Field Emission Scanning Electron Microscopy Research Articles

Next-Generation BiOCl/MXene Nanocomposites: Optimized for Dye Removal and Supercapacitor Applications.

The study focuses on the development of an efficient and sustainable solution for synthetic dye degradation through the hydrothermal synthesis of BiOCl and BiOCl/MXene heterostructures. Structural and compositional properties were analyzed by using X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), field emission scanning electron microscopy (FESEM), and X-ray photoelectron spectroscopy (XPS) techniques. A significant reduction in the band gap of BiOCl/MXene to 2.97 eV from 3.62 eV for BiOCl was observed via UV spectroscopy, leading to enhanced photocatalysis with 89% degradation efficiency in just 12 min. The mechanism involved and reactive species were confirmed by LC-HRMS and radical trapping tests, while ICP-MS verified metal content in water before and after degradation. Additionally, the nanocomposite demonstrated a specific capacitance of 431.24 F g-1 at a current density of 1 mA cm-2, with an excellent capacitance retention of 94.35% after 2000 cycles. This study highlights BiOCl/MXene as a promising material for both photodegradation and supercapacitor applications.

Microstructural and biological characterization of 3D printed PEEK scaffolds coated with alginate/CNT for bone regeneration applications

The main aim of bone tissue engineering is to develop novel scaffold structures that integrate biological functionality with sufficient mechanical strength and properties. In this study, bone scaffolds were fabricated using polyether ether ketone (PEEK) via 3D printing, resulting in three different porous designs. To enhance their biological attributes, these scaffolds were coated with an alginate and carbon nanotube (CNT) composite using a freeze-drying technique. The biological characteristics of fabricated samples, such as biocompatibility and bioactivity, were evaluated in simulated body fluid (SBF). Field emission scanning electron microscopy (FE-SEM) analysis showed that the 3D-printed PEEK scaffolds had a porous, uniform, and interconnected architecture with pore sizes between 321–378 µm. Energy-dispersive X-ray spectroscopy (EDS) and X-ray diffraction (XRD) confirmed the formation of hydroxyapatite (HA) and bioactive calcium phosphate (Ca-P) on the scaffold surfaces, indicating their bioactivity. Cell biocompatibility was assessed using the MTT assay, which revealed a high cell viability rate of approximately 97% and no significant toxicity. Consequently, the 3D-printed PEEK scaffold coated with Alginate/0.3%wt CNT demonstrated promising microstructure, bioactivity, and biocompatibility, making it suitable for bone tissue regeneration.Graphical abstract

Synthesis and Characterization of cellulose-derived superabsorbent hydrogel and its applications in the treatment of wastewater containing heavy metal ions

A cellulose xanthate (CX) based polymer hydrogel has been synthesized using free radical graft polymerization technique. Two monomers Acrylic Acid (AA) and Acrylonitrile (AN) were reacted with cellulose xanthate to synthesize the desired hydrogel CX-g-poly(AA-co-AN). The synthesized hydrogel has been characterized by various techniques viz. Thermo-gravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR), UV-visible spectroscopy (UV), Field emission scanning electron microscope (FESEM) and Point zero charge (PZC). This hydrogel has been employed for the removal of toxic metal ions from wastewater. The maximum percentage removal has been found to be 97.5 (±4.87)% for Cu2+ ions and 96.1 (±4.80)% for Co2+ ions under optimum pH 6. The calculated adsorption capacities have been found to be 330.03 (±35.3) mg/g for Cu2+ ions and 325.73 (±22.4) mg/g for Co2+ ions using the Langmuir Adsorption isotherm model. The thermodynamic parameters depicted that the process was endothermic, and spontaneous. The adsorption kinetics data shows excellent fit with pseudo-second-order kinetic model. The synthesized hydrogel exhibits a high swelling ratio of 846.85 (±42.36) g/g and retention ratio of 50.12 (±2.50) % in distilled water. Also, the synthesized hydrogel showed good reusability, exhibiting percentage removal 83.2% for Cu2+ ions and 81.3% for Co2+ ions in the fifth cycle.

