Search Results (3,485)

Poly (3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) stands out as a renowned commercial conducting polymer composite, boasting extensive and promising applications in the realm of film electronics. In this study, we have made a concerted effort to overcome the inherent drawbacks of PEDOT:PSS films (especially, high moisture absorption, mechanical damage vulnerability, insufficient substrate adhesion ability, etc.) by uniformly blending them with polydimethylsiloxane polyurea (PDMS-PUa) and silica (SiO₂) nanoparticles through a feasible mechanical stirring process, which effectively harnesses the intermolecular interactions, as well as the morphological and structural characteristics, among the various components. The Si−O bonds within PDMS-PUa and the −CH₃ groups attached to Si atoms significantly enhance the hydrophobicity of the composite film (as evidenced by a water contact angle of 132.89° under optimized component ratios). Meanwhile, SiO₂ microscopically modifies the surface morphology, resulting in increased surface roughness. This composite film not only maintains high conductivity (1.21 S/cm, in contrast to 0.83 S/cm for the PEDOT:PSS film) but also preserves its hydrophobicity and electrical properties under rigorous conditions, including high-temperature exposure (60–200 °C), ultraviolet (UV) aging (365.0 nm, 1.32 mW/cm²), and abradability testing (2000 CW abrasive paper, drag force of approximately 0.98 N, 40 cycles). Furthermore, the film demonstrates enhanced resistance to both acidic (1 mol/L, 24 h) and alkaline (1 mol/L, 24 h) environments, along with excellent self-cleaning and de-icing capabilities (−6 °C), and satisfactory adhesion (Level 2). Notably, the dried composite film can be re-dispersed into a solution with the aid of isopropanol through simple magnetic stirring, and the sequentially coated films also exhibit good surface hydrophobicity (136.49°), equivalent to that of the pristine film. This research aims to overcome the intrinsic performance drawbacks of PEDOT:PSS-based materials, enabling them to meet the demands of complex application scenarios in the field of organic electronics while endowing them with multifunctionality. Full article

The flammability and volatility of conventional lithium hexafluorophosphate (LiPF₆)-based electrolytes with organic carbonate solvents remain critical issues to the safety and thermal stability of lithium-ion batteries (LIBs). This study investigates the incorporation of phosphate-based additives including ammonium dihydrogen phosphate (ADP), trimethyl phosphate (TMP), and trimethyl phosphite (TMPi) into LiPF₆ electrolytes for improving the ionic conductivity, safety, and electrochemical performance of LIBs. Self-extinguishing time (SET) measurements demonstrated that the ADP-based LiPF₆ electrolyte significantly reduced flammability, achieving a shorter SET of 04 min 53 s, compared to 12 min for the pristine LiPF₆ electrolyte. The ADP-based LiPF₆ electrolyte possessed the highest ionic conductivity (14.08 mS·cm⁻¹) with an excellent lithium-ion transference number of 0.0076. Electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (C-V) analyses demonstrated that ADP lowered interfacial resistance and stabilized long-term cycling behavior. In particular, the 1% ADP-based LiPF₆ electrolyte maintained improved charge-discharge profiles and Coulombic efficiency over 200 cycles. These results highlight ADP’s dual functionality in suppressing gas-phase flammability and enhancing condensed-phase electrochemical stability, making it a promising candidate for next-generation, high-safety, high-performance LIB electrolytes. Full article

Theoretical studies have indicated that borophene is a promising two-dimensional material characterized by remarkable chemical, mechanical, and electrical properties. Nonetheless, its practical applications in areas such as catalysis and gas sensing are hindered by the limited density of reactive sites in its pristine form. To address this limitation, the present study explores the controlled fluorination of borophene nanoflakes as a strategy to modify their surface chemistry and enhance the availability of active sites. Furthermore, it is anticipated that surface fluorination will improve hydrophobicity, which is crucial for reducing humidity-related interference in sensing applications. In this study, we report the successful functionalization of borophene nanoflakes with fluorine using a plasma arc discharge technique for the first time. Borophene nanolayers were synthesized via a sonochemical-assisted exfoliation method, yielding nanosheets with an average lateral dimension of approximately 100 nm. The fluorinated samples were characterized using X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and high-resolution transmission electron microscopy (HRTEM). A systematic investigation of plasma exposure durations demonstrated that fluorine was effectively introduced as a dopant while maintaining the crystallinity of the borophene lattice. Full article

