Search Results (388)

The loosening or fracture of the prosthetic abutment screw is the most frequently reported complication in implant dentistry. Thin diamond-like carbon (DLC) films offer a low friction coefficient and high wear resistance, functioning as a solid lubricant to prevent the weakening of the implant–abutment system. This study evaluated the effects of DLC nanofilms on the reverse torque of prosthetic abutments after simulated chewing. Abutments with 8° and 11° taper connections, with and without DLC or silver-doped DLC coatings, were tested. The films were deposited through the plasma enhanced chemical vapor deposition process. After two million cycles of mechanical loading, reverse torque was measured. Analyses with scanning electron microscopy were conducted on three samples of each group before and after mechanical cycling to verify the adaptation of the abutments. Tribology, Raman and energy-dispersive spectroscopy analyses were performed. All groups showed a reduction in insertion torque, except the DLC-coated 8° abutments, which demonstrated increased reverse torque. The 11° taper groups experienced the most torque loss. The nanofilm had no significant effect on maintaining insertion torque, except for the DLC8 group, which showed improved performance. Full article

Amoxicillin (AMX) is utilized in the treatment of several infectious diseases, and its concentration in wastewater has increased quite significantly over the years, posing high health hazards for humans and other living organisms. Investigations are in progress globally to eliminate AMX and other related pollutants using several methods that include adsorption, photolysis, photocatalytic degradation, photoelectrocatalytic degradation, and electrochemical conversion. AMX can be eliminated efficiently from the environment using photodegradation, either by photolysis or a photocatalytic process. Several types of semiconductor NMs have been used to eliminate AMX and other related drugs present in wastewater. This review spans the photodegradation studies conducted during the years 2018–2024 to degrade and eliminate AMX in aquatic systems. Several studies have been reported to eliminate AMX from different water streams. These studies are categorized into TiO₂-containing and non-TiO₂-based catalysts for better comparison. A section on photolysis is also included, showing the use of UV alone or with H₂O₂ or PS without using any nanomaterial. A tabulated summary of both types of catalysts showing the catalysts, reaction conditions, and degradation efficiency is presented. Researchers have used a variety of reaction conditions that include radiation types (UV, solar, and visible), pH of the solution, concentration of AMX, number of nanomaterials, presence of other additives and activators such as H₂O₂ as oxidant, and the influence of different salts like NaCl and CaCl₂ on the photodegradation efficiency. TiO₂ was the best nanomaterial found that achieved the highest degradation of AMX in ultraviolet irradiation. TiO₂ doped with other nanomaterials showed very good performance under visible light. WO₃ was also used by several investigators and found quite effective for AMX degradation. Other metal oxides used for AMX elimination were derived from molybdenum, zinc, manganese, copper, cerium, silver, etc. Some researchers have used UV and/or visible irradiation or sunlight, without using solid catalysts, in the presence of oxidants such as H₂O₂. A summarized description of earlier published reviews is also presented. Full article

Graphene oxide-silver poly(vinylidene fluoride) membranes (PVDF@GO-Ag) were successfully synthesized by the electrospinning method, which exhibited a high catalytic activity using the hydrogenation of 4-nitrophenol (4-NP) as a model reaction in a batch reaction study. The hybrid membranes doped with 1 wt% GO and 2 wt% Ag (PVDF-1-2) exhibited the most desired performance for the catalytic reduction of 4-NP. Importantly, PVDF-1-2 exhibited excellent cycling stability in 10 catalytic cycle tests and was highly amenable to separation. This property effectively addresses the significant challenges associated with the practical application of nanocatalysts. Furthermore, density-functional theory (DFT) calculations have demonstrated that the GO-Ag nanocomposites exhibit the strongest adsorption capacity for 4-NP⁻ when a specific ratio of GO and Ag is achieved, accompanied by the loading of Ag nanoclusters onto GO. Additionally, the study demonstrated that an increase in temperature significantly accelerated the reaction rate, in line with the van’t Hoff rule. This study provides an effective and environmentally friendly solution for the treatment of 4-NP in wastewater. Full article

