Dispersion Of Nanoparticles Research Articles

Solid Lipid Nanoparticles Incorporated with Retinol and Pentapeptide-18-Optimization, Characterization, and Cosmetic Application.

Solid lipid nanoparticles (SLNs) incorporated with retinol and oligopeptide can have a full spectrum of effects on the skin as a compatible combination of ingredients with broad anti-aging properties. The research's main objective was to ensure the stability of lipid nanocarriers containing retinol and peptide due to the planned use of this dispersion as a cosmetic raw material. To confirm the effectiveness of method optimization (high shear homogenization, HSH) and proper selection of substrates, SLN dispersions were obtained in three combinations: 1-non-incorporated SLNs; 2-SLNs containing only retinol; 3-SLNs containing retinol and pentapeptide-18; these were then stored at different temperatures (4, 25, 45 °C) for 4 weeks. The desired values of the physicochemical parameters of the optimized dispersion of lipid nanoparticles incorporated with retinol and oligopeptide over the required storage period were confirmed: mean particle size (Z-Ave) = 134.7 ± 0.3 nm; polydispersity index (PDI) = 0.269 ± 0.017 [-]; zeta potential (ZP) = 42.7 ± 1.2 mV (after 4 weeks at 25 °C). The results confirmed the proper selection of the SLN production method and the effectiveness of the optimization performed. The possibility of using the obtained raw material as an ingredient in cosmetic products with anti-aging properties was indicated.

Surfactant-Free Preparation of Conjugated Polymer Nanoparticles in Aqueous Dispersions Using Sulfate Functionalized Fluorene Monomers.

Conjugated polymer nanoparticles (CPNs) can be synthesized by a Suzuki-Miyaura cross-coupling miniemulsion polymerization to give stable dispersions with a high concentration of uniform nanoparticles. However, large amounts of added surfactants are required to stabilize the miniemulsion and prevent the aggregation of the nanoparticles. Removal of the excess surfactant is challenging, and residual surfactant in thin films deposited from these dispersions can reduce the performance of optoelectronic devices. We report a novel approach to prepare stable dispersions with no added surfactant using a fluorene monomer, 2,7-dibromo-9,9-bis(undecanesulfate)-9H-fluorene, with alkyl side chains terminated by negatively charged sulfate groups. This functionality mimics the structure of one of the most commonly used surfactants, sodium dodecyl sulfate (SDS). This charged monomer effectively stabilizes the miniemulsion through electrostatic repulsion without the use of any additional surfactant in molar ratios ranging from 2.0 to 20.0 mol % of total monomer content for the preparation of poly(9,9-dioctylfluorene) (PFO) and poly(9,9-dioctylfluorene-alt-bithiophene) (PF8T2). Incorporation of 5.0 mol % of the amphiphilic monomer gave stable dispersions with a surface potential below -40 mV and, and polymers with molar mass (Mn) above 10 kg mol-1. This method should be generally applicable to the preparation of dispersions of polyfluorenes for application in organic electronic and optoelectronic devices without the requirement for time-consuming processes to remove residual surfactant.

Catalytic hydrodeoxygenation of lignin enhanced by selectively etching ZSM-5

Cyclanes, a major component of aviation fuel, can be obtained from the catalytic hydrodeoxygenation (HDO) of lignin, which not only reduces the dependence on fossil resources, but also makes lignin refining economically viable. The adsorption capacity and dwell times of reactants and H2 on the catalyst play a key role in the HDO of lignin. It remains a difficult challenge to enhance the adsorption capacity of the catalyst for reactants and H2 and to prolong their extended dwell times on the catalyst. Based on this, a nickel-based catalyst with moderate corrosion was prepared by the dissolution of ZSM-5 single crystals induced by ammonia, and was used for value-added conversion of lignin. It was confirmed by experiments and complementary characterizations that the corrosion of Ni/ZSM-5 for etching 2 h (Ni/ZSM-52) enhanced the adsorption capacity of H2 and extended the dwell times of the reactant and H2. Furthermore, the uniformly dispersed Ni nanoparticles stimulated the intrinsic catalytic activity and efficiently generated H…H and H+, which synergistically promote the HDO of lignin with the cyclanes yield up to 58.6 %. As a result, BOB was completely converted to cyclanes over Ni/ZSM-52 at 140 °C under 2 MPa of H2 for 4 h, suggesting Ni/ZSM-52 exhibits excellent HDO activity under mild conditions.

