Structure-Function Relationship of Iron Oxide Nanoflowers: Optimal Sizes for Magnetic Hyperthermia Depending on Alternating Magnetic Field Conditions.

Iron oxide nanoflowers (IONFs) that display singular magnetic properties can be synthesized through a polyol route first introduced almost 2 decades ago by Caruntu et al, presenting a multi-core morphology in which several grains (around 10 nm) are attached together and sintered. These outstanding properties are of great interest for magnetic field hyperthermia, which is considered as a promising therapy against cancer. Although of significantly smaller diameter, the specific adsorption rate (SAR) of IONFs reach values as large as for "magnetosomes" that are natural magnetic nanoparticles typically ~40 nm found in certain bacteria, which can be grown artificially but with much lower yield compared to chemical synthesis such as the polyol route. This work aims at better understanding the structure-property relationships, linking the internal IONF nanostructure as observed by HR-TEM to their magnetic properties. A library of mono- and multicore IONFs is presented, with diameters ranging from 11 to 30 nm in a narrow size distribution. More particularly, by relating their structural features to their magnetic properties investigated by utilizing AC magnetometry over a wide range of alternating magnetic field conditions, we showed that the SAR values of all synthesized batches vary with overall diameter and number of constituting cores.

Investigating the optical and electrical performance of rod coated silver nanowire-based transparent conducting films.

Silver nanowires (Ag NWs) are highly promising building blocks for developing transparent conducting films (TCFs) due to their high electrical conductivity and good optical transparency. The large-scale production of Ag NW-based high-quality TCFs using low-cost processing methods can replace the traditional oxide based TCFs. Therefore, developing a reliable technique for large-scale fabrication of Ag NW-based TCFs is vital. This work involves the synthesis of Ag NWs, the fabrication of large-area Ag NW-based TCFs using a simple rod coating process, its optimization, and the performance analysis of the fabricated TCFs, including their demonstration as transparent heaters. The polyol synthesis method produces Ag NWs of lengths ranging from 25-110µm and diameters from 80-180 nm. The effect of Ag NW length, the number of coating passes, and the volume of the NW dispersion used per coating pass on the electrical and optical properties of the TCFs are studied by quantifying sheet resistance(Rs)and transmittance (T) of the film. The performance of the fabricated film is evaluated by estimating the figure of merit (FoM) in both percolative and bulk regimes. The TCF made with NWs of length 25.7µm and diameter 85.1 nm had the largest value of bulk FoM (101.3), percolative FoM (43.9), and, conductivity exponent (0.6). This elucidated the superior performance of the fabricated TCFs over those fabricated by other techniques. The critical thickness of the film (tmin), at the crossover between the percolation and bulk, scales with the shortest dimension of the NW, namely its diameter. The percolative FoM showed an increase, with a decrease in both sheet resistance and diameter of the NWs, with lowern. The fabricated TCF is tested as a transparent heater and the demonstration proves that rod coated Ag NW-based TCFs can be used for transparent electrode applications.

Optimizing silver nanowire dimensions by the modification of polyol synthesis for the fabrication of transparent conducting films.

Transparent conducting films (TCFs) made by the assembly/deposition of silver nanowires (Ag NWs) are widely used to manufacture flexible electronics such as touch screens, heaters, displays, and organic light-emitting diodes. Controlling the dimensions (length and diameter) of the nanowires is key in obtaining TCFs with the desired optoelectronic properties, namely sheet resistance and optical transparency. This work describes a combined experimental and theoretical investigation on the optimization of the NW dimensions to fabricate high-quality TCFs. Ag NWs of different dimensions are synthesized by the modified polyol method and the average diameter and length of the wires are tailored over a wide range, 35-150 nm and 12-130µm respectively, by controlling the synthesis parameters such as reaction conditions, stabilizing agents, and growth promoters. The synthesized NWs are spin coated on glass substrates to form TCFs. Comparing the films with different lengths, but identical diameters, enabled the quantification of the effect of length on the optoelectronic properties of the TCFs. Similarly, the effect of NW diameter is also studied. A non-uniformity factor is defined to evaluate the uniformity of the TCF and the transmittance of the NW network is shown to be inversely proportional to its area coverage. The sheet conductance versus the normalized number density is plotted for the different concentrations of NWs to extract a conductivity exponent that agrees well with the theoretical predictions. For thin film networks, the relation between the transmittance and sheet resistance provides the percolative figure of merit (FoM) as a fitting parameter. A large FoM is desirable for a good-performing TCF and the synthesis conditions to achieve this are optimized.

