Chemical Solution Deposition Technique Research Articles

PZT based dual energy harvester using chemical solution deposition technique

The present finding reports the state-of-art thin film based dual energy harvester which can harvest both mechanical as well as magnetic energies. Dual energy harvester is realised with the help of Lead Zirconium Titanate (PZT) thin film and nickel (Ni) foil. Ferroelectric PZT has been grown with the help of chemical solution deposition technique under optimised conditions on Nickel cantilevers. The effect of damping mass on the resonating frequency of the PZT-60/Ni dual cantilever has been studied. The maximum power and voltage generated by dual energy harvester at the matching load impedance of 100 kΩ under resonance condition were about 117 × 102 mW/m3 and 52 mV respectively corresponding to an applied acceleration of 1.0 g. A change of about 0.5 mV/Oe voltage was achieved for PZT-60/Ni cantilever in the presence of magnetic field. The dual energy harvester prepared with the help of chemical solution technique is found to have profound response and hence enables the realization of self powered electronic devices by scavenging an ambient magnetic and mechanical energies for various wireless electronic applications ranging from medical implant to health monitoring areas.

Investigating mechanism of photo refractivity in Mg substituted ZnO thin films using pump and probe technique

In the current investigation magnesium (Mg) has been incorporated in the ZnO matrix to induce photo refractivity thereby adding an extra dimension to its already present multi-functionality. Undoped and MgxZn1-xO (x = 0.25, 0.30, 0.35, 0.40, 0.45) thin films have been grown using Chemical Solution Deposition (CSD) technique. Obtained X-Ray Diffraction (XRD) spectra exhibits a slight shift in the peak value along (002) plane whereas UV–visible spectra indicates corresponding widening of ZnO band gap values (3.24–3.64 eV) with increase in Mg content. Mg substituted ZnO films were then investigated for their ferroelectric properties using a P-E hysteresis loop tracer. It was noted that ZnO film with 35 % Mg content (x = 0.35) exhibited the high values for saturation (Ps = 1.8 μC/cm2) and remnant (Pr = 0.7 μC/cm2) polarization. Hence the ZnO with same Mg concentration was investigated for nonlinear optical properties (two wave mixing phenomenon) using pump and probe technique. In order to enhance the beam amplification gain and impart stability Au micro-dots were thermally evaporated onto MgxZn1-xO (x = 0.35) films. The maximum beam amplification gain was noted to shoot up to 2.7 post patterning of MgxZn1-xO (x = 0.35) film surface by Au micro-dots.

Plasmonic electro-optic modulators on lead zirconate titanate platform

Abstract The advancement in material platforms exhibiting strong and robust electro-optic effects is crucial for further progress in developing highly efficient and miniaturized optoelectronic components with low power consumption for modern optical communication systems. In this work, we investigate thin-film lead zirconate titanate (PZT) substrates grown by a chemical solution deposition technique as a potential platform for on-chip plasmonic electro-optic modulators. A high modulation depth (>40 %) is achieved with 15 μm-long electro-optic directional coupler modulators. An unusual cutoff in the modulation frequency response at ∼200 kHz is observed and further studied with respect to possible reorientation effects. Second-harmonic generation signals are found influenced by the externally applied electric field, indicating that the domain reorientation effect can be responsible for the unusual frequency response observed.

Remote epitaxy-based atmospherically stable hybrid graphene template for fast and versatile transfer of complex ferroelectric oxides onto Si

