Search Results (147)

The flexible transparent conductive films (TCFs) of a ZnS/Cu/Ag/TiO₂ multilayered structure were deposited on a flexible PET substrate with high surface roughness using magnetic sputtering, and the effects of structural characteristics on the performance of the films were analyzed. The TCFs with TiO₂/Cu/Ag/TiO₂ and ZnS/Cu/Ag/ZnS symmetric structures were also prepared for comparison. The TCF samples were deposited using ZnS, TiO₂, Cu and Ag targets, and they were analyzed using scanning electronic microscopy, atomic force microscopy, grazing incidence X-ray diffraction, spectrophotometry and a four-probe tester. The TCFs exhibit generally uniform surface morphology, excellent light transmittance and electrical conductivity with optimized structure. The optimal values are 84.40%, 5.52 Ω/sq and 33.19 × 10⁻³ Ω⁻¹ for the transmittance, sheet resistance and figure of merit, respectively, in the visible spectrum. The satisfactory properties of the asymmetric multilayered TCF deposited on a rough-surface substrate should be mainly attributed to the optimized structure parameters and reasonable interfacial compatibilities. Full article

Tomatoes are a fundamental part of the daily diet, rich in carbohydrates, vitamins, minerals, carotenoids, and polyphenols. Nonetheless, optimal fruit yield and quality typically depend on the application of synthetic agrochemicals. However, the irrational use of these agrochemicals has caused various environmental problems. Therefore, it is necessary to develop alternatives to conventional agrochemical products. Applying nanomaterials as fertilizers in tomato production is emerging as a promising approach, with documented improvements in germination, vegetative development, and fruit yield. Therefore, we present a comprehensive review of recent developments (2015–2024) in the application of nanomaterials in tomato crops, with a particular emphasis on the significance of nanomaterial characteristics in their role as fertilizers. Several types of nanomaterials, such as ZnO, Ag, TiO₂, Si, hydroxyapatite, P, Zn, Se, CuO, Cu, Fe, Fe₂O₃, CaO, CaCO₃, and S, have been evaluated as fertilizers for tomato crops, with ZnO nanoparticles being the most extensively studied. However, it is pertinent to conduct further research on the less-explored nanomaterials to gain a deeper understanding of their effects on seed germination, plant growth, and fruit quality and quantity. Full article

The efficient simultaneous removal of NO_x and CO from sintering flue gas under low-temperature conditions (110–180 °C) in iron and steel enterprises remains a significant challenge in the field of environmental catalysis. In this study, we present an innovative strategy to enhance the performance of CuSmTi catalysts through silver modification, yielding a bifunctional system capable of oxygen structure regulation and demonstrating superior activity for the combined NH₃-SCR and CO oxidation reactions under low-temperature, oxygen-rich conditions. The modified AgCuSmTi catalyst achieves complete NO conversion at 150 °C, representing a 50 °C reduction compared to the unmodified CuSmTi catalyst (T_100% = 200 °C). Moreover, the catalyst exhibits over 90% N₂ selectivity across a broad temperature range of 150–300 °C, while achieving full CO oxidation at 175 °C. A series of characterization techniques, including XRD, Raman spectroscopy, N₂ adsorption, XPS, and O₂-TPD, were employed to elucidate the Ag-Cu interaction. These modifications effectively optimize the surface physical structure, modulate the distribution of acid sites, increase the proportion of Lewis acid sites, and enhance the activity of lattice oxygen species. As a result, they effectively promote the adsorption and activation of reactants, as well as electron transfer between active species, thereby significantly enhancing the low-temperature performance of the catalyst. Furthermore, in situ DRIFTS investigations reveal the reaction mechanisms involved in NH₃-SCR and CO oxidation over the Ag-modified CuSmTi catalyst. The NH₃-SCR process predominantly follows the L-H mechanism, with partial contribution from the E-R mechanism, whereas CO oxidation proceeds via the MvK mechanism. This work demonstrates that Ag modification is an effective approach for enhancing the low-temperature performance of CuSmTi-based catalysts, offering a promising technical solution for the simultaneous control of NO_x and CO emissions in industrial flue gases. Full article