In this study, the biosynthesis of polyhydroxyalkanoates (PHAs) was carried out using Pseudomonas putida and Pseudomonas aeruginosa. These PHAs were produced using reagent-grade glycerol and crude glycerol as the carbon sources. The objective was to compare the production of PHAs and to functionalize these polymers with silver nanoparticles to provide antibacterial properties for potential biomedical applications. The findings from the physical and chemical analyses confirmed the successful synthesis and extraction of PHAs, achieving comparable yields using both crude glycerol and reagent-grade glycerol as carbon sources across both strains. Approximately 16% higher PHAs production was obtained using Pseudomonas putida compared to Pseudomonas aeruginosa, and no significant difference was observed in the production rate of PHAs between the two carbon sources used, which means that crude glycerol could be utilized even though it has more impurities. Notably, PHAs functionalized with silver nanoparticles showed improved antibacterial effectiveness, especially those derived from reagent-grade glycerol and the Pseudomonas aeruginosa strain. Full article

The advancement in performance in the domain of flexible wearable strain sensors has become increasingly significant due to extensive research on laser-induced graphene (LIG). An innovative doping modification technique is required owing to the limited progress achieved by adjusting the laser parameters to enhance the LIG’s performance. By pre-treating with AgNO₃, we successfully manufactured LIG with a uniform dispersion of silver nanoparticles across its surface. The experimental results for the flexible strain sensor exhibit exceptional characteristics, including low resistance (183.4 Ω), high sensitivity (426.8), a response time of approximately 150 ms, and a relaxation time of about 200 ms. Moreover, this sensor demonstrates excellent stability under various tensile strains and remarkable repeatability during cyclic tests lasting up to 8000 s. Additionally, this technique yields favorable results in finger bending and hand back stretching experiments, holding significant reference value for preserving the inherent characteristics of LIG preparation in a single-step and in situ manner. Full article

BiVO₄ is an important n-type semiconductor used in photocatalysis due to its high capacity to absorb solar light in the 400–700 nm range, abundance, high chemical stability, non-toxicity, and low cost. However, research on physicochemical modifications to increase its catalytic activity via simple procedures is limited. In this work, the influence of different synthesis parameters, such as calcination temperatures or silver doping, on the structural and physicochemical characteristic of the BiVO₄-based photocatalysts and their photocatalytic performance in degrading sulfamethoxazole from aqueous solution under blue-LED irradiation was evaluated. BiVO₄-based photocatalysts were synthesized using a solvothermal method. The monoclinic phase (m-s) was successfully kept stable even after the thermal treatments at 300, 450, and 600 °C and the corresponding silver doping. The low bandgap of 2.40 eV and the average particle size of 18 nm of the BiVO₄ catalyst treated at 300 °C seems to be the key. Afte doping, Ag/BiVO₄ photocatalyst treated at the optimal found calcination temperature (300 °C) showed the best photocatalytic behavior. Full article

This research introduces a novel approach using silver (Ag) nanostructures generated through electrochemical deposition and photo-reduction of Ag on fluorine-doped tin oxide glass substrates (denoted as X-Ag-Ag_yFTO, where ‘X’ and ‘y’ represent the type of light source and number of deposited cycles, respectively) for surface-enhanced Raman spectroscopy (SERS). This study used malachite green (MG) as a Raman probe to evaluate the enhancement factors (EFs) in SERS-active substrates under varied fabrication conditions. For the substrates produced via electrochemical deposition, we determined a Raman EF of 6.15 × 10⁴ for the Ag₂FTO substrate. In photo-reduction, the impact of reductant concentration, light source, and light exposure duration were examined on X-Ag nanoparticle formation to achieve superior Raman EFs. Under optimal conditions (9.0 mM sodium citrate, 460 nm blue-LED at 10 W for 90 min), the combination of blue-LED-reduced Ag (B-Ag) and an Ag₂FTO substrate (denoted as B-Ag-Ag₂FTO) exhibited the best Raman EF of 2.79 × 10⁵. This substrate enabled MG detection within a linear range of 0.1 to 1.0 µM (R² = 0.98) and a detection limit of 0.02 µM. Additionally, the spiked recoveries in aquaculture water samples were between 90.0% and 110.0%, with relative standard deviations between 3.9% and 6.3%, indicating the substrate’s potential for fungicide detection in aquaculture. Full article