Heterogenous integration of complex epitaxial oxides onto Si and other target substrates is recently gaining traction. One of the popular methods involves growing a water-soluble and highly reactive sacrificial buffer layer, such as Sr3Al2O6 (SAO), at the interface and a functional oxide on top of this. To improve the versatility of layer transfer techniques, it is desired to utilize stable (less reactive) sacrificial layers without compromising on the transfer rates. In this study, we utilized a combination of chemical vapor deposited (CVD) graphene as a 2D material at the interface and pulsed laser deposited (PLD) water-soluble SrVO3 (SVO) as a sacrificial buffer layer. We then exploit the well-known enhancement of liquid diffusivities by monolayer graphene to enhance the dissolution rate of SVO over ten times without compromising its atmospheric stability. We demonstrate the versatility of our hybrid- graphene-SVO- template by growing ferroelectric BaTiO3 (BTO) via PLD and Pb(Zr, Ti)O3 (PZT) via Chemical Solution Deposition (CSD) technique and transferring them onto the target substrates and establishing their ferroelectric properties. Our hybrid templates allow for the realization of the potential of complex oxides in a plethora of device applications for MEMS, electro-optics, and flexible electronics.

Enhanced piezoelectric properties in europium-doped lead lanthanum zirconate titanate thin films

This paper investigates the effect of europium (Eu3+) doping on the crystal structure, dielectric and piezoelectric properties of lead lanthanum zirconate titanate (PLZT) thin film. For the present study, Pb0·92(La1-yEuy)0·08(Zr0·52Ti0·48)O3 (PLEZT) compositions with various Eu concentrations (y = 0.0, 0.3, 0.5 and 0.7) were prepared on Si/SiO2/Ti/Pt substrates by chemical solution deposition technique. The X-ray diffraction and Raman spectroscopy studies revealed the structural distortions in PLZT films with Eu doping. The piezoelectric charge coefficient showed significant enhancement with Eu doping for y = 0.5 composition, with good room temperature frequency stability. This improvement in the piezoelectric characteristics of PLEZT films is the result of stronger intrinsic contributions brought in by bigger c/a ratios and higher extrinsic contributions from non-180° domain wall motions.

Sol-gel synthesis and Opto-electrical properties study of double perovskite oxide Dy2NiMnO6 thin film

Thin film of double perovskite oxide Dy2NiMnO6 (DNMO) has been synthesised by the simple and cost-effective chemical solution deposition technique. The room temperature X-ray diffraction pattern and Raman spectroscopy confirm the monoclinic (space group - P21/n) crystal structure of polycrystalline DNMO thin film. The optical and electrical properties of DNMO thin film are investigated to study the detailed photo physical properties of DNMO thin film. The direct band gap and temperature dependant impedance spectroscopy confirm its semiconductor behaviour. Impedance spectroscopy also shows two types of dielectric relaxation behaviour and the nature of conductivity reveals the electron hopping conduction mechanism. Moreover, the chemical solution deposited DNMO film shows promising photo response under white light.

Tunable resistive nature of LaMnO3 / Nd0.7Sr0.3MnO3 interfaces: Role of swift heavy ion irradiation

In the present communication, high crystalline quality LaMnO3/Nd0.7Sr0.3MnO3/SrTiO3 (LMO/NSMO/STO) structures were fabricated using low cost chemical solution deposition (CSD) technique to perform swift heavy ion (SHI) irradiation using 100 MeV O+7 ions. X–ray diffraction (XRD) θ–2θ, XRD φ–scan and XRD ω–scan results show a single phase nature having finite and ion fluence influenced strain state, four–fold lattice symmetry with epitaxial growth and an effective influence of ion fluence on the crystalline granular structure of LMO/NSMO/STO structure. Atomic force microscopy (AFM) images suggest an effect of ion fluence on the surface morphology through the creation of defects and local annealing effect. Zero field cooled (ZFC) protocol based LMO/NSMO interface resistivity suggests that transport nature of the LMO/NSMO interface of all studied LMO/NSMO/STO structures is strongly governed by lattice strain between LMO//NSMO layers and STO substrate, strain across LMO and NSMO manganite layers, crystalline granular structure, grain size, grain boundary density and grain boundary nature of the LMO and NSMO manganite thin layers. ZFC protocol followed by field cooled cooling (FCC) and field cooled warming (FCW) protocols for the realization of LMO/NSMO interface resistivity behaviors have been understood on the bases of freezing and trapping of tiny high temperature high resistive insulating clusters within the coexisting low temperature low resistive metallic phase fraction. Observed LMO/NSMO interface resistivity behaviors have been understood using the percolation model fits to the recorded experimental LMO/NSMO interface resistivity data in addition to irradiation influences. Obtained fitting parameters have been discussed in detail based on their variations with different employed resistivity measurement protocols for all pristine and irradiated LMO/NSMO/STO structures.

