Electrochemical performance of reduced graphene oxide in Spiro‐(1, 1')‐bipyrrolidinium tetrafluoroborate electrolyte

This paper investigates the relationship between structure and electrochemical performance of reduced graphene oxide (RGO) prepared via heat treatment and chemical reduction method. Structure and morphology of RGO was characterized by means of Fourier transform infrared spectroscopy, scanning electron microscopy, X‐ray diffraction and Brunauer–Emmett–Teller. Electrochemical performance of RGO electrode supercapacitor was investigated in the organic electrolyte by cyclic voltammetry, galvanostatic charge–discharge and electrochemical impedance. The results show heat treatment RGO has high graphitization degree, less surface oxygen‐containing groups, good charge–discharge efficiency and stable life cycle. The chemical reduced RGO has single‐graphene structure, high specific surface area, high specific capacitance and low internal resistance. The ascorbic acid reduction RGO exhibits good comprehensive electrochemical performance: Its specific capacitance was 220.7 F g^?1, internal resistance was 3.0 Ω and charge–discharge efficiency was 97.0% after 2000 cycles of charging/discharging tests. Copyright © 2016 John Wiley & Sons, Ltd.     

Physical and mechanical properties of a reversible adhesive for automotive applications

In this work, a hot-melt adhesive used by automotive industries for bonding plastic components has been modified with three different percentages of nanofiller (iron oxide) in order to make the adhesive electromagnetically sensitive and to perform adhesive joint separations. Fe₃O₄ particles with a weight concentration of 3%, 5% and 10% were embedded in the adhesive matrix. Single Lap Joint (SLJ) tests showed that a slight increase of the maximum load and a more ductile behaviour are obtained. The sensitivity of these modified adhesive performance to the induction heating process was studied with respect to some relevant parameters: the current (or power), the frequency of the electromagnetic induction field and the shape of the coil. Furthermore, the diameter of the hollow copper coil was modified in order to understand whether the coil temperature has an effect on the separation time. The separation time, that is an index of the time needed to reach the melt of the adhesive and the consequent SLJ separation, together with the temperature profile of the adhesives have been used to evaluate the sensitivity of these adhesives to the process parameters. The analysis on the temperature and separation time showed that the most influencing parameter is the frequency of the electromagnetic induction field. As expected, also the shape of the coil influences the separation time, in particular, the adhesive joint separated with the pancake coil showed lower values of the separation time compared to the solenoidal coils. Scanning Electron Microscope (SEM) showed that iron oxide particles tend to form small agglomerate that resulted well dispersed in the adhesive matrix. Thermogravimetric analysis (TGA) was used to verify that the separation procedure do not degrades these modified adhesives.     

Synthesis and characterization of poly(ethylene tetrasulfide)/graphene oxide nanocomposites by in situ polymerization method

Poly(ethylene tetrasulfide) (PSP) is synthesized via interfacial polycondensation of 1,2 dichloroethane and sodium tetrasulfide, in the presence of graphene oxide (GO). This process resulted in homogeneously dispersed PSP/GO nanocomposites. Nanocomposites of 0.3 and 0.5?wt% of GO are synthesized and their morphology, chemical characteristics behavior are studied employing field emission scanning electron microscopy, Fourier transform infrared spectroscopy and X-ray diffraction techniques. Thermal characterization of composites is performed by differential scanning calorimetry and thermogravimetry analysis. Results indicate that the addition of only small amounts (0.5?wt%) of well-dispersed GO can increase the melting point more than 16°C resulting in better thermal properties for the composite. The solubility of nanocomposite is also studied and results show that the solubility depends on solvent concentration in addition to reinforcement (GO) deals.     

