Marta Gajewska

Hierarchically structured ZSM-5 obtained by optimized mesotemplate-free method as active catalyst for methanol to DME conversion

In the presented studies, a new method for the synthesis of hierarchical porous materials with ZSM-5 zeolite properties was applied. The proposed method is based on the acidification of the zeolite seeds slurry using HCl solution, followed by hydrothermal treatment, enabling the aggregation of zeolite nanoseeds with the formation of the interparticle mesoporous structure. The influence of the duration of zeolite parent mixture aging before and after acidification on the resulting properties of the samples was investigated. The physicochemical properties of the obtained micro-mesoporous samples were analyzed using techniques such as N2-sorption measurements, X-ray diffraction, TG analysis, NH3-TPD and electron microscopy. In the second part of the studies, the influence of the modified zeolite sample parameters (such as porosity, acidity and crystallinity) on their catalytic activity for dimethyl ether (DME) synthesis from methanol was studied. DME is considered as a future clean alternative to diesel fuel and the development of methods for its synthesis is currently of high scientific interest. It was shown that modification of the porous structure and acidity of the zeolitic samples strongly influences their catalytic activity, selectivity and stability for the DME synthesis process. The micro-mesoporous samples, despite their significantly lower acidity, exhibited high catalytic activity (similar to conventional ZSM-5 zeolite) and enhanced selectivity towards DME, as well as higher stability in a long term catalytic test (higher resistance to the formation of coke deposits) in comparison to standard MFI-type zeolites.

Formation and stability of manganese-doped ZnS quantum dot monolayers determined by QCM-D and streaming potential measurements

Manganese-doped ZnS quantum dots (QDs) stabilized by cysteamine hydrochloride were successfully synthesized. Their thorough physicochemical characteristics were acquired using UV-Vis absorption and photoluminescence spectroscopy, X-ray diffraction, dynamic light scattering (DLS), transmission electron microscopy (HR-TEM), energy dispersive spectroscopy (EDS) and Fourier transform infrared (FT-IR) spectroscopy. The average particle size, derived from HR-TEM, was 3.1nm, which agrees with the hydrodynamic diameter acquired by DLS, that was equal to 3-4nm, depending on ionic strength. The quantum dots also exhibited a large positive zeta potential varying between 75 and 36mV for ionic strength of 10-4 and 10-2M, respectively (at pH 6.2) and an intense luminescent emission at 590nm. The quantum yield was equal to 31% and the optical band gap energy was equal to 4.26eV. The kinetics of QD monolayer formation on silica substrates (silica sensors and oxidized silicon wafers) under convection-controlled transport was quantitatively evaluated by the quartz crystal microbalance (QCM) and the streaming potential measurements. A high stability of the monolayer for ionic strength 10-4 and 10-2M was confirmed in these measurements. The experimental data were adequately reflected by the extended random sequential adsorption model (eRSA). Additionally, thorough electrokinetic characteristics of the QD monolayers and their stability for various ionic strengths and pH were acquired by streaming potential measurements carried out under in situ conditions. These results were quantitatively interpreted in terms of the three-dimensional (3D) electrokinetic model that furnished bulk zeta potential of particles for high ionic strengths that is impractical by other experimental techniques. It is concluded that these results can be used for designing of biosensors of controlled monolayer structure capable to bind various ligands via covalent as well as electrostatic interactions.

Electrochemically deposited nanocrystalline InSb thin films and their electrical properties

We present an electrochemical route to prepare nanocrystalline InSb thin films that can be transferred to an industrial scale. The morphology, composition, and crystallinity of the prepared uniform and compact thin films with a surface area of around 1 cm2 were investigated. The essential electrical characteristics such as conductivity, Seebeck coefficient, the type, concentration and mobility of charge carriers have been examined and compared with InSb nanowires obtained in the same system for electrochemical deposition (fixed pulse sequence, temperature, electrolyte composition, and system geometry). Moreover, obtained thin films show much higher band gap energy (0.53 eV) compared to the bulk material (0.17 eV) and InSb nanowires (0.195 eV).

Organotitania-based nanostructures as a suitable platform for the implementation of binary, ternary and fuzzy logic systems

Titanium dioxide nanocomposites were synthesized in hierarchical architectures through the use of a 1,4-dihydroxyanthraquinone photosensitizer. In the first step, the dye was either incorporated into the TiO2 core or adsorbed on its surface. In the subsequent phase, both structures were covered with an outer layer of titanium dioxide. The structure, morphology, aggregation, spectroscopic, and electrochemical properties of the synthesized TiO2 -based materials are presented with emphasis on the photosensitization and the photocurrent switching phenomena, which are also discussed within the context of the optical logic gates implementation and fuzzy logic systems operation. We present three different interpretations of the photocurrent action spectra yielding binary, ternary, or fuzzy logic circuits.

Sol–gel synthesis, structural and electrical properties of Li2CoSiO4 cathode material

Polyanionic cathode materials for lithium-ion batteries start to be considered as potential alternative for layered oxide materials. Among them, Li2CoSiO4, characterized by outstanding capacity and working voltage, seems to be an interesting substitute for LiFePO4 and related systems. In this work, structural and electrical investigations of Li2CoSiO4 obtained by sol–gel synthesis were presented. Thermal decomposition of gel precursor was studied using EGA (FTIR)-TGA method. Chemical composition of the obtained material was confirmed using X-ray diffraction and energy-dispersive X-ray spectroscopy. The morphology of β-Li2CoSiO4 was studied using transmission electron microscopy. High temperature electrical conductivity of Li2CoSiO4 was measured for the first time. Activation energies of the electrical conductivity of two Li2CoSiO4 polymorphs (β and γ) were determined. The room temperature electrical conductivity of those materials was estimated as well.

Multifunctional carbon aerogels derived by sol–gel process of natural polysaccharides of different botanical origin

In this manuscript, we describe the results of our recent studies on carbon aerogels derived from natural starches. A facile method for the fabrication of carbon aerogels is presented. Moreover, the complete analysis of the carbonization process of different starch aerogels (potato, maize, and rice) was performed using thermogravimetric studies combined with a detailed analysis of evolved decomposition products. The prepared carbon aerogels were studied in terms of their morphology and electrical properties to relate the origin of starch precursor with final properties of carbon materials. The obtained results confirmed the differences in carbon aerogels’ morphology, especially in materials’ specific surface areas, depending on the botanical origin of precursors. The electrical conductivity measurements suggest that carbon aerogels with the best electrical properties can be obtained from potato starch.

Preliminary study of structural changes in Li2MnSiO4 cathode material during electrochemical reaction

In this paper, we present exsitu observations of a structure of particular Li2MnSiO4 grains at different states of charge (SOC). The goal of these studies is structural analysis of Li2MnSiO4 cathode material for Li-ion batteries at different stages of electrochemical reaction using transmission electron microscopy. Performed analysis suggests that amorphