Precursor Concentration Research Articles

Revealing Enhanced Optical Modulation and Coloration Efficiency in Nanogranular WO3 Thin Films Through Precursor Concentration Modifications

Electrochromic (EC) materials allow for dynamic tuning of optical properties via an applied electric field, presenting great potential in energy-efficient technologies, such as smart windows for effective light and temperature regulation. The precise control of precursor concentration has proven to be a powerful approach in tailoring the physicochemical properties of semiconducting metal oxides. In this study, we employed a one-step electrodeposition technique to fabricate tungsten oxide (WO3) thin films, systematically exploring how varying precursor concentrations influence the material’s characteristics. X-ray diffraction analysis revealed significant changes in diffraction patterns, reflecting subtle structural modifications due to concentration variations. Additionally, scanning electron microscopy revealed significant changes in the microstructure, showing a progression from small nanogranules to larger agglomerations within the film matrix. The W-25 mM thin film delivered exceptional EC performance, efficiently accommodating lithium ions while showcasing superior EC properties. The optimized electrode, denoted as W-25 mM, showcased exceptional EC metrics, featuring the highest optical modulation at 82.66%, outstanding reversibility at 99%, and a notably high coloring efficiency of 83.01 cm2/C. These findings emphasize the importance of precursor concentration optimization in enhancing the EC properties of WO3 thin films, contributing to the advancement of high-performance, energy-efficient materials.

Tailoring the Wettability of Bacterial Cellulose Magnetobots via the Assembly of In Situ Synthesized and Surfactant-Coated Magnetic Nanoparticles.

This study showcases the possibility of tailoring the wettability of magnetic bacterial cellulose (m-BC) composites by the combined effect of in situ synthesized magnetic nanoparticles (MNPs) distribution and simultaneous oleic acid (OA) coating within the BC matrix. This combined effect of MNPs and OA resulted in m-BC composites exhibiting solvent-dependent and time-dependent surface-wetting behavior, which was not observed in either individual cases of BC that have been modified with OA or BC that has MNPs adsorbed on its fibers. This tailored wettability in m-BCs was achieved via varying the concentrations of iron precursors, which governed the arrangement and morphology of MNPs (uniformly or clustered) on the BC membrane, although the same fraction of MNPs was observed in both the m-BCs. Finally, we have achieved delayed water absorption in m-BC_x (synthesized in a comparatively lower precursor concentration) and no absorption of water in m-BC_4x (synthesized in a 4-times-higher precursor concentration). The m-BC_4x composite maintained its hydrophobic characteristics in diverse environments, ranging from highly acidic conditions (pH 1.2) to physiological environments at pH 4, 5.5, and 7.4. The MNP agglomerates on the BC nanofibers in the m-BC_4x composite were found to be instrumental in attaining a stable cyclic absorption performance with structural integrity. Additionally, the magnetic-inducing heat generation efficiency of the m-BCs can be extended for evaporating low-boiling-point solvents. The present study expands the frontiers of BC-based magnetic composites by emphasizing the assembly of surfactant-coated magnetic nanostructures in their responsiveness to polar/nonpolar liquids with stable performance even in complex scenarios.

Synthesis and properties of tailored β‐tricalcium phosphate for bone filler applications

AbstractThe present work reports the synthesis of highly phase pure (> 95%) β‐TCP and its subsequent conversion into granules for bone graft applications, using an industrial scale proprietary manufacturing route. Following the wet chemical approach, several process parameters, were adjusted for large volume synthesis, including pH, precursor concentration, and ripening time. The granulation process is tailored to facilitate the scalibility and control over morphology, porosity, and pore size. X‐ray diffraction analysis confirms the presence of pure β‐TCP phase where as Ca/P molar ratio of 1.497 was determined using ICP‐OES. Fourier transform infrared spectroscopy depicts the presence of PO43− as a major molecular group. Scanning electron microscopy (SEM) images of the β‐TCP powders reveal necking features, a characteristic morphology of β‐TCP. SEM images of the β‐TCP granules reveal microporosity, which aids in triggering a biological response. The TGA‐DTA curve suggests that the weight loss in pure β‐TCP is twice as compared with β‐TCP containing hydroxyapatite. Furthermore, these β‐TCP granules were clinically tested in a few orthopedic and spine surgeries. In all the treated patients, β‐TCP granules did not induce any pus formation or infection at the surgical sites, thereby establishing clinically relevant biocompatibility properties.