Synthesis of PEDOT: PSS thin film doped with silver nanoparticles via green approach and study their refractive indices and dispersive parameters using Wemple–DiDomenico (WDD) single oscillator model

Silver nanoparticles (AgNPs) synthesised via green synthesis using clove extract were incorporated into PEDOT:PSS polymers using the chemical solution deposition technique (CSD), and the effect of surface plasmon resonance in the nanocomposites was investigated. To assess the effect of Silver nanoparticles (AgNPs) (and surface plasmon resonance) on the polymer, TEM, UV–Visible spectroscopy, FTIR, Ellipsometry, and Photoluminescence are used. The surface plasmon peak of the curves in UV–Vis spectroscopy study of these films has shifted towards the infrared region, which may be useful in increasing the efficiency of optical devices. The optical band gap calculated using UV–Vis results reduced from 1.77eV for pure PEDOT: PSS to 1.53eV for the nanocomposite. Ellipsometry data is used to calculate Ψ, Δ values and thickness of films. The Wemple-DiDomenico (WDD) single oscillator model was used to analyse and estimate the dispersion parameters of these films. Refractive indices the films were calculated in the range 1.256–1.643 using the Ellipsometry data.

Control of Columnar Grain Microstructure in CSD LaNiO3 Films.

Conductive LaNiO3 (LNO) films with an ABO3 perovskite structure deposited on silicon wafers are a promising material for various electronics applications. The creation of a well-defined columnar grain structure in CSD (Chemical Solution Deposition) LNO films is challenging to achieve on an amorphous substrate. Here, we report the formation of columnar grain structure in LNO films deposited on the Si-SiO2 substrate via layer-by-layer deposition with the control of soft-baking temperature and high temperature annealing time of each deposited layer. The columnar structure is controlled not by typical heterogeneous nucleation on the film/substrate interface, but by the crystallites' coalescence during the successive layers' deposition and annealing. The columnar structure of LNO film provides the low resistivity value ρ~700 µOhm·cm and is well suited to lead zirconate-titanate (PZT) film growth with perfect crystalline structure and ferroelectric performance. These results extend the understanding of columnar grain growth via CSD techniques and may enable the development of new materials and devices for distinct applications.

THE SUBTRACTIVE PROCESS OF FORMING A METALLIZATION SYSTEM.

The subtractive process of forming a metallization system for integrated circuits has been studied. Structures with aluminum and copper conductors with different pitches were used as models. The gaps between the conductors were filled using the chemical solution deposition technique. The formed organosilicate layers provided complete or partial planarization of the relief. Electrical measurements indicated a decrease in capacitance and leakage currents in structures with nanoporous dielectric layers.

Chemical and Microstructural Nanoscale Homogeneity in Superconducting YBa2Cu3O7-x Films Derived from Metal-Propionate Fluorine-free Solutions.

Research involved in developing alternative energy sources has become a necessity to face global warming. In this context, superconductivity is an appealing solution to enhance clean electrical energy provided that lower production costs can be attained. By implementation of chemical solution deposition techniques and high-throughput growth methods, low-cost nanostructured epitaxial cuprate superconductors are timely candidates. Here, we present a versatile and tunable solution method suitable for the preparation of high-performance epitaxial cuprate superconducting films. Disregarding the renowned trifluoroacetate route, we center our focus on the transient liquid-assisted growth (TLAG) that meets the requirement of being a greener chemical process together with ultrafast growth rates beyond 100 nm/s. We developed a facile, fast, and cost-effective method, starting from the synthesis of metal-propionate powders of Y, Ba, and Cu of high purity and high yields, being the precursors of the fluorine-free solutions, which enable the chemical and microstructural nanoscale homogeneity of YBa2Cu3O7-x (YBCO) precursor films. These solutions present endured stability and enable precise tunability of the composition, concentration, porosity, and film thickness. Homogeneous precursor films up to thicknesses of 2.7 μm through eight layer multidepositions are demonstrated, thus establishing the correct basis for epitaxial growth using the fast kinetics of the TLAG process. YBCO films of 500 nm thickness with a critical current density of 2.6 MA/cm2 at 77 K were obtained, showing the correlation of precursor film homogeneity to the final YBCO physical properties.

