Search Results (65)

Thin films of bismuth(III) sulfide (Bi₂S₃) on fluorine doped tin oxide (FTO) coated glass slides were successfully formed by the chemical bath deposition (CBD) method. In this work, a new sulfur precursor L-cysteine was used instead of the typical sulfur precursors, such as urea, thiosulfate, or thioacetamide, used for the formation of the Bi₂S₃ films by the CBD method. The synthesized Bi₂S₃ thin film on the FTO substrate was subjected to characterization techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), and UV–Visible spectroscopy analysis. An X-ray diffraction analysis showed that, initially, Bi₂S₃ films of an amorphous structure with elemental sulfur impurities were formed on the FTO surface. During the annealing of the samples, amorphous Bi₂S₃ was transformed into its crystalline phase with an average crystallite size of about 22.06 nm. The EDS studies confirmed that some of the sulfur that was not part of the Bi₂S₃ was removed from the films during annealing. The influence of the morphology of Bi₂S₃ films on their optical properties was confirmed by studies in the UV-visible range. Full article

The present study employed the spin-coating method for the preparation of nanostructured crystalline zinc oxide (ZnO) thin films on FTO glass substrates. Subsequently, cadmium selenide (CdSe) layers were deposited on the surfaces using two distinct chemical methods: successive ionic layer adsorption and reaction (SILAR) and chemical bath deposition (CBD). The obtained films were then characterized by a variety of analytical methods, including XRD, SEM, AFM, EDX spectroscopy, UV–vis spectrophotometry, and linear sweep voltammetry. The XRD and SEM studies demonstrated that all of the films exhibited a polycrystalline nature, with the crystallinity of the cadmium selenide thin films prepared using the SILAR method exceeding that obtained by the CBD method. The SEM and AFM images revealed the uniformity of the cadmium selenide films on the FTO substrates, with no visible cracks or pores. The EDX spectra confirmed the presence of the expected elements in the thin films. The optical band gaps (E_g) for CdSe prepared with the SILAR or CBD method were determined to be 1.85 and 1.97 eV, respectively. Full article

This study explored the controlled formation of chiral copper(II) oxide (CuO) crystals using chiral amino acids as chirality-inducing agents. Utilizing chemical bath deposition (CBD) as the fabrication method, we achieved simple, reproducible synthesis suitable for industrial-scale applications. Our characterization of the induced chirality through high-performance liquid chromatography (HPLC), circular dichroism (CD), and isothermal titration calorimetry (ITC) revealed distinctive chiral features. These findings not only advance our understanding of chirality control in inorganic nanostructures but also establish CBD as a viable technique for the large-scale production of chiral materials. Full article

In this work, bismuth sulfide (Bi₂S₃) thin films were deposited by a chemical bath deposition (CBD) technique (called soft chemistry), while titanium dioxide (TiO₂) nanoparticles were synthesized by sol–gel and zinc oxide (ZnO) nanoparticles were extracted from alkaline batteries. The resulting nanoparticles were then deposited on the Bi₂S₃ thin films by spin coating at 1000 rpm for 60 s each layer to create heterojunctions of Bi₂S₃/ZnO and Bi₂S₃/TiO₂. These materials were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive X-ray spectroscopy (EDX). The optical and contact angle analyses were undertaken by UV–Vis spectroscopy and a contact microscopy angle meter, respectively. The calculated band gap values were found to be between 1.9 eV and 2.45 eV. The Bi₂S₃ presented an orthorhombic structure, the TiO₂ nanoparticles presented an anatase structure, and the ZnO nanoparticles presented a wurtzite hexagonal crystal structure. Furthermore, heterogeneous solar photocatalysis was performed using the Bi₂S₃, Bi₂S₃/ZnO, and Bi₂S₃/TiO₂ thin film combinations, which resulted in the degradation of Congo red increasing from 8.89% to 30.80% after a 30 min exposure to sunlight. Full article

The chemical bath deposition (CBD) process enables the deposition of ZnO nanowires (NWs) on various substrates with customizable morphology. However, the hydrogen-rich CBD environment introduces numerous hydrogen-related defects, unintentionally doping the ZnO NWs and increasing their electrical conductivity. The oxygen-based plasma treatment can modify the nature and amount of these defects, potentially tailoring the ZnO NW properties for specific applications. This study examines the impact of the average ion energy on the formation of oxygen vacancies (V_O) and hydrogen-related defects in ZnO NWs exposed to low-pressure oxygen plasma. Using X-ray photoelectron spectroscopy (XPS), 5 K cathodoluminescence (5K CL), and Raman spectroscopy, a comprehensive understanding of the effect of the oxygen ion energy on the formation of defects and defect complexes was established. A series of associative and dissociative reactions indicated that controlling plasma process parameters, particularly ion energy, is crucial. The XPS data suggested that increasing the ion energy could enhance Fermi level pinning by increasing the amount of V_O and favoring the hydroxyl group adsorption, expanding the depletion region of charge carriers. The 5K CL and Raman spectroscopy further demonstrated the potential to adjust the ZnO NW physical properties by varying the oxygen ion energy, affecting various donor- and acceptor-type defect complexes. This study highlights the ability to tune the ZnO NW properties at low temperature by modifying plasma process parameters, offering new possibilities for a wide variety of nanoscale engineering devices fabricated on flexible and/or transparent substrates. Full article

