Oxide Nanopowders Research Articles

Antibacterial Properties and Biocompatibility of Multicomponent Titanium Oxides: A Review

The simple oxides like titania, zirconia, and ZnO are famous with their antibacterial (or even antimicrobial) properties as well as their biocompatibility. They are broadly used for air and water filtering, in food packaging, in medicine (for implants, prostheses, and scaffolds), etc. However, these application fields can be broadened by switching to the composite multicomponent compounds (for example, titanates) containing in their unit cell, together with oxygen, several different metallic ions. This review begins with a description of the synthesis methods, starting from wet chemical conversion through the manufacturing of oxide (nano)powders toward mechanosynthesis methods. The morphology of these multicomponent oxides can also be very different (like thin films, complicated multilayers, or porous scaffolds). Further, we discuss in vitro tests. The antimicrobial properties are investigated with Gram-positive or Gram-negative bacteria (like Escherichia coli or Staphylococcus aureus) or fungi. The cytotoxicity can be studied, for example, using mouse mesenchymal stem cells, MSCs (C3H10T1/2), or human osteoblast-like cells (MG63). Other human osteoblast-like cells (SaOS-2) can be used to characterize the cell adhesion, proliferation, and differentiation in vitro. The in vitro tests with individual microbial or cell cultures are rather far away from the real conditions in the human or animal body. Therefore, they have to be followed by in vivo tests, which permit the estimation of the real applicability of novel materials. Further, we discuss the physical, chemical, and biological mechanisms determining the antimicrobial properties and biocompatibility. The possible directions of future developments and novel application areas are described in the concluding section of the review.

Outstanding Activity and Durability of Supported NiCo2O4 Nanoparticles for Direct Ethanol Fuel Cells

ABSTRACTThe rational design of noble metal‐free electrocatalysts represents one of the basic stones for fuel cell development. With the exploration of eco‐friendly nanomaterials for the investigated alcohol oxidation process, nickel‐based electrodes have been recognized as the most auspicious anodes with promoted activity and stability. In this work, a series of NiCo2O4 nanoparticles were deposited onto graphite sheets (NiCo2O4/T) introducing varied proportions of cobalt oxide species. Co‐precipitation protocol of the respective metallic hydroxides onto the carbonaceous support was followed with consecutive annealing in an air atmosphere at 400°C. The fabricated mixed metallic oxide nanopowder was physically studied using X‐ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X‐ray analysis (EDX), X‐ray photoelectron spectroscopy (XPS), and selected area electron diffraction (SAED). Uniformly arranged nanoparticles were observed on graphite surface as evidenced by SEM and TEM. The cubic lattice structure of formed NiCo2O4 crystals was also confirmed by XRD through the defined peaks of binary metallic oxides clarifying their successful preparation scheme. The electrocatalytic properties of these NiCo2O4/T nanocatalysts were evaluated for oxidizing ethanol molecules in basic solution. Pronounced oxidation current densities were remarkably measured at NiCo2O4/T electrodes in relation to that at NiO/T. Differing the introduced cobalt oxide content into the synthesized nanocatalyst significantly controlled its catalytic performance. NiCo2O4/T‐20 exhibited the highest activity and stability among the prepared nanomaterials. Much decreased charge transfer resistances were also recorded at this electrode demonstrating its promoted electron transfer characteristics. This work could provide a reasonable route for the simple synthesis of comparable transition metallic oxides with promising attitudes for energy generation purposes.

Photocatalytic performance of pristine NiO and Ni6MnO8 nanopowders in degradation of Rose Bengal dye.