Exposure of LIB materials to ambient conditions with some level of humidity, either accidentally owing to imperfect fabrication or cell damage, or deliberately due to battery opening operations for analytical or recycling purposes, is a rather common event. As far as humidity-induced damage is concerned, on the one hand the general chemistry is well known, but on the other hand, concrete structural details of these processes have received limited explicit attention. The present study contributes to this field with an investigation centered on the use of Raman spectroscopy for the assessment of structural modifications using common lithium iron phosphate (LFP) and nickel–cobalt–manganese/lithium–manganese oxide (NCM-LMO) cathodes. The impact of humidity has been followed through the observation of differences in Raman bands of pristine and humidity-exposed cathode materials. Vibrational spectroscopy has been complemented with morphological (SEM), chemical (EDS), and electrochemical analyses. We have thus pinpointed the characteristic morphological and compositional changes corresponding to corrosion and active material dissolution. Electrochemical tests with cathodes reassembled in coin cells allowed for the association of specific capacity losses with humidity damaging. Full article

In this study, we assessed soil pollutants and surveyed the bacterial communities using 16S rRNA sequencing to better understand how to improve rehabilitation strategies for nickel-laterite mines in the Philippines. Representative soil samples and rhizospheres from Saccharum spontaneum L. in three post-mining sites rehabilitated in 2015, 2017, and 2019 were collected and analyzed. X-ray diffraction (XRD) identified iron oxyhydroxides, silicates, and clays as major soil components. Based on the pollution load index and contamination degree, the 2015A and 2015B sites were classified as “pristine” and had a “low degree of pollution”, while the remaining sites (2017A, 2017B, 2019A, and 2019B) were considered “moderately contaminated” with nickel, chromium, cobalt, lead, zinc, and copper. An analysis of the bacterial community composition revealed that the phyla Proteobacteria and Actinobacteria, along with the genus Ralstonia, were the most abundant groups across both control and rehabilitated sites. Our results showed that the soil pH and organic matter contents were strongly linked to specific bacterial community composition. These taxa have potential for inoculation in nickel-laterite soils to promote the growth of hyperaccumulator plants. Our results also showed a significant correlation between the structure of the bacterial communities and nickel, chromium, and manganese soil contents, but not with rehabilitation time. Furthermore, we identified the genera Diaphorobacter as potential bioindicators because they are sensitive to nickel and chromium. This study provides valuable baseline data on heavy metal pollution and microbial diversity in a rehabilitated Ni-laterite mine site. Full article

Cu-BTC (HKUST-1) metal–organic framework (MOF) is widely recognized for its carbon capture capability due to its unsaturated copper sites, high surface area, and well-defined porous structure. This study developed mixed matrix membranes (MMMs) using cellulose triacetate (CTA), incorporating bimetallic Ni-Cu-BTC MOFs for CO₂/CH₄ separation, and benchmarked them against membranes fabricated with monometallic Cu-BTC. CTA was selected for its biodegradability, membrane-forming properties, and cost-effectiveness. The optimized membrane with 10 wt.% Ni-Cu-BTC achieved a CO₂ permeability of 22.9 Barrer at 25 °C and 5 bar—more than twice that of pristine CTA—with a CO₂/CH₄ selectivity of 33.8. This improvement stems from a 51.66% increase in fractional free volume, a 49.30% rise in the solubility coefficient, and a 51.94% boost in the diffusivity coefficient. Dual-sorption model analysis further confirmed enhanced solubility and adsorption mechanisms. These findings establish CTA/Ni-Cu-BTC membranes as promising candidates for high-performance CO₂ separation in natural gas purification and related industrial processes. Full article