In this work, we present the area-selective growth of zinc oxide nanowire (NW) arrays on patterned surfaces of a silicon (Si) substrate for a piezoelectric nanogenerator (PENG). ZnO NW arrays were selectively grown on patterned surfaces of a Si substrate using a devised microelectromechanical system (MEMS)-compatible chemical bath deposition (CBD) method. The fabricated devices measured a maximum peak output voltage of ~7.9 mV when a mass of 91.5 g was repeatedly manually placed on them. Finite element modeling (FEM) of a single NW using COMSOL Multiphysics at an applied axial force of 0.9 nN, which corresponded to the experimental condition, resulted in a voltage potential of −6.5 mV. The process repeated with the same pattern design using a layer of SU-8 polymer on the NWs yielded a much higher maximum peak output voltage of ~21.6 mV and a corresponding peak power density of 0.22 µW/cm³, independent of the size of the NW array. The mean values of the measured output voltage and FEM showed good agreement and a nearly linear dependence on the applied force on a 3 × 3 µm² NW array area in the range of 20 to 90 nN. Full article

Analytical methods for the early detection of the neurodegenerative biomarker for Parkinson’s disease (PD), α-synuclein, are time-consuming and invasive, and require skilled personnel and sophisticated and expensive equipment. Thus, a pain-free, prompt and simple α-synuclein biosensor for detection in plasma is highly demanded. In this paper, an α-synuclein electrochemical biosensor based on hierarchical polyglutamic acid/ZnO nanowires decorated by gold nanoparticles, assembled as nanostars (NSs), for the determination of α-synuclein in human plasma is proposed. ZnO NSs were prepared by chemical bath deposition (CBD) and decorated with electrodeposited Au nanoparticles (Au NPs). Then, electro-polymerized glutamic acid was grown and functionalized with anti-α-synuclein. A synergistic enhancement of electrode sensitivity was observed when Au NPs were embedded into ZnO NSs. The analytical performance of the biosensor was evaluated by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS), using the Fe(II)(CN)₆⁴⁻/Fe(III)(CN)₆³⁻ probe. The charge transfer resistance after α-synuclein recognition was found to be linear, with a concentration in the range of 0.5 pg·mL⁻¹ to 10 pg·mL⁻¹, a limit of detection of 0.08 pg·mL⁻¹, and good reproducibility (5% variation) and stability (90%). The biosensor was also shown to reliably discriminate between healthy plasma and PD plasma. These results suggest that the proposed biosensor provides a rapid, quantitative and high-sensitivity result of the α-synuclein content in plasma, and represents a feasible tool capable of accelerating the early and non-invasive identification of Parkinson’s disease. Full article

This research article provides a comprehensive investigation into the optoelectronic characteristics of three distinct types of cadmium sulfide (CdS) thin films, namely: (a) conventionally prepared CdS thin films using chemical bath deposition (CBD-CdS), (b) CdS thin films produced via chemical bath deposition with the inclusion of zinc (CBD-Cd_(1−x)Zn_xS, x = 0.3), and (c) CdS thin films synthesized using a seed-assisted approach, treated with ethylenediaminetetraacetic acid (EDTA), and incorporating zinc (ED/CBD + EDTA-Cd_(1−x)Zn_xS). The investigation reveals that the crystallite size of these thin films decreases upon the addition of EDTA to the reaction solution, leading to an increase in the inter-planar spacing and dislocation density. Furthermore, a blue shift in the transmittance edge of the ED/CBD + EDTA-Cd_(1−x)Zn_xS samples compared to CBD-CdS implies modifications in the band gaps of the deposited films. The incorporation of Zn²⁺ into the reaction solution results in an increased band gap value of up to 2.42 eV. This suggests that Cd_(1−x)Zn_xS thin films permit more efficient photon transmission compared to conventional CdS. Among the three types of films studied, ED/CBD + EDTA-Cd_(1−x)Zn_xS exhibits the highest optical band gap of 2.50 eV. This increase in the optical band gap is attributed to the smaller crystallite size and the splitting of the tail levels from the band structure. Additionally, the increment in the optical band gap leads to reduced light absorption at longer wavelengths, thereby enhancing the electrical properties. Notably, ED/CBD + EDTA-Cd_(1−x)Zn_xS thin films demonstrate improved photovoltaic performance in a photoelectrochemical (PEC) cell, characterized by enhanced open-circuit voltage (363 mV, V_OC), short-circuit current (35.35 μA, I_SC), and flat-band voltage (−692 mV, V_fb). These improvements are attributed to the better adhesion of CdS to the fluorine-doped tin oxide (FTO) substrate and improved inter-particle connectivity. Full article