Enhanced lead adsorption by eco-hydroxyapatite derived from marble sludge: Optimization and kinetic study

In this study, eco-hydroxyapatite (e-HAP) was synthesized from marble sludge via a hydrothermal process for utilization as an adsorbent in the removal of Pb2+ ions from wastewater. X-ray powder diffraction (XRD) and thermal field emission scanning electron microscope (FE-SEM) revealed that increasing the Ca/P molar ratio (CPMR) and hydrothermal temperature (HT) increased crystallinity and that the influence of HT was more apparent. An increase in crystallinity, crystal length, and peak intensity was observed following an increase in the CPMR. Adsorption studies show that when the HT was 393 K, the CPMR was 0.67, the initial Pb2+ ion concentration was 100 mg/L, the equilibrium time was 20 min, and the adsorbent dosage was 0.6 g/L. The resulting removal efficiency (99.99 %) and maximum adsorption capacity (166.65 mg/g) are both very high. Adsorption kinetics are well described using a pseudo-second-order kinetic model. This paper presents a facile and economically sustainable approach to the synthesis of e-HAP from marble sludge for use in removing of Pb2+ from wastewater.

Covalent Lysozyme Immobilization on Enzymatic Cellulose Nanocrystals.

Nanostructured materials represent promising substrates for biocatalyst immobilization and activation. Cellulose nanocrystals (CNCs), accessible from waste and/or renewable sources, are sustainable and biodegradable, show high specific surface area for anchoring a high number of enzymatic units, and high thermal and mechanical stability. In this work, we present a holistic enzyme-based approach to functional antibacterial materials by bioconjugation between the lysozyme from chicken egg white and enzymatic cellulose nanocrystals. The neutral CNCs were prepared by endoglucanase hydrolysis from Avicel. We explore the covalent immobilization of lysozyme on enzymatic CNCs and on their TEMPO oxidized derivatives (TO-CNCs), comparing immobilization yields, material properties, and enzymatic activities. The materials were characterized by X-ray diffractometry (XRD), attenuated total reflectance Fourier Transform infrared spectroscopy (ATR-FTIR), bicinchoninic acid (BCA) assay, field-emission scanning electron microscopy (FE-SEM) and dynamic light scattering (DLS). We demonstrate the higher overall efficiency of the immobilization process carried out on TO-CNCs, based on the success of covalent bonding and on the stability of the isolated bioconjugates.

Magnetic structure and colossal dielectric properties in Ga3+ substituted Zn2Y hexaferrites by chemical co-precipitation method

Y-type Ba0.5Sr1.5Zn2Fe12-xGaxO22 (x = 0.0, 0.2, 0.4, 0.6, 0.8 and 1.0) hexaferrites are prepared through modified chemical co-precipitation method. X-ray diffraction (XRD) results reveal that these samples are single-phase and the space group is R3‾m. The field-emission scanning electronic microscope (FE-SEM) measurements indicate that the grains are hexagonal-plate with a diameter of 2–5 μm. In the M-T diagrams, various magnetic structures are modulated, including proper-screw, longitudinal conical (LC), mixed conical (MC), and collinear ferrimagnetic (collinear FIM). In this series of samples, the values of dielectric constant (ε′) achieve an order increase from 102 to 104. For the best x = 0.8 sample, the ε′ is as high as 1804.76 at 1 MHz and 300 K. In conclusion, Ba0.5Sr1.5Zn2Fe12-xGaxO22 with controllable magnetic structures and colossal dielectric constant are potential materials for miniaturization of modern electronic devices.

Enhancing Herbal Efficacy: Synthesis and Evaluation of Nanosuspension from Withania somnifera Root Extract