The structural, optical and electrical properties of the flexible, asymmetric TiO₂/Cu/Ag/ZnS and ZnS/Cu/Ag/TiO₂ transparent conductive films (TCFs) were studied. The multilayered TCFs were magnetron sputtered onto the flexible PET substrate layer-wise, with TiO₂, ZnS, Cu and Ag targets. The atomic force microscope, scanning electronic microscope, X-ray diffractometer, ultraviolet-visible spectrophotometer and four-probe tester were utilized to characterize the samples. The photoelectric property of the multilayers varies with the adjustment in structural parameters. The ZnS/Cu/Ag/TiO₂ samples demonstrate a more uniform surface morphology and better optical and electrical properties than the TiO₂/Cu/Ag/ZnS counterparts. The optimal sheet resistance and average transmittance of the ZnS/Cu/Ag/TiO₂ films are 5.56 Ω/sq and 88.46% in the visible spectrum, with the corresponding figure of merit reaching 52.76 × 10⁻³ Ω⁻¹. The bottom ZnS layer reveals superior percolation function for the bimetallic layer, forming with good continuity and homogeneity, although the original surface roughness is higher than that of TiO₂. The top TiO₂ layer demonstrates a smooth morphology and dense structure, beneficial to the high transparency and stability of the multilayer. Full article

This study attempts to use fly ash as the brazing filler additive to increase the sustainable use of coal-fired power plant by-product materials. The experimental results show that adding 5 wt% fly ash into the Ag paste filler contributes to the interfacial reactions in heterogeneous reactive air brazing (RAB) of the ZrO₂ and Crofer alloy. The Ag-rich phase dominates the brazed zone. The interfacial reaction layers contain oxidation of the Cu-Ti coating layer, Crofer alloy, and the Si/Al-rich oxides from the fly ash particles. The 5% fly ash RAB joint maintained airtightness for 280 h under 2 psig helium at room temperature. When the test temperature was raised to 600 °C for 24 h, the pressure of the joint assembly still did not drop. When the fly ash addition was increased to 10 wt%, the joint assembly was no longer leak-free at room temperature. Many visible voids and cracks exist in the brazed zone and at the ZrO₂/braze and braze/Crofer interfaces. A high volume fraction of the fly ash particles results in many brittle Si/Al-rich oxides in the joint after RAB, and the fracture of these oxides significantly deteriorates the airtightness of the joint. This study shows the feasibility and potential of introducing 5 wt% fly ash particles to the Ag-rich paste filler during the RAB of ZrO₂ and Crofer for airtight applications. Full article

Photocatalytic H₂ production is one of the most promising approaches for sustainable energy. The literature presents a plethora of carefully designed systems aimed at harnessing solar energy and converting it into chemical energy. However, the main drawback of the reported photocatalysts is their stability. Thus, the development of a cost-effective and stable photocatalyst, suitable for real-world applications remains a challenge. An ideal photocatalyst for H₂ production must possess appropriate band-edge energy positions, an effective sacrificial agent, and a suitable cocatalyst. Among the various photocatalysts studied, TiO₂ stands out due to its stability, abundance, and non-toxicity. However, its efficiency in the visible spectrum is limited by its wide bandgap. Metal doping is an effective strategy to enhance electron–hole separation and improve light absorption efficiency, thereby boosting H₂ synthesis. Common metal cocatalysts used as TiO₂ dopants include platinum (Pt), gold (Au), copper (Cu), nickel (Ni), cobalt (Co), ruthenium (Ru), iron (Fe), and silver (Ag), as well as bimetallic combinations such as Ni-Fe, Ni-Cu, Nb-Ta, and Ni-Pt. In all cases, doped TiO₂ exhibits higher H₂ production performance compared to undoped TiO₂, as metals provide additional reaction sites and enhance charge separation. The use of bimetallic dopants further optimizes the hydrogen evolution reaction. Additionally, porphyrins, with their strong visible light absorption and efficient electron transfer properties, have demonstrated potential in TiO₂ photocatalysis. Their incorporation expands the photocatalyst’s light absorption range into the visible spectrum, enhancing H₂ production efficiency. This review paper explores the principles and advancements in metal- and porphyrin-doped TiO₂ photocatalysts, highlighting their potential for sustainable hydrogen production. Full article

The polyol method under a single pot has successfully produced a coating of CuO, TiO₂, and the combination of CuO/TiO₂ around Ag NWs under sequential addition. The Ag NWs and their coating with a pure metal oxide and a hybrid of metal oxide were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM) coupled with EDX, X-ray photoelectron spectroscopy (XPS), UV–Visible, photoluminescent (PL) spectroscopy, and cyclic voltammetry (CV). The formation of ultra-thin NWs was also been seen in the presence of the TiO₂ coating. The ultra-thin and co-axial coating of each metal oxide and their hybrid form preserved the SPR of the Ag NWs and demonstrated photon harvesting from the 400–800 nm range. The band gap hybridization was confirmed by CV for the Ag@CuO/TiO₂ design, which made the structure a reliable catalyst. Therefore, the material expresses excellent photocatalytic activities for carcinogenic textile dyes such as turquoise blue (TB), sapphire blue (SB), and methyl orange (MO), with and without the reagent H₂O₂. The hybrid form (i.e., Ag@CuO/TiO₂) exhibited degradation within 6 min in the presence of H₂O₂. Additionally, the material showed antibacterial activities against various bacteria (Pseudomonas aeruginosa, Escherichia coli, Staphylococcus aureus, Bacillus subtilis, and Bacillus pumilus) when assayed using broth media. Therefore, the materials have established degrading and disinfection roles suitable for environmental perspectives. The role of coating with each metal oxide and their hybrid texture further improved the growth of Ag NWs. The preparatory route possibly ensued metal–metal oxide and metal–hybrid metal oxide Schottky junctions, which would expectedly transform it into a diode material for electronic applications. Full article

