Towards stable and highly active IrO2 catalysts supported on doped tin oxides for the oxygen evolution reaction in acidic media

Iridium oxide is the preferred catalyst for water oxidation but it is required to maximize its utilization to deploy Proton Exchange Membrane Water Electrolyzers (PEMWEs) into the large-scale applications panorama. A promising pathway for dispersing this precious catalyst is on an electric conductive and stable support. However, there is a lack of understanding how the support-catalyst interactions affect the stability/activity of the electrocatalyst under anodic conditions. This work discloses a modified, easy-scalable, polyol synthesis protocol to produce a highly active and stable iridium-based catalyst, supported on metal-doped tin oxides. The loading of Ir was reduced 30 wt.% compared to the reference IrO2, and dispersed on Sb-SnO2 (IrOx/ATO), In-SnO2 (IrOx/ITO) and SnO2 supports. All synthesized electrocatalysts not only surpassed the OER-mass activity of a commercial catalyst (IrO2) – reference – but also reached higher electrochemical active surface areas and enhanced stability under the OER conditions. The highest performance was achieved with Ir NPs supported on ITO (176 A/gIr vs. 15.5 A/gIr for the reference catalyst @ 1.51 V vs. RHE) and both IrOx/ITO and IrOx/SnO2 catalysts demonstrated remarkable stability after cycling the electrode and performing long-term chronopotentiometry. ITO is, therefore, an auspicious support to serve Ir-based catalysts as it favors a good bargain between activity and stability, while drastically reducing the amount of noble metal.

Single step polyol synthesis of highly stable Pt/C/SiO2 catalysts for use in PEMFCs: effects of pH, temperature and W/EG ratio

Hybrid supports have been proposed as a new alternative to increase the stability of ORR catalysts used in PEMFCs for automotive applications since they are known to be stable under harsh conditions. In this work, Pt nanoparticles were deposited over C/SiO2, via single-step polyol method, to take advantage of the corrosion-resistance properties of silica nanoparticles. In fact, the synthesis parameters, namely, pH, temperature, and glycol concentration had a remarkable impact on the Pt size-distribution, crystallinity, and dispersion over the C/SiO2 supports. A maximum ORR activity and stability was obtained for Pt/C/SiO2 catalysts produced at 1:6 W/EG (v/v). The addition of SiO2 nanoparticles to the carbon structure showed their ability to effectively inhibit support corrosion and Pt nanoparticles detachment and/or growth, with the pH adjustments being critical for obtaining highly stable C/SiO2 supports. Pt/C/SiO2 synthetized under acidic conditions revealed the highest stability when subjected to accelerated stress tests (ASTs), losing only 30 % of the initial electrochemically active surface area (ECSA) of Pt after 4 000 cycles from 0.6 to 1 V (vs RHE), whereas the commercial Pt/C revealed > 50 % of ECSA loss.

Suberinic Acids as a Potential Feedstock for Polyol Synthesis: Separation and Characterization

Global sustainability challenges prompt the world to modify its strategies and shift from a fossil-fuel-based economy to a bio-resources-based one and to the production of renewable biomass chemicals. Depolymerized suberinic acids (SA) were considered as an alternative resource to develop bio-polyols that can be further used in polyurethane (PU) material production. Birch (Betula pendula) outer bark was used as a raw material to obtain the SA, extracted with ethanol, and depolymerized with potassium hydroxide ethanol solution. By acidifying the filtrate to pH 5.0, 3.0, and 1.0 and drying it at 50 °C and 130 °C, 12 different SA potential feedstocks were obtained and characterized using chemical (total phenolics content, solubility in DMSO, acid, hydroxyl, and saponification number) and instrumental analytical methods (GC-MS, SEC-RID, DSC, and FTIR). Several bio-polyols were synthesized from the SA sample acidified to pH 1 and dried at 130 °C. Acid number and hydroxyl number values, the apparent viscosity and moisture content were measured. It was concluded that SA have a high enough saponification and acid value to investigate the polyol synthesis route via the esterification reaction. Moreover, SA had OH groups in their structure, which can be exploited for PU material development. The majority of SA compounds had relatively low molecular weight with <1300 Da that are suited for bio-polyol synthesis applied for rigid PU foam development. The synthesized bio-polyols had high hydroxyl number values necessary for bio-polyols to be used for rigid PU foam production.