Roles of Exogenous 5-Aminolevulinic Acid and Dihydroporphyrin Iron in Chlorophyll Precursor Synthesis and Chlorophyll-Related Enzyme Activities in Wheat Under Different Light Intensities

Aminolevulinic acid (5-ALA) and dihydroporphyrin iron chelates (DHFe) play roles in plant growth regulation under normal and stressful conditions. However, definitive data on their roles in regulating chlorophyll synthesis in wheat are lacking. In this study, the optimal concentrations for foliar-spray application of 5-ALA and DHFe to promote wheat seedling growth and leaf chlorophyll content were assessed. The optimal concentrations of 5-ALA or DHFe (50 mg/L and 0.01 mg/L, respectively) were applied as foliar sprays to seedlings of wheat ‘Bainong 4199’ (high light efficient) and ‘Zhoumai No. 18’ (average light efficient) under different light intensities. Chlorophyll precursor contents and activities of three chlorophyll synthesis-related enzymes were altered, and the combined application of 5-ALA and DHFe more strongly increased the leaf chlorophyll content. 5-ALA significantly increased the contents of the chlorophyll precursors porphobilinogen, uroporphyrinogen III, protoporphyrin IX, and magnesium-protoporphyrin IX, and the activities of 5-amino-ketovalerate dehydratase and uroporphyrinogen III synthase. DHFe resulted in an increase in chlorophyll content but a significant decrease in chlorophyllase activity and protochlorophyllide content. 5-ALA promoted the synthesis of chlorophyll precursors by regulating the activities of 5-amino-ketovalerate dehydratase and uroporphyrinogen III synthase. DHFe decreased chlorophyllase activity, thereby slowing chlorophyll degradation and increasing the chlorophyll content.

Size-Resolved Shape Evolution in Inorganic Nanocrystals Captured via High-Throughput Deep Learning-Driven Statistical Characterization.

Precise size and shape control in nanocrystal synthesis is essential for utilizing nanocrystals in various industrial applications, such as catalysis, sensing, and energy conversion. However, traditional ensemble measurements often overlook the subtle size and shape distributions of individual nanocrystals, hindering the establishment of robust structure-property relationships. In this study, we uncover intricate shape evolutions and growth mechanisms in Co3O4 nanocrystal synthesis at a subnanometer scale, enabled by deep-learning-assisted statistical characterization. By first controlling synthetic parameters such as cobalt precursor concentration and water amount then using high resolution electron microscopy imaging to identify the geometric features of individual nanocrystals, this study provides insights into the interplay between synthesis conditions and the size-dependent shape evolution in colloidal nanocrystals. Utilizing population-wide imaging data encompassing over 441,067 nanocrystals, we analyze their characteristics and elucidate previously unobserved size-resolved shape evolution. This high-throughput statistical analysis is essential for representing the entire population accurately and enables the study of the size dependency of growth regimes in shaping nanocrystals. Our findings provide experimental quantification of the growth regime transition based on the size of the crystals, specifically (i) for faceting and (ii) from thermodynamic to kinetic, as evidenced by transitions from convex to concave polyhedral crystals. Additionally, we introduce the concept of an "onset radius," which describes the critical size thresholds at which these transitions occur. This discovery has implications beyond achieving nanocrystals with desired morphology; it enables finely tuned correlation between geometry and material properties, advancing the field of colloidal nanocrystal synthesis and its applications.