All-Chemical YBCO-Based Architecture Using a Simplified Multilayer Buffer Deposition

Chemical solution deposition (CSD) is a versatile and cheap technique widely used for both buffer layer and YBa <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2</sub> Cu <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">3</sub> O <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">7−<i>δ</i></sub> (YBCO) epitaxial film growth. One of the main limits hindering the widespread use of the CSD technique in the field of coated conductors is the limited film thickness that can be reached without degradation. Among the different strategies adopted to obtain thicker film by CSD, increase of precursor solution concentration and viscosity can be mentioned. Another interesting approach is the use of multilayer deposition in order to overcome the limits of CSD technique. Multilayer deposition has been so far realized by performing a complete heat treatment - or at least a pyrolysis step - after each deposited layer, resulting in increased processing time and overall cost. In this contribution, we show that an epitaxial multilayer buffer can be easily obtained by means of multiple successive depositions, in which after each layer only a fast drying step of the precursor solution is carried out. In this way, only a single conversion heat treatment can be used. This approach not only allows a significant reduction on the processing time but also it is more suitable for the growth on metallic template. The viability of this approach is shown by using multilayer Zr-doped CeO <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2</sub> buffer deposition on single crystalline YSZ substrate. It is shown that, up to 8 layers, no significant structural and morphological degradation of the buffer layer occurs. Further, YBCO film grown by CSD was used to test the suitability of multilayer buffer. YBCO film grown on multilayer buffer shows excellent superconducting properties, with zero-resistance critical temperature up to 92 K and a critical current density exceeding 1 MA/cm2 at 77 K in self field.

Influence of morphology on photoanodic behaviour of WO3 films in chloride and sulphate electrolytes

Photoelectrochemical (PEC) synthesis is gaining an increasing interest amongst the advanced oxidation processes, which can convert solar energy to chemical energy in the form of value-added oxidants suitable for water treatment and disinfection. To ensure the efficient generation of desired product, careful engineering of semiconductor/electrolyte interface is required. In this study the effect of surface morphology on the competition between the photoanodic oxidation of water molecules and anions occurring on the surface of tungsten (VI) oxide electrodes in sulphate and chloride electrolytes is analysed. Four WO3 coatings composed of plate-like particles, similar in shape but of different sizes, were prepared using chemical solution deposition technique and methanol, ethanol, isopropanol or butanol as reductants. Crystalline structure, morphology, surface chemical composition and optical properties of the coatings were characterised applying X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy and photoluminescence spectroscopy techniques. The photoelectrochemical performance of WO3 layers was studied using the methods of electrochemical impedance spectroscopy, cyclic voltammetry and chronoamperometry. Possible photoanodic processes are analysed on the basis of the proposed potential-assisted photochemical approach, which takes into consideration high oxidizing power of photogenerated holes in WO3 and formation of radicals as intermediates. Significant role of specific adsorption of chloride ions as well as intermediate products of their oxidation (Cl·, Cl2˙−) in lowering the photocurrent onset potential, trapping the photogenerated charge carriers as well as protecting WO3 surface from accumulation of hydroxo species is revealed. Influence of morphology on the competition between certain photoanodic reactions occurring at the semiconductor/electrolyte interface in the PEC systems investigated is explained considering the effects of steric hindrance as well as electrostatic interactions between adsorbing/reacting species at rough electrified interfaces.

