Marta Prześniak-Welenc

The influence of nanostructure size on V2O5 electrochemical properties as cathode materials for lithium ion batteries

In this paper, V2O5 nanostructures with a size depending on the annealing temperature are successfully synthesized by a sol–gel method. The crystal structure and morphology of the samples are characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), selected area electron diffraction (SEAD) and scanning electron microscopy (SEM), respectively. Electrochemical testing such as discharge–charge cycling (CD) and cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) are employed in evaluating their electrochemical properties as cathode materials for lithium ion batteries. One-dimensional nanostructures are successfully synthesized with the same structure, composition and similar shape. The results reveal that for one-dimensional nanostructures, next to the thickness which must be as small as possible, the length of the nanocrystals is crucial and should be above 2 μm. The longer nanostructures obtained at 650 °C deliver a discharge specific capacity of 281 mA h g−1 at a current rate of C/5 which is over 95.5% of the theoretical capacity for two Li+ ion intercalation (294 mA h g−1) within a voltage window of 2.0–4.0 V.

Fully scalable one-pot method for the production of phosphonic graphene derivatives

Graphene oxide was functionalized with simultaneous reduction to produce phosphonated reduced graphene oxide in a novel, fully scalable, one-pot method. The phosphonic derivative of graphene was obtained through the reaction of graphene oxide with phosphorus trichloride in water. The newly synthesized reduced graphene oxide derivative was fully characterized by using spectroscopic methods along with thermal analysis. The morphology of the samples was examined by electron microscopy. The electrical studies revealed that the functionalized graphene derivative behaves in a way similar to chemically or thermally reduced graphene oxide, with an activation energy of 0.014 eV.

Mechanism of reduced sintering temperature of Al2O3–ZrO2 nanocomposites obtained by microwave hydrothermal synthesis

A novel method to obtain Al₂O₃⁻ZrO₂ nanocomposites is presented. It consists of the co-precipitation step of boehmite (AlO(OH)) and ZrO₂, followed by microwave hydrothermal treatment at 270 °C and 60 MPa, and by calcination at 600 °C. Using this method, we obtained two nanocomposites: Al₂O₃⁻20 wt % ZrO₂ and Al₂O₃⁻40 wt % ZrO₂. Nanocomposites were characterized by Fourier transformed infrared spectroscopy, Raman spectroscopy, X-ray diffraction, and transmission electron microscopy. Sintering behavior and thermal expansion coefficients were investigated during dilatometric tests. The sintering temperatures of the nanocomposites were 1209 °C and 1231 °C, respectively-approximately 100 °C lower than reported for such composites. We attribute the decrease of the sintering temperature to the specific nanostructure obtained using microwave hydrothermal treatment instead of conventional calcination. Microwave hydrothermal treatment resulted in a fine distribution of intermixed highly crystalline nanoparticles of boehmite and zirconia. Such intermixing prevented particle growth, which is a factor reducing sintering temperature. Further, due to reduced grain growth, stability of the θ-Al₂O₃ phase was extended up to 1200 °C, which enhances the sintering process as well. For the Al₂O₃⁻20 wt % ZrO₂ composition, we observed stability of the zirconia tetragonal phase up to 1400 °C. We associate this stability with the mutual separation of zirconia nanoparticles in the alumina matrix.

Bis-phosphonated carbon nanotubes: One pot synthesis and their application as efficient adsorbent of mercury

ABSTRACT Effective, one-pot method of CNTs phosphonylation is presented. Cheap and readily available reagents are used, so the process can be easily transferred to large-scale production. The product was analyzed using spectroscopic methods (FTIR, UV-vis, XPS). Thermal properties of the bis-phosphonated nanotubes are reported for the first time. Newly obtained material was tested as an adsorbent for mercury removal from water. The sorption capacity for newly developed adsorbent was as high as 223.7 mg/g. The adsorption kinetics were studied within framework of Lagergren model, and Langmuir and Freundlich isotherms have been described. The effect of pH on the adsorption process has been evaluated and the optimal environmental conditions were determined to be neutral. The presence of bivalent ions Cd2+, Ni2+ in the solution did not affect adsorption efficiency of novel materials.