconducting properties is demonstrated. The epitaxial growth of (Ba,K)Fe2As2 was enabled by implementing an undoped BaFe2As2 buffer layer between the SrTiO3 substrate and (Ba,K)Fe2As2 film. The film exhibits a high Tc of 38.0 K and an extremely high Jc of 14.3 MA/cm2 at 4.2 K. Artificial grain boundaries of (Ba,K)Fe2As2 were also successfully achieved on bicrystals with misorientation angles up to 36.8° by the same preparation methods. The artificial grain boundaries exhibited an identical Tc of 38.0 K and an excellent transfer of the grain orientation from the bicrystal substrates with high crystallinity comparable to that of the high-quality Ba(Fe,Co)2As2 films. This enables the investigation of the intrinsic (Ba,K)Fe2As2 grain boundary nature, which will clarify its potential for superconducting applications, like Josephson junctions, wires, and magnets.

Enabling 2D Electron Gas with High Room-Temperature Electron Mobility Exceeding 100cm2 Vs-1 at a Perovskite Oxide Interface.

In perovskite oxide heterostructures, bulk functional properties coexist with emergent physical phenomena at epitaxial interfaces. Notably, charge transfer at the interface between two insulating oxide layers can lead to the formation of a 2D electron gas (2DEG) with possible applications in, e.g., high-electron-mobility transistors and ferroelectric field-effect transistors. So far, the realization of oxide 2DEGs is, however, largely limited to the interface between the single-crystal substrate and epitaxial film, preventing their deliberate placement inside a larger device architecture. Additionally, the substrate-limited quality of perovskite oxide interfaces hampers room-temperature (RT) 2DEG performance due to notoriously low electron mobility. In this work, the controlled creation of an interfacial 2DEG at the epitaxial interface between perovskite oxides BaSnO3 and LaInO3 is demonstrated with enhanced RT electron mobility values up to 119 cm2 Vs-1-the highest RT value reported so far for a perovskite oxide 2DEG. Using a combination of state-of-the-art deposition modes during oxide molecular beam epitaxy, this approach opens up another degree of freedom in optimization and in situ control of the interface between two epitaxial oxide layers away from the substrate interface. Thus this approach is expected to apply to the general class of perovskite oxide 2DEG systems and to enable their improved compatibility with novel device concepts and integration across materialsplatforms.

Electroanalysis with Carbon Paste Electrodes: A Look Behind the Scientific-Research Activities of the Electroanalytical Group in Pardubice

In this article, a retrospective view of the research activities of the electroanalytical group at the University in Pardubice (UPCE) is presented, offering a concise overview on the development, continuing work, and significant achievements in electrochemical measurements with carbon paste electrodes (CPEs). At the very beginning, a brief history of the field is provided and the state-of-the-art in a global view outlined. Second, research activities with CPEs and related configurations in the former Czechoslovakia and the succeeding Czech Republic are also summarised and the respective publications cited. The introductory section ends with a historical survey of the activities of the electroanalytical group at the UPCE, characterising the individual time periods with CPEs from the mid-1980s up until now and highlighting the most important achievements and the corresponding publications. The pivotal part of the text then gathers five various examples representing some of the truly key-themes that have made electroanalysis at UPCE well-known and, at the same, distinctive. Namely, overviewed, commented, and illustrated in selected figures are (i) carbon paste mixtures with atypical binders from liquid esters, (ii) extractive pre-concentration onto the carbon paste bulk and determination of iodine, (iii) method for determination of Ag(I) ions at a CPE with extraordinary analytical performance, (iv) carbon pastes as substrates for mercury, gold, bismuth, and antimony films, and (v) recent applications of CPEs prepared from carbonaceous materials of natural origin.