Background: Ayurveda emphasizes the balance of mind, body, and spirit, drawing on ancient texts that highlight the medicinal properties of herbs like Withania somnifera, known for its wide range of therapeutic applications and pharmacological benefits. Commonly referred to as Indian ginseng or Ashwagandha, Withania somnifera, demonstrates a variety of therapeutic effect , including anti-inflammatory, antitumor, sedative, hypnotic, deobstruent effects, narcotic, antioxidant, tonic, antistress, diuretic, aphrodisiac, immunomodulatory, and rejuvenating properties. Nanotechnology, particularly through the development of nanosuspensions, offers a significant advancement in medicine, addressing challenges like poor solubility and low bioavailability of lipophilic drugs. Nanosuspensions can enhance drug safety and efficacy by improving solubility and altering pharmacokinetics. Methods: This study focuses on formulating and characterizing a nanosuspension using an ethanolic extract of Withania somnifera roots. The nanosuspension (NSWS) underwent comprehensive characterization, utilizing techniques such as FT-IR spectroscopy, particle size analysis, zeta potential measurement, polydispersity index (PDI) assessment, Field emission scanning electron microscopy (FESEM), X-ray diffraction analysis, pH measurement, and stability testing. This study seeks to explore the potential of nanosuspensions, aiming to integrate nanotechnology with herbal medicine to improve the safety and efficacy of herbal formulations. Results: The nanosuspension (NSWS) shown particle size about 133.09 nm, and its uniform particle distribution was indicated by a Polydispersity Index (PDI) about 0.27. Stability and uniformity were further supported by the zeta potential, particle size, and PDI values. Conclusion: Nanosuspension formulations represents a versatile strategy to improve the therapeutic efficacy of hydrophobic drugs across various routes of administration. Keywords: Withania somnifera, Nanosuspension, Characterization, FT-IR, PDI, FESEM

The Influence of Temperature on the Spatial Distribution of AuNPs on a Ceramic Substrate for Biosensing Applications

In this study, we investigated the spatial distribution and homogeneity of gold nanoparticles (AuNPs) on an alumina (Al2O3; AAO) substrate for potential application as surface-enhanced Raman scattering (SERS) sensors. The AuNPs were synthesized through thermal treatment at 450 °C at varying times (5, 15, 30, and 60 min), and their distribution was characterized using field-emission scanning electron microscopy (FE-SEM) and scanning transmission electron microscopy (STEM). The FE-SEM and STEM analyses revealed that the size and interparticle distance of the AuNPs were significantly influenced by the duration of thermal treatment, with shorter times promoting smaller and more closely spaced nanoparticles, and longer times resulting in larger and more dispersed particles. Raman spectroscopy, using Rhodamine 6G (R6G) as a probe molecule, was employed to evaluate the SERS enhancement provided by the AuNPs on the AAO substrate. Raman mapping (5 µm × 5 µm) was conducted on five sections of each sample, demonstrating improved homogeneity in the SERS effect across the substrate. The topological features of the AuNPs before and after R6G incubation were analyzed using atomic force microscopy (AFM), confirming the correlation between a decrease in surface roughness and an increase in R6G adsorption. The reproducibility of the SERS effect was quantified using the maximum intensity deviation (D), which was found to be below 20% for all samples, indicating good reproducibility. Among the tested conditions, the sample synthesized for 15 min exhibited the most favorable characteristics, with the smallest average nanoparticle size and interparticle distance, as well as the most consistent SERS enhancement. These findings suggest that AuNPs on AAO substrates, particularly those synthesized under the optimized condition of 15 min at 450 °C, are promising candidates for use in SERS-based sensors for detecting cancer biomarkers. This could be attributed to temperature propagation promoted at the time of synthesis. The results also provide insights into the influence of thermal treatment on the spatial distribution of AuNPs and their subsequent impact on SERS performance.

Enhancing sensitivity in wireless capacitive pressure sensors via highly flexible LC circuits utilizing porous polydimethylsiloxane dielectric layer

In this study, we introduce a highly flexible LC circuit-based wireless capacitive pressure sensor (CPS) that utilizes porous polydimethylsiloxane (PDMS) as a dielectric layer, demonstrating its transformative potential in tactile sensing, physiological monitoring, and flexible electronics. To optimize sensor performance, various porous PDMS thin films (100 μm) with different porosities (ranging from 0 % to 75 %) were prepared using a novel steaming method, and their properties were thoroughly analyzed using field emission scanning electron microscopy (FE-SEM) and capacitance measurements. Remarkably, the sensor with a 75 % porous PDMS film demonstrated enhanced sensitivity up to 11 times compared to the 0 % porous (pristine) PDMS film when subjected to a 300 g weight. High sensitivities of 0.046 kPa^-1, 0.036 kPa^-1, and 0.028 kPa^-1 were attained for the pressure sensor in the pressure ranges of 0–9.8 kPa, 0–19.6 kPa, and up to 29.4 kPa, respectively. Additionally, a real-time resonance frequency analysis was conducted using a network analyzer, allowing the detection of tiny pressure changes in an artificial blood vessel. Finally, the flexibility of the wireless CPS was investigated by studying various parameters, including body temperature, facial expressions such as smiling, selected speech characters (M, N, T, L), and swallowing actions.

