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Abstract The demand for modern electronics and semiconductors has increased throughout the years, which has enabled the innovation and exploration of solution-processed deposition. Solution-based processes have gained a lot of interest due to the low-cost fabrication and the large fabrication areas without the need for high-vacuum equipment. In this study, we utilized the ZnO ink for inkjet printer ink to fabricate a thin film via Electrohydrodynamic printing. Three different ink solutions were prepared for experimentation. The EHD printing technique demonstrated the ink’s compatibility with and without the modifications. The outcomes of the EHD printed materials were comparable with the spin-coated thin films. The EHD-printed films demonstrated better results in comparison to spin-coated films. Ra and Rq of the EHD film measured at 3.651 nm and 4.973 nm, respectively. It improved the absorbance up to two-fold at 360 nm wavelength and electrical conductivity up to 40% compared to the spin-coated films. Furthermore, the optimization of the printing parameters can lead to the improved morphology and thickness of the EHD thin films.

Thin film solar cells are gaining popularity as an affordable, efficient, and flexible substitute for traditional silicon solar cells . This success is closely tied to the deposition techniques used to fabricate their layers. This review explores and analyzes the advances in the major deposition techniques for solar cell applications, offering insights into their underlying principles, associated advantages, drawbacks, and suitability for diverse materials and device architectures. The two primary deposition for thin film solar cells are PVD and CVD. In PVC materials are physically ejecting from a target, and depositing it onto a substrate. While, CVD entails the reaction of gases or vapour precursors to creating film on a substrate. The ability to achieve high purity, control over film properties, scalability, and compatibility with flexible substrates are notable advantages. However, challenges such as high costs and complexity can impact the commercial viability of certain techniques. Recent advancements in the technology of thin film deposition for solar cells include the discovery of novel materials with enhanced light absorption and electronic charge transport capabilities, emerging deposition processes such as pulsed laser deposition, and atomic layer deposition scalable and low-cost processes like roll-to-roll processing, and integration with other technologies like perovskite solar cells and tandem devices. Understanding these techniques and staying informed about recent advancements and future directions empowers researchers and engineers to innovate and create improved thin film solar cells, contributing significantly to a more sustainable future through enhanced solar energy harvesting technologies. [ABSTRACT FROM AUTHOR]

The demand for modern electronics and semiconductors has increased throughout the years, which has enabled the innovation and exploration of solution-processed deposition. Solution-based processes have gained a lot of interest due to the low-cost fabrication and the large fabrication areas without the need for high-vacuum equipment. In this study, we utilized the ZnO ink for inkjet printer ink to fabricate a thin film via Electrohydrodynamic printing. Three different ink solutions were prepared for experimentation. The EHD printing technique demonstrated the ink's compatibility with and without the modifications. The outcomes of the EHD printed materials were comparable with the spin-coated thin films. The EHD-printed films demonstrated better results in comparison to spin-coated films. Ra and Rq of the EHD film measured at 3.651 nm and 4.973 nm, respectively. It improved the absorbance up to two-fold at 360 nm wavelength and electrical conductivity up to 40% compared to the spin-coated films. Furthermore, the optimization of the printing parameters can lead to the improved morphology and thickness of the EHD thin films. [ABSTRACT FROM AUTHOR]

In this work, copper oxide (CuO) thin films were prepared using the pulsed laser deposition (PLD) technique. The effect of laser beam energy and pulse number on the structural, morphological, and topographical characteristics was investigated. X-ray diffraction (XRD) results indicate the presence of characteristic peaks for CuO with a crystalline growth orientation at the (111) plane and an increase in crystallite size (D) when the laser power and number of pulses increase. EDX results indicate the presence of distinct energy peaks for the copper and oxygen elements that form CuO, and the weight percentage (wt.%) of Cu increases with increasing laser energy. The atomic force microscope (AFM) results showed the dependence of the roughness on the laser energy used, as the roughness decreased from 31.18 to 20.89 nm when the energy increased from 700 to 820 mJ. It increases with the increase in the number of laser pulses at the same energy (700 mJ). Field emission scanning electron microscopy (FESEM) confirms the presence of sub-spherical nanoparticles, and increasing laser energy and pulses increases nanoparticle size. [ABSTRACT FROM AUTHOR]