Three hundred sixty‐degree viewable linear grooves 3D display

AbstractWe proposed a linear grooves 3D display that can display 360° viewable 3D images by creating linear grooves that correspond to the viewpoint positions. In the conventional method, arc‐shaped grooves are drawn on a flat substrate of transparent film. However, depending on the viewing position, the image may be distorted. In addition, when a flat substrate is bent into a curved shape, the image is more affected than one observed in a flat shape. Furthermore, the conventional method of arc 3D display method cannot display a 3D image that corresponds to the viewpoint position. In this paper, we propose design and fabrication methods that reduce the image distortion for both flat and curved shapes. A 3D image displayed by the proposed method can change depending on the viewpoint position, and a natural 3D image with motion parallax can be observed. In the experiment, our proposed method fabricated a 360° 3D display by calculating the linear grooves and presented natural 3D images with smooth motion parallax.

A new method for growing epitaxial films on foreign substrates − Bent epitaxy

In recent years, to mitigate the effects of climate change, countries’ transition to the green economy has accelerated, and thereby, the demand of semiconductor industry for wide-gap semiconductors such as SiC and GaN has increased dramatically. These semiconductors are expensive. To reduce the price of the final product, industrial production of thin epitaxial films of sought-after semiconductors on accessible and cheap substrates, such as Si and sapphire, is being developed. When growing epitaxial films on foreign substrates, the resulting heterostructure bends, becomes concave or convex, due to a mismatch between the coefficients of thermal expansion (CTE) of the substrate and the epitaxial film. As a result, the quality of the epitaxial film deteriorates and further processing of the resulting heterostructures in production lines becomes difficult or even impossible. The essence of the proposed new method is that the epitaxial film is grown not on a flat, but on a pre-curved substrate with the expectation that after cooling the fabricated heterostructure to room temperature, the heterostructure will take a flat shape due to the difference in the CTE of the epitaxial film and the substrate. A round bimetallic plate, located under the substrate, bends the substrate in the required direction to the desired value at the growth temperature, and gradually reduces the bend of the fabricated heterostructure during cooling, in proportion to the thermal contraction of the epitaxial film. This allows obtaining qualitative and flat epitaxial films, regardless of the material of the substrate or epitaxial film and the diameter of the substrate or thickness of the epitaxial film, without any buffer layers or carrying out any additional operations and costs.

STUDY ON THE PROPERTIES OF DIAMOND FILMS ON CEMENTED CARBIDE SUBSTRATES BY SURFACE IMPLANTATION PRETREATMENT PROCESS

The deposition of diamond films on tungsten carbide-based tools can greatly improve the life and performance of cutting tools. However, the deposition of diamond coatings on cemented carbide (WC-Co) suffers from poor film-base bond strength. In this paper, diamond coatings were deposited of phytocrystalline metal micropowders (pure, Nb, Ti, Ta) pretreatment method and the properties of diamond films were analyzed by energy spectrometry (EDS), scanning electron microscopy (SEM), Raman spectroscopy and bonding strength test of diamond films. The results show that through the experiment of the pretreatment process of surface implanted crystal metal micropowder, the best implanted crystal metal micropowder was obtained, the surface quality of implanted crystal titanium (Ti) coating was improved, the diamond Raman peaks were sharp and the indentation cracks had a crack diameter of 389 [Formula: see text]m, which is small and has the highest bond strength. The pretreatment process of phytocrystalline diamond micropowder can deposit high-performance diamond coatings and improve the bonding strength between the coating and the substrate film base.

Flexible substrate-based mass spectrometry platform for in situ non-destructive molecular imaging of living plants.

Monitoringand localizing molecules on living plants is critical for understanding their growth, development and disease. However, current techniques for molecular imaging of living plants often lack spatial information or require tedious pre-labelling. Here, we proposed a novel molecular imaging platform that combines sliver nanowire-doped Ti3C2 MXene (AgNWs@MXene) flexible film substrate with laser desorption/ionization mass spectrometry imaging (AMF-LDI-MSI) to study the spatial distribution of biomolecules on the surface of living plants. This platform overcomes the MSI challenges posed by difficult-to-slice plant tissues (e.g., tough or water-rich roots and fragile flowers) and enables precisely transfer and visualize the molecule. Comparisons of the measurement results to those from matrix-assisted LDI-MSI (MALDI-MSI) technology demonstrate the accuracy and reliability of the platform. Biocompatibility evaluations indicated that the platform without observable adverse effects on the health of living plants. The distribution of growth and disease-associated signalling molecules, such as choline, organic acids and carbohydrates, can be in situ non-destructively detected on the surfaces of living plants, which is important for tracking the health of plants and their diseased areas. AMF-LDI-MSI platform can serve as a promising tool for label-free, in situ and non-destructive monitoring of functional biomolecules and plant growth from a spatial perspective.