Magneto-electrochemical water splitting performance of graphene oxide/nickel aluminum-layered double hydroxide nanocomposites

Designing efficient, cheap catalysts for oxygen production is very important for water electrolysis and green hydrogen production. Here, synthesis and electrocatalytic performance of graphene oxide (GO)/nickel-aluminum layered double hydroxide (NiAl-LDH) composites were investigated for water-splitting applications. The composition, microstructure, and morphology of the nanocomposites were confirmed by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), and field emission scanning electron microscopy (FE-SEM), and their water oxidation performance was examined in 0.1 M potassium hydroxide solution in the presence and absence of magnetic field. The results show that optimized GO/NiAl-LDH nanocomposite (GO-1 %/NiAl-LDH) exhibits the lowest overpotential compared with other prepared nanocomposites. This performance demonstrates comparable electroactivity to well-developed electrocatalysts like the perovskite-based electrodes, it also shows an improved electrocatalytic activity compared to NiAl-LDHs due to the presence of graphene oxide in the composite. We interpreted this significant performance to improve electron transform and high active site at the synthesized GO/NiAl-LDH composites. The best electrocatalytic activity with an overpotential of 443 and 473 mV at the current density 10 mA.cm−2 were evidenced for GO-1 %/NiAl-LDH nanocomposite in the presence and absence of external magnetic field, respectively. Furthermore, the tafel slope were reported about 54 and 162 mV.dec−1 in the presence and absence of magnetic field, respectively. This improved water oxidation can be attributed to the magneto-hydrodynamic effect and the increased number of metal sites on LDHs under the magnetic field.

Enhanced wound healing with biogenic zinc oxide nanoparticle-incorporated carboxymethyl cellulose/polyvinylpyrrolidone nanocomposite hydrogels.

Contemporary wound dressings lack antibacterial properties, exhibit a low water vapour transmission rate, and demonstrate inadequate porosity. In order to overcome these limitations, scientists have employed water hyacinth to produce carboxymethyl cellulose (CMC). CMC/PVP nanocomposite films containing biogenic zinc oxide nanoparticles (nZnOs) were synthesised using cost effective solution-casting technique. As the proportion of nZnOs in the film increased, swelling and water permeability decreased, whereas mechanical stability improved. Dynamic light scattering testing and transmission electron microscopy confirmed that the particle size was around 50.7 nm. Field emission scanning electron microscopy (FESEM) images showed that nZnOs were distributed uniformly in the polymer matrix. Cell viability against Vero cells was greater than 94%, and a substantial zone of inhibition against S. aureus and E. coli bacteria was observed. Wounds of albino mice were treated with CMC/PVP and CMC/PVP/nZnO (6%) nanocomposite hydrogels and healed in 20 and 12 days, respectively, as demonstrated by wound healing assay and histological staining. In vitro and in vivo studies revealed that the novel nanocomposite hydrogels exhibit improved cell viability and wound healing features. Therefore, they could be exploited as promising skin wound dressing materials.

Energy band gap tuning of Ba-Ca hexagonal ferrite by Dy3+ ion substitution (0 ≤ x ≤ 0.2) to improve spectral, structural, dielectric and photocatalytic properties

In the present study, Dy3+ substituted M-type Ba0.5Ca0.5DyxFe12-xO19 (0.00 ≤ x ≤ 0.20) hexagonal ferrites were synthesized using sol-gel auto-combustion method with lemon extract as a fuel. The single hexaferrite phase with space group P63/mmc is revealed by the X-ray powder diffraction (XRD) patterns. The Field emission scanning electron microscopy (FESEM) exhibits the agglomeration of nanoplates with vacancies at some places. Energy dispersive X-ray photoelectron spectroscopy (EDAX) mapping confirmed the presence of Ba, Ca, Fe, O, and Dy in the hexaferrite. Fourier Transform Infrared (FTIR) spectroscopy exhibits two characteristic bands at 579 and 429 cm−1 corresponding to tetrahedral and octahedral metal ions-oxygen stretching, revealing the occurrence of the ferrite phase. The optical energy band gap calculated using the Tauc plots was found to increase with the increase in dysprosium substitution to fall within the range of 2.8–3.5 eV. The Raman spectra confirmed the Raman vibration modes and M-type structures of hexagonal ferrites (HFs). The dielectric constant values drop rapidly with increasing frequency up to a few KHz and then gradually for the further higher frequencies. The occurrence of Ba and Ca with 2+, while Dy, and Fe with 3+ oxidation states is confirmed using X-ray photoelectron spectroscopy (XPS). The HFs exhibit remarkable efficiency by degrading the Reactive Brown dye to 99.3 % in just 15 min, equivalent to a high degradation reaction rate constant (k) value of up to 0.0396 min−1. Consequently, the catalyst shows promising potential for environmental remediation.