Solid oxide cell technologies play a pivotal role in the realm of renewable energy storage, guiding us through the journey toward decarbonization. Understanding how electrocatalytic materials behave under high‐temperature conditions is an absolute necessity to push these technologies forward. Operando spectroscopic investigations, such as near‐ambient pressure X‐ray photoelectron spectroscopy (NAP–XPS), offer insights into the chemical nature of active working electrodes, including the dynamic response of redox states and adsorbate chemistry to changing electrochemical conditions. Mixed ceramic–metallic electrodes exhibit a limited region with electrochemically active triple‐phase‐boundary (TPB) sites, which are located close to the electrolyte/electrode interface. To monitor this specific region spectroscopically, metallic (Ni) and bimetallic (NiCu) network‐like structures are synthesized on a yttria‐stabilized zirconia electrolyte and the electrochemical state and performance are studied by using operando NAP–XPS. In the experiments, the surface oxidation states under different polarizations are revealed, the gas composition dependent Nernst shift is confirmed, electrocatalytic activities are unraveled, and hydrogen evolution is correlated with the applied potential. The findings demonstrate, the effectiveness of thin‐film model cells with spectroscopically accessible TPB regions for probing interfacial states and electrochemical processes. The obtained fundamental knowledge can provide valuable insights for the advancement of renewable energy storage technologies. [ABSTRACT FROM AUTHOR]

Solid oxide cell technologies play a pivotal role in the realm of renewable energy storage, guiding us through the journey toward decarbonization. Understanding how electrocatalytic materials behave under high‐temperature conditions is an absolute necessity to push these technologies forward. Operando spectroscopic investigations, such as near‐ambient pressure X‐ray photoelectron spectroscopy (NAP–XPS), offer insights into the chemical nature of active working electrodes, including the dynamic response of redox states and adsorbate chemistry to changing electrochemical conditions. Mixed ceramic–metallic electrodes exhibit a limited region with electrochemically active triple‐phase‐boundary (TPB) sites, which are located close to the electrolyte/electrode interface. To monitor this specific region spectroscopically, metallic (Ni) and bimetallic (NiCu) network‐like structures are synthesized on a yttria‐stabilized zirconia electrolyte and the electrochemical state and performance are studied by using operando NAP–XPS. In the experiments, the surface oxidation states under different polarizations are revealed, the gas composition dependent Nernst shift is confirmed, electrocatalytic activities are unraveled, and hydrogen evolution is correlated with the applied potential. The findings demonstrate, the effectiveness of thin‐film model cells with spectroscopically accessible TPB regions for probing interfacial states and electrochemical processes. The obtained fundamental knowledge can provide valuable insights for the advancement of renewable energy storage technologies.

Hafnium zirconium oxide (HZO) is an ideal candidate for the implementation of ferroelectric memristive devices, due to its compatibility with the complementary metal‐oxide‐semiconductor technology. Ferroelectricity in HZO films is significantly influenced by the properties of electrode/HZO interfaces. Here, the impact of the interfacial microstructure and chemistry on the ferroelectricity of 6 nm‐thick HZO‐based capacitors, realized by sputtering, with titanium nitride or tungsten electrode materials, is investigated. The results highlight a strong correlation between the structural properties of electrode/HZO interfaces and the HZO ferroelectric performance. Interface effects become significant at low HZO thickness, thus the precise control over the quality of electrode/HZO interfaces allows the remarkable improvement of HZO ferroelectric properties. A double remanent polarization of 40 µC cm−2 is achieved. This work is a new step towards high quality ultra‐thin HZO films with enhanced ferroelectricity for the implementation of ferroelectric tunnel junctions for brain‐inspired computing. [ABSTRACT FROM AUTHOR]

Despite enormous progress in the field of surface plasmon resonance (SPR) imaging sensor technology in the past three decades, noble metals like Au and Ag, despite their drawbacks, continue to be the metals of choice for plasmonic sensing layers. The conventional architecture of the SPR sensor based on gold/silver and glass prism hinders scaling, portability, and industrial manufacturing. In this contribution, we present a novel architecture of SPR sensor using copper on polycarbonate prism as a cost-effective, scalable, and mass-producible alternative. Various optimization techniques, such as interface layer, protective encapsulation, and 2D affinity layer are explored to address the challenges related to the practical application of copper in a plasmonic sensor. Our results show that optimized architectures of SPR sensor based on copper has a sensitivity of 235.01°/RIU. From a quantitative analysis of the interrelationships among various performance parameters, we have derived a comprehensive sensing parameter that integrates signal quality and sensitivity. The proposed architecture of the copper based SPR sensor can lead to inexpensive, compact, and handy probes that do not sacrifice accuracy or reliability.