Effective tuning of bandgap of transition metal oxides is a promising approach in improving their photocatalytic activity towards organic pollutant removal from water. The present paper describes synthesis of nickel oxide and Ni6MnO8 nanopowders by simple hydrothermal technique. During the synthesis of nickel oxide by hydrothermal process, addition of Mn source resulted in the formation of Ni6MnO8. X-ray diffraction analysis has confirmed the formation of nickel oxide and Ni6MnO8 both having cubic structures. The average crystallite size decreases from 20 to 12nm on increasing Mn source concentration during the synthesis of nickel oxide. Rectangular, hexagonal, and triangular faceted structures are revealed from the scanning electron microscopic images. HRTEM also indicated formation of cubical shaped structure with average sizes of 32 and 21nm for pristine NiO and Ni6MnO8 nanopowders. In the case of Ni6MnO8 nanopowder, inter-connected cubes are seen. Modification in Ni6MnO8 nanopowder is found to display multiple optical band gaps at 1.21, 1.82, and 2.65eV. The formation of Ni6MnO8 phase was further confirmed by XPS studies due to the presence of + 4 oxidation state of Mn. The photocatalytic properties of synthesized nickel oxide and Ni6MnO8 nanopowders are measured by using Rose Bengal dye under UV illumination. Enhancement in the photocatalytic activity is noticed in the case of Ni6MnO8 nanopowder as compared to nickel oxide nanopowder. Nearly 90% dye degradation is observed on utilizing Ni6MnO8 nanopowder.

Photocatalytic degradation of acetaminophen, ciprofloxacin and amoxicillin using UV/ZnO in a suspended photocatalytic reactor

Abstract This study aims at evaluation of the photocatalytic degradation of pharmaceutical compounds acetaminophen (ATM), ciprofloxacin (CXN), and amoxicillin (AMX) using zinc oxide (ZnO) nano powder as a photocatalyst in a suspended reactor using a 16 W UV lamp. Operating parameters pH, catalyst dosage, and pollutant concentration were optimised for a working volume of 1.3 litres of model pharmaceutical compounds. The photo degradation efficiency was 95% at pH 6 after 5 h of irradiation for ATM, 98% at pH 6 after 2 h of irradiation for CXN, and 100% at pH 10 after 3 h of irradiation for AMX. The reaction kinetics for the degradation of ATM, CXN, and AMX followed pseudo-first order with the rate constants in the order of kAMX>kCXN>kATM 0.0321 min−1, 0.0232 min−1 and 0.0070 min−1 respectively. TOC (Total Organic Carbon) analysis was carried out for the model compounds, among which compound amoxicillin was found having a higher rate constant of about 0.0108 min−1, which is 1.2 times higher than ciprofloxacin and 2.5 times greater than acetaminophen. This study concludes that ZnO nano powder is efficient in degrading the model pharmaceutical compounds ATM, CXN, and AMX by utilising the UV light, which is evident from the results of the UV–vis spectrophotometer, HPLC analysis, and mineralisation study. In addition, ANOVA was performed on the results obtained from optimisation studies, which confirms the substantial influence of the operating parameters on the degradation of the compounds.

Synthesis of gamma aluminum oxide nano-powder for adsorptive removal of nitrate from aqueous solutions

Nitrate pollution of surface and groundwater could be a worldwide issue resulting in the threat to the environment and public health. The removal of nitrate from water was carried out using gamma aluminum oxide (γ-Al2O3) nano powder. The nano powder was synthesized from aluminum oxide powder using the aqueous-based reflux method and applied for nitrate removal. The surface properties of the activated γ-Al2O3 were characterized using FTIR, XRD, and BET surface area analysis. Analysis of variance (ANOVA) was used to analyze nitrate removal to determine the appropriate regression model, which was found to be the quadratic model with a coefficient of determination (R2 = 0.99). The adsorption process was observed to be dependent on initial nitrate concentration, adsorbent dose, and time. The optimized nitrate removal efficiencies were 97.01% using a dose of 2.26 gL−1, an initial nitrate concentration of 10 mgL−1, and a contact time of 45 min. Additionally, the kinetics of nitrate ion adsorption was discussed based on pseudo-first order and pseudo-second order kinetic models. The experimental data fitted well with the pseudo-second order kinetic model, indicating that the adsorption mechanism is chemisorption. The equilibrium adsorption of nitrate experimental data followed the both Freundlich and Langmuir isotherm (R2 = 0.95), implying a homogeneous nature of the γ-Al2O3 surface sites. These results suggest further consideration of the practical application of γ-Al2O3 for nitrate treatment for domestic purposes.