A Machine Learning Assisted Non-Enzymatic Electrochemical Biosensor to Detect Urea Based on Multi-Walled Carbon Nanotube Functionalized with Copper Oxide Micro-Flowers.

Detecting urea is crucial for diagnosing related health conditions and ensuring timely medical intervention. The addition of machine learning (ML) technologies has completely changed the field of biochemical sensing, providing enhanced accuracy and reliability. In the present work, an ML-assisted screen-printed, flexible, electrochemical, non-enzymatic biosensor was proposed to quantify urea concentrations. For the detection of urea, the biosensor was modified with a multi-walled carbon nanotube-zinc oxide (MWCNT-ZnO) nanocomposite functionalized with copper oxide (CuO) micro-flowers (MFs). Further, the CuO-MFs were synthesized using a standard sol-gel approach, and the obtained particles were subjected to various characterization techniques, including X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), and Fourier transform infrared (FTIR) spectroscopy. The sensor's performance for urea detection was evaluated by assessing the dependence of peak currents on analyte concentration using cyclic voltammetry (CV) at different scan rates of 50, 75, and 100 mV/s. The designed non-enzymatic biosensor showed an acceptable linear range of operation of 0.5-8 mM, and the limit of detection (LoD) observed was 78.479 nM, which is well aligned with the urea concentration found in human blood and exhibits a good sensitivity of 117.98 mA mM-1 cm-2. Additionally, different regression-based ML models were applied to determine CV parameters to predict urea concentrations experimentally. ML significantly improves the accuracy and reliability of screen-printed biosensors, enabling accurate predictions of urea levels. Finally, the combination of ML and biosensor design emphasizes not only the high sensitivity and accuracy of the sensor but also its potential for complex non-enzymatic urea detection applications. Future advancements in accurate biochemical sensing technologies are made possible by this strong and dependable methodology.

Development of zeolite 5A-incorporated polyvinyl alcohol membrane for desalination by pervaporation

Abstract With the rapid depletion of potable and useable water resources globally due to population growth and the effects of global warming, the desalination of seawater – the world’s largest source of water – to acceptable quality levels is critical to meeting future water needs. This study investigates the use of zeolite 5A-incorporated polyvinyl alcohol membranes to produce fresh water from seawater for industrial and domestic use and evaluates the application of the pervaporation process on the separation performance. Polyvinyl alcohol and polyvinyl alcohol/zeolite 5A mixed matrix membranes were prepared by solution-casting technique, and their morphological, structural, and mechanical properties were analyzed by field emission scanning electron microscopy, thermogravimetric analysis, Fourier transform infrared spectroscopy, and tensile strength tests. The swelling behavior and pervaporation performance of the membranes were investigated at different temperatures (30, 45, and 60 °C) using synthetic seawater containing 35 g L−1 NaCl, and membrane–solvent interactions were determined using data from sorption experiments. The membrane produced water flux and salt rejection values at 60 °C of 5.82 kg m−2 h−1 and >99.9 %, respectively.

Green Approach for the Synthesis of 2-Phenyl-2H-indazoles and Quinazoline Derivatives Using Sustainable Heterogeneous Copper Oxide Nanoparticles Supported on Activated Carbon and OER Study.