Microstructural evolution of diamond thin film grown on a silicon substrate via a surface-wave plasma system: Identification of intermediated phase

Diamond thin films are promising for diverse applications because of their exceptional properties. Understanding the interface between diamond films and substrates is crucial for optimizing the film quality and functionality. In this study, a diamond thin film was grown on a Si(100) substrate using a microwave-based surface-wave plasma system and subjected to transmission electron microscopy (TEM) and electron energy-loss spectroscopy (EELS). The formation of a SiC interlayer was identified at the interface between the diamond thin film and Si substrate through cross-sectional TEM and EELS. Analysis of the atomic structure and crystalline properties indicated that the interlayer was β-SiC and that the orientation relationships [110]β-SiC//[110]Si and (111)β-SiC//(111)Si existed at the β-SiC/Si interface. The β-SiC interlayer exhibited the {111} extra half-planes, because they were more easily formed by the {111} planes than the {110} extra half-planes generated on {001} planes through 60° misfit dislocations. Many stacking faults and microtwins were observed in the diamond grains; such planar defects were likely attributed to strain behavior and complex contrasts at the nanoscale.

Role of growth temperature on microstructural and electronic properties of rapid thermally grown MoTe2 thin film for infrared detection

In the field of electronic and optoelectronic applications, two-dimensional materials are found to be promising candidates for futuristic devices. For the detection of infrared (IR) light, MoTe2possesses an appropriate bandgap for which p-MoTe2/n-Si heterojunctions are well suited for photodetectors. In this study, a rapid thermal technique is used to grow MoTe2thin films on silicon (Si) substrates. Molybdenum (Mo) thin films are deposited using a sputtering system on the Si substrate and tellurium (Te) film is deposited on the Mo film by a thermal evaporation technique. The substrates with Mo/Te thin films are kept in a face-to-face manner inside the rapid thermal-processing furnace. The growth is carried out at a base pressure of 2 torr with a flow of 160 sccm of argon gas at different temperatures ranging from 400 °C to 700 °C. The x-ray diffraction peaks appear around 2θ= 12.8°, 25.5°, 39.2°, and 53.2° corresponding to (002), (004), (006), and (008) orientation of a hexagonal 2H-MoTe2structure. The characteristic Raman peaks of MoTe2, observed at ∼119 cm-1and ∼172 cm-1, correspond to the in-plane E1gand out-of-plane A1gmodes of MoTe2, whereas the prominent peaks of the in-plane E12gmode at ∼234 cm-1and the out-of-plane B12gmode at ∼289 cm-1are also observed. Root mean square (RMS) roughness is found to increase with increasing growth temperature. The bandgap of MoTe2is calculated using a Tauc plot and is found to be 0.90 eV. Electrical characterizations are carried out using current-voltage and current-time measurement, where the maximum responsivity and detectivity are found to be 127.37 mA W-1and 85.21 × 107Jones for a growth temperature of 600 °C and an IR wavelength illumination of 1060 nm.

A comprehensive study of thermocapillary rupture of liquid layer

There is a lack of understanding of the physical mechanisms involved in the rupture of a liquid film on a solid surface. This is in part due to the large number of parameters of the liquid film—substrate system on which this complex process is dependent. Due to the thermocapillary effect, local heating can have a destabilizing effect on the stability of the film. In this work, using a numerical model verified by the experimental data, the influence of parameters not available for variation in the experiment has been studied. It was found that the formation of dry spots in a locally heated liquid film occurs only under the influence of thermocapillary forces. In turn, the expansion of the dry spots takes place under the influence of the capillary forces. Thus, until the dry spot appears, the rupture does not differ on either hydrophilic or superhydrophobic substrates, but the contact line velocity during dry spot growth is extremely sensitive to the contact angle.