Unlocking nature’s brilliance: using Antarctic extremophile Shewanella baltica to biosynthesize lanthanide-containing nanoparticles with optical up-conversion

Both lanthanide-containing and fluorine-containing nanomaterials present challenging targets for microbial biosynthesis because these elements are toxic to most bacteria. Here, we overcome these challenges by using an Antarctic Shewanella baltica strain that tolerates these elements and report the first biosynthesis of lanthanide-doped fluoride nanoparticles (NPs) from them. NaYF4 NPs doped with Er3+/Yb3+ are prototypical lanthanide-based upconverting nanoparticles (UCNPs) with upconverted luminescence at visible wavelengths under infrared excitation. However, their synthesis employs high precursor concentrations, organic solvents, and elevated temperatures. Microbial biosynthesis offers a greener alternative but has not been explored for these materials. Here, we harness an extremophile S. baltica strain to biosynthesize UCNPs at room temperature, based upon its high tolerance for fluoride and lanthanide ions and the observation that tolerance of lanthanides increased in the presence of fluoride. Our biosynthesis produces electron-dense nanostructures composed of Na, Y, F, Yb, and Er in the bacterial periplasm, adhered to the outer cell membrane, and dispersed extracellularly, which exhibited up-converted emission under 980 nm excitation. This suggests that extracellular or periplasmic mineralization of lanthanides as fluorides protects the bacteria from lanthanide toxicity. Subsequent heating both enhanced upconverted emission from UCNPs and allowed observation of their crystallinity in transmission electron microscopy (TEM). This work establishes the first biosynthesis of NaYF4:Yb: Er UCNPs, advancing both nanotechnology and biotechnology.Graphical

High-responsivity photoelectrochemical ultraviolet photodetector based on SnO2 nanosheets-Ga2O3

Abstract Tin oxide (SnO2) has garnered significant attention for its high spectral selectivity when used as an ultraviolet photodetector. In this study, SnO2 nanosheets (NSs) were synthesized via a hydrothermal method, followed by spin-coating a layer of Ga2O3 thin film to construct a heterojunction photoelectrochemical ultraviolet photodetector (PEC UV PD). Initially, we investigated the effect of precursor composition on the properties of the Ga2O3 thin films. It was observed that the thickness of the films increased with higher precursor concentrations, while the optical bandgap decreased. Based on these findings, we successfully fabricated the SnO2 NSs-Ga2O3 PEC UV PD. Electrochemical analysis revealed that as the precursor concentration used for spin-coating Ga2O3 increased, the device's responsivity and detectivity initially increased and then decreased. After optimization, the device prepared with a 0.2M Ga(NO3)3 solution spin-coated on SnO2 exhibited excellent spectral selectivity (R 265nm/R 420nm ~ 4472), a responsivity of 4.86 mA W-1, and a detectivity of 2.72×109 Jones. This study demonstrates that coating Ga2O3 is an effective approach to constructing high-performance SnO2-based UV PDs.

Exploring grapevine canopy management: effects of removing main leaves or lateral shoots before flowering

Over the course of a six-year trial, we investigated the physiological response of the Swiss white cultivar Vitis vinifera Petite Arvine, rich in varietal thiols, to the following canopy removal treatments from the cluster area, i.e. from the shoot base to the sixth leaf of each shoot: A) lateral shoots only, B) lateral shoots + 50 % main leaves, C) lateral shoots + 100 % main leaves or D) main leaves only. All leaf removal (LR) treatments were performed at the pre-flowering stage. Intensive pre-flowering removal of both lateral shoots + 100 % main leaves from the cluster area (C) strongly reduced yield potential (‒47 % on average) and tended to reduce the concentration of 3-mercaptohexanol precursors (Cys-3MH) in the must (‒21 %; p-value < 0.10). The effect of LR on berry set and must composition was modulated by removing fewer main leaves (‒24 % in yield potential and ‒6 % in Cys-3MH concentration). Climate conditions primarily influenced yield and grape composition. Main leaves and lateral shoots played different physiological roles: removal of main leaves only (D) resulted in a larger leaf area (+15 %) due to the development of lateral shoots in the cluster area and a lower yield potential (‒12 %) due to fewer berries per cluster when compared one-to-one with removal of lateral shoots only (A). In the must at harvest, treatment D had higher concentrations of malic acid (+12 %), yeast-assimilable nitrogen (+10 %) and glutathione (+8 %), but there were no significant trends for TSS, pH, Cys-3MH or Folin index. The overall effects of pre-flowering LR on wine composition were negligible in the context of this trial. The study highlighted the different physiological roles of the main leaves and lateral shoots, suggesting that pre-flowering leaf removal should be used cautiously, taking into account the plant’s resilience to environmental conditions. This research is part of a broader project on grapevine canopy management in temperate climates in Switzerland.