Disinfection by ultrasound and carbon nanotubes (CNTs) provides attractive alternatives to conventional methods for water and wastewater treatment. This study explored the inactivation of Escherichia coli (E. coli) by 5 mg/L pristine short and long multi-walled CNTs (MWCNTs) and 20 kHz ultrasound individually or in combinations in DI water, Suwannee River natural organic matter (SRNOM), and sodium dodecyl sulfate (SDS) solution, respectively. The results indicated that the dispersity of MWCNTs was the single most important factor determining the inactivation rate of E. coli. The dispersity of short MWCNTs in solutions increased in the order of DI water <10 mgC/L SRNOM < 2 mM SDS. Correspondingly, the greatest log inactivation of E. coli was achieved in SDS when short MWCNTs were used alone (0.67 ± 0.12) and combined with ultrasound (1.80 ± 0.02) for 10 min. Short MWCNTs alone had a slightly greater inactivation (0.29 ± 0.07) in SRNOM solution than in DI water (0.18 ± 0.05). However, long MWCNTs had a slightly higher inactivation in DI water (0.24 ± 0.03) than short ones (0.18 ± 0.05), because of better dispersity in DI. The observed synergistic inactivation when ultrasound and short MWCNTs were used together in 2 mM SDS shows that ultrasound energized the MWCNTs more effectively when they were well dispersed, although SDS and MWCNTs can occupy the reaction sites at the cavitational bubble–water interfacial regions and scavenge •OH radicals. The results suggest that sonophysical effects are more important to inactivate E. coli than sonochemical effects. Ultrasound inactivates E. coli and/or energizes MWCNTs through the mechanisms of acoustic streaming, microstreaming, microstreamers, transient cavitation collapse-generated shock waves and microjets (transitional forms), and localized hot temperatures. The results of this study indicate that the cytotoxicity of CNTs includes impinging bacterial cells and/or direct contact with the bacteria. Full article

Commercial hydrophobic membranes encounter severe problems such as membrane wetting and membrane fouling under extreme conditions, which affect membrane separation performance. To enhance the anti-fouling abilities of hydrophobic membranes, a composite membrane with omniphobic characteristics was fabricated successfully in this paper. Titanium dioxide (TiO₂) nanoparticles were in-situ grown via the hydrothermal synthesis method, and then fluorosilane with low surface energy was grafted on polyvinylidene fluoride (PVDF) membranes. Subsequently, the morphologies, chemical compositions, wetting properties and structural parameters of composite membranes were characterized systematically. Various contaminants were added to the feed to investigate the anti-fouling and anti-wetting performances of the composite membrane in membrane distillation tests. The results showed that butyl titanate was first hydrolyzed to form titanium hydroxide (Ti(OH)₄) and then it was dehydrated to form TiO₂ in the hydrothermal environment. TiO₂ crystals continued to grow and formed rough morphology with micro-nano synergistic distribution, which is similar to a “sunflower” disk composed of cubic clusters and nanopillars. Meanwhile, fluorosilane successfully was grafted onto TiO₂. The contact angles of deionized water, 0.4 mM sodium dodecyl sulfate (SDS) solution and 0.2% v/v mineral oil emulsion on the composite membrane surface were 167.3°, 162.0° and 158.5°, respectively, endowing the composite membrane with excellent omniphobic features. In direct contact membrane distillation (DCMD) tests, the composite membrane exhibited a relatively stable membrane permeate flux, and the salt rejection rate almost reached 100%. The mixture, consisting of inorganic salts, organic substances, surfactants and oil emulsions, was used as feed. In contrast, the commercial PVDF membrane flux decreased drastically and even dropped to 0 due to the membrane fouling and wetting. As for the pristine PVDF membrane, the membrane surface was covered with pollutants and membrane pores were blocked. Therefore, it was proved that the omniphobic composite membrane possesses outstanding anti-fouling and anti-wetting performance. Full article