Simple and Fast High-Yield Synthesis of Silver Nanowires.

Silver nanowires (AgNWs) combine high electrical conductivity with low light extinction in the visible and are used in a wide range of applications, from transparent electrodes, to temperature and pressure sensors. The most common strategy for the production of AgNWs is the polyol synthesis, which always leads to the formation of silver nanoparticles as byproducts. These nanoparticles degrade the performance of AgNWs' based devices and have to be eliminated by several purification steps. Here, we report a simple and fast synthesis of AgNWs with minimal formation of byproducts, as confirmed by the spectral purity of the final solution. Our synthetic strategy relies on the use of freshly prepared AgCl and on the minimization of gas evolution inside the reaction vessel. The observed synthetic improvements can be of general validity for the polyol synthesis of metallic nanostructures of different shapes and compositions.

One-Pot Seed-Mediated Growth of Co Nanoparticles by the Polyol Process: Unraveling the Heterogeneous Nucleation.

The one-step seed-mediated synthesis is widely used for the preparation of ferromagnetic metal nanoparticles (NPs) since it offers a good control of particle morphology. Nevertheless, this approach suffers from a lack of mechanistic studies because of the difficulties of following in real time the heterogeneous nucleation and predicting structure effects with seeds that are generated in situ. Here, we propose a complete scheme of the heteronucleation process involved in one-pot seed-mediated syntheses of cobalt nanoparticles in liquid polyols, relying on geometrical phase analysis (GPA) of high-resolution high-angle annular dark field (HAADF)-STEM images and in situ measurements of the molecular hydrogen evolution. Cobalt particles of different shapes (rods, platelets, or hourglass-like particles) were grown by reducing cobalt carboxylate in liquid polyols in the presence of iridium or ruthenium chloride as the nucleating agent. A reaction scheme was established by monitoring the H2 evolution resulting from the decomposition of metal hydrides, formed in situ by ß-elimination of metal alkoxides, and from the polyol dehydrogenation, catalytically activated by the metal particles. This is a very good probe for both the noble metal nucleation and the heterogeneous nucleation of cobalt, showing a good separation of these two steps. Ir and Ru seeds with a size in the range 1-2 nm were found exactly in the center of the cobalt particles, whatever the cobalt particle shape, and high-resolution images revealed an epitaxial growth of the hcp Co on fcc Ir or hcp Ru seeds. The microstructure analysis around the seeds made evident two different ways of relaxing the lattice mismatch between the seeds and the cobalt, with the presence of dislocations around the Ir seeds and compression zones of the cobalt lattice near the Ru seeds. The relationship between the nature of the nucleating agent, the reaction steps, and the microstructure is discussed.

Synthesis of Silver Nanowires with Reduced Diameters Using Benzoin-Derived Radicals to Make Transparent Conductors with High Transparency and Low Haze.

Reducing the diameter of silver nanowires has been proven to be an effective way to improve their optoelectronic performance by lessening light attenuation. The state-of-the-art silver nanowires are typically around 20 nm in diameter. Herein we report a modified polyol synthesis of silver nanowires with average diameters as thin as 13 nm and aspect ratios up to 3000. The success of this synthesis is based on the employment of benzoin-derived radicals in the polyol approach and does not require high-pressure conditions. The strong reducing power of radicals allows the reduction of silver precursors to occur at relatively low temperatures, wherein the lateral growth of silver nanowires is restrained because of efficient surface passivation. The optoelectronic performance of as-prepared 13 nm silver nanowires presents a sheet resistance of 28 Ω sq-1 at a transmittance of 95% with a haze factor of ∼1.2%, comparable to that of commercial indium tin oxide (ITO).

Branched silver nanowires on fluorine-doped tin oxide glass for simultaneous amperometric detection of H2O2 and of 4-aminothiophenol by SERS.