Emerging Application of Magnetic Nanoparticles for Diagnosis and Treatment of Cancer

Cancer is a disease that has resulted in millions of deaths worldwide. The current conventional therapies utilized for the treatment of cancer have detrimental side effects. This led scientific researchers to explore new therapeutic avenues with an improved benefit to risk profile. Researchers have found nanoparticles, particles between the 1 and 100 nm range, to be encouraging tools in the area of cancer. Magnetic nanoparticles are one of many available nanoparticles at present. Magnetic nanoparticles have increasingly been receiving a considerable amount of attention in recent years owing to their unique magnetic properties, among many others. Magnetic nanoparticles can be controlled by an external magnetic field, signifying their ability to be site specific. The most popular approaches for the synthesis of magnetic nanoparticles are co-precipitation, thermal decomposition, hydrothermal, and polyol synthesis. The functionalization of magnetic nanoparticles is essential as it significantly increases their biocompatibility. The most utilized functionalization agents are comprised of polymers. The synthesis and functionalization of magnetic nanoparticles will be further explored in this review. The biomedical applications of magnetic nanoparticles investigated in this review are drug delivery, magnetic hyperthermia, and diagnosis. The diagnosis aspect focuses on the utilization of magnetic nanoparticles as contrast agents in magnetic resonance imaging. Clinical trials and toxicology studies relating to the application of magnetic nanoparticles for the diagnosis and treatment of cancer will also be discussed in this review.

Green Synthesis and Characterization of Nickel Tungsten Bimetallic Oxide Nanoparticles via Microwave Irradiation Technique

Nickel tungsten bimetallic oxide nanoparticles were synthesised in ethylene glycol using microwave irradiation technique. Nickel and tungsten oxide nanoparticles were synthesised separately using microwave assisted polyol synthesis method. The respective systems are combined together in ratio 1:1 molar and are subjected to microwave irradiation to get Ni-W bimetallic oxide. The structure and composition of nanoparticles were characterised by UV-Visible Spectroscopy, FT-IR Spectroscopy, X-Ray Diffraction (XRD), Energy Dispersion Spectroscopy (EDS), Transmission Electron Microscopy (TEM), Photoluminescence Spectroscopy (PL) and Magnetic Susceptibility measurements. From the XRD and FTIR measurements, nanocrystalline Wolframite structure of Ni-W bimetallic oxide nanoparticles was established. The emperical formula of the nanoparticle is found as Ni0.4W0.6O2.6. The composition may be varied by changing the ratio of Ni and W. A maximum absorbance of 385nm was obtained in UV-Visible spectrum and three emission peaks were obtained in the visible region of photoluminescent studies. Further studies can be done on the catalytic and electrochromic properties of the substance.

A review: Development of magnetic nano vectors for biomedical applications

The study of magnetic nanoparticles (MNPs) is an emergent field of science in this era due to their widespread utilization in the various fields of biomedical science. Developing concerns of magnetic nanoparticles in the researcher’s field led to design a huge number of MNPs including individual or binary metallic particles, oxides, (ferrites), biopolymer coated composites, metallic carbides and graphene mediated nanoparticles. Numerous synthetic routes are defined in literature to attain the desired size, crystal structure, morphology and magnetic properties. To build up biocompatibility, MNPs subjected to surface treatments by coating with some suitable organic or inorganic biomaterials which not only improves its physical characteristics but also elevate its chemical stability. These biomaterials coat either isolatly or in a combined state to enhance the colloidal stability, magnetic properties as well as prevent it cytotoxicity and surface corrosion in the biological media. These properties are essential for the particles and empowering their effectiveness in various biomedical science i.e., drug delivery Magnetic resonance imaging (MRI), hyperthermia, biosensors and gene therapy etc. Current review recapitulates the verdicts of previous research on the subject of magnetic nanoparticles. It will also explain the recent advancements of biomaterials that execute a dynamic role in various medical treatments. Our main focus is to report the particle types, design and properties as well as discussing various synthetic routes including sol gel, co-precipitation, microemulsion, green synthesis, sonochemical method and polyol synthesis etc. These methods produced particles of excellent yield with unique magnetic properties, coercivity and crystallinity and enhanced biocompatibility as compared to traditional methods used to develop MNPs.

Anion Dependent Particle Size Control of Platinum Nanoparticles Synthesized in Ethylene Glycol

The polyol synthesis is a well-established method to form so-called “surfactant-free” nanoparticles (NPs). In the present study, the NP size resulting from the thermal reduction of the precursors H2PtCl6, H2Pt(OH)6, or Pt(acac)2 in presence of the bases NaOH or Na(acac) at different concentrations is studied. It is shown that the size control depends more strongly on the nature of the precursor (metal salt) than on the anion present in the base. The latter is surprising as the concentration of the base anion is often an important factor to achieve a size control. The reduction of H2PtCl6 or H2Pt(OH)6 in presence of NaOH and Na(acac) confirm the observation that the NP size is determined by the OH−/Pt molar ratio and expands it to the base anion/Pt molar ratio. In contrast, the reduction of Pt(acac)2 in presence of the bases NaOH (previous reports) or Na(acac) (shown in the present work) leads to larger NPs of ca. 3 nm, independent of the concentration of the base anions. Hence, the anion effect observed here seems to originate predominantly from the nature of the precursor (precursor anion dependence) and only for certain precursors as H2PtCl6 or H2Pt(OH)6 the size control depends on the base anion/Pt molar ratio.