Solution-Crystalized AgBiS2 Films for Solar Cells Generating a Photo-Current Density Over 31mA cm-2.

In response to the toxic heavy metal absorbers in perovskite solar cells (PSCs), this work focuses on the development of an environmentally friendly simple solution-processed infrared (IR) absorber. In this work, a simple solution-crystallized IR-absorbing AgBiS2 film is reported by spin-coating silver, bismuth nitrates, and thiourea dissolved in dimethylformamide (DMF) to produce thick AgBiS2 film. Extensive optimization of the precursor concentrations thicknesses and conductive substrates used allow for obtaining 250nm AgBiS2 film with different crystal sizes. When applied as an absorber in solar cells, solution-crystalized AgBiS2 thick film delivers an extraordinarily high current density of over 31mA cm-2. The devices show high stability under continuous 100mW cm-2 illumination and when stored in the dark for more than six months. When the AgBiS2 layer is fabricated in a gradient fashion combining one layer of 0.25m and three layers of 0.5m precursor concentrations, the efficiency of 5.15% is registered which is the highest reported for the simple solution-crystallized AgBiS2 films.

Impact of precursor content on microstructure and properties of in-situ synthesized Ni60A-xTiC ceramic composite coating

To improve the surface properties of copper components, Ni60A-xTiC composite coatings with different precursor (TiFe and Cr3C2) contents were fabricated on copper surface by plasma cladding in this paper. The surface of all composite coatings forms a ceramic film composed of a dense layer (TiO2 and Ti2O3) and a loose layer (Fe2O3 and FeO). As the precursor content increases, the number and size of TiC particles in the composite coating have a tendency to increase, resulting in a gradual increase in microhardness. The wear resistance of the composite coating increases first and then decreases. Too high precursor content (20 wt. %) can lead to poor interface connection and wear resistance deterioration of the coating. Furthermore, the melting loss resistance of the composite coating is significantly better than that of the Ni60A coating due to the barrier effect of the ceramic film, and it becomes better with the increase of precursor content. To sum up, the composite coating with 15 wt. % precursor content is more suitable because of its smooth appearance, good interface connection and excellent comprehensive performance.

City-scale impacts of PFAS from normal and elevated temperature landfill leachates on wastewater treatment plant influent

The influence of elevated temperatures on PFAS leaching in municipal solid waste (MSW) landfills has not been well characterized in the published scientific literature. This study systematically examined the compositions and concentrations of per- and polyfluoroalkyl substances (PFAS) and precursors content in both normal temperature landfill and elevated temperature landfill (ETLF) leachates and compared to a municipal wastewater and to a WWTP influent with and without introduced leachates. The characterization of the samples involved the analysis of 71 PFAS target compounds before and after applying the total oxidizable precursor (TOP) assay, along with measuring fluorotelomer alcohols (FTOHs) and adsorbable organofluorine (AOF) levels. Summed PFAS concentrations in leachates were driven largely by fluorotelomer carboxylic acids (FTCAs), short-chain and ultrashort-chain perfluorinated carboxylic acids and sulfonic acids. Summed PFAS concentrations in ETLF leachate were significantly higher than in normal leachate for precursors and terminal PFAS products. TOP assay data demonstrated that ETLF leachate contained significantly higher concentrations of oxidizable PFAS precursors than normal leachate. PFAS profiles in leachates were distinct from municipal wastewater and from WWTP influent, suggesting diverse PFAS inputs to the WWTP. The presence of unknown precursors revealed by the TOP assay and AOF analyses highlights the complexity of PFAS sources impacting sewer networks, warranting further study to better characterize PFAS inputs to the WWTP on a city-wide scale.