This study introduces a two-step method for the deposition of branched silver nanowires (AgNWs) on fluorine-doped tin oxide (FTO) glass. This material serves as both an active surface-enhanced Raman-scattering (SERS) substrate and as an enzyme-free electrochemical sensor for H2O2. This dual functionality is systematically studied. The AgNWs as the main trunk were first deposited on FTO by spray-coating. Silver branches were then electrochemically produced on the preformed NWs. Scanning electron microscopy, X-ray diffraction and X-ray photoelectron spectrometry were employed to characterize morphology, composition and microstructure. SERS experiments show that the branched AgNW/FTO substrate exhibits excellent performance in detecting 4-aminothiophenol at an ultra-low concentration of 0.1 fM. Simultaneously, this material displays an excellent electrocatalytic response to H2O2 reduction at a concentration as low as 1 µM. The sensor has a rapid response and two linear analytical ranges that extend from 0.25 to 300 µM, and from 0.3 to 2.6 mM of H2O2, respectively. The ultrahigh sensitivity and satisfactory reproducibility highlights the merit of this hierarchical AgNW dendritic structure for sensing applications. Graphical abstract Branched silver nanowires can serve as both an active surface-enhanced Raman scattering substrate and as an electrochemical sensor for H2O2. This dual functionality is systematically investigated.

Continuous Polyol Synthesis of Metal and Metal Oxide Nanoparticles Using a Segmented Flow Tubular Reactor (SFTR).

Over the last years a new type of tubular plug flow reactor, the segmented flow tubular reactor (SFTR), has proven its versatility and robustness through the water-based synthesis of precipitates as varied as CaCO3, BaTiO3, Mn(1-x)NixC2O4·2H2O, YBa oxalates, copper oxalate, ZnS, ZnO, iron oxides, and TiO2 produced with a high powder quality (phase composition, particle size, and shape) and high reproducibility. The SFTR has been developed to overcome the classical problems of powder production scale-up from batch processes, which are mainly linked with mass and heat transfer. Recently, the SFTR concept has been further developed and applied for the synthesis of metals, metal oxides, and salts in form of nano- or micro-particles in organic solvents. This has been done by increasing the working temperature and modifying the particle carrying solvent. In this paper we summarize the experimental results for four materials prepared according to the polyol synthesis route combined with the SFTR. CeO2, Ni, Ag, and Ca3(PO4)2 nanoparticles (NPs) can be obtained with a production rate of about 1-10 g per h. The production was carried out for several hours with constant product quality. These findings further corroborate the reliability and versatility of the SFTR for high throughput powder production.

Improved selectivity of electrochemical aniline sensing using one-dimensional silver nanorods with high aspect ratio synthesized by ascorbic acid assisted method.

BACKGROUND: Aniline serves as a pivotal precursor in many industries such as pesticides, pharmaceuticals, and chemicals. However, its ingestion can lead to severe health consequences, including the potential to induce cancer, respiratory tract irritation, and adverse effects on the nervous and digestive systems in the human body. The widespread use of aniline in industrial processes, coupled with inadequate wastewater management that allows for the direct release of aniline into the environment, leads to surface and groundwater contamination. Therefore, it becomes crucial to devise a reliable electrochemical sensor capable of detecting even trace amounts of aniline. RESULTS: This study presents a modified polyol synthesis method for producing silver nanorods (AgNRs, length: 861-1345 nm, diameter: 66-107 nm) with preferential growth along the (111) crystal plane. Immobilizing AgNRs on a glassy carbon (GC) electrode with Nafion as a binder decreases its charge transfer resistance from 3040 to 129 kΩ and increases its electroactive area from 0.034 to 0.101 cm2. AgNRs/GC electrode exhibited an aniline detection limit of 0.032 µM and sensitivity of 1.4841 µA.M-1cm-2 within a linear range of 0-10 µM using square wave voltammetry (SWV). The reaction rate constant of aniline sensing was determined to be 0.08697 s-1. Chlorobenzene, acephate, and chlorpyrifos could not interfere aniline detection, and 26 % decrease in peak response was observed after the 10th cycle of aniline sensing. The sensor demonstrated ∼100 % recovery for aniline, comparable to the performance of high-performance liquid chromatography when applied to real-world samples like tap and river water. SIGNIFICANCE: The electrochemical sensing of aniline is notably efficient in tap and river water within the acceptable limit, by utilizing one dimensional AgNRs functionalized GC electrode. Importantly, the presence of interferents does not compromise the sensitivity of the sensor. Therefore, one dimensional AgNRs synthesized via a modified polyol route emerge as a promising electrocatalyst for the in-situ detection and determination of aniline.