Study of the Structure and Properties of Magnetic Nanopowders of Magnetite-Maggemite Series Solid Solutions by SAPNS

Nanopowders of the magnetite-maggemite series were synthesized by both aqueous precipitation and using sol-gel technology. A comprehensive comparative study of the structure of the synthesized powders was carried out using the methods of X-ray phase analysis (XPA), scanning electron microscopy (SEM), low-temperature nitrogen adsorption and small-angle polarized neutron scattering (SAPNS). It has been established that the synthesized iron oxide nanopowders are porous systems that, depending on the synthesis method, have a one-level or two-level (for powders obtained by aqueous synthesis) and three-level (for powders obtained by the sol-gel method) hierarchical structure organization with different characteristic scales and types of aggregation for each from structural levels, and the characteristic size for the larger level in both cases exceeds 45 nm. It was revealed that the magnetic structure of the obtained iron oxide powders, regardless of the synthesis method, consists of superparamagnetic particles with a characteristic magnetic radius RМ ≈ 4 nm and magnetic-nuclear cross-correlations RMN ≈ 3 nm for powders obtained by the sol-gel method; and with RM ≈ 5–11 nm and RMN ≈ 4–8 nm for powders obtained by aqueous synthesis, depending on the production conditions.

Formation of Bismuth Doped Cerium Oxide Nanopowder with Thermal Stability and UV Absorption Properties

Formation of Bismuth Doped Cerium Oxide Nanopowder with Thermal Stability and UV Absorption Properties

Influence of Gamma-Phase Aluminum Oxide Nanopowder and Polyester-Glass Recyclate Filler on the Destruction Process of Composite Materials Reinforced by Glass Fiber.

Recycling of composite materials is an important global issue due to the wide use of these materials in many industries. Waste management options are being explored. Mechanical recycling is one of the methods that allows obtaining polyester-glass recyclate in powder form as a result of appropriate crushing and grinding of waste. Due to the fact that the properties of composites can be easily modified by adding various types of fillers and nanofillers, this is one of the ways to improve the properties of such complex composite materials. This article presents the strength parameters of composites with the addition of fillers in the form of polyester-glass recyclate and a nanofiller in the form of gamma-phase aluminum nanopowder. To analyze the obtained results, Kolmogorov-Sinai (K-S) metric entropy was used to determine the transition from the elastic to the viscoelastic state in materials without and with the addition of nanoaluminum, during a static tensile test. The tests included samples with the addition of fillers and nanofillers, as well as a base sample without any additives. The article presents the strength parameters obtained from a testing machine during a static tensile test. Additionally, the acoustic emission method was used during the research. Thanks to which, graphs of the effective value of the electrical signal (RMS) were prepared as a function of time, the parameters were previously identified as extremely useful for analyzing the destruction process of composite materials. The values obtained from the K-S metric entropy method and the acoustic emission method were plotted on sample stretching graphs. The influence of the nanofiller and filler on these parameters was also analyzed. The presented results showed that the aluminum nanoadditive did not increase the strength parameters of the composite with recyclate as a result of the addition of aluminum nanofiller; however, its addition influenced the operational parameters, which is reflected in a 5% increase in the UTS value (from 55% to 60%).

Graphene Supported Silicon Nanocomposites As Anode for Lithium-Ion Batteries

This work indicates Silicon/Grphene (Si/G) nanocomposites anode on the performance in lithium-ion batteries (LIBs).The self-assembled graphene aerogel and silicon (Si/G) anode materials with some surface defects have been successfully prpared by hydrothermal synthesis using chemically modified graphene oxide and commercial Si nanopowder (about 50 nm) as precursor. The morphologies and textural properties of as-obtained Si/G were investigated by scanning electron microscopy, X-ray photoelectron spectroscopy, and other sturucture techniques. The surface defects and electrical conductivities of Si/G can be controlled by adjusting the amount of Si nanopowder. The results indicate that Si/G with Si amount of half exhibits excellent stability and reversible capacity and superior rate capability with excellent cycling stability. It is demonstrated that the 3D porous network with increased defect density, as well as the considerable electrical conductivity, results in the excellent electrochemical performance of the as-made Si/G anodes in LIBs.