Green Synthesis of Iron-Based Nanoparticles Using Pomegranate Leaf Extracts: Characterization, Biomolecules and Indole Removal

This study investigates the synthesis of iron-based nanoparticles (Fe NPs) using pomegranate leaf extracts and their application in removing indole, a persistent organic pollutant commonly found in wastewater. The physicochemical properties of the synthesized Fe NPs and the active biomolecules in the pomegranate leaf extracts were comprehensively characterized. Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM) analyses revealed that the Fe NPs exhibited quasi-spherical shapes, with sizes ranging from 75 to 105 nm. Energy-Dispersive X-ray Spectroscopy (EDS) confirmed a homogeneous distribution of elements, including C, O, Fe, and S, on the nanoparticle surfaces, with weight percentages of 43.59%, 42.95%, 12.58%, and 0.88%, respectively. Fourier-transform infrared spectroscopy (FTIR) identified key functional groups like −OH, −COOH, and −C=O, which are essential for the capping and stabilization of the nanoparticles. Biomolecules such as ellagic acid (C14H6O8) and gallic acid (C7H6O5) functioned as reducing agents, improving nanoparticle dispersion and preventing aggregation. The synthesized Fe NPs quickly achieved 45.5% removal of indole within just 20 min and maintained a stable removal efficiency of approximately 51.4% after 90 min. This performance was attributed to the synergetic interaction between the biomolecules and the nanoparticles, with the monolayer adsorption of indole molecules on the Fe NP surfaces likely setting an upper limit on the maximum achievable removal efficiency. It appears from this study that pomegranate leaf extracts can be effectively utilized to synthesize Fe NPs as a novel and eco-friendly approach, demonstrating promising potential for the rapid removal of indole from aqueous solutions.

Nanocomposites of Poly(n-Butyl Acrylate) with Fe3O4: Crosslinking with Hindered Urea Bonds, Reprocessing and Related Functional Properties.

In this contribution, we reported the synthesis of the nanocomposites of poly(n-butyl acrylate) with Fe3O4 nanoparticles (NPs) via dynamic crosslinking of poly(n-butyl acrylate)-grafted Fe3O4 NPs with hindered urea bonds (HUBs). Towards this end, the surfaces of Fe3O4 NPs were grafted with poly(n-butyl acrylate-ran-2-(3-tert-butyl-3-ethylureido)ethyl acrylate) chains [denoted as Fe3O4-g-P(BA-r-TBEA)] via living radical polymerization. Thereafter, 1,2-bis(tert-butyl)ethylenediamine was used as a crosslinker to afford the organic-inorganic networks with variable contents of Fe3O4 NPs and crosslinking densities. It was found that the fine dispersion of Fe3O4 NPs in the matrix of poly(n-butyl acrylate) was achieved. The nanocomposites exhibited excellent reprocessing properties, attributed to the introduction of HUBs. Owing to the crosslinking, the nanocomposites displayed excellent shape memory properties. Further, the nanocomposites possessed photo- and magnetic-thermal properties, which were inherited from Fe3O4 NPs. These functional properties allow triggering the shape shifting of the nanocomposites in an uncontacted fashion.

Computational study on cilia transport of Prandtl nanofluid (blood-Fe3O4) enhancing convective heat transfer along microorganisms under electroosmotic effects in wavy capillaries