Unravelling the formation of characteristic aroma of traditional braised pork through untargeted and targeted flavoromics

Untargeted flavoromics and targeted quantitative analysis of key aroma compounds, and analysis of dynamic change of aroma precursors concentration were used to investigate the aroma evolution of traditional braised pork and the underlying mechanism. The results indicated that lipid oxidation dominated at early cooking stage (0th–45th min), resulting in an increased concentration of most aldehydes, alcohols, ketones, such as hexanal, heptanal, octanal, nonanal, (E)-2-octenal, benzaldehyde, 1-octen-3-ol, and 2,3-octanedione, accompanied with an enhanced unpleasant fatty odor. From 45th to 73rd min, the seasonings alleviated excessive oxidation of unsaturated fatty acids accompanied with decreased aldehydes. Moreover, the diffusion of glucose and amino acids from seasonings to lean meat promoted the consumption of endogenous ribose and amino acids in meat through Maillard reaction, and facilitated the formation of dimethyl trisulfide, dimethyl disulfide, methanethiol, and 2-furfural, which contributed to the meaty, sauce-like, and sweety aroma, thus formed the characteristic aroma of traditional braised pork.

Multienzyme Immobilization on PVDF Membrane via One-Step Mussel-Inspired Method: Enhancing Fouling Resistance and Self-Cleaning Efficiency.

Immobilizing different enzymes on membranes can result in biocatalytic active membranes with a self-cleaning capacity toward a complex mixture of foulants. The membrane modification can reduce fouling and enhance filtration performance. Protease, lipase, and amylase were immobilized on poly(vinylidene fluoride) (PVDF) microfiltration membranes using a polydopamine coating in a one-step method. The concentrations of polydopamine precursor and enzymes were optimized during the immobilization. The higher hydrolytic activities were obtained using 0.2 mg/mL of dopamine hydrochloride and 4 mg/mL of enzymes: 0.90 mgstarch/min·cm2 for amylase, 10.16 nmoltyrosine/min·cm2 for protease, and 20.48 µmolp-nitrophenol/min·cm2 for lipase. Filtration tests using a protein, lipid, and carbohydrate mixture showed that the modified membrane retained 41%, 29%, and 28% of its initial water permeance (1808 ± 39 L/m2·h·bar) after three consecutive filtration cycles, respectively. In contrast, the pristine membrane (initial water permeance of 2016 ± 40 L/m2·h·bar) retained only 23%, 12%, and 8%. Filtrations of milk powder solution were also performed to simulate dairy industry wastewater: the modified membrane maintained 28%, 26%, and 26% of its initial water permeance after three consecutive filtration cycles, respectively, and the pristine membrane retained 34%, 21%, and 7%. The modified membrane showed increased fouling resistance against a mixture of foulants and presented a similar water permeance after three cycles of simulated dairy wastewater filtration. Membrane fouling is reduced by the immobilized enzymes through two mechanisms: increased membrane hydrophilicity (evidenced by the reduced water contact angle after modification) and the enzymatic hydrolysis of foulants as they accumulate on the membrane surface.

Electrodeposition of Aluminum-Silicon Films in Chloroaluminate Ionic Liquids

Electrodeposition of aluminum-silicon films in 1-ethyl-3-methylimidazolium chloride: aluminum chloride (1:1.5 molar ratio) was studied in the presence of different silicon halides. The silicon content in the deposited films was investigated as a function of the type and the concentration of various Si precursors. Using pulse plating technique, Al-Si films with Si content between 2 - 12.9 at. % could be obtained on copper substrates at room temperature.

In vitro and in vivo efficacy of zinc oxide green nanoparticles against multidrug-resistant Salmonella Typhi.

Antibiotic resistance is an increasing threat, requiring novel therapeutic solutions. Metal nanoparticles e.g., zinc oxide nanoparticles (ZnO NPs) exhibited the potential against many bacterial pathogens. Strains of Salmonella enterica serovar Typhi resistant to ceftriaxone were reported first from Pakistan in 2016. Since then, S. Typhi is a pathogen of concern globally owing to its rapidly emerging resistance potential against many last resort antibiotics. In the present study, in vitro and in vivo antimicrobial activity of ZnO NPs against multidrug resistant (MDR) and extensively drug resistant (XDR) Salmonella Typhi strains from Pakistan was evaluated. Zinc oxide green nanoparticles (ZnO GNPs), synthesized from Aloe vera, were characterized by SEM, XRD, UV-vis and Raman spectroscopy. In vitro antibacterial activity of two different concentrations of ZnO GNPs (7 and 15%) was checked using agar well diffusion method. Further, broth microdilution and time kill assays were performed using the ZnO GNPs. In vivo assays were conducted in BALB/c mice sepsis models. In all the three methods, agar well diffusion assay broth microdilution and time kill assay, different zinc oxide dihydrate precursor concentrations had shown the antibacterial activity. The minimum inhibitory concentration (MIC) of ZnO GNPs nanoparticles against MDR and XDR S. Typhi strains was found as 16 to 64µg/ml. In vivo experiment has shown a significant decrease in CFU/ml in the mice treated with ZnO GNPs as compared to the control group. Our findings have revealed that ZnO GNPs have significant antibacterial activity against MDR and XDR S. Typhi, both in vitro and in vivo.