Cytotoxicity and antioxidant activity of iron oxide nanopowders synthesized by radiation-chemical method using different precursors

The study revealed a correlation between the cytotoxicity and antioxidant activity of iron oxide nanopowders produced by the radiation-chemical method and the choice of precursors (iron (III) nitrate or iron(II) sulfate), and the temperature of pre-annealing of the synthesized product, and also irradiation with accelerated electrons. Notably, high and lowabnormal cytotoxicity of aqueous suspensions of samples S300 and S400, respectively, annealed at temperatures of 300 and 400 °C, was observed for the first time at all concentrations (0.1–1.0 ml/mg). The likely cause of this abnormal cytotoxicity was identified as alterations in the textural and structural properties of NP after annealing.Furthermore, a significant impact of electron beam irradiation on the antibacterial and antioxidant properties of both unannealed and annealed iron oxide NP was discovered with irradiated samples exhibited lower cytotoxicity compared to non-irradiated ones. Additionally, the deposition of nanosilver on the surface of iron oxide powders was found to significantly influence their biological properties, with the survival of Vero cell cultures being dependent on the composite concentration in the aqueous suspension.A study of the oxidative stress of composites based on iron oxides coated with silver showed that they significantly increased cell viability, and at a concentration of 1 mg/ml provided complete mitigation of oxidative stress in cells.

Synthesis and Characterization of ZnO and TiO2 Hybrid Coatings for Textile UV Anti-Aging Protection.

The aim of this study was to prepare and characterize thin hybrid films on polyurethane-coated knitted fabrics and to achieve satisfactory color fastness to artificial light. Sol-gel-derived hybrid thin films were deposited via the dip-coating of 3-glycidoxypropiltrimethoxysilane. Titanium dioxide (TiO2) and zinc oxide (ZnO) nanopowders were added to compensate for the insufficient aging resistance, which manifests itself in low color fastness and is one of the most frequent complaints from manufacturers of coated marine fabrics (yachts, boats, etc.). The optimum processing conditions were determined by varying the concentration of precursors and auxiliaries, the mass concentration of TiO2 and ZnO nanopowders, the drawing speed, and the methods and process of fabric treatment. The hybrid films were also characterized using scanning electron microscopy and Fourier transform infrared spectroscopy with attenuated total internal reflection, while Spectraflash SF 300 investigated color fastness. After 300 h of exposure in a xenon chamber, the thin hybrid films showed good color fastness and good resistance to washing cycles. The sol-gel treatment proved to be a successful answer to the manufacturers' need for the post-treatment of polyurethane-coated knitted fabrics against UV radiation for use in the marine sector (yachts, speedboats, etc.).

Laser synthesis of oxide nanoparticles with controlled gas condensation

In this work, the oxide nanopowders of Al2O3, ZrO2, Y2O3, Gd2O3, CeO2, and SiO2 were synthesized by CW CO2 laser vaporization technique with controlled gas condensation in an inert atmosphere. Methods for controlling the size of the resulting nanoparticles by adjusting the gas composition and pressure during the vaporization process have been demonstrated. The potential for producing ultrasmall oxide nanoparticles with dimensions less than 5 nm has been shown. The size distribution of nanoparticles taken from different parts of the evaporation-condensation tract was studied using scanning (SEM) and transmission (TEM) electron microscopy methods. The effect of synthesis conditions (pressure and composition of the inert gas) on characteristics of the nanoparticles is discussed. Using a wide class of simple oxides as the example, it is shown that the powders synthesized by the laser method consist of three types of particles: target spherical particles with a diameter of 3–20 nm (more than 98%), larger spherical particles with a diameter of 50–200 nm, and shapeless large particles with sizes more than 200 nm. The possibility of separating large particles from the main particles using the original labyrinth system for gas pumping is shown. The obtained particles with controlled sizes can be effectively used in various applications, in particular, for the preparation of catalysts and adsorbents.