Purpose This study aims to focuse on the flow behavior of a specific nanofluid composed of blood-based iron oxide nanoparticles, combined with motile gyrotactic microorganisms, in a ciliated channel with electroosmosis. Design/methodology/approach This study applies a powerful mathematical model to examine the combined impacts of bio convection and electrokinetic forces on nanofluid flow. The presence of cilia, which are described as wave-like motions on the channel walls, promotes fluid propulsion, which improves mixing and mass transport. The velocity and dispersion of nanoparticles and microbes are modified by the inclusion of electroosmosis, which is stimulated by an applied electric field. This adds a significant level of complexity. Findings To ascertain their impact on flow characteristics, important factors such as bio convection Rayleigh number, Grashoff number, Peclet number and Lewis number are varied. The results demonstrate that while the gyrotactic activity of microorganisms contributes to the stability and homogeneity of the nanofluid distribution, electroosmotic forces significantly enhance fluid mixing and nanoparticle dispersion. This thorough study clarifies how to take advantage of electroosmosis and bio convection in ciliated micro channels to optimize nanofluid-based biomedical applications, such as targeted drug administration and improved diagnostic processes. Originality/value First paper discussed “Numerical Computation of Cilia Transport of Prandtl Nanofluid (Blood-Fe3O4) Enhancing Convective Heat Transfer along Micro Organisms under Electroosmotic effects in Wavy Capillaries”.

Enhanced nanofluid stability of Zn-doped iron oxide: Applications of ascorbic acid nanofluid in enhanced oil recovery

Ascorbic acid-coated, transition metal-doped Fe3O4 nanoparticles were successfully synthesized via coprecipitation. The synthesized Zn-doped Fe3O4 nanoparticles have an average diameter of approximately 30 nm. These nanoparticles exhibit ferromagnetic properties at room temperature, with the highest saturation magnetization approaching 40 emu/g and decreasing coercivity. The surface was functionalized with ascorbic acid, which served as a surfactant to ensure high dispersibility and stability of the Fe3O4 nanoparticles in a brine solution containing 30,000 ppm NaCl. Zeta potential and interfacial tension (IFT) measurements were conducted to assess the suspension quality, confirming the effectiveness of the ascorbic acid coating in stabilizing the nanoparticles.

Hierarchically structured nanospherical fibrous silica-supported bimetallic catalysts: An enhanced performance in methane decomposition

Hydrogen production by methane catalytic decomposition is a promising method that also allows the formation of valuable carbon nanomaterials which can be utilized in transportation fuels, chemical synthesis, and fuel cell technology. In this study, bimetallic 3d transition metal (Ni, Fe, Co) catalysts supported on spherical mesoporous nanofibrous silica (KCC1) were successfully synthesized using a hydrothermal method followed by sono co-impregnation. The catalysts were evaluated for their performance in the catalytic decomposition of methane. Comprehensive characterization of the catalysts was conducted utilizing XRD, FTIR, SEM, TEM, STEM, XPS, H2-TPR, and BET techniques. XRD and TEM analyses confirmed the formation of Ni–Fe, Ni–Co, and Co–Fe bimetallic alloys on the nanofibrous silica without compromising its dendrimeric hierarchical structure. STEM HAADF imaging revealed a uniform dispersion of bimetallic nanoparticles within the spherical fibrous framework. Catalytic tests demonstrated that all bimetallic catalysts showed high stability and activity for methane cracking at 700 °C over 180 min of time on stream (TOS). Among them, Fe-based catalysts Ni–Fe/KCC1 and Co–Fe/KCC1 achieved the highest hydrogen yields of 80% and 60%, respectively. Methane conversion was 1.56 and 2.23 times higher in Ni–Fe/KCC1 compared to Co–Fe/KCC1 and Ni–Co/KCC1, respectively. Post-reaction characterization of the spent catalysts was performed using XRD, Raman spectroscopy, SEM, TEM, and TGA. XRD and Raman spectroscopy were used to evaluate the degree of graphitization and crystallinity in the carbon nanotubes (CNTs) produced on the catalysts, enabling a correlation with the catalyst properties. TEM examination was used to investigate the structural morphology and growth methods of the CNTs, including tip or base growth and chain-like or parallel-wall types. TGA results revealed that all bimetallic catalysts exhibited no amorphous carbon during methane cracking reaction.

Coherent Phonon Dynamics in Plasmonic Gold Tetrahedral Nanoparticle Ensembles.