Abstract Hafnium zirconium oxide (HZO) is an ideal candidate for the implementation of ferroelectric memristive devices, due to its compatibility with the complementary metal‐oxide‐semiconductor technology. Ferroelectricity in HZO films is significantly influenced by the properties of electrode/HZO interfaces. Here, the impact of the interfacial microstructure and chemistry on the ferroelectricity of 6 nm‐thick HZO‐based capacitors, realized by sputtering, with titanium nitride or tungsten electrode materials, is investigated. The results highlight a strong correlation between the structural properties of electrode/HZO interfaces and the HZO ferroelectric performance. Interface effects become significant at low HZO thickness, thus the precise control over the quality of electrode/HZO interfaces allows the remarkable improvement of HZO ferroelectric properties. A double remanent polarization of 40 µC cm−2 is achieved. This work is a new step towards high quality ultra‐thin HZO films with enhanced ferroelectricity for the implementation of ferroelectric tunnel junctions for brain‐inspired computing.

The continuously increasing interest in flexible and integrated photonics requires new strategies for device manufacturing on arbitrary complex surfaces and with smallest possible size, respectively. Terahertz (THz) technology can particularly benefit from this achievement to make compact systems for emission, detection and on-demand manipulation of THz radiation. Here, we present a novel fabrication method to realize conformable terahertz metasurfaces. The flexible and versatile character of polymeric nanomembranes is combined with direct laser writing via two-photon polymerization to develop free-standing ultra-thin quasi-perfect plasmonic absorbers with an unprecedentedly high level of conformability. Moreover, revealing new flexible dielectric materials presenting low absorption and permittivity in the THz range, this work paves the way for the realization of ultra-thin, conformable hybrid or all-dielectric devices to enhance and enlarge the application of THz technologies, and flexible photonics in general.

Erbium-doped silica films were synthesized using a two-step sol–gel methodology that involved acid and base catalysts, with erbium concentration ranging from 0.2% to 6% and annealing temperatures varying from 500 °C to 900 °C. The photoluminescence spectra showed that the samples exhibiting efficient emission were annealed at 800 °C and 900 °C and doped with 3% and 6% erbium. The X-ray diffraction analysis revealed that the internal structure of the films was influenced by the different annealing temperatures and the doping concentrations. Samples with dominant 4f transitions were modelled. The results suggest that the proposed method is a promising approach for the synthesis of erbium-doped silica films with potential applications in optical devices. [ABSTRACT FROM AUTHOR]

The effect of nitrogen (N2) partial pressure on the structure and bandgap tunability of RF magnetron sputtered Cadmium Sulphide (CdS) thin films is investigated by varying N2 partial pressure in Ar/N2 mixture. In presence of N2, films have a polycrystalline structure with (002) preferential orientation, which leads to defect-free, continuous, dense, and fibrous structures with increased roughness. The average optical transmittance increased to > 80 at 500–2500 nm for 30 % N2 partial pressure, whereas the band gap decreases from 2.45 eV to 2.30 eV with increasing N2 concentration. This work shows that the bandgap of sputtered CdS thin films can be tuned with the variation of N2 concentration for customized applications.