The Kongco area of Nima in the northern part of the Lhasa terrane has a suite of alkaline granitic porphyry dykes associated with Early Cretaceous granites and accompanied by Cu/Mo mineralization. LA-ICP-MS ²⁰⁶Pb/²³⁸U zircon geochronology performed on the dykes produced an age of 104.15 ± 0.94 Ma (MSWD = 0.98), indicating the Early Cretaceous emplacement of the dykes. The dykes exhibit high silica (SiO₂ = 76.22~77.90 wt.%), high potassium (K₂O = 4.97~6.21 wt.%), high alkalinity (K₂O + Na₂O = 8.07~8.98 wt.%), low calcium (CaO = 0.24~0.83 wt.%), low magnesium (MgO = 0.06~0.20 wt.%), and moderate aluminum content (Al₂O₃ = 11.93~12.45 wt.%). The Rieterman index (σ) ranges from 1.93 to 2.34. A/NK (molar ratio Al₂O₃/(Na₂O + K₂O)) and A/CNK (molar ratio Al₂O₃/(CaO + Na₂O + K₂O)) values of the dykes range from 1.06 to 1.18 and 0.98 to 1.09, respectively. The dykes are relatively enriched in Rb, Th, U, K, Ta, Ce, Nd, Zr, Hf, Sm, Y, Yb, and Lu, and they show a noticeable relative depletion in Ba, Nb, Sr, P, Eu, and Ti, as well as an average differentiation index (DI) of 96.42. The dykes also exhibit high FeO_T/MgO ratios (3.60~10.41), Ga/Al ratios (2.22 × 10⁻⁴~3.01 × 10⁻⁴), Y/Nb ratios (1.75~2.40), and Rb/Nb ratios (8.36~20.76). Additionally, they have high whole-rock Zr saturation temperatures (884~914 °C), a pronounced Eu negative anomaly (δEu = 0.04~0.23), and a rightward-sloping “V-shaped” rare earth element pattern. These characteristics suggest that the granitic porphyry dykes can be classified as A2-type granites formed in a post-collisional tectonic environment and that they are weakly peraluminous, high-potassium, and Calc-alkaline basaltic rocks. Positive ε_Hf(t) values = 0.43~3.63 and a relatively young Hf crustal model age (T_DM2 = 826~1005 Ma, ⁸⁷Sr/⁸⁶Sr ratios = 0.7043~0.7064, and ε_Nd(t) = −8.60~−2.95 all indicate lower crust and mantle mixing. The lower crust and mantle mixing model is also supported by (²⁰⁶Pb/²⁰⁴Pb)t = 18.627~18.788, (²⁰⁷Pb/²⁰⁴Pb)t = 15.707~15.719, (²⁰⁸Pb/²⁰⁴Pb)t = 39.038~39.110). Together, the Hf, Sr and Pb isotopic ratios indicate that the Kongco granitic porphyry dykes where derived from juvenile crust formed by the addition of mantle material to the lower crust. From this, we infer that the Kongco granitic porphyry dykes are related to a partial melting of the lower crust induced by subduction slab break-off and asthenospheric upwelling during the collision between the Qiangtang and Lhasa terranes and that they experienced significant fractional crystallization dominated by potassium feldspar and amphibole. These dykes are also accompanied by significant copper mineralization (five samples, copper content 0.2%), suggesting a close relationship between the magmatism associated with these dykes and regional metallogenesis, indicating a high potential for mineral exploration. Full article