Coherent phonon modes supported by plasmonic nanoparticles offer prospective applications in chemical and biological sensing. Whereas the characterization of these phonon modes often requires single-particle measurements, synthetic routes to narrow size distributions of nanoparticles permit ensemble investigations. Recently, the synthesis of highly monodisperse gold tetrahedral nanoparticles with tunable edge lengths and corner sharpnesses has been developed. Herein, we characterize a size series of these nanoparticles in colloidal dispersion via transient absorption spectroscopy to examine their mechanical and plasmonic responses upon photoexcitation. Oscillations of transient absorption signals are observed in the plasmon resonance and correspond to the lowest-order radial breathing modes of the nanoparticles, the frequencies of which are affected by the edge length and truncation of the corners. Homogeneous quality factor values ranging from 24 to 34 are observed for the oscillations that convey potential utility in mass-sensing and plasmon-exciton-coupling photonics schemes. Finite-difference time domain and finite element analysis calculations establish specific optically relevant phonon modes.

Coating effect of polyurethane-layered double hydroxide nanocomposite on steel

The motivation behind this work is the preparation of polyurethane-magnesium aluminum layered double hydroxide (PU-LDH) nanocomposite and its application as a coating for steel protection. The coating was prepared with different doses of LDH, ranging from 0 to 2% of the coating weight. The effect of different concentrations on the mechanical, adhesion, and surface properties of PU coating is studied. Firstly, LDH was prepared via the coprecipitation process and then distributed in PU matrix. The nanocomposites were then crosslinked in the form of coating layers on steel. The preparation of the thermally stable crystalline LDH nanoparticles with 89 nm particle size was confirmed by FTIR, XRD, DLS, and TGA. SEM photos showed the dispersed and intercalated structure. The coating characteristics demonstrate that addition of LDH decreased the drying time and increased the dry film thickness of PU up to 1.5% due to the crosslinking between the large surface area nanofiller and polyurethane matrix. Furthermore, the prepared LDH nanofiller increased the adhesion strength, impact resistance, abrasion resistance, modulus, and flexibility of PU due to the strong polymeric network structure. The 2% nanocomposite coating shows poor properties due to the excess concentration and heterogeneous dispersion of nanoparticles within the PU polymer. The resistance to fire and some chemicals was supported by the thermally and physically stable LDH nanoclay. The former characterizations state that the proposed PU-LDH nanocomposite is an enhanced and applicable coating.

Zein nanoencapsulation enhances the antifungal activity of thymol for postharvest decay control in bananas

AbstractThe current work describes a nanoparticle system-based approach to enhance the antifungal activity of thymol, a ubiquitous natural antifungal phenolic compound, in postharvest control against banana anthracnose. Thymol was encapsulated within the amphiphilic protein zein by high-shear emulsification, yielding highly dispersible thymol-loaded zein nanoparticles with a high encapsulation efficiency (70%). These particles have an average diameter of 300 nm with spherical morphology, smooth interface, and matrix-type internal structure, as supported by comprehensive structural characterization (dynamic light scattering, transmission electron microscopy and atomic force microscopy). Based on a 40-d storage stability test, thymol was effectively retained within the nanoparticles at 4 °C and ambient room temperature (99% and 97% retention, respectively), despite thymol’s instability and volatility. Antifungal activity assessment against Colletotrichum musae, one of the predominant pathogens that cause banana anthracnose, showed a 200- to 300-fold improvement in the in vitro antifungal activity of thymol. Moreover, the application of thymol-loaded zein nanoparticles as a spray component for banana postharvest treatment demonstrated the efficacy of thymol-loaded zein nanoparticles in preventing and delaying the formation of initial symptoms of banana anthracnose. This appears to arise from the thymol-loaded zein nanoparticles depositing as a film on the banana epidermis, as revealed by atomic force microscopy. Overall, this nanoparticle system offers a new avenue for the design of effective antifungal materials with potential applications in combatting postharvest diseases. Graphical abstract

Enhanced sonophoto-catalytic and adsorption capabilities of Fe3O4@MC/MWCNT-CuO/Ag for petrochemical organic pollutants degradation from industrial process streams