Carbon black nanocomposites are complex systems that show potential for engineering applications. Understanding the influence of preparation methods on the engineering properties of these materials is critical for widespread deployment. In this study, the fidelity of a stochastic fractal aggregate placement algorithm is explored. A high-speed spin-coater is deployed for the creation of nanocomposite thin films of varying dispersion characteristics, which are imaged via light microscopy. Statistical analysis is performed and compared to 2D image statistics of stochastically generated RVEs with comparable volumetric properties. Correlations between simulation variables and image statistics are examined. Future and current works are discussed. [ABSTRACT FROM AUTHOR]

Due to their high optical efficiency, low-cost fabrication and wide variety in composition and bandgap, halide perovskites are recognized nowadays as real contenders for the development of the next generation of optoelectronic devices, which, among others, often require high quality over large areas which is readily attainable by vacuum deposition. Here, we report the amplified spontaneous emission (ASE) properties of two CsPbBr3 films obtained by single-step RF-magnetron sputtering from a target containing precursors with variable compositions. Both the samples show ASE over a broad range of temperatures from 10 K up to 270 K. The ASE threshold results strongly temperature dependent, with the best performance occurring at about 50 K (down to 100 µJ/cm2), whereas at higher temperatures, there is evidence of thermally induced optical quenching. The observed temperature dependence is consistent with exciton detrapping up to about 50 K. At higher temperatures, progressive free exciton dissociation favors higher carrier mobility and increases trapping at defect states with consequent emission reduction and increased thresholds. The reported results open the way for effective large-area, high quality, organic solution-free deposited perovskite thin films for optoelectronic applications, with a remarkable capability to finely tune their physical properties. [ABSTRACT FROM AUTHOR]

Zero-biased photodetectors have desirable characteristics for potentially next-generation devices, including high efficiency, rapid response, and low power operation. In particular, the detector efficiency can be improved simply by changing the electrode contact geometry or morphological structure of materials, which give unique properties such as energy band bending, photo absorbance and electric field distribution. In addition, several combinations of materials enable or disable the operation of selective wavelengths of light detection. Herein, such recent progresses in photodetector operating at zero-bias voltage are reviewed. Considering the advantages and promises of these low-power photodetectors, this review introduces various zero-bias implementations and reviews the key points. [ABSTRACT FROM AUTHOR]

Aluminum nitride (AlN) has gained wide interest owing to its high values of elastic modulus, band gap, dielectric strength, resistivity, thermal conductivity and acoustic velocities, especially because it retains most of its properties and versatility in the thin-film form. This review focuses on applications where the CMOS integration of AlN MEMS has been effectively demonstrated. First, the fundamental concepts of piezoelectricity on polycrystalline $c$ -axis oriented thin-films are introduced and AlN is compared to other common piezoelectric materials, namely LiNbO3, LiTaO3, quartz, lead zirconate titanate (PZT), ZnO and GaN by thoroughly discussing the material properties, processing and technological implications. After presenting the possible MEMS-CMOS integration strategies, recent demonstrations of AlN-based devices are reviewed, namely energy harvesters, film bulk acoustic resonators (FBAR), contour mode resonators (CMR), gas sensors, imagers, microphones, transducers for chip-scale communication and calorimetric sensors. Finally, other recent applications/integration opportunities are outlined for AlN-based micro-mirrors, flexible sensors and transducers for liquid media and harsh environments. [2022-0006] [ABSTRACT FROM AUTHOR]

Starting from solid-solutions (SS) of AlCoCrFeNix high-entropy alloys (HEAs) that have been produced with high purity constituent elements by vacuum arc remelting (VAR) method varying the nickel molar ratio x from 0.2 to 2.0, we investigated the synthesis of protective thin films of HEAs and high-entropy nitrides (HENs) with the aid of the pulsed laser deposition (PLD) system. The structure of all ten available bulk targets have been examined by means of X-Ray Diffraction (XRD), as well as their elemental composition by means of energy dispersion X-ray spectroscopy (EDS). Three targets with nickel molar composition x = 0.4, 1.2 and 2.0 corresponding to BCC, mixed BCC and FCC, and finally FCC structures were used for thin film depositions using a KrF excimer laser. The depositions were performed in residual low vacuum (10−7 mbar) and under N2 (10−4 mbar) at room temperature (RT~25 °C) on Si and glass substrates. The deposited films' structure was investigated using grazing incidence XRD, their surface morphology, thickness and elemental composition by scanning electron microscopy (SEM), EDS and X-ray photoelectron spectroscopy (XPS), respectively. A homemade four-point probe (4PP) set-up was applied to determine layers electrical resistance. Besides, a Nanoindentation (NI) was employed to test films' mechanical properties. XRD results showed that all deposited films, regardless of the initial structure of targets, were a mixture of FCC and BCC structures. Additionally, the quantitative and qualitative EDS and XPS results showed that the elemental composition of films was rather close to that of the targets. The depositions under an N2 atmosphere resulted in the inclusion of several percentage nitrogen atoms in a metallic nitride type compound into films, which may explain their higher electrical resistivity. The Young's modulus, nanohardness and friction coefficient values showed that the deposited films present good mechanical properties and could be used as protective coatings to prevent damage in harsh environments. [ABSTRACT FROM AUTHOR]