Nickel hydroxide β-Ni(OH)₂ nanolamellae with high aspect ratios were grown via chemical bath deposition (CBD) on both smooth and textured nickel foil. Depending on bath composition and/or the presence of an additive, thin foam-like nanolamellae to stacked lamellae were obtained. The used CBD method is highly cost-effective, as it is faster and requires less chemicals than typical hydrothermal methods, and it is readily implementable for large-scale production. The influence of surface texture on the final morphology and its effect on capacitive performance was investigated. Herein, we show how subtle changes in the concentration can drastically influence the morphology, which, in turn, drastically impacts the supercapacitive performance of the electrode. Also, the use of a textured surface significantly impacts the morphology, with vastly better cycling performance than samples made on a relatively smooth substrate. The measured specific capacitance values of the best sample were 1961 Fg⁻¹ at 5 mVs⁻¹ and 1998 Fg⁻¹ at 1 Ag⁻¹ under potentiostatic and galvanostatic conditions, respectively. This sample also retained 100% of its initial specific capacitance when discharged at a very high current density of 40 Ag⁻¹. These values are substantially enhanced compared to previously reported data using a nearly analogous method (CBD with higher reagent conc.), with our method, cost-wise, offering economic advantages relative to results obtained with similar materials and other methods (e.g., hydrothermal). Full article

ZnO inverse opals combine the outstanding properties of the semiconductor ZnO with the high surface area of the open-porous framework, making them valuable photonic and catalysis support materials. One route to produce inverse opals is to mineralize the voids of close-packed polymer nanoparticle templates by chemical bath deposition (CBD) using a ZnO precursor solution, followed by template removal. To ensure synthesis control, the formation and growth of ZnO nanoparticles in a precursor solution containing the organic additive polyvinylpyrrolidone (PVP) was investigated by in situ ultra-small- and small-angle X-ray scattering (USAXS/SAXS). Before that, we studied the precursor solution by in-house SAXS at T = 25 °C, revealing the presence of a PVP network with semiflexible chain behavior. Heating the precursor solution to 58 °C or 63 °C initiates the formation of small ZnO nanoparticles that cluster together, as shown by complementary transmission electron microscopy images (TEM) taken after synthesis. The underlying kinetics of this process could be deciphered by quantitatively analyzing the USAXS/SAXS data considering the scattering contributions of particles, clusters, and the PVP network. A nearly quantitative description of both the nucleation and growth period could be achieved using the two-step Finke–Watzky model with slow, continuous nucleation followed by autocatalytic growth. Full article

In this study, ZnO nanorods with a porous structure were successfully prepared using the chemical bath deposition (CBD) method. According to the surface and cross-sectional images photographed by scanning electron microscopy, we found that the diameters of samples with concentrations of 10, 30, 50, and 70 mM were 90, 141, 214, and 259 nm, respectively, with 6 h of deposition. The height of the nanorods was maintained at approximately 1.3 μm. The EDS material analysis showed that the ratio of zinc atoms and oxygen atoms in samples with different concentrations changed with the concentration of the growth solution. The column diameter of the zinc oxide nanorods prepared by the chemical bath deposition method was closely related to the concentration of the growth solution. The higher the concentration, the larger the column diameter. The height of the nanorods was directly proportional to the deposition time and was not influenced by solution concentration. Full article

Chalcogenides semiconductors are currently being studied as active layers in the development of electronic devices in the field of applied technology. In the present paper, cadmium sulfide (CdS) thin films containing nanoparticles of the same material as the active layer were produced and analyzed for their application in fabricating optoelectronic devices. CdS thin films and CdS nanoparticles were obtained via soft chemistry at low temperatures. The CdS thin film was deposited via chemical bath deposition (CBD); the CdS nanoparticles were synthesized via the precipitation method. The construction of a homojunction was completed by incorporating CdS nanoparticles on CdS thin films deposited via CBD. CdS nanoparticles were deposited using the spin coating technique, and the effect of thermal annealing on the deposited films was investigated. In the modified thin films with nanoparticles, a transmittance of about 70% and a band gap between 2.12 eV and 2.35 eV were obtained. The two characteristic phonons of the CdS were observed via Raman spectroscopy, and the CdS thin films/CdS nanoparticles showed a hexagonal and cubic crystalline structure with average crystallite size of 21.3–28.4 nm, where hexagonal is the most stable for optoelectronic applications, with roughness less than 5 nm, indicating that CdS is relatively smooth, uniform and highly compact. In addition, the characteristic curves of current-voltage for as-deposited and annealed thin films showed that the metal-CdS with the CdS nanoparticle interface exhibits ohmic behavior. Full article