Sn99Ag0.3Cu0.7–TiO2 composite solder joints and their influence on thermal parameters of power components

PurposeThis paper aims to investigate the influence of composite solder joint preparation on the thermal properties of metal-oxide-semiconductor field-effect transistors (MOSFETs) and the mechanical strength of the soldered joint.Design/methodology/approachReinforced composite solder joints with the addition of titanium oxide nanopowder (TiO2) were prepared. The reference alloy was Sn99Ag0.3Cu0.7. Reinforced joints differed in the weight percentage of TiO2, ranging from 0.125 to 1.0 Wt.%. Two types of components were used for the tests. The resistor in the 0805 package was used for mechanical strength tests, where the component was soldered to the FR4 substrate. For thermal parameters measurements, a power element MOSFET in a TO-263 package was used, which was soldered to a metal core printed circuit board (PCB) substrate. Components were soldered in batch IR oven.FindingsShear tests showed that the addition of titanium oxide does not significantly increase the resistance of the solder joint to mechanical damage. Titanium oxide addition was shown to not considerably influence the soldered joint’s mechanical strength compared to reference samples when soldered in batch ovens. Thermal resistance Rthj-a of MOSFETs depends on TiO2 concentration in the composite solder joint reaching the minimum Rthj at 0.25 Wt.% of TiO2.Research limitations/implicationsMechanical strength: TiO2 reinforcement shows minimal impact on mechanical strength, suggesting altered liquidus temperature and microstructure, requiring further investigation. Thermal performance: thermal parameters vary with TiO2 concentration, with optimal performance at 0.25 Wt.%. Experimental validation is crucial for practical application. Experimental confirmation: validation of optimal concentrations is essential for accurate assessment and real-world application. Soldering method influence: batch oven soldering may affect mechanical strength, necessitating exploration of alternative methods. Thermal vs mechanical enhancement: while TiO2 does not notably enhance mechanical strength, it improves thermal properties, highlighting the need for balanced design in power semiconductor assembly.Practical implicationsIncorporating TiO2 enhances thermal properties in power semiconductor assembly. Optimal concentration balancing thermal performance and mechanical strength must be determined experimentally. Batch oven soldering may influence mechanical strength, requiring evaluation of alternative techniques. TiO2 composite solder joints offer promise in power electronics for efficient heat dissipation. Microstructural analysis can optimize solder joint design and performance. Rigorous quality control during soldering ensures consistent thermal performance and mitigates negative effects on mechanical strength.Social implicationsThe integration of TiO2 reinforcement in solder joints impacts thermal properties crucial for power semiconductor assembly. However, its influence on mechanical strength is limited, potentially affecting product reliability. Understanding these effects necessitates collaborative efforts between researchers and industry stakeholders to develop robust soldering techniques. Ensuring optimal TiO2 concentration through experimental validation is essential to maintain product integrity and safety standards. Additionally, dissemination of research findings and best practices can empower manufacturers to make informed decisions, fostering innovation and sustainability in electronic manufacturing processes. Ultimately, addressing these social implications promotes technological advancement while prioritizing consumer trust and product quality in the electronics industry.Originality/valueThe research shows the importance of the soldering technology used to assemble MOSFET devices.

Chitosan/MgO NPs/CQDs bionanocomposite coating: Fabrication, characterization and determination of antimicrobial efficacy

The development of new polymer nanocomposites or antibacterial coatings is crucial in combating drug-resistant infections, particularly bacterial infections. In this study, a new chitosan polymer based nanocomposite reinforced with magnesium oxide nanopowders and carbon quantum dots was fabricated by sol-gel technique and coated on 316 L stainless steel. In order to gaining the optimal amount of components to achieve the maximum antibacterial properties, the effect of concentration of nanocomposite components on its antibacterial properties was investigated. Crystal structure, microstructure, elemental dispersion, size distribution, chemical composition and morphology of nanocomposite and coating were characterized with various analyses. The obtained results exhibited that the carbon quantum dot and magnesium oxide nanopowders were distributed uniformly and without agglomeration in the chitosan matrix and created a uniform coating. The antibacterial properties of the synthesized samples against Staphylococcus aureus bacteria (gram positive) were evaluated using disk diffusion and minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) antibacterial tests. The inhibition growth zone formed around the antibiotic and nanocomposite 25 mg/ml under dark and light was about 32 and 14, 11 mm, respectively. Also, MIC and MBC values for final nanocomposite were 62.5 and 125 μg/ml, respectively.