Dissolved oxygen (DO) is a crucial parameter in water quality monitoring because it directly affects the health of aquatic ecosystems. This study explored electrodeposited Cu₂O thin-film semiconductors for DO sensing. Cu₂O was chosen for its low cost, eco-friendliness, and non-toxic nature. Cu₂O films were electrodeposited on titanium (Ti) substrates using an acetate bath (0.1 M sodium acetate and 0.01 M cupric acetate) at −200 mV versus Ag/AgCl for 30 min, with a bath temperature of 55 °C, stirred at 50 rpm. The bath pH was systematically adjusted from 5.8 to 6.8 in 0.2 steps using NaOH and Acetic acid. A range of analyses including synchrotron X-ray diffraction (SXRD), scanning electron microscopy (SEM), surface wettability, capacitance–voltage (C-V), Raman spectroscopy, Fourier-transform infrared (FTIR) spectrum, and Electrochemical Impedance Spectroscopy (EIS) was performed to assess their properties and sensing performance. The results showed that Cu₂O films deposited at pH 6.4 exhibited optimal performance for DO sensing, with a strong linear response, marking this pH, deposition time, and temperature as ideal for creating effective DO sensors. This study introduces a novel, cost-effective approach to dissolved oxygen sensing using electrodeposited n-Cu₂O thin-film semiconductors, marking the first application of this material in such sensors and showcasing its potential for scalable and environmentally sustainable sensing technologies. Full article

TiO₂ is widely utilized as an excellent photocatalyst in energy production. However, its rapid electron and hole recombination confers poor photocatalytic activity. Cocatalysts are essential for increasing photocatalytic efficacy by introducing improved electron transmission and enlarging the active site. Herein, the photocatalytic degradation of aqueous methanol solution to generate hydrogen was studied with the simultaneous in situ deposition of metals (M = Ag, Cu, Ni, Pd, and Pt) on the TiO₂ surface. Adding methanol to water and incorporating a bimetallic cocatalyst enhanced hydrogen production by reducing the electron–hole pair recombination. The studied metal ions could be reduced by the conduction band electrons of TiO₂ for the in situ simultaneous deposition of metal. The larger work function value of the studied metals favored the Schottky junction formation, which contributed to increasing photocatalytic efficiency. Among these simultaneous metal-deposited photocatalysts, maximal photocatalytic hydrogen production was achieved with NiPt/TiO₂. The optimal component was 0.01 wt.% Ni/1.0 wt.% Pt for TiO₂. The hydrogen evolution with NiPt/TiO₂ was approximately 341 and 1.3 times better than that with pure TiO₂ and Pt/TiO₂, respectively. A potential reaction pathway for photocatalytic hydrogen production from an aqueous methanol solution over NiPt/TiO₂ photocatalyst has also been proposed. Full article

Improving the performance of TiO₂ photoanodes via the inclusion of metal particles on the electrode surface could provide significant advantages for the development of dye-sensitized solar cells (DSSCs). We studied a TiO₂/Cu film electrode prepared by electrodepositing Cu particles on a TiO₂ film on an indium-doped tin oxide (ITO) substrate. Cu particles were electrodeposited on a TiO₂ electrode at −700 mV vs. a Ag/AgCl electrode in an acetate bath, with the pH adjusted between 6.3 and 7.7 in 0.2 increments to optimize the deposition conditions. TiO₂/Cu thin-film electrodes were tested as a photo anode in a natural DSSC consisting of a carbon counter electrode, Vitis vinifera dye, and a KI/I₂-based electrolyte. Film characterization was performed using hard X-ray photoelectron spectroscopy (HAXPES), grazing incidence X-ray diffraction (GIXD), scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, electrochemical impedance spectroscopy (EIS), ultraviolet–visible spectroscopy (UV–Vis), and photocurrent density–voltage (J–V) measurements. DSSCs with Cu particles containing TiO₂ electrodes prepared using an acetate bath of pH 7.3 resulted in a 370% improvement in efficiency compared to the DSSCs without Cu particles. Thus, this study revealed that incorporating Cu particles into the surface of the TiO₂ electrode enhances the photovoltaic performance of DSSCs. Full article

Energy generation and storage are critical challenges for developing economies due to rising populations and limited access to clean energy resources. Fossil fuels, commonly used for energy production, are costly and contribute to environmental pollution through greenhouse gas emissions. Quantum dot-sensitized solar cells (QDSSCs) offer a promising alternative due to their stability, low cost, and high-power conversion efficiency (PCE) compared to other third-generation solar cells. Kesterite materials, known for their excellent optoelectronic properties and chemical stability, have gained attention for their potential as hole transport layer (HTL) materials in solar cells. In this study, the SCAPS-1D numerical simulator was used to analyze a solar cell with the configuration FTO/TiO₂/MoS₂/HTL/Ag. The electron transport layer (ETL) used was titanium dioxide (TiO₂), while Cu₂FeSnS₄ (CFTS), Cu₂ZnSnS₄ (CZTSe), Cu₂NiSnS₄ (CNTS), and Cu₂ZnSnSe₄ (CZTSSe) kesterite materials were evaluated as HTLs. MoS₂ quantum dot served as the absorber, with FTO as the anode and silver as the back metal contact. The CFTS material outperformed the others, yielding a PCE of 25.86%, a fill factor (FF) of 38.79%, a short-circuit current density (J_SC) of 34.52 mA cm⁻², and an open-circuit voltage (V_OC) of 1.93 V. This study contributes to the advancement of high-performance QDSSCs. Full article