To address the problem of petrochemical organic pollutants in water, specifically monoethylene glycol (MEG) present in industrial process streams, in this research, we synthesized and evaluated a multifunctional nanocomposite, Fe3O4@MC/MWCNT-CuO/Ag. The nanocomposite was produced by combining magnetic Fe3O4 nanoparticles, methylcellulose (MC), multi-walled carbon nanotubes (MWCNTs), and CuO/Ag nanoparticles by an integrated synthesis process. A consistent dispersion of nanoparticles, with diameters ranging from 30-40 nm, was discovered by FESEM analysis, showing effective integration without aggregation. Effective synthesis was demonstrated by well-doped and evenly dispersed CuO and Ag nanoparticles. Functional groups that improve electrostatic interactions with contaminants hence enhancing catalytic performance and adsorption efficiency, were validated by FTIR analysis. XRD indicated an unchanged crystal structure with an average crystallite size of 8.67 nm. The anticipated elemental composition was verified by EDS & mapping. A VSM study revealed magnetic characteristics (9.33 emu/g) that simplify nanocomposite separation and reuse. TGA proved thermal stability to be up to 600 °C. A BET study showed a highly specific surface area of 67.661 m2/g, enhancing adsorption. According to DRS and PL studies, the bandgap was lowered by 1.31 eV, which led to better optical absorption. The nanocomposite exhibited notable MEG removal efficiency, with 72 % in adsorption, 65 % in photocatalysis, and 56 % in sonocatalysis. This makes it a promising alternative for the remediation of organic pollutants in water treatment.

Preparation and characterization of a new food-grade Pickering emulsion stabilized by mulberry-leaf protein nanoparticles.

Food-grade Pickering particles, particularly plant proteins, have attracted significant interest due to their bio-based nature, environmental friendliness, and edibility. Mulberry-leaf protein (MLP) is a high-quality protein with rich nutritional value and important functional properties. It has special amphoteric and emulsifying characteristics, making it valuable for use in Pickering emulsions. This study aimed to investigate the feasibility of using MLP nanoparticles as solid particles to stabilize Pickering emulsions. The particle size of MLP nanoparticles was less than 300 nm under neutral and alkaline conditions. At pH 9, the zeta potential value reached -34.3 mV, indicating the electrostatic stability of the particles. As ion concentration increased, the particle size of MLP nanoparticles increased, and the zeta potential decreased. Throughout the storage process, no obvious aggregation or precipitation was observed in the dispersion of MLP nanoparticles, indicating strong stability. The particle size of the Pickering emulsion decreased with the increase in protein concentration. When the protein concentration was low, the particles on the oil-water interface became sparse, resulting in poor stability of the prepared emulsion and making it susceptible to aggregation and thus larger particle sizes. Increasing the oil-phase ratio to 70% (v/v) promotes the formation of Pickering emulsions, which exhibit exceptional stability when MLP nanoparticles are fixed at a concentration of 20 mg mL-1. The overall findings indicated that MLP nanoparticles have potential as food-grade materials for Pickering emulsions, marking a novel application of these nanoparticles in the food industry. © 2024 Society of Chemical Industry.

Multifunctional SERS Substrate for Simultaneous Detection of Multiple Contaminants and Photothermal Removal of Pathogenic Bacteria.

In this work, a boric-acid-modified Fe3O4@Au@BA-MOF composite material as a multifunctional SERS substrate was ingeniously constructed for detecting both pathogens and antibiotics as well as photothermally inactivating the pathogens. Through improving the dispersity and stability of gold nanoparticles (Au NPs), leveraging the specificity of boric acid (BA) groups in recognizing cis-diol structures, and the ability of SERS technology to provide unique fingerprint spectra of targets, the sensitive and stable detection of pathogens and antibiotics was achieved. Compared with Au NPs and Fe3O4@Au, the SERS enhancement factor of Fe3O4@Au@BA-MOF was 4.31 × 106, which was about 400 times and 16 times higher than the former two, respectively. Among the existing work, the limit of detection for pathogens was lower or comparable, and it exhibited good stability, maintaining consistent performance for 23 days. Additionally, this substrate achieved efficient photothermal inactivation of pathogens under both near-infrared light and natural light excitation. Within 8 min of near-infrared light irradiation, the bactericidal rates for Staphylococcus aureus and Escherichia coli reach 100% and 99.3%, respectively.