[Display omitted] • First comprehensive examination of the reaction mechanism in nanoZr-based thermite compositions. • Predominance of a low-temperature exothermic event in Zr/CuO redox reaction. • Zr undergoes a sequential three-step oxidation process below 475 °C. • Zr/CuO demonstrates a 400-fold reduction in ignition delay compared to Al/CuO. In this report, we examine the intricate details of the mechanism driving Zr/CuO thermite system, shedding new light on the exceptional reactivity of Zr fuel with oxygen. Magnetron-sputtered Zr/CuO reactive multilayers were deposited, and thermo-physical techniques were employed to characterize the progression of the chemical reaction upon heating. Unlike commonly used Al fuel, Zr/CuO exhibited 100% heat release below 500 °C, contrasting with the ∼5% observed for conventional Al/CuO system. This enhanced reactivity at low temperature is attributed to the rapid oxygen consumption behavior of Zr, due to the poor barrier of ZrO x to oxygen diffusion. The oxidizing behavior of Zr was quantitatively analyzed using electron microscopy and spectroscopy. Our observations reveal a three-step process of Zr oxidation facilitated by a rapid reduction of CuO to metallic Cu accompanied by the formation of an intermediate Cu 2 O phase: (i) a preliminary low-temperature mass transport initiating at 275 °C, (ii) partial Zr oxidation forming ZrO 2 and oxygen enriched Zr and finally (iii) complete conversion to zirconia at 450 °C. Finally, Zr/CuO reactive thin-films demonstrated a very high reactivity with an ignition delay time of 0.04 ± 0.016 ms and a burn rate of 3.5 m.s−1, in stark contrast to the same volume of Al/CuO, which failed to ignite and burn altogether. This study not only deepens our comprehension of Zr-based thermite system but also underscores its potential for diverse applications in energetic materials. [ABSTRACT FROM AUTHOR]

Erbium-doped silica films were synthesized using a two-step sol–gel methodology that involved acid and base catalysts, with erbium concentration ranging from 0.2% to 6% and annealing temperatures varying from 500 °C to 900 °C. The photoluminescence spectra showed that the samples exhibiting efficient emission were annealed at 800 °C and 900 °C and doped with 3% and 6% erbium. The X-ray diffraction analysis revealed that the internal structure of the films was influenced by the different annealing temperatures and the doping concentrations. Samples with dominant 4f transitions were modelled. The results suggest that the proposed method is a promising approach for the synthesis of erbium-doped silica films with potential applications in optical devices.

Carbon black nanocomposites are complex systems that show potential for engineering applications. Understanding the influence of preparation methods on the engineering properties of these materials is critical for widespread deployment. In this study, the fidelity of a stochastic fractal aggregate placement algorithm is explored. A high-speed spin-coater is deployed for the creation of nanocomposite thin films of varying dispersion characteristics, which are imaged via light microscopy. Statistical analysis is performed and compared to 2D image statistics of stochastically generated RVEs with comparable volumetric properties. Correlations between simulation variables and image statistics are examined. Future and current works are discussed.

Due to their high optical efficiency, low-cost fabrication and wide variety in composition and bandgap, halide perovskites are recognized nowadays as real contenders for the development of the next generation of optoelectronic devices, which, among others, often require high quality over large areas which is readily attainable by vacuum deposition. Here, we report the amplified spontaneous emission (ASE) properties of two CsPbBr3 films obtained by single-step RF-magnetron sputtering from a target containing precursors with variable compositions. Both the samples show ASE over a broad range of temperatures from 10 K up to 270 K. The ASE threshold results strongly temperature dependent, with the best performance occurring at about 50 K (down to 100 µJ/cm2), whereas at higher temperatures, there is evidence of thermally induced optical quenching. The observed temperature dependence is consistent with exciton detrapping up to about 50 K. At higher temperatures, progressive free exciton dissociation favors higher carrier mobility and increases trapping at defect states with consequent emission reduction and increased thresholds. The reported results open the way for effective large-area, high quality, organic solution-free deposited perovskite thin films for optoelectronic applications, with a remarkable capability to finely tune their physical properties.