Smart Nanocomposite in the SiC-Si-Al-Al2O3-Geopolymer System

Goal-obtaining of composite in the SiC-Si-Al-Al2O3 (nanopowder)-geopolymer system with the metal-thermal method in the nitrogen medium. Method- In the present paper nanocomposite with SiALON was obtained through alum-thermal process in the nitrogen medium on the base of Geopolymer (kaolin and pology cley – Ukraine), SiC, alumina oxide nanopowder, aluminum nanopowder and Si powder with small additives of glas perlite (Aragatz, Armenia) by the reactive baking method. The advantage of this method is that compounds, which are newly formed thanks to interaction going on at thermal treatment: Si3N4, Si, AlN are active, which contributes to SiALON formation at relatively low temperature, at 1250-13000C. Results-ß-SiAlON was formed at the sintering of SiC-aluminium and silicium powder, geopolymer at 14500C. Porosity of carbide SiAlON composite obtained by reactive sintering, according to water absorption, equals to 13-15%. The samples were fragmented in a jaw-crusher and were powdered in attrition mill till micro-powder dispersion was obtained. Then samples were hot-pressed at 16200C under 30 MPa pressure. Hold-time at the final temperature was 8 min. Sample water absorption, according to porosity, was less than 0.4%. Further studies were continued on these samples. Conclusion-the paper offers processes of formation of SiC-SiAlON composites and their physical and technical properties. Phase composition of the composites was studied by X-ray diffraction method, while the structure was studied by the use of optic and electron microscope. Electric properties showed that the specimen A obtained by hot-compression is characterized by 2 signs lower resistance than the porous material B, which was used to receive this specimen. Probably this should be connected with transition of the reactively baked structure of the hot-compressed material into compact structure. Obtained materials are used in protecting jackets of thermo couples used for melted metal temperature measuring (18-20 measuring) and for constructions used for placing objects in factory furnaces.

Alumina - Stabilized SEI and CEI in Potassium Metal Batteries.

Aluminum oxide (Al2O3) nanopowder is spin-coated onto both sides of commercial polypropene separator to create artificial solid-electrolyte interphase (SEI) and artificial cathode electrolyte interface (CEI) in potassium metal batteries (KMBs). This significantly enhances the stability, including of KMBs with Prussian Blue (PB) cathodes. For example, symmetric cells are stable after 1,000 cycles at 0.5 mA/cm2-0.5 mAh/cm2 and 3.0 mA/cm2-0.5 mAh/cm2. Alumina modified separators promote electrolyte wetting and increase ionic conductivity (0.59 vs. 0.2 mS/cm) and transference number (0.81 vs. 0.23). Cryo-stage focused ion beam (cryo-FIB) analysis of cycled modified anode demonstrates dense and planar electrodeposits, versus unmodified baseline consisting of metal filaments (dendrites) interspersed with pores and SEI. Alumina-modified CEI also suppresses elemental Fe crossover and reduces cathode cracking. Mesoscale modeling of metal - SEI interactions captures crucial role of intrinsic heterogeneities, illustrating how artificial SEI affects reaction current distribution, conductivity and morphological stability.