Ultrasound-Driven enhancement of Pt/C catalyst stability in oxygen reduction reaction.

Polymer electrolyte membrane fuel cells (PEMFCs) have reached the commercialization phase, representing a promising approach to curbing carbon emissions. However, greater durability of PEMFCs is of paramount importance to ensure their long-term viability and effectiveness, and catalyst development has become a focal point of research. Pt nanoparticles supported on carbon materials (Pt/C) are the primary catalysts used in PEMFCs. Accomplishing both a high dispersion of uniform metal particles on the carbon support and robust adhesion between the metal particles and the carbon support is imperative for superior stability, and will thereby, advance the practical applications of PEMFCs in sustainable energy solutions. Ultrasound-assisted polyol synthesis (UPS) has emerged as a suitable method for synthesizing catalysts with a well-defined metal-support structure, characterized by the high dispersion and uniformity of metal nanoparticles. In this study, we focused on the effect of ultrasound on the synthesis of Pt/C via UPS and the resulting enhanced stability of Pt/C catalysts. Therefore, we compared Pt/C synthesized using a conventional polyol synthesis (Pt/C_P) and Pt/C synthesized via UPS (Pt/C_U) under similar synthesis conditions. The two catalysts had a similar Pt content and the average particle size of the Pt nanoparticles was similar; however, the uniformity and dispersion of Pt nanoparticles in Pt/C_U were better than those of Pt/C_P. Moreover, ex/in-situ analyses performed in a high-temperature environment, in which nanoparticles tend to agglomerate, have revealed that Pt/C_U exhibited a notable improvement in the adhesion of Pt particles to the carbon support compared with that of Pt/C_P. The enhanced adhesion is crucial for maintaining the stability of the catalyst, ultimately contributing to a better durability in practical applications. Ultrasound was applied to the carbon support without the Pt precursor under the same UPS conditions used to synthesize Pt/C_U to identify the reason for the increased adhesion between the Pt particles and the carbon support in Pt/C_U, and we discovered that oxygen functional groups (C-O, C = O, and O-C = O) for anchoring site of Pt particles were generated in the carbon support. Pt/C_U displayed an increase in stability in an electrochemical accelerated stress test (AST) in an acidic electrolyte. The physical and chemical effects of ultrasound on the synthesis of Pt/C via UPS were identified, and we concluded that UPS is suitable for synthesizing carbon supported electrocatalysts with high stability.

Design of Pt-Sn-Zn Nanomaterials for Successful Methanol Electrooxidation Reaction.

This work highlights the potential for the synthesis of new PtSnZn catalysts with enhanced efficiency and durability for methanol oxidation reaction (MOR) in low-temperature fuel cells. In this research, PtZn and PtSnZn nanoparticles deposited on high surface area Vulcan XC-72R Carbon support were created by a microwave-assisted polyol method. The electrochemical performances of synthesized catalysts were analyzed by cyclic voltammetry and by the electrooxidation of adsorbed CO and the chronoamperometric method. The physicochemical properties of obtained catalysts were characterized by transmission electron microscopy (TEM), thermogravimetric (TGA) analysis, energy dispersive spectroscopy (EDS) and by X-ray diffraction (XRD). The obtained findings showed the successful synthesis of platinum-based catalysts. It was established that PtSnZn/C and PtZn/C catalysts have high electrocatalytic performance in methanol oxidation reactions. Catalysts stability tests were obtained by chronoamperometry. Stability tests also confirmed decreased poisoning and indicated improved stability and better tolerance to CO-like intermediate species. According to activity and stability measurements, the PtSnZn/C catalyst possesses the best electrochemical properties for the methanol oxidation reaction. The observed great electrocatalytic activity in the methanol oxidation reaction of synthesized catalysts can be attributed to the beneficial effects of microwave synthesis and the well-balanced addition of alloying metals in PtSnZn/C catalysts.

Self-Heating Flower-like Nanoconstructs with Limited Incorporation of Yttrium in Maghemite: Effect of Chemical Composition on Heating Efficiency, Cytotoxicity and Genotoxicity.