In this work we will study the dynamics of a thin layer of a viscous fluid which is embedded in the interior of another viscous fluid. The resulting flow can be approximated by means of the solutions of a free boundary problem for the Stokes equation in which one of the unknowns is the shape of a curve which approximates the geometry of the thin layer of fluid. We also derive the equation yielding the thickness of this fluid. This model, that will be termed as the Geometric Free Boundary Problem , will be derived using matched asymptotic expansions. We will prove that the Geometric Free Boundary Problem is well posed and the solutions of the thickness equation are well defined (in particular they do not yield breaking of fluid layers) as long as the solutions of the Geometric Free Boundary Problem exist. [ABSTRACT FROM AUTHOR]

The aim of this work is to investigate the preparation, the optical properties, and the stability over time of a colloidal organic-inorganic hybrid perovskite (CH3NH3PbBr3)/random copolymer P(MMA-co-DMAEMA) system. Different ratios of perovskite to copolymer were used to study its effect on stability and properties. The optical properties were investigated by UV-Vis and fluorescence spectroscopy. Dynamic light scattering was used to determine the size, and the size polydispersity of the colloidal hybrid particles; while morphology was investigated by transmission electron microscopy. Photoluminescence decay studies revealed the interaction of the random copolymer with the perovskite. Finally, thin-films were prepared, to investigate the optical properties of the samples in the absence of the solvent. High temporal stability of the optical properties of thin hybrid films was observed under certain conditions. [ABSTRACT FROM AUTHOR]

Zero-biased photodetectors have desirable characteristics for potentially next-generation devices, including high efficiency, rapid response, and low power operation. In particular, the detector efficiency can be improved simply by changing the electrode contact geometry or morphological structure of materials, which give unique properties such as energy band bending, photo absorbance and electric field distribution. In addition, several combinations of materials enable or disable the operation of selective wavelengths of light detection. Herein, such recent progresses in photodetector operating at zero-bias voltage are reviewed. Considering the advantages and promises of these low-power photodetectors, this review introduces various zero-bias implementations and reviews the key points.

Lifetime and reliability in realistic operating conditions are important parameters for the application of thin-film piezoelectric microelectromechanical systems (piezoMEMS) based on lead zirconate titanate (PZT). Humidity can induce time-dependent dielectric breakdown at a higher rate compared to dry conditions, and significantly alter the dynamic behavior of piezoMEMS-devices. Here we assess the lifetime and reliability of PZT-based micromirrors with and without humidity barriers operated at 23°C in an ambient of 0 and 95 % relative humidity. The correlation of the dynamic response, as well as the ferroelectric, dielectric, and leakage properties, with degradation time was investigated. In humid conditions, the median time-to-failure was increased from ${2.7\times }{10}^{4}{[1.9\times }{10}^{4}{-4.0\times }{10}^{4}{]}$ s to ${1.1\times }{10}^{6}{[0.9\times }{10}^{6}{-1.5\times }{10}^{6}{]}$ s at 20 $\text{V}_{{\mathrm {AC}}}$ continuous unipolar actuation, by using a 40 nm thick Al2O3 humidity barrier. However, the initial maximum angular deflection, polarization, and dielectric permittivity decreased by about 6, 11, and 12 %, respectively, for Al2O3 capped devices. For both bare and encapsulated devices, the onset of electrothermal breakdown-events was the dominant cause of degradation. Severe distortions in the device’s dynamic behavior, together with failure from loss of angular deflection, preceded time-dependent dielectric breakdown in 95% relative humidity. Moreover, due to the film-substrate stress transfer sensitivity of thin-film devices, water-induced degradation affects the reliability of thin-film piezoMEMS differently than bulk piezoMEMS. [2020-0228] [ABSTRACT FROM AUTHOR]