The primary objective of this investigation was to synthesize a resin incorporating nanoparticles of hydroxyapatite and silver (HA-NpsAg) to enhance biocompatibility and antimicrobial efficacy, thereby facilitating potential implementation within the dental industry. These enhancements aim to ensure reliable, durable, functional, and aesthetically pleasing restorations while concurrently reducing susceptibility to bacterial colonization within the oral cavity. Hydroxyapatite powders were prepared using the sol–gel method and doped with silver nanoparticles obtained by chemical reduction. The crystalline amorphous calcium phosphate powder had a particle size of 279 nm, and the silver nanoparticles had an average diameter of 26.5 nm. Resin spheres containing HA-NpsAg (RHN) were then synthesized at two concentrations (0.5% and 1%) by dissolving the initial monomer mixture in tetrahydrofuran. Subsequent antimicrobial evaluations were conducted via agar diffusion and turbidimetry, employing three strains of Gram-negative bacteria (E. coli, K. oxytoca, and P. aeruginosa) and three strains of Gram-positive bacteria (S. mutans, S. aureus, and B. subtilis). The findings revealed that P. aeruginosa exhibited maximum susceptibility to RHN powder at a concentration of 0.5%, while RHN powder at 1% concentration demonstrated maximal inhibition against S. aureus and S. mutans. Overall, our study highlights the successful synthesis of a dental resin with hydroxyapatite and silver nanoparticles, exhibiting bactericidal properties at low silver concentrations. These findings hold promise for enhancing dental materials with improved antimicrobial efficacy and clinical performance. Full article

Weak doping can broaden, shift, and quench plasmon peaks in nanoparticles, but the mechanistic intricacies of the diverse responses to doping remain unclear. In this study, we used the time-dependent density functional theory (TD-DFT) to compute the excitation properties of transition-metal Pd- or Pt-doped gold and silver atomic arrays and investigate the evolution characteristics and response mechanisms of their plasmon peaks. The results demonstrated that the Pd or Pt doping of the off-centered 10 × 2 atomic arrays broadened or shifted the plasmon peaks to varying degrees. In particular, for Pd-doped 10 × 2 Au atomic arrays, the broadened plasmon peak significantly blueshifted, whereas a slight red shift was observed for Pt-doped arrays. For the 10 × 2 Ag atomic arrays, Pd doping caused almost no shift in the plasmon peak, whereas Pt doping caused a substantial red shift in the broadened plasmon peak. The analysis revealed that the diversity in these doping responses was related to the energy positions of the d electrons in the gold and silver atomic clusters and the positions of the doping atomic orbitals in the energy bands. The introduction of doping atoms altered the symmetry and gap size of the occupied and unoccupied orbitals, so multiple modes of single-particle transitions were involved in the excitation. An electron transfer analysis indicated a close correlation between excitation energy and the electron transfer of doping atoms. Finally, the differences in the symmetrically centered 11 × 2 doped atomic array were discussed using electron transfer analysis to validate the reliability of this analytical method. These findings elucidate the microscopic mechanisms of the evolution of plasmon peaks in doped atomic clusters and provide new insights into the rational control and application of plasmons in low-dimensional nanostructures. Full article

The ceramic Sr(NiNb)_0.5O₃, incorporating silver doping in the A site, was synthesized using a sol–gel route and subjected to comprehensive analysis through various experimental techniques. X-ray diffraction data analysis indicates a rhombohedral crystal structure. Scanning electron microscopy (SEM) examination reveals densely packed grains with minimal surface porosity. A thorough investigation of electrical properties, encompassing dielectric constant, loss tangent, electrical impedance, modulus, conductivity, etc., was conducted across a wide frequency range (10³–10⁶ Hz) and temperature range (260–340 K). This analysis provided valuable insights into structure–property relationships and conduction mechanisms. The discussion highlights the significance of interface effects, space charge polarization, and Maxwell–Wagner dielectric relaxation in achieving the material’s high dielectric constant at low frequencies and elevated temperatures. Examination of temperature dependence through Nyquist plots elucidates the contributions of grain behavior to the material’s resistive and capacitive properties. The dielectric permittivity, dissipation of energy, and electrical characteristics like impedance, modulus and conductivity are notably influenced by the frequency of the applied electric field and temperature. Overall, the material exhibits promising potential for industrial applications such as energy storage, given its intriguing properties. Full article