Antibiotic contaminants such as tetracycline (TC) from agricultural production have become widely distributed and persistently accumulated in aquatic environments (rivers, lakes, and oceans), posing severe threats to ecological security and human health. This study developed a modified rice-straw-derived biochar through NaOH activation and ball-milling-assisted Fe₃O₄ loading, which simultaneously enhanced TC adsorption capacity and enabled magnetic recovery. The Box–Behnken design (BBD) response surface methodology was employed to optimize three key preparation parameters: ball-milling time (A, 39.95 min), frequency (B, 57.23 Hz), and Fe₃O₄/biochar mass ratio (C, 2.85:1), with TC adsorption capacity as the response value. The modified biochar was systematically characterized using SEM, BET, FTIR, XRD, and XPS, while adsorption mechanisms were elucidated through kinetic studies, isotherm analyses, and pH-dependent experiments. The results demonstrate that modification via ball-milling with Fe₃O₄ loading significantly enhanced the biochar’s tetracycline adsorption capacity. The maximum adsorption capacity of the modified biochar reached 102.875 mg/g, representing a 114.85% increase from the initial value of 47.882 mg/g observed for the pristine biochar. Furthermore, the modified biochar exhibited excellent stability, maintaining robust adsorption performance across a wide pH range. The primary adsorption mechanisms involved metal coordination complexation, supplemented by hydrogen bonding, π-π interactions, and pore filling. Full article

The engineering of porous transport layer (PTL)–catalyst layer (CL) interfacial architecture plays a critical role in optimizing the performance of proton exchange membrane water electrolyzers (PEMWEs). Particularly, at the PTL-CL interface, our results reveal that anode catalyst loadings affect the modulation of the PTL surface structure on the overpotentials of PEMWEs. Under high anode catalyst loadings, the magnitude of overpotentials is predominantly governed by the electronic conductivity and mass transport resistance within the CL, where the modifying effects of PTL-CL interfacial contact characteristics become negligible. However, when the catalyst loading is reduced, the PTL-CL interfacial contact characteristics become critical for electron conduction, mass transport, and kinetic reaction. Under low catalyst loadings, the etched PTL demonstrates a maximum reduction of 59 mV compared to the pristine PTL at 4 A/cm², with the former exhibiting a 10 mΩ·cm² reduction. Meanwhile, the etched PTL integrated with a cell demonstrates superior performance in both mass transport and kinetic overpotentials compared to a pristine PTL. This clearly indicates that the surface structure of the PTL plays an increasingly significant role in regulating the overpotentials of PEMWEs as the catalyst loadings decrease. Full article

Developing cost-effective, sustainable, and high-performance air electrode catalysts for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) remains a significant challenge in the advancement of rechargeable zinc–air batteries (ZABs). Herein, we successfully construct a vacancy-rich heterogeneous perovskite La_0.85Y_0.15Ni_0.7Fe_0.3O₃ (LYNF) hybridized with Co₃O₄ spinel nanoparticles using a simple chemical bath-assisted method. The Co₃O₄ composite LYNF material is systematically evaluated as the bifunctional catalyst for ZABs in the proportion of 25 wt%, 50w t%, and 75 wt% (denoted as LYNF-xCo₃O₄, x = 0.25, 0.5, 0.75). The results confirm an intimate coupling between the perovskite and spinel phases, along with a significant increase in oxygen vacancy concentration. Among the composites, LYNF-0.5Co₃O₄ exhibits the best performance, achieving an ORR onset potential of 0.813 V vs. RHE at −0.1 mA cm⁻² and a lower OER overpotential of 441 mV at 10 mA cm⁻². When applied as the air electrode catalyst in ZABs, LYNF-0.5Co₃O₄ displays the highest discharge voltage and a peak power density of 115 mW cm⁻², representing a 20% improvement over pristine LYNF. The enhanced performance of the LYNF-0.5Co₃O₄ composite is attributed to the accumulation of Co₃O₄ nanoparticles within the LYNF matrix, which introduces numerous electrochemically active sites and facilitates the charge and mass transport during the catalytic process in ZABs. Full article