One of the emerging and environmentally friendly technologies is the photoelectrochemical generation of green hydrogen; however, the cheap cost of production and the need for customizing photoelectrode properties are thought to be the main obstacles to the widespread adoption of this technology. The primary players in hydrogen production by photoelectrochemical (PEC) water splitting, which is becoming more common on a worldwide basis, are solar renewable energy and widely available metal oxide based PEC electrodes. This study attempts to prepare nanoparticulate and nanorod-arrayed films to better understand how nanomorphology can impact structural, optical, and PEC hydrogen production efficiency, as well as electrode stability. Chemical bath deposition (CBD) and spray pyrolysis are used to create ZnO nanostructured photoelectrodes. Various characterization methods are used to investigate morphologies, structures, elemental analysis, and optical characteristics. The crystallite size of the wurtzite hexagonal nanorod arrayed film was 100.8 nm for the (002) orientation, while the crystallite size of nanoparticulate ZnO was 42.1 nm for the favored (101) orientation. The lowest dislocation values for (101) nanoparticulate orientation and (002) nanorod orientation are 5.6 × 10⁻⁴ and 1.0 × 10⁻⁴ dislocation/nm², respectively. By changing the surface morphology from nanoparticulate to hexagonal nanorod arrangement, the band gap is decreased to 2.99 eV. Under white and monochromatic light irradiation, the PEC generation of H₂ is investigated using the proposed photoelectrodes. The solar-to-hydrogen conversion rate of ZnO nanorod-arrayed electrodes was 3.72% and 3.12%, respectively, under 390 and 405 nm monochromatic light, which is higher than previously reported values for other ZnO nanostructures. The output H₂ generation rates for white light and 390 nm monochromatic illuminations were 28.43 and 26.11 mmol.h⁻¹cm⁻², respectively. The nanorod-arrayed photoelectrode retains 96.6% of its original photocurrent after 10 reusability cycles, compared to 87.4% for the nanoparticulate ZnO photoelectrode. The computation of conversion efficiencies, H₂ output rates, Tafel slope, and corrosion current, as well as the application of low-cost design methods for the photoelectrodes, show how the nanorod-arrayed morphology offers low-cost, high-quality PEC performance and durability. Full article

CdS thin films were deposited on glass substrates employing low-cost and low-temperature chemical bath deposition (CBD). The effect of deposition time on the fabricated sample’s properties was investigated by XRD, SEM, EDX, Raman, UV-vis spectrophotometry, and PL spectroscopy. XRD results indicate the formation of cubic and hexagonal structures of CdS thin films. The calculated average crystal size ranged from 21–50 nm. SEM results indicate the formation of hierarchical nanoflakes where the nanoflakes are entangled with one another like plant roots. Raman study confirmed that the fabricated thin films have two distinct peaks that are centered at 298 cm⁻¹ and 599 cm⁻¹, which are characteristic vibration modes for CdS thin film. UV-vis absorption spectra indicate absorption band edges near 500 nm, which are related to the band gap values of CdS thin films. The estimated Eg of CdS thin films was reduced from 2.4 to 2.22 eV as the deposition time increased from 5 to 60 min. PL results show the main peak centered at 537 nm, its intensity decreasing as deposition time increases, indicating lower recombination of charge carriers. Our results reveal that CdS thin films are an excellent candidate for optoelectronic applications. Full article

Zinc sulfide (ZnS) thin films prepared using the chemical bath deposition (CBD) method have demonstrated great viability in various uses, encompassing photonics, field emission devices, field emitters, sensors, electroluminescence devices, optoelectronic devices, and are crucial as buffer layers of solar cells. These semiconducting thin films for industrial and research applications are popular among researchers. CBD appears attractive due to its simplicity, cost-effectiveness, low energy consumption, low-temperature compatibility, and superior uniformity for large-area deposition. However, numerous parameters influence the CBD mechanism and the quality of the thin films. This study offers a comprehensive review of the impact of various parameters that can affect different properties of ZnS films grown on CBD. This paper provides an extensive review of the film growth and structural and optical properties of ZnS thin films influenced by various parameters, which include complexing agents, the concentration ratio of the reactants, stirring speed, humidity, deposition temperature, deposition time, pH value, precursor types, and annealing temperature environments. Various studies screened the key influences on the CBD parameters concerning the quality of the resulting films. This work will motivate researchers to provide additional insight into the preparation of ZnS thin films using CBD to optimize this deposition method to its fullest potential. Full article