Chemical solution deposition of epitaxial indium- and aluminum-doped Ga2O3 thin films on sapphire with tunable bandgaps

Compared to the vacuum-required deposition techniques, the chemical solution deposition (CSD) technique is superior in terms of low cost and ease of cation adjustment and upscaling. In this work, highly epitaxial indium- and aluminum-doped Ga2O3 thin films are deposited using a novel CSD technique. The 2θ, rocking curve, and φ-scan modes of x-ray diffraction (XRD) measurements and high-resolution transmission electron microscopy suggest that these thin films have a pure beta phase with good in- and out-of-plane crystallization qualities. The effect of incorporating indium and aluminum into the crystallization process is studied using high-temperature in situ XRD measurements. The results indicate that indium and aluminum doping can shift the crystallization of the thin films to lower and higher temperatures, respectively. Additionally, ultraviolet-visible spectroscopy measurements indicate that the bandgap of the sintered thin films can be tuned from 4.05 to 5.03 eV using a mixed precursor solution of In:Ga = 3:7 and Al:Ga = 3:7. The photodetectors based on the (InGa)2O3, pure Ga2O3, and (AlGa)2O3 samples exhibit the maximum photocurrents at 280, 255, and 230 nm, respectively. The results suggest that the described CSD technique is promising for producing high-quality bandgap tunable deep-ultraviolet photoelectrical and high-power devices.

High electro-optic coefficient lead zirconate titanate films toward low-power and compact modulators

Developing strong electro-optic (EO) effect materials and devices is vital for high-speed optical communications and integrated photonics. In this work, we explored a chemical solution deposition technique to grow pure perovskite lead zirconate titanate (PZT) films on sapphire substrates. The grown PZT films demonstrated a preferential orientation and a broadband optical transmission window ranging from 600 to 2500 nm. Based on the high-quality film, we subsequently designed and fabricated a PZT Mach-Zehnder interference waveguide EO modulator. The measured half-wave voltage Vπ is 3.6 V at the wavelength of 1550 nm, corresponding to an in-device EO coefficient as high as ∼133 pm/V. The response of the PZT modulator from 6 to 12 GHz has been measured. We foresee that our work may pave the way towards power-efficient, ultra-compact integrated devices, including modulators, switches and sensors.

Comparison of Ferroelectric Photovoltaic Performance in BFO/BTO Multilayer Thin Film Structure Fabricated Using CSD &amp; PLD Techniques

Multilayer thin film structures of BFO/BTO possessing a distinct count of layers were prepared by chemical solution deposition and pulsed laser deposition techniques. These two different deposition techniques have been explored to investigate the effect of deposition technique on ferroelectric-photovoltaic properties of the BFO/BTO system in detail. Multilayers prepared using both the techniques exhibit pure perovskite structure showing the tetragonal and rhombohedral phases of BTO/BFO respectively obtained using XRD analysis. The multilayer thin film of BTO/BFO structures possessed enhanced ferroelectric and ferromagnetic properties, which is found to be increasing as the number of layers increases. The maximum values of Ps = 99.80 μC/cm2 and Ms = 94.70 emu/cm3 were obtained for the six-layer system prepared using the PLD technique. The six-layer PLD-grown PV cell upon irradiation with 405-nm wavelength light with 160 mW/cm2 intensity, showed a large increase in photocurrent from 4.5 × 10−7A to 3.84 × 10−4A as compared to the PV cell grown using CSD. The obtained magnitudes of short-circuit photocurrent density (Jsc) and open circuit voltage (Voc) were 0.384 mA/cm2 and − 0.40 individually with 0.098% light-to-electricity conversion efficiency for a six-layer PLD-grown PV cell.

Unravelling the Crystallization Process in Solution-Derived YBa2Cu3O7-δ Nanocomposite Films with Preformed ZrO2 Nanocrystals via Definitive Screening Design.