The increasing demand for smart bone substitutes has boosted the implementation of biomaterials possibly endowed with both pro-osteogenic and pro-angiogenic capabilities, among which bioactive glasses hold great potential. Hence, two Poly(ε-caprolactone) (PCL)-based composites were loaded at 10 wt.%, with either pristine (SBA3) or copper-doped (SBA3_Cu) silica-based bioactive glasses, through a solvent casting method with chloroform. Neat PCL was used as a control. Samples produced by 3D printing underwent SEM and EDX analyses, and the following were measured: tensile strength and hardness, surface roughness, ion release through ICP-OES, surface free energy, and optical contact angle. Adipose-derived mesenchymal stem cells (ASCs) and human microvascular endothelial cells (HMEC-1) were used to test the biocompatibility of the materials through cell adhesion, spreading, and viability assays. A significant improvement in tensile strength and hardness was observed especially with Cu-doped composites. Both SBA3 and SBA3_Cu added to the PCL favored the early adhesion and the proliferation of HMEC-1 after 3 and 7 days, while ASCs proliferated significantly the most on the SBA-containing composite, at all the time points. Cellular morphology analysis highlighted interesting adaptation patterns to the samples. Further biological characterizations are needed to understand thoroughly how specific bioactive glasses may interact with different cellular types. Full article

The utility of nanostructured TiO₂ in the degradation of organic compounds and the disinfection of pathogenic microorganisms represents an important endeavor in photocatalysis. However, the low photocatalytic efficiency of TiO₂ remains challenging. Herein, we report a robust photocatalytic route to benzene removal rendered by enhancing its adsorption capacity via rationally designed mesoporous SiO₂-coated TiO₂ colloids. Specifically, amorphous, mesoporous SiO₂-coated TiO₂ nanoparticles (denoted T@S NPs) are produced via a precipitation-gel-hydrothermal approach, possessing an increased specific surface area over pristine TiO₂ NPs for improved adsorption of benzene. Notably, under UV irradiation, the degradation rate of benzene by T@S NPs reaches 89% within 30 min, representing a 3.1-fold increase over that achieved by pristine TiO₂. Moreover, a 99.5% degradation rate within 60 min is achieved and maintains a stable photocatalytic activity over five cycles. Surface coating of TiO₂ with amorphous SiO₂ imparts the T@S composite NPs nearly neutral characteristic due to the formation of Ti-O-Si bonds, while manifesting enhanced light harvesting, excellent stability, adhesion, and photocatalytic bacteriostatic effects. Our study underscores the potential of T@S composites for practical applications in photocatalysis over pristine counterparts. Full article

Groundwater, a critical source of drinking water, plays an essential role in global biogeochemical cycles, yet its microbial ecosystems remain insufficiently characterized, particularly in pristine karst aquifers. This study conducted high-resolution profiling of microbial communities and environmental parameters in two representative alpine karst aquifers in Slovenia: Idrijska Bela and Krajcarca. Monthly groundwater samples from the Krajcarca spring and Idrijska Bela borehole over a 14-month period were analyzed using whole-metagenome sequencing (WMS), UV-Vis spectroscopy, inductively coupled plasma mass spectrometry (ICP-MS), and isotopic analysis. The results revealed stable hydrochemical conditions with clear spatial differences driven by bedrock composition and groundwater residence time. Bacterial communities displayed strong correlations with hydrochemical parameters, while archaeal communities exhibited temporal stability. Functional gene profiles mirrored bacterial patterns, emphasizing the influence of environmental gradients on metabolic potential. No significant temporal changes were detected across two sampling campaigns (2016–2023), highlighting the resilience of these aquifers. This work establishes a valuable baseline for understanding pristine groundwater microbiomes and informs future monitoring and water quality management strategies. Full article

Amorphous indium gallium zinc oxide (a-IGZO) is widely used as an oxide semiconductor in the electronics industry due to its low leakage current and high field-effect mobility. However, a-IGZO suffers from notable limitations, including crystallization at temperatures above 600 °C and the high cost of indium. To address these issues, nitrogen-doped zinc oxynitride (ZnON), which can be processed at room temperature, has been proposed. Nitrogen in ZnON effectively reduces oxygen vacancies (V_O), resulting in enhanced field-effect mobility and improved stability under positive bias stress (PBS) compared to IGZO. In this study, selective deep ultraviolet femtosecond (DUV fs) laser annealing was applied to the channel region of ZnON thin-film transistors (TFTs), enabling rapid threshold voltage (Vth) modulation within microseconds, without the need for vacuum processing. Based on the electrical characteristics of both Vth-modulated and pristine ZnON TFTs, an NMOS inverter was fabricated, demonstrating reliable performance. These results suggest that laser annealing is a promising technique, applicable to various logic circuits and electronic devices. Full article