Alumina – Stabilized SEI and CEI in Potassium Metal Batteries

AbstractAluminum oxide (Al2O3) nanopowder is spin‐coated onto both sides of commercial polypropene separator to create artificial solid‐electrolyte interphase (SEI) and artificial cathode electrolyte interface (CEI) in potassium metal batteries (KMBs). This significantly enhances the stability, including of KMBs with Prussian Blue (PB) cathodes. For example, symmetric cells are stable after 1,000 cycles at 0.5 mA/cm2–0.5 mAh/cm2 and 3.0 mA/cm2–0.5 mAh/cm2. Alumina modified separators promote electrolyte wetting and increase ionic conductivity (0.59 vs. 0.2 mS/cm) and transference number (0.81 vs. 0.23). Cryo‐stage focused ion beam (cryo‐FIB) analysis of cycled modified anode demonstrates dense and planar electrodeposits, versus unmodified baseline consisting of metal filaments (dendrites) interspersed with pores and SEI. Alumina‐modified CEI also suppresses elemental Fe crossover and reduces cathode cracking. Mesoscale modeling of metal – SEI interactions captures crucial role of intrinsic heterogeneities, illustrating how artificial SEI affects reaction current distribution, conductivity and morphological stability.

Simple synthesis and supercapacitor characterization of cobalt molybdate/graphene oxide nanopowders

Simple synthesis and supercapacitor characterization of cobalt molybdate/graphene oxide nanopowders

Physiochemical and electrical activities of nano copper oxides synthesised via hydrothermal method utilising natural reduction agents for solar cell application

Abstract The aim of this study is to explore the potential compatibility of copper oxide nano-powders synthesised via hydrothermal method for solar cell applications by triggering a reaction between copper acetate and various reducing agents derived from natural resources, including Arabic gum, molasses, starch, and vinegar. X-ray diffraction analysis revealed the crystalline phases of the synthesised materials, indicating the successful synthesis of copper oxide material, which was confirmed by identifying patterns that matched specific copper oxide phases. Fourier transform infrared spectroscopy was employed to analyse the molecular vibrations and chemical compounds present in the reducing agents. The reducing properties of the selected materials and their capacity to convert copper acetate into copper oxide were validated. Field-emission microscopy and transmission electron microscopy analyses of the synthesised copper oxide nanoparticles (NPs) revealed variations in particle size and morphology. These variations were dependent on the particular reducing agent utilised during synthesis. Moreover, the carrier concentration, mobility, and resistivity were evaluated as the electrical properties of the spin-coated copper oxide thin films. Hall effect analysis determined that the choice of reducing agent significantly influenced the carrier concentration (n) and mobility (µ) of the films. Remarkably, nano copper oxide films synthesised using starch exhibited irregular spherical grains with porous surfaces. Starch-synthesised samples showed the highest conductivity of n = 1.2 × 1019 cm−3 when compared with those synthesised with other reducing agents. This suggests that the porous surfaces in the starch-synthesised films may have contributed to their enhanced conductivity compared to films synthesised with alternative reducing agents. In summary, the findings emphasised the influence of the reducing agent on the size, morphology, and electrical conductivity of the copper oxide NPs.

Fabrication of Functional Coating Layer for Emerging Transparent Electrodes using Antimony Tin Oxide Nano-colloid

This study fabricated a functional coating layer for transparent electrodes using antimony tin oxide nanopowder. The wet grinding method was employed to create a stable dispersion solution of antimony tin oxide nanopowder with aminopropyl tri-methoxysilane and acetyl acetone as primary dispersing agents. Various concentrations of these dispersing agents were used to determine optimal conditions, followed by a gel reaction to form a stable solution. The primary objective was to provide a viable alternative to indium-based transparent electrodes, specifically indium tin oxide, by incorporating antimony oxide. This approach not only addresses limitations associated with indium, but also enhances mechanical properties. The methodology involves the utilization of antimony tin oxide nanopowder and various solvents including ethanol and aforementioned dispersing agents to create a stable antimony tin oxide sol through wet grinding. Effects of dispersant concentration and milling time on the secondary particle size of the antimony tin oxide sol were thoroughly evaluated. Furthermore, this study examined sheet resistance of resulting coating layers by conducting a comparative analysis between antimony tin oxide and indium tin oxide under similar conditions. Findings of this study meticulously detailed in subsequent sections of the manuscript provide valuable insights into optimizing the entire process, encompassing synthesis, coating, heat treatment, and the production of high-quality transparent conductive coatings. These techniques and outcomes can significantly contribute to the development of more sustainable and cost-effective alternatives to traditional indium-based transparent electrodes.