This research work reports the synthesis of copper oxide (CuO) nanoparticles supported on activated carbon by a simple impregnation method using 2-propanol as a green solvent, followed by calcination. The synthesized CuO@C is used as an efficient heterogeneous nanocatalyst for the synthesis of 2H-indazoles and quinazolines utilizing commercially available 2-bromobenzaldehydes, primary amines, and sodium azide under ligand-free and base-free conditions. The present methodology demonstrates the formation of new N-N, C-N, and C═N bonds under one-pot reaction conditions using PEG-400 as a green solvent. The reaction pathways are supported by control experiments and mechanistic elucidation. Further, the synthesized catalyst was characterized by a range of microscopic and spectroscopic techniques such as powdered X-ray diffraction, fourier transform infrared spectroscopy, field emission scanning electron microscopy, energy-dispersive X-ray, UV-vis, X-ray photoelectron spectroscopy, high-resolution transmission electron microscopy, and BET-BJH analysis. Importantly, the study focused on the recyclability of the catalyst and successfully showed gram-scale production. Significantly, our active catalyst exhibited an outstanding performance in the oxygen evolution reaction, with an overpotential of 290 mV and a swallow Tafel slope of 91 mV dec-1.

Direct Growth of Bio-Graphene Using Modified-Chemical Vapor Deposition For Straight-Forward Characterization

Oil Palm Shell (OPS) is subjected to heating, resulting in gaseous compound release. These compounds are deposited on the substrate to produce Bio-Graphene. Through Chemical Vapor Deposition (CVD), the process is optimized by growing environment parameters during the production process. This process involves the controlled deposition of gaseous compounds onto a substrate under two different positions of the alumina boat (ABC-1 and ABC-2). Direct deposition on silicon wafers eliminated etching and transfer sequences, simplifying Bio-Graphene characterization. Field Emission Scanning Electron Microscope, Atomic Force Microscope, Raman Spectroscopy, X-ray diffraction, and I-V measurement were employed to characterize the Bio-Graphene. The findings revealed that the better-closed settings (ABC-2) facilitated the growth of high-quality Bio-Graphene with better crystallinity, detectable growth spurt, estimated few-layer thickness, larger growth area, and lower surface roughness. Optimizing the deposition environment at ABC-2 significantly enhances the quality and crystallinity of Bio-Graphene from OPS, paving the way for future applications.

In vitro assessment of corrosion, antibacterial properties, and degradation behavior of zirconia-coated polyetheretherketone (PEEK)

The medical industry often uses ceramic and polymeric coatings to safeguard metal substrates. However, more investigation is required to explore the implementation of ceramic coatings on polymer substrates and to determine their degradation and in vitro characteristics. This work involves applying zirconia coating onto the 3D-printed PEEK polymer substrate using the RF magnetron sputtering technique. With varying layer thickness and printing speed parameters, PEEK samples (S1, S2, S3, and S4) were 3D printed and coated with zirconia. The coated and uncoated samples were immersed in Fusayama artificial saliva solution for 30 days. Following immersion in artificial saliva, this study examined the corrosion of 3D-printed PEEK samples with and without coatings. Elemental mapping, field emission scanning electron microscopy, and X-ray photoelectron spectroscopy were employed to evaluate sample morphology and estimate the binding energy of possible compounds generated in the artificial saliva solution. In vitro assessments such as antibacterial studies were performed against E. coli and S. aureus, and cytotoxic analysis was performed using Human Wharton’s jelly-derived mesenchymal stem cells (WJ-MSCs) to determine cell proliferation. The results indicated that sample S3, printed with 0.15 mm layer thickness and 20 mm/s print speed coated with zirconia showed a better degradation rate of 9.01% whereas the other three samples S1, S2, and S4 coated with zirconia showed deterioration rates of 36.4%, 33% and 16% respectively. Sample S3 showed a better antibacterial activity as biofilm formation was absent and also showed cell viability of about 79% and hence can be considered as a viable option for dental applications.

Influence of the annealing temperature on the self-powered CuO/ZnO NRs heterojunction photodetector