Functionalised hybrid Poly(ether ether ketone) containing MnO2: Investigation of operative conditions for hydrogen sorption

A composite material synthesis, based on Manganese oxide (MnO₂) anchored to a functionalized polymeric matrix, was optimized. For this investigation two different MnO₂ loadings were selected (16 and 80 wt%) in order to understand the relation between the oxide content, chemical-physical characteristic and the H₂ sorption properties. SEM, XRD were carried out and the obtained results were correlated to the H₂ sorption/desorption characterizations by Sievert apparatus.From these measurements at 50 °C/40 bar, the sample containing 16 wt% of metal oxide content has revealed a low H₂ sorption capability (0,04 wt%), while the 80 wt% sample showed a very high H₂ storage value (3 wt%). A short sorption/desorption cycles were carried out and a good reversibility was revealed.A modelling study, ab-initio Density Functional Theory (DFT) calculations, was carried out. The starting unit cell was MnO₂ while Mn₂₄O₄₈ was considered as a supercell. The number of H atoms was gradually increased and desorption energy was calculated. Desorption energy starts from 366 kJ/mol and decreases by increasing the number of H atoms. For the experimental H₂ sorption value (1,7 wt%) it was calculated the number of the respective H atoms (36) and the corresponding desorption energy (150 kJ/mol).     

Identification of Toxin Inhibitors Using a Magnetic Nanosensor‐Based Assay

A magnetic nanosensor‐based method is described to screen a library of drugs for potential binding to toxins. Screening is performed by measuring changes in the magnetic relaxation signal of the nanosensors (bMR nanosensors) in aqueous suspension upon addition of the toxin. The Anthrax lethal factor (ALF) is selected as a model toxin to test the ability of our bMR nanosensor‐based screening method to identify potential inhibitors of the toxin. Out of 30 molecules screened, sulindac, naproxen and fusaric acid are found to bind LF, with dissociation constants in the low micromolar range. Further biological analysis of the free molecules in solution indicate that sulindac and its metabolic products inhibited LF cytotoxicity to macrophages with IC₅₀ values in the micromolar range. Meanwhile, fusaric acid is found to be less effective at inhibiting LF cytotoxicity, while naproxen does not inhibit LF toxicity. Most importantly, when the sulindac and fusaric acid‐bMR nanosensors themselves are tested as LF inhibitors, as opposed to the corresponding free molecules, they are stronger inhibitors of LF with IC₅₀ values in the nanomolar range. Taken together, these studies show that a bMR nanosensors‐based assay can be used to screen known drugs and other small molecules for inhibitor of toxins. The method can be easily modified to screen for inhibitors of other molecular interactions and not only the selected free molecule can be study as potential inhibitors but also the bMR nanosensors themselves achieving greater inhibitory potential.     

Influence of doctor blade gap on the properties of tape cast NiO/YSZ anode supports for solid oxide fuel cells

In this study, various tape cast NiO/YSZ anode support layers with similar geometric properties are fabricated by varying the doctor blade from 100?µm to 200?µm with an increment of 25?µm. The mechanical properties of the anode support layers are investigated by three point bending tests of 30 samples for each doctor blade gap. The reliability curves of the flexural strength data are also obtained via two-parameter Weibull distribution method. The effects of the doctor blade gap on the microstructure and the electrochemical performance of the anode support layers are determined via SEM investigations and single cell performance-impedance tests, respectively. The apparent porosities of the samples are also measured by Archimedes’ principle. The results indicate that the doctor blade gap or the resultant tape thickness influences the microstructure of tape cast NiO/YSZ anode supports significantly, yielding different mechanical and electrochemical characteristics. At a reliability level of 70%, the highest flexural strength of 110.20?MPa is obtained from the anode support layer with a doctor blade gap of 175?µm and the 16?cm² active area cell with this anode support layer also exhibits the highest peak performance of 0.483?W/cm² at an operating temperature of 800?°C. Thus, a doctor blade gap of 175?µm is found to have such a microstructure that provides not only better mechanical strength but also higher electrochemical performance.     