Highly effective ruthenium catalyst support on La2Zr2O7 for ammonia decomposition to COx-free hydrogen

Pyrochlore-type La2Zr2O7 was prepared through a sol–gel route and served as a Ru-based catalyst support for ammonia decomposition to produce H2 without COx emission. The NH3 conversion over Ru/La2Zr2O7 could reach 69.5 % at 450 °C under the pure NH3 gas hourly space velocity (GHSV) of 30 000 mL.gcat-1h−1, which is approximately 3.1 times of that over Ru/ZrO2 and 2.2 times of Ru/La2O3 under the same conditions, respectively. It was found that the presence of oxygen vacancies on La2Zr2O7 surface can strongly interact with Ru particles to form the electronic strong metal-support interaction (EMSI), increasing the dispersion of Ru nanoparticles. Additionally, the mobile electrons are effectively transferred from La2Zr2O7 to the surface of Ru particles through the EMSI effect, consequently boosting the recombination desorption of N and ultimately contributing to the exceptional catalytic activity of Ru/La2Zr2O7.

A cation exchange strategy to construct highly dispersed copper-doped CdS nanoparticles for photocatalytic hydrogen production

Developing facile methods to modulate the structure and performance of photocatalysts plays a pivotal role in the potential large-scale application of photocatalytic hydrogen production. Herein, a series of uniformly sized and highly dispersed copper-doped cadmium sulfide (CdS) nanoparticles (NPs) were successfully synthesized through a facile cation exchange strategy. The resulting Cu-doped CdS samples exhibited a remarkable photocatalytic hydrogen production rate of 2459.3 μ mol·h−1g−1, nearly 11 times that of pure CdS. The introduction of Cu+ ions effectively reduced the band gap, leading to enhanced light absorption, as well as improved charge carrier separation and transfer efficiency. Meanwhile, the theoretical investigation further confirmed that Cu+ doping substantially decreased the free energy of hydrogen adsorption and provided more suitable active sites, thereby promoting the photocatalytic hydrogen production activity on CdS NPs. This work provides compelling evidence for the exploration of novel transition metal-doped photocatalysts for hydrogen production using the cation exchange method.

Effect of degree of substitution of octenyl succinate on starch micelles for synthesis and stability of selenium nanoparticles: Towards selenium supplements

To develop a promising selenium supplement that overcomes the instability and poor water dispersibility of selenium nanoparticles (SeNPs), we synthesized a series of amphiphilic octenyl succinic anhydride starch (OSAS) through esterification. As the degree of substitution (DS) increased, the particle size of OSAS micelles and the critical micelle concentration (CMC) decreased. FTIR and XRD analysis confirmed the successful introduction of octenyl succinic anhydride groups onto starch. Subsequently, OSAS micelles were used as carriers to synthesize SeNPs via in situ chemical reduction, forming SeNPs-loaded self-assembled starch nano-micelles (OSAS-SeNPs). The OSAS-SeNPs exhibited spherical dispersion in water with an average diameter of 116.1 ± 2.3 nm, contributed to enhanced hydrophobic interactions. TEM images showed a core-shell structure with SeNPs as the core and OSAS as the shell. FTIR results indicated hydrogen bonding interactions between OSAS and SeNPs. Due to the negatively charged OSAS shell and hydrogen bonding (OH⋯Se), OSAS-SeNPs remained non-aggregated for one month at room temperature, demonstrating remarkable stability. This study suggests that using OSAS can address the synthesis and stability issues of SeNPs, making it a potential selenium supplement candidate for further evaluation as an anticancer agent.