Partial cation substitution can significantly change the physical properties of parent compounds. By controlling the chemical composition and knowing the mutual relationship between composition and physical properties, it is possible to tailor the properties of materials to those that are superior for desired technological application. Using the polyol synthesis procedure, a series of yttrium-substituted iron oxide nanoconstructs, γ-Fe2-xYxO3 (YIONs), was prepared. It was found that Y3+ could substitute Fe3+ in the crystal structures of maghemite (γ-Fe2O3) up to a limited concentration of ~1.5% (γ-Fe1.969Y0.031O3). Analysis of TEM micrographs showed that crystallites or particles were aggregated in flower-like structures with diameters from 53.7 ± 6.2 nm to 97.3 ± 37.0 nm, depending on yttrium concentration. To be investigated for potential applications as magnetic hyperthermia agents, YIONs were tested twice: their heating efficiency was tested and their toxicity was investigated. The Specific Absorption Rate (SAR) values were in the range of 32.6 W/g to 513 W/g and significantly decreased with increased yttrium concentration in the samples. Intrinsic loss power (ILP) for γ-Fe2O3 and γ-Fe1.995Y0.005O3 were ~8-9 nH·m2/Kg, which pointed to their excellent heating efficiency. IC50 values of investigated samples against cancer (HeLa) and normal (MRC-5) cells decreased with increased yttrium concentration and were higher than ~300 µg/mL. The samples of γ-Fe2-xYxO3 did not show a genotoxic effect. The results of toxicity studies show that YIONs are suitable for further in vitro/in vivo studies toward to their potential medical applications, while results of heat generation point to their potential use in magnetic hyperthermia cancer treatment or use as self-heating systems for other technological applications such as catalysis.

Microporous 3D-Structured Hierarchically Entangled Graphene-Supported Pt3Co Alloy Catalyst for PEMFC Application with Process-Friendly Features.

To improve the oxygen reduction reaction (ORR) performance in a proton-exchange membrane fuel cell (PEMFC) cathode with respect to mass activity and durability, a suitable electrocatalyst design strategy is essentially needed. Here, we have prepared a sub-three nm-sized platinum (Pt)-cobalt (Co) alloy (Pt3Co)-supported N-doped microporous 3D graphene (Pt3Co/pNEGF) by using the polyol synthesis method. A microwave-assisted synthesis method was employed to prepare the catalyst based on the 3D porous carbon support with a large pore volume and dense micro-/mesoporous surfaces. The ORR performance of Pt3Co/pNEGF closely matches with the state-of-the-art commercial Pt/C catalyst in 0.1 M HClO4, with a small overpotential of 10 mV. The 3D microporous structure of the N-doped graphene significantly improves the mass transport of the reactant and thus the overall ORR performance. As a result of the lower loading of Pt in Pt3Co/pNEGF as compared to that in Pt/C, the alloy catalyst achieved 1.5 times higher mass activity than Pt/C. After 10,000 cycles, the difference in the electrochemically active surface area (ECSA) and half-wave potential (E1/2) of Pt3Co/pNEGF is found to be 5 m2 gPt-1 (ΔECSA) and 24 mV (ΔE1/2), whereas, for Pt/C, these values are 9 m2 gPt-1 and 32 mV, respectively. Finally, in a realistic perspective, single-cell testing of a membrane electrode assembly (MEA) was made by sandwiching the Pt3Co/pNEGF-coated gas diffusion layers as the cathode displayed a maximum power density of 800 mW cm-2 under H2-O2 feed conditions with a clear indication of helping the system in the mass-transfer region (i.e., the high current dragging condition). The nature of the I-V polarization shows a progressively lower slope in this region of the polarization plot compared to a similar system made from its Pt/C counterpart and a significantly improved performance throughout the polarization region in the case of the system made from the Pt3Co/NEGF catalyst (without the microwave treatment) counterpart. These results validate the better process friendliness of Pt3Co/pNEGF as a PEMFC electrode-specific catalyst owing to its unique texture with 3D architecture and well-defined porosity with better structural endurance.

Surface modification and antibacterial properties of superelastic Ti-Zr-based alloys for medical application.