Leveraging in-situ formation of Ni–Fe nanoparticles to promote the catalytic performance of Ruddlesden-Popper based electrode for symmetrical solid oxide fuel cells

Ruddlesden?Popper layered oxide, La_0.25Sr_2.75FeNiO_7-δ (LSFN) is evaluated as a potential electrode material for symmetrical solid oxide fuel cells. The in-situ formation of Ni–Fe alloy nanoparticles on the LSFN surface in reducing atmosphere can be believed to enhance the activity towards hydrogen oxidation reaction. LSFN exhibit maximum conductivity of 221.2 S/cm and 0.206 S/cm in air and hydrogen environment. Furthermore, LSFN is mixed with GDC powder to form a composite electrode for symmetric solid oxide fuel cells (SSOFC). Results show that with the combination of GDC, the maximum power density of YSZ-based SSOFC enlarges from 232.3 mW cm^?2 to 348.5 mW cm^?2, and related polarization resistance reduces from 0.359 Ω cm² to 0.108 Ω cm². The improved performance is attributed to the enlarged triple-phase boundary with the mixing of GDC. In addition, YSZ-based SSOFC with the LSFN-GDC composite electrode shows a stable performance in intermediate-temperature SSOFCs within 200 h, which indicates that LSFN-GDC composite material is a prospective symmetrical electrode for SSOFC.     

Rational design and synthesis of upconversion luminescence-based optomagnetic multifunctional nanorattles for drug delivery

Optomagnetic multifunctional composite based on upconversion luminescence nanomaterial is regarded as a promising strategy for bioimaging,disease diagnosis and targeted delivery of drugs.To explore a mesoporous nanostructure with excellent water dispersibility and high drug-loading capacity,a novel nanorattle-structured Fe3O4@SiO2@NaYF4∶Yb,Er magnetic upconversion nanorattle (MUCNR) was suc-cessfully designed by using Fe3O4 as core and NaYF4∶Yb,Er nanocrystals as shell.The microstructures and crystal phase of the as-prepared MUCNRs were evaluated by transmission electron microscopy,X-ray powder diffraction and N2 adsorption/desorption isotherms.The Kirkendall effect was adapted to explain the formation mechanism of the MUCNRs.The loading content and encapsulation efficiency of doxorubicin hydrochloride (DOX) could reach as high as 18.2％ and 60.7％,respectively.Moreover,the DOX loading MUCNR (DOX-MUCNR) system showed excellent sustained drug release and strong pH-dependent performance,which was conducive to drug release at the slightly acidic microenvironment of tumor.Microcalorimetry was used to quantify the interactions between the carrier structure and drug release rate directly.The heat release rates in the heat-flow diagrams are basically consistent with the DOX release rate,thereby showing that microcalorimetry assay not only provides a unique thermody-namic explanation for the structure-activity relationship of Fe3O4@SiO2@NaYF4∶Yb,Er MUCNRs but also provides powerful guidance to avoid the blind selection or design of drug carriers.Therefore,our work firmly provided a comprehensive perspective for using Fe3O4@SiO2@NaYF4∶Yb,Er MUCNRs as a remark-able magnetic targeted drug carrier.     

A comparative theoretical study of CO oxidation reaction by O2 molecule over Al- or Si-decorated graphene oxide

Using density functional theory calculations, the probable CO oxidation reaction mechanisms are investigated over Al- or Si-decorated graphene oxide (GO). The equilibrium geometry and electronic structure of these metal decorated-GOs along with the O₂/CO adsorption configurations are studied in detail. The relatively large adsorption energies reveal that both Al and Si atoms can disperse on GO quite stably without clustering problem. Hence, both Al- and Si-decorated GOs are stable enough to be utilized in catalytic oxidation of CO by molecular O₂. The two possible reaction pathways proposed for the oxidation of CO with O₂ molecule are as follows: O₂ + CO → CO₂ + O_ads and CO + O_ads → CO₂. The estimated energy barriers of the first oxidation reaction on Si-decorated GOs, following the Eley–Rideal (ER) reaction, are lower than that on Al-decorated ones. This is most likely due to the larger atomic charge on the Si atom than the Al one, which tends to stabilize the corresponding transition state structure. The results of this study can be useful for better understanding the chemical properties of Al- and Si-decorated GOs, and are valuable for the development of an automobile catalytic converter in order to remove the toxic CO molecule.