Critical stages in pea photosynthesis impaired by tetracycline as an environmental contaminant.

The widespread use of antibiotics in intensive animal husbandry, and the agricultural utilization of manure from such farms, imposes a significant burden on the environment. Consequently, the effects of antibiotics should be studied not only in animals and humans but also in all components of biocenoses and agrocenoses. In our study, we analyze the impact of four different concentrations of tetracycline present in soil (0, 5, 50, and 500mg/kg of soil) on the growth and key photosynthesis parameters of pea seedlings: chlorophyll concentration, aminolevulinic acid concentration, aminolevulinic acid dehydrogenase activity, and ribulose bisphosphate carboxylase-oxygenase (RuBisCO) activity. At the lowest tetracycline concentration, chlorophyll content decreased by 13% compared to the control (0 tetracycline), while at the highest antibiotic concentration, it decreased by as much as 27%. Similarly, the decrease in aminolevulinic acid (a chlorophyll precursor) concentration was significant, amounting to 34%. However, the activity of the dehydrogenase enzyme, which consumes this precursor, decreased even more drastically by 51%, indicating significant disturbances in the light phase of photosynthesis. However, the activity of RuBisCO in pea plants subjected to tetracycline was even more severely affected, dropping by 58%, 69%, and 70% in soils with increasing concentrations of tetracycline. The reduction in enzyme activity could only partially be explained by a less pronounced decrease in the quantity of RuBisCO (large subunit) protein, which amounted to 6.5%, 11%, and 35% for tetracycline concentrations of 5, 50, and 500mg/kg of soil, respectively.

Hydroxy salt induced CoAl-LDH nanosheet composite membrane for pervaporation desalination

Pervaporation is a promising desalination technology. Developing high-performance and stable pervaporation membranes with high continuity structure remains a significant challenge. This study reports the development of a novel layered double hydroxide (LDH) nanosheet composite membrane fabricated using a hydroxyl salt induction method. This approach facilitated the in-situ nucleation and growth of the CoAl-LDH nanosheets on polyvinylidene fluoride (PVDF) substrate, reducing precursor concentration and enhancing preparation efficiency. The resulting cross-compatible architecture closely integrated the dense LDH nanosheet separation layer with the flexible PVDF support. The microstructure and morphology of the hydroxyl salt layer and its transformed CoAl-LDH composite membrane were comprehensively investigated. The optimized membrane was applied for pervaporation desalination (3 wt% NaCl, 50 °C), achieving a high flux of 38.4 kg·m−2·h−1 and exceptional NaCl rejection of 99.9 %. It also demonstrated excellent tolerance to a wide salinity range, maintaining 99.6–99.9 % rejection even at 20 wt% NaCl, while the flux remained stable at 26.7 kg·m−2·h−1. Long-term testing confirmed the consistent separation performance and operational stability, underscoring the great potential of this advanced membrane material for practical pervaporation desalination applications.

Magnetic Nanoparticles with On-Site Azide and Alkyne Functionalized Polymer Coating in a Single Step through a Solvothermal Process.