TiO2 and ZnO Nanoparticles Immobilized on Magnetic Sulfonated Melamine‐Formaldehyde: Structure Identification and Performance as Recyclable Catalysts for the Biginelli Reaction

AbstractSulfonated melamine‐formaldehyde (SMF) containing high dispersed TiO2 and ZnO nanoparticles were fabricated into magnetic nanocomposites by two different method material incorporation protocols, including calcination and wet impregnation. Their catalytic performance was investigated toward Biginelli reaction. For the preparation of the first catalyst series, a two‐step protocol was used. Initially, Fe3O4 nanoparticles were coated with SMF (Fe3O4/SMF). Subsequently, they were decorated consecutively with TiO2 (Fe3O4/SMF/TiO2) and ZnO (Fe3O4/SMF/ZnO). The second set of catalysts was prepared using a two‐step process. Fe3O4 nanoparticles were first used to modify SMF (SMF/Fe3O4). Following the initial step, the surface of SMF/Fe3O4 was decorated with both TiO2 (SMF/Fe3O4/TiO2) and ZnO (SMF/Fe3O4/ZnO). To understand the characteristics of the synthesized nanocomposites, a variety of characterization techniques were employed. New catalysts enabled the rapid synthesis (30–45 min) of a range of biologically active 3,4‐dihydropyrimidinones based on the Biginelli reaction with high yields (70–95 % isolated).

Impact of Nickel on Iridium-Ruthenium Structure and Activity for the Oxygen Evolution Reaction under Acidic Conditions.

Proton exchange membrane water electrolysis (PEMWE) is a promising technology to produce hydrogen directly from renewable electricity sources due to its high power density and potential for dynamic operation. Widespread application of PEMWE is, however, currently limited due to high cost and low efficiency, for which high loading of expensive iridium catalyst and high OER overpotential, respectively, are important reasons. In this study, we synthesize highly dispersed IrRu nanoparticles (NPs) supported on antimony-doped tin oxide (ATO) to maximize catalyst utilization. Furthermore, we study the effect of adding various amounts of Ni to the synthesis, both in terms of catalyst structure and OER activity. Through characterization using various X-ray techniques, we determine that the presence of Ni during synthesis yields significant changes in the structure of the IrRu NPs. With no Ni present, metallic IrRu NPs were synthesized with Ir-like structure, while the presence of Ni leads to the formation of IrRu oxide particles with rutile/hollandite structure. There are also clear indications that the presence of Ni yields smaller particles, which can result in better catalyst dispersion. The effect of these differences on OER activity was also studied through rotating disc electrode measurements. The IrRu-supported catalyst synthesized with Ni exhibited OER activity of up to 360 mA mgPGM -1 at 1.5 V vs RHE. This is ∼7 times higher OER activity than the best-performing IrO x benchmark reported in the literature and more than twice the activity of IrRu-supported catalyst synthesized without Ni. Finally, density functional theory (DFT) calculations were performed to further elucidate the origin of the observed activity enhancement, showing no improvement in intrinsic OER activity for hollandite Ir and Ru compared to the rutile structures. We, therefore, hypothesize that the increased activity measured for the IrRu supported catalyst synthesized with Ni present is instead due to increased electrochemical surface area.

Three-dimensional gel network structure of agarose interlayer dispersed Pd nanoparticles in copper foam electrode for electrocatalytic degradation of doxycycline hydrochloride

In this study, we successfully prepared palladium/agarose/copper foam (Pd/AG/CF) composite electrodes by utilizing the three-dimensional network structure agarose (AG), a green material derived from biomass, and homogeneously immobilizing palladium (Pd) atoms on a copper foam (CF) substrate through a facile route. The electrode showed excellent performance in the electrocatalytic degradation of doxycycline (DOX), with a high DOX degradation rate of 92.19 % in 60 min. In-depth studies revealed that palladium can form metal-metal interactions with the CF substrates, which enhances the electron transfer on the catalyst surface. In addition, the introduction of agarose effectively prevented the agglomeration of palladium nanoparticles. In addition, the hydroxyl functional groups in the molecular structure of agarose facilitate interactions between water molecules and the electrode interface through the formation of hydrogen bonds, thereby further enhancing the efficiency of the electrocatalytic reaction. In addition to good stability and reusability. Microbial toxicity test results show that the degraded wastewater has minimal impact on the environment. Also, possible degradation pathways of DOX were explored in this study. Finally, a novel continuous flow reactor was designed, featuring a unique design that ensures full contact between wastewater and the composite electrodes, thereby achieving continuous and efficient treatment of antibiotic wastewater.