In recent years, nanomaterials have gained special attention for removing contaminants from wastewater. Nanoparticles (NPs), such as carbon-based materials and metal oxides, exhibit exceptional adsorption capacity and antimicrobial properties for wastewater treatment. Their unique properties, including reactivity, high surface area, and tunable surface functionalities, make them highly effective adsorbents. They can remove contaminants such as organics, inorganics, pharmaceuticals, medicine, and dyes by adsorption mechanisms. In this review, the effectiveness of different types of carbon-based NPs, including carbon nanotubes (CNTs), graphene-based nanoparticles (GNPs), carbon quantum dots (CQDs), carbon nanofibers (CNFs), and carbon nanospheres (CNSs), and metal oxides, including copper oxide (CuO), zinc oxide (ZnO), iron oxide (Fe₂O₃), titanium oxide (TiO₂), and silver oxide (Ag₂O), in the removal of different contaminants from wastewater has been comprehensively evaluated. In addition, their synthesis methods, such as physical, chemical, and biological, have been described. Based on the findings, CNPs can remove 75 to 90% of pollutants within two hours, while MONPs can remove 60% to 99% of dye in 150 min, except iron oxide NPs. For future studies, the integration of NPs into existing treatment systems and the development of novel nanomaterials are recommended. Hence, the potential of NPs is promising, but challenges related to their environmental impact and their toxicity must be considered. Full article

The formation of conductive copper patterns on mica holds promise for developing cost-effective flexible electronics and sensing devices, though it is challenging due to the low adhesion of mica’s atomically flat surface. Herein, we present a wet-chemical method for copper patterning on flexible mica substrates via electroless copper deposition (Cu-ELD). The process involves pre-functionalizing 50 µm thick muscovite mica with a titanium dioxide (TiO₂) layer, via a sol–gel dip-coating method with a titanium acetylacetonate-based sol. Photolithography is employed to selectively activate the TiO₂-coated mica substrates for Cu-ELD, utilizing in situ photodeposited silver (Ag) nanoclusters as a catalyst. Copper is subsequently plated using a formaldehyde-based Cu-ELD bath, with the duration of deposition primarily determining the thickness and electrical properties of the copper layer. Conductive Cu layers with thicknesses in the 70–130 nm range were formed within 1–2 min of deposition, exhibiting an inverse relationship between plating time and sheet resistance, which ranged from 600 to 300 mΩ/sq. The electrochemical thickening of these layers to 1 μm further reduced the sheet resistance to 27 mΩ/sq. Finally, the potential of Cu-ELD patterning on TiO₂-functionalized mica for creating functional sensing devices was demonstrated by fabricating a functional resistance temperature detector (RTD) on the titania surface. Full article

This study proposes a method to enhance the airtightness of the joint between the ZrO₂ and Crofer alloy using coating technology. With the aid of vacuum sputtering technology, a titanium–copper alloy layer with a thickness between 1.5 μm and 6 μm was first deposited on the surface of ZrO₂ and Crofer, respectively. The chemical composition of the deposited reaction layer was 70.2 Cu and 29.8 Ti in at%. Then, using silver as the base material in the reactive air brazing (RAB) process, we explore the use of this material design to improve the microstructure and reaction mechanism of the joint surface between ceramics and metal, compare the effects of different pretreatment thicknesses on the microstructure, and evaluate its effectiveness through air tightness tests. The results show that a coating of Cu-Ti alloy on the ZrO₂ substrate can significantly improve bonding between the Ag filler and ZrO₂. The Cu-Ti metallization layer on the ZrO₂ substrate is beneficial to the RAB. After the brazing process, the coated Cu-Ti layers form suitable reaction interfaces between the filler, the metal, the filler, and the ceramic. In terms of coating layer thickness, the optimized 3 μm coated Cu-Ti alloy layer is achieved from the experiment. Melting and dissolving the Cu-Ti coated layer into the ZrO₂ substrate results in a defect-free interface between the Ag-rich braze and the ZrO₂. The air tightness test result shows no leakage under 2 psig at room temperature for 28 h. The pressure condition can still be maintained even under high-temperature conditions of 600 °C for 24 h. Full article