To date, significant progress has been achieved in the development of biomedical superelastic Ti-based alloys with high mechanical properties. In view of the high probability of implant-associated infection, an urgent task is to impart bactericidal properties to the material. Herein, advanced superelastic Ti-18Zr-15Nb alloys were surface-etched in a piranha solution, and then Ag nanoparticles were deposited on their surface using a polyol process. This led to the formation of a porous surface layer with a thickness of approximately 100 nm and pore size of less than 20 nm, filled with metallic Ag nanoparticles with an average size of 14 nm. The surface-modified samples showed superior antibacterial activity against E.coli cells. The enhanced bactericidal efficiency is explained by the combination of a higher rate of Ag+ ions release and direct contact of E.coli cells with Ag nanoparticles.

The Polyol Process and the Synthesis of ζ Intermetallic Compound Ag5Sn0.9.

The present work concerns the intermetallic compound (IMC) existing in the Ag-Sn system and its potential use in electronics as attachment materials allowing the adhesion of the chip to the substrate forming the power module. First, we present the synthesis protocol in polyol medium of a compound with the chemical formula Ag5Sn0.9 belonging to the solid solution of composition located between 9 and 16 at.% Sn, known as solid solution ζ (or ζ-Ag4Sn). This phase corresponds to the peritectic invariant point at 724 °C. Differential thermal analysis and X-ray dispersive analysis confirm the single-phased (monocrystalline) nature of the Ag5Sn0.9 powder issued after synthesis. Scanning electron microscopy shows that Ag5Sn0.9 particles are spherical, and range in submicronic size of around 0.18 µm. X-ray diffraction analysis reveals that the ζ phase mostly exists under the two allotropic varieties (orthorhombic symmetry and hexagonal symmetry) with however a slight excess of the hexagonal variety (60% for the hexagonal variety and 40% for the orthorhombic variety). The lattice parameters resulting from this study for the two allotropic varieties are in good agreement with the Hume-Rothery rules.

Polyvinylpyrrolidone-Capped Silver Nanoparticles for Highly Sensitive and Selective Optical Fiber-Based Ammonium Sensor.

Herein, aqueous ammonium sensing characteristics of polyvinylpyrrolidone (PVP) capped silver nanoparticles (Ag-NPs) coated optical fiber-based sensors are presented. The PVP-capped Ag-NPs were prepared using cold and modified polyol synthesis methods. Aqueous ammonium detection was carried out by the surface plasmon resonance (SPR) effect observed in the Ag-NPs coated optical fiber system. The effect of cold and modified polyol synthesis methods on optical sensing performance was studied. The optical fiber cladding was modified with PVP-capped Ag-NPs according to the standard protocol for sensing investigation. The probe sensing response was analyzed for varying concentrations of ammonium ions on red, green, and blue LEDs. The sensor characteristics, viz., sensing response, repeatability, calibration curve, and ambient light effect, were investigated for PVP capped Ag-NPs coated optical fiber-based sensor. The PVP capped Ag-NPs synthesized via the polyol synthesis method showed a detection limit of 48.9 mM, 1.33 mV/M sensitivity, and an excellent linear relationship (R2 = 0.9992) between voltage and ammonium ion concentration in the range of 0.054-13.4 M concentration. On the other hand, PVP capped Ag-NPs synthesized using the cold synthesis method showed a detection limit of 159.4 mM, a sensitivity of 0.06 mV/M, and a poor linear relationship (R2 = 0.4588) between voltage and ammonium ion concentration in the range of 0.054-13.4 M concentration. The results indicate that the PVP-capped Ag-NPs synthesized using the polyol synthesis method exhibit enhanced ammonium ion sensing compared to the cold synthesis method.

Stable Iron Oxide Nanoflowers with Exceptional Magnetic Heating Efficiency: Simple and Fast Polyol Synthesis.

Magnetically induced hyperthermia has reached a milestone in medical nanoscience and in phase III clinical trials for cancer treatment. As it relies on the heat generated by magnetic nanoparticles (NPs) when exposed to an external alternating magnetic field, the heating ability of these NPs is of paramount importance, so is their synthesis. We present a simple and fast method to produce iron oxide nanostructures with excellent heating ability that are colloidally stable in water. A polyol process yielded biocompatible single core nanoparticles and nanoflowers. The effect of parameters such as the precursor concentration, polyol molecular weight as well as reaction time was studied, aiming to produce NPs with the highest possible heating rates. Polyacrylic acid facilitated the formation of excellent nanoheating agents iron oxide nanoflowers (IONFs) within 30 min. The progressive increase of the size of the NFs through applying a seeded growth approach resulted in outstanding enhancement of their heating efficiency with intrinsic loss parameter up to 8.49 nH m2 kgFe-1. The colloidal stability of the NFs was maintained when transferring to an aqueous solution via a simple ligand exchange protocol, replacing polyol ligands with biocompatible sodium tripolyphosphate to secure the IONPs long-term colloidal stabilization.