A low-cost chemical solution deposition technique was employed to prepare YBa2Cu3O7-δ (YBCO) nanocomposite films starting from a colloidal solution containing preformed ZrO2 nanocrystals. As previous publications revealed, an increase in the amount of nanocrystals results in a progressive deterioration of the film properties. The parameters that control this process and their interplay are still unknown in detail. Using definitive screening design (DSD), a design-of-experiments approach, allowed determining which of the multiple growth parameters play a key role for improving the superconducting properties of YBCO nanocomposite films even with a large concentration of nanocrystals. In order to show the potential of DSD, it has been applied for the optimization of two different properties: the critical temperature Tc and the full width at half-maximum of the (005) YBCO reflection. This work shows that DSD is a powerful and efficient method that allows optimizing certain processes with a minimal number of experiments.

Electronic and Magnetic Properties of Chemical Solution Deposited BiFeO3 Thin Film: a Soft X-ray Magnetic Circular Dichroism Study

In this work, we report the electronic and magnetic properties of epitaxial BiFeO3 (BFO) thin film deposited on SrTiO3 (001) substrate via the chemical solution deposition technique. These properties of pure BFO thin films were characterized by X-ray absorption spectroscopy (XAS) and X-ray magnetic circular dichroism techniques (XMCD). The large magnetization at Fe-edge could be due to annealing in nitrogen. Annealing in nitrogen atmosphere increases the grain size and porosity which lead to create more oxygen vacancy. The presence of oxygen vacancies which compensate the bismuth vacancies created due to bismuth volatilization. The origin of large orbital momentum in BFO thin film is also discussed. The O K-edge spectra display large spectral variation depending on the polarization vector E. The structural distortion at oxygen octahedral induces large anisotropy due to Fe 3d–O 2p hybridization. The hybridized Fe 3d orbitals contribute a much larger orbital momentum in BFO thin film.

Texture and terahertz analysis of YBa2Cu3O7 grown onto LaAlO3 by the chemical solution deposition technique

ABSTRACT We analyze in-plane and out-of-plane texture and terahertz analysis of a YBa2Cu3O7-δ (YBCO) film deposited by chemical solution deposition technique onto LaAlO3 (100) substrate. X-ray diffraction reveals the presence of (00l) reflections for the YBCO phase. The out-of-plane texture, measured by a rocking curve, shows two sub-layers with Δω = 0.45° and 1.8°. The value of the c-axis fraction of the crystallites is 81%. Also, the in-plane texture was studied by ϕ–scan measurements of (102) reflection, displaying mostly a colony of c-axis oriented grains, and two colonies of a-axis oriented grains onto the YBCO surface. In addition, the temperature dependence of the magnetization measurement revealed a critical temperature of 90 K, typical for YBCO superconductor material. From the temperature-dependent optical conductivity of YBCO, we observe an absorption feature at ≈1.57 THz, which redshifts with increasing temperature.

Influence of BiFeO3 perovskite on the structure and magnetic properties of lead-free Bi0.5Na0.4K0.1TiO3 films

Lead-free (1-x)Bi0.5Na0.4K0.2TiO3-xBiFeO3 (abbreviated as BNKT-xBFO) ferroelectric films with x in the range from 0.00 to 0.10, were synthesized by the chemical solution deposition technique on Pt/Ti/SiO2/Si substrates. The microstructures and magnetic behaviors of BNKT-xBFO films were analyzed in detail as a function of BFO concentration. X-ray diffraction patterns indicated that BNKT-xBFO films were grown with a single-phase perovskite structure. The pure films showed an antiferromagnetic behavior. The magnetic properties of the films were gradually transferred from antiferromagnetic to ferromagnetic properties when BFO concentration was raised. The saturated magnetization (M S) reached the highest value of 10.3 emu cm−3 at the BFO-doped concentration x = 0.10. Our work will contribute to illuminate the impact of BFO (ABO3 perovskite structure) on the magnetic properties of BNKT materials at room temperature.