High sensitivity and selectivity and short response and recovery times are important for practical conductive polymer gas sensors. However, poor stability, poor selectivity, and long response times significantly limit the applicability of single-phase conducting polymers, such as polypyrrole (PPy). In this study, PPy/MoS₂ composite films were prepared via chemical polymerization and mechanical blending, and flexible thin-film resistive NO₂ sensors consisting of copper heating, fluorene polyester insulating, and PPy/MoS₂ sensing layers with a silver fork finger electrode were fabricated on a flexible polyimide substrate using a flexible electronic printer. The PPy/MoS₂ composite films were characterized using X-ray diffraction, Fourier-transform infrared spectroscopy, and field-emission scanning electron microscopy. A home-built gas sensing test platform was built to determine the resistance changes in the composite thin-film sensor with temperature and gas concentration. The PPy/MoS₂ sensor exhibited better sensitivity, selectivity, and stability than a pure PPy sensor. Its response to 50 ppm NO₂ was 38% at 150 °C, i.e., 26% higher than that of the pure PPy sensor, and its selectivity and stability were also higher. The greater sensitivity was attributed to p–n heterojunction formation after MoS₂ doping and more gas adsorption sites. Thus, PPy/MoS₂ composite film sensors have good application prospects. Full article

This study investigates the surface plasmon resonance (SPR)-induced UV photoresponse of zinc oxide (ZnO) derived from zeolitic imidazolate framework-8 (ZIF-8) to assess the influence of silver nanoparticles (Ag NPs) on the photoresponse behavior of metal–organic framework (MOF)-derived ZnO. The initial synthesis involved a thermal treatment in air to convert ZIF-8 into ZnO. We noted enhanced optical absorption both in the UV and visible spectra with the deposition of Ag NPs onto the ZIF-8-derived ZnO. Additionally, the presence of Ag NPs in the ZnO resulted in a substantial increase in current, even without any light exposure. This increase is attributed to the transfer of electrons from the Ag NPs to the ZnO. Photocurrent measurements under UV illumination revealed that the photocurrent with Ag NPs was significantly higher—by two orders of magnitude—compared with that without Ag NPs. This demonstrates that SPR-induced absorption markedly boosted the photocurrent, although the current rise and decay time constants remained comparable to those observed with ZnO alone. Although Ag NPs contribute electrons to ZnO, creating a “pre-doping” effect that heightens baseline conductivity (even in the absence of light), this does not necessarily alter the recombination dynamics of the photogenerated carriers, as indicated by the similar rise and decay time constants. The electron transfer from Ag to ZnO increases the density of charge carriers but does not significantly influence their recombination. Full article

Silicon (Si) shows great potential as an anode material for lithium-ion batteries. However, it experiences significant expansion in volume as it undergoes the charging and discharging cycles, presenting challenges for practical implementation. Nanostructured Si has emerged as a viable solution to address these challenges. However, it requires a complex preparation process and high costs. In order to explore the above problems, this study devised an innovative approach to create Si/C composite anodes: micron-porous silicon (p-Si) was synthesized at low cost at a lower silver ion concentration, and then porous silicon-coated carbon (p-Si@C) composites were prepared by compositing nanohollow carbon spheres with porous silicon, which had good electrochemical properties. The initial coulombic efficiency of the composite was 76.51%. After undergoing 250 cycles at a current density of 0.2 A·g⁻¹, the composites exhibited a capacity of 1008.84 mAh·g⁻¹. Even when subjected to a current density of 1 A·g⁻¹, the composites sustained a discharge capacity of 485.93 mAh·g⁻¹ even after completing 1000 cycles. The employment of micron-structured p-Si improves cycling stability, which is primarily due to the porous space it provides. This porous structure helps alleviate the mechanical stress caused by volume expansion and prevents Si particles from detaching from the electrodes. The increased surface area facilitates a longer pathway for lithium-ion transport, thereby encouraging a more even distribution of lithium ions and mitigating the localized expansion of Si particles during cycling. Additionally, when Si particles expand, the hollow carbon nanospheres are capable of absorbing the resulting stress, thus preventing the electrode from cracking. The as-prepared p-Si utilizing metal-assisted chemical etching holds promising prospects as an anode material for lithium-ion batteries. Full article