In this study, the fabrication and comprehensive analysis of CuO/ZnO nanorod (NR) heterojunction photodetectors were carried out, focusing on the influence of annealing temperatures (400 °C, 500 °C, and 600 °C) on their structural, optical, and electrical characteristics. The ZnO nanorods were synthesized via a hydrothermal method, followed by a spin-coating deposition of CuO thin films. The resultant heterojunctions were subjected to different annealing treatments to determine the optimal conditions for enhanced photodetector performance. Characterization techniques such as Field Emission Scanning Electron Microscopy (FE-SEM), Energy Dispersive x-ray Spectroscopy (EDX), x-ray Diffraction (XRD), and UV–vis spectroscopy were employed to assess the quality and composition of the heterostructures. The analyses revealed a polycrystalline structure with monoclinic phases for CuO and wurtzite phases for ZnO. Photodetectors annealed at 400 °C exhibited the highest performance metrics, achieving a photoresponse ratio (Iph/Idark) of 26.3, photosensitivity (Sph%) of 2531.6, and a specific detectivity (D*) of 4.58 × 1010 Jones under 405 nm UV light illumination. These devices also demonstrated rapid response times of 0.8 s without any external bias, indicating effective exciton separation and charge transport facilitated by the built-in electric field at the heterojunction interface. The study underscores the critical role of annealing temperature in optimizing the photodetector properties of CuO/ZnO NRs, positioning these self-powered devices as promising candidates for future ultraviolet sensor applications in optoelectronics.

Investigating Gold Deposition with High-Power Impulse Magnetron Sputtering and Direct-Current Magnetron Sputtering on Polystyrene, Poly-4-vinylpyridine, and Polystyrene Sulfonic Acid.

Fabricating thin metal layers and particularly observing their formation process in situ is of fundamental interest to tailor the quality of such a layer on polymers for organic electronics. In particular, the process of high power impulse magnetron sputtering (HiPIMS) for establishing thin metal layers has sparsely been explored in situ. Hence, in this study, we investigate the growth of thin gold (Au) layers with HiPIMS and compare their growth with thin Au layers prepared by conventional direct current magnetron sputtering (dcMS). Au was chosen because it is an inert noble metal and has a high scattering length density. This allows us to track the growing nanostructures via grazing incidence scattering. In particular, Au deposition on the polymer polystyrene (PS) with the respective structural analogues poly-4-vinlypyridine (P4VP) and polystyrene sulfonic acid (PSS) is studied. Additionally, the nanostructured layers on these different polymer films are further probed by field emission scanning electron microscopy (FESEM), atomic force microscopy (AFM), X-ray reflectometry (XRR), and four-point probe measurements. We report that HiPIMS leads to smaller island-to-island distances throughout the whole sputter process. Moreover, an increased cluster density and an earlier percolation threshold are achieved compared to dcMS. Additionally, in the early stage, we observe a significant increase in coverage by HiPIMS, which is favorable for the improvement of the polymer-metal interface.

Two-Dimensional TiS2 Nanosheet- and Conjugated Polymer Nanoparticle-Based Composites for Sensing Applications.

The assessment of phenolic compounds in food samples, environmental samples, and medical applications has gained importance recently. Here, we present research on novel conjugated polymer nanoparticles (P-PimBzBt NPs) and their composites with two-dimensional titanium disulfide nanosheets (2D-TiS2) for electrochemical tyrosinase (TYR)-based catechol detection. P-PimBzBt NPs are decorated with 2D-TiS2 to enhance the electrochemical performance for biosensing. In addition, the interaction of P-PimBzBt NPs with TiS2 was investigated at the molecular level by employing van der Waals (vdW) dispersion-corrected density functional theory (DFT) calculations and classical all-atom molecular dynamics simulations. According to the theoretical studies, the presence of the TiS2 layer increases the interfacial interaction with the conjugated polymer via electrostatic interactions. Using cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), field emission scanning electron microscopy (FE-SEM), and energy-dispersive X-ray spectroscopy (EDS) analyses, the production of SPE/TiS2@P-PimBzBt NPs/TYR nanobiosensors was examined. With a detection range of 3.0-27.5 μM, 0.33 μM LOD, and 3.89 μA/μM·cm2 sensitivity values, the sensing layer based on the TiS2@P-PimBzBt NP composites has a targeting ability toward catechol. Its selectivity was investigated using commonly used interfering ions and compounds such as citric acid, urea, glucose, uric acid, KCl, and NaCl. Application of nanobiosensors to actual samples (tap water and black tea) was carried out with high accuracy. The fabricated biosensing platform demonstrates that P-PimBzBt NPs with 2D-TiS2 nanomaterial functionalization are appropriate as electrode materials and could be used to create an inexpensive, fast-response, and highly selective electrochemical biosensor for the detection of catechol in actual samples.