Background/Objectives: Magnetic Fe3O4 nanoparticles (MNPs) are becoming more important every day. We prepared MNPs in a simple one-step reaction by following the solvothermal method, assisted by azide and alkyne functionalized polyethylene glycol (PEG400) polymers, as well as by PEG6000 and the polyol β-cyclodextrin (βCD), which played a crucial role as electrostatic stabilizers, providing polymeric/polyol coatings around the magnetic cores. Methods: The composition, morphology, and magnetic properties of the nanospheres were analyzed using Transmission Electron and Atomic Force Microscopies (TEM, AFM), Nuclear Magnetic Resonance (NMR), X-ray Diffraction Diffractometry (XRD), Fourier-Transform Infrared Spectroscopy (FT-IR), Matrix-Assisted Laser Desorption/Ionization (MALDI) and Vibrating Sample Magnetometry (VSM). Results: The obtained nanoparticles (@Fe3O4-PEGs and @Fe3O4-βCD) showed diameters between 90 and 250 nm, depending on the polymer used and the Fe3O4·6H2O precursor concentration, typically, 0.13 M at 200 °C and 24 h of reaction. MNPs exhibited superparamagnetism with high saturation mass magnetization at room temperature, reaching values of 59.9 emu/g (@Fe3O4-PEG6000), and no ferromagnetism. Likewise, they showed temperature elevation after applying an alternating magnetic field (AMF), obtaining Specific Absorption Rate (SAR) values of up to 51.87 ± 2.23 W/g for @Fe3O4-PEG6000. Additionally, the formed systems are susceptible to click chemistry, as was demonstrated in the case of the cannabidiol-propargyl derivative (CBD-Pro), which was synthesized and covalently attached to the azide functionalized surface of @Fe3O4-PEG400-N3. Prepared MNPs are highly dispersible in water, PBS, and citrate buffer, remaining in suspension for over 2 weeks, and non-toxic in the T84 human colon cancer cell line, Conclusions: indicating that they are ideal candidates for biomedical applications.

Structural, morphological, and optical properties of CuO nanoblade-decorated TiO2 nanotubular photoelectrodes

Titania (TiO2) nanotubular photoelectrodes are a competitive component of titania-based photoelectrochemical water splitting systems. However, TiO2 actively absorbs light in the UV region, which limits its usefulness in solar water splitting, a fast-growing clean energy alternative. In this study, the structural, morphological and optical properties of CuO/TiO2 nanostructures on conductive transparent F-doped SnO2 (FTO) coated glass substrates are engineered for potential application in solar water splitting. The efficacy of a three-step anodization synthesis process to develop free-standing high-fidelity nanotubular TiO2 thin films (∼8μm) is demonstrated. CuO nanoblades were deposited on TiO2/FTO by a successive ionic layer adsorption reaction (SILAR). An increase in the precursor concentration and number of immersion cycles influenced the adsorption of CuO and the resultant red shift in the absorption range. SEM and TEM analyses confirm the formation of a heterostructure, with evidence of CuO nanostructures within the TiO2 nanotubular arrays and on the top of the tubes.

Heteronanotrimers by Selective Photodeposition of Gold Nanodots on Janus-Type Cu2‒ xS/CuInS2 Heteronanocrystals.

This study focuses on the development of environmentally friendly Au-Cu2-xS/CuInS2 heteronanotrimers. The chosen strategy relies on the laser photodeposition of a single gold nanodot (ND) onto Janus Cu2- xS/CuInS2 heteronanocrystals (HNCs). This method offers precise control over the number, location, and size (5 to 8nm) of the Au NDs by adjusting laser power for the career production, concentration of hole scavenger for charge equilibration in redox reactions, and gold precursor concentration, and exposure time for the final ND size. The photoreduction of gold ions onto HNCs starts systematically at the Cu2- xS tip. The Au deposition then depends on the CuInS2 segment length. For short HNCs, stable Au-Cu2- xS/CuInS2 heteronanotrimers form, while long HNCs undergo a secondary photo-induced step: the initial Au ND is progressively oxidized, with concomitant deposition of a second gold ND on the CuInS2 side, to yield Au2S-Cu2- xS/CuInS2-Au heteronanotrimers. Results are rationalized by quantitative comparison with a model that describes the growth kinetics of NDs and Au-Cu2- xS transformation and emphasizes the importance of charge separation in predicting selective deposition in heteronanotrimer production. The key parameter controlling Au-Cu2‒ xS/CuInS2 HNCs is the photoinduced electric field gradient generated by charge separation, which is tailored by controlling the CuInS2 segment size.