With the rapid development of industrialization, the emission of nitrogen oxides (NO_x) has become a global environmental issue. Uranium is the primary fuel used in nuclear power generation. However, the production of uranium, typically based on the uranyl nitrate method, usually generates large amounts of nitrogen oxides, particularly NO₂, with concentrations in the exhaust gas exceeding 10,000 ppm. High concentrations of nitrogen dioxide are also produced during silver electrolysis processing and the treatment of waste electrolyte solutions. Traditional V-W/TiO₂ NH₃-SCR catalysts typically exhibit high catalytic activity at temperatures ranging from 300 to 400 °C, under conditions of low NO_x concentrations and high gas hourly space velocity. However, their performance is not satisfying when reducing high concentrations of NO₂. This study aims to optimize the traditional V-W/TiO₂ catalysts to enhance their catalytic activity under conditions of high NO₂ concentrations (10,000 ppm) and a wide temperature range (200–400 °C). On the basis of 3 wt% Mo/TiO₂, various loadings of V₂O₅ were selected, and their catalytic activities were tested. Subsequently, the optimal ratios of active component vanadium and additive molybdenum were explored. Simultaneously, doping with WO₃ for modification was selected in the V-Mo/TiO₂ catalyst, followed by activity testing under the same conditions. The results show that: the NO_x conversion rates of all five catalysts increase with temperature at range of 200–400 °C. Excessive loading of MoO₃ decreased the catalytic performance, with 5 wt% being the optimal loading. The addition of WO₃ significantly enhanced the low-temperature activity of the catalysts. When the loadings of WO₃ and MoO₃ were both 3 wt%, the catalyst exhibited the best denitrification performance, achieving a NO_x conversion rate of 98.8% at 250 °C. This catalyst demonstrates excellent catalytic activity in reducing very high concentration (10,000 ppm) NO₂, at a wider temperature range, expanding the temperature range by 50% compared to conventional SCR catalysts. Characterization techniques including BET, XRD, XPS, H₂-TPR, and NH₃-TPD were employed to further study the evolution of the catalyst, and the promotional mechanisms are explored. The results revealed that the proportion of chemisorbed oxygen (O_α) increased in the WO₃-modified catalyst, exhibiting lower V reduction temperatures, which are favorable for low-temperature denitrification activity. NH₃-TPD experiments showed that compared to MoO_x species, surface WO_x species could provide more acidic sites, resulting in stronger surface acidity of the catalyst. Full article

The aim of this study was to obtain three experimental resin-based cements containing GO and HA-Ag for posterior restorations. The samples (S0, S1, and S2) shared the same polymer matrix (BisGMA, TEGDMA) and powder mixture (bioglass (La₂O₃ and Sr-Zr), quartz, GO, and HA-Ag), with different percentages of graphene oxide (0%, 0.1%, 0.2% GO) and silver-doped hydroxyapatite (10%, 9.9%, 9.8% HA-Ag). The physical–chemical properties (water absorption, degree of conversion), mechanical properties (DTS, CS, FS), structural properties (SEM, AFM), and antibacterial properties (Staphylococcus aureus, Enterococcus faecalis, Streptococcus mutans, Porphyromonas gingivalis, and Escherichia coli) were investigated. The results showed that the mechanical properties, except for the diametral tensile test, increased with the rise in the %GO. After 28 days, water absorption increased with the rise in the %GO. The surface structure of the samples did not show major changes after water absorption for 28 days. The antibacterial effects varied depending on the samples and bacterial strains tested. After increasing the %GO and decreasing the %HA-Ag, we observed a more pronounced antibacterial effect. The presence of GO, even in very small percentages, improved the properties of the tested experimental cements. Full article