Synthesis of biocompatible silver nanoparticles by a modified polyol method for theranostic applications: Studies on red blood cells, internalization ability and antibacterial activity.

Recently, there has been ongoing research in the field of nanotechnology and nanomedicine aiming at developing multifunctional biomaterials using noble metals. The unique properties of silver (Ag) are known from ancient times and thus are being explored for their behavior on the nano scale. Silver shows high antimicrobial activity against different microorganisms, while modification of the surface of its nanostructures can be useful in active targeting regarding cancer treatment. During the synthetic procedure, in order to obtain a more uniform sample of silver nanoparticles (Ag NPs) with spherical morphology, a stabilizer is essential. The stabilizers used not only control the progression of the reaction, but also increases the biocompatibility of the NPs. Thus, we managed to synthesize spherical and rod-like Ag NPs via a polyol method and stabilize them with polyvinylpyrrolidone (PVP). The resulted Ag NPs were characterized morphologically with Transmission Electron Microscopy (TEM) and further confirmed by their structural characterization (FT-IR, UV-Vis, Dynamic Light Scattering (DLS) and Zeta Potential). For their biocompatibility profile, we studied their interaction with red blood cells (RBCs) through hemolysis assay and we monitored their structural alterations through SEM. The antimicrobial activity was tested with the agar diffusion disc assay for Gram negative and Gram positive microorganisms E. coli and S. aureus respectively. Nanoparticles' (NPs) internalization and localization studies in cancer cells were monitored with fluorescence microscopy in MCF-7 and U87-MG. According to our results it is worth it to investigate the potential of these nanomaterials since they can have a significant role in applications of theranostics in nanomedicine.

Facile polyol-triggered anatase-rutile heterophase TiO2-x nanoparticles for enhancing photocatalytic CO2 reduction.

Solar-driven CO2 photoreduction into fuels has great potential in addressing the environmental and energy crisis. Heterophase TiO2 has attracted increasing attention in photoenergy applications owing to its fascinating properties, but much more attention has been paid on photodegradation and photocatalytic water splitting than that of photocatalytic CO2 reduction. Herein, anatase-rutile heterophase TiO2 nanoparticles with oxygen vacancy (TiO2-x) were successfully synthesized by involving proper amounts of polyols (EG, DEG, TEG, etc.) into the reaction system. The heterophase TiO2-x nanoparticles could accelerate the electron-hole separation and exhibit superior photocatalytic activity for reducing CO2 into methane. This work offers an alternative approach to simply fabricate TiO2-x-based heterophase photocatalyst towards efficient CO2 photoreduction.

Enhanced Thermoelectric Performance of Novel Reaction Condition-Induced Bi2S3-Bi Nanocomposites.

This is the first report on the enhanced thermoelectric (TE) properties of novel reaction-temperature (TRe) and duration-induced Bi2S3-Bi nanocomposites synthesized using a facile one-step polyol method. They are well characterized as nanorod composites of orthorhombic Bi2S3 and rhombohedral Bi phases in which the latter coats the former forming Bi2S3-Bi core-shell-like structures along with independent Bi nanoparticles. A very significant observation is the systematic reduction in electrical resistivity ρ with a whopping 7 orders of magnitude (∼107) with just reaction temperature and duration increase, revealing a promising approach for the reduction of ρ of this highly resistive chalcogenide and hence resolving the earlier obstacles for its thermoelectric application potentials in the past few decades. Most astonishingly, a TE power factor at 300 K of the highest Bi content nanocomposite pellet, made at 27 °C using ∼900 MPa pressure, is 3 orders of magnitude greater than that of hot-pressed Bi2S3. Its highest ZT at 325 K of 0.006 is over twice of that of similarly prepared CuS or Ag2S-based nanocomposites. A significantly improved TE performance potential near 300 K is demonstrated for these toxic-free and rare-earth element-free TE nanocomposites, making the present synthesis method as a pioneering approach for developing enhanced thermoelectric properties of Bi2S3-based materials without extra sintering steps.