Karolina Wenelska

Electrochemical Characteristics of Discrete, Uniform, and Monodispersed Hollow Mesoporous Carbon Spheres in Double-Layered Supercapacitors

Core-shell-structured mesoporous silica spheres were prepared by using n-octadecyltrimethoxysilane (C18TMS) as the surfactant. Hollow mesoporous carbon spheres with controllable diameters were fabricated from core-shell-structured mesoporous silica sphere templates by chemical vapor deposition (CVD). By controlling the thickness of the silica shell, hollow carbon spheres (HCSs) with different diameters can be obtained. The use of ethylene as the carbon precursor in the CVD process produces the materials in a single step without the need to remove the surfactant. The mechanism of formation and the role played by the surfactant, C18TMS, are investigated. The materials have large potential in double-layer supercapacitors, and their electrochemical properties were determined. HCSs with thicker mesoporous shells possess a larger surface area, which in turn increases their electrochemical capacitance. The samples prepared at a lower temperature also exhibit increased capacitance as a result of the Brunauer-Emmett-Teller (BET) area and larger pore size.

Nanoconfinement induced formation of core/shell structured mesoporous carbon spheres coated with solid carbon shell.

A novel method for the fabrication of core/shell structured mesoporous carbon spheres with solid shell using a template method has been presented. The unique molecular nanostructures are characterized by XRD, TEM, TGA, and nitrogen adsorption/desorption measurement. The formation mechanism of the mesostructured carbon spheres with a carbon shell is proposed according to the experimental results. Nanoconfinement effect, occurring in the core/shell structured template, is believed to play a key role in mediating the formation of these hierarchical carbon mesostructures, with SnO2 as a template and C2H4 as a carbon source of a mesoporous carbon core. This synthesis method is simple, straightforward, and suitable for the preparation of various nanostructures that are unique scaffolds in catalytic and electrochemical applications.

Preparation, thermal conductivity, and thermal stability of flame retardant polyethylene with exfoliated MoS2/MxOy

In this work, exfoliated molybdenum disulfide (MoS2) modified by a metal oxide (MoS2/MxOy) was prepared by a hydrothermal method and characterized by atomic force microscopy (AFM), Raman spectroscopy and transmission electron microscopy (TEM). The samples were used in polymer composite (polyethylene) preparation by using an extruder blending method. Nanocomposites of polyethylene (PE) with MoS2/MxOy were obtained. The morphology, thermal properties, fire resistant properties and thermal conductivity of the PE nanocomposites were studied. We observed an excellent flame retardance for all PE composites. The peak of heat release rate (pHRR) was reduced by 40% for PE_MoS2 with respect to pristine PE. The lowest CO emission was observed for the PE/MoS2 composite containing 2% Fe3O4. All composites with exfoliated MoS2 exhibit greater potential for preparation of smart and functional nanomaterials with good thermal and fire resistant properties.

Facile synthesis N-doped hollow carbon spheres from spherical solid silica

Nitrogen-doped core/shell carbon nanospheres (NHCS are prepared and their capability as an anode material in lithium-ion batteries is investigated. The synthesis methodology is based on a fast template route. The resulting molecular nanostructures are characterized by X-ray diffraction, transmission electron microscopy, thermal analysis, and nitrogen adsorption/desorption measurement as well as by cyclic voltammetry and galvanostatic cycling. The core/shell structure provides a rapid lithium transport pathway and boasts a highly reversible capacity. For undoped HCS the BET specific surface area is 623m2/g which increases up to 1000m2/g upon N-doping. While there is no significant effect of N-doping on the electrochemical performance at small scan rates, the doped NHCS shows better specific capacities than the pristine HCS at elevated rates. For instance, the discharge capacities in the 40th cycle, obtained at 1000mA/g, amount to 170mAh/g and 138mAh/g for NHCS and HCS, respectively.

Time Dependent Influence of Rotating Magnetic Field on Bacterial Cellulose

The aim of the study was to assess the influence of rotating magnetic field (RMF) on the morphology, physicochemical properties, and the water holding capacity of bacterial cellulose (BC) synthetized by Gluconacetobacter xylinus. The cultures of G. xylinus were exposed to RMF of frequency that equals 50 Hz and magnetic induction 34 mT for 3, 5, and 7 days during cultivation at 28°C in the customized RMF exposure system. It was revealed that BC exposed for 3 days to RMF exhibited the highest water retention capacity as compared to the samples exposed for 5 and 7 days. The observation was confirmed for both the control and RMF exposed BC. It was proved that the BC exposed samples showed up to 26% higher water retention capacity as compared to the control samples. These samples also required the highest temperature to release the water molecules. Such findings agreed with the observation via SEM examination which revealed that the structure of BC synthesized for 7 days was more compacted than the sample exposed to RMF for 3 days. Furthermore, the analysis of 2D correlation of Fourier transform infrared spectra demonstrated the impact of RMF exposure on the dynamics of BC microfibers crystallinity formation.

From Hollow to Solid Carbon Spheres: Time-Dependent Facile Synthesis

Here, we report a facile route for obtaining carbon spheres with fully tunable shell thickness. Using a hard template in chemical vapor deposition (CVD), hollow carbon spheres, solid carbon spheres, and intermediate structures can be obtained with optimized process time. The resulting carbon spheres with particle diameters of ~400 nm, as well as a controllable shell thickness from 0 to 70 nm, had high Brunauer–Emmett–Teller (BET) specific surface area (up to 344.8 m2·g−1) and pore volume (up to 0.248 cm3·g−1). The sphere formation mechanism is also proposed. This simple and reproducible technique can deliver carbon materials for various applications, e.g., energy storage and conversion, adsorption, catalytic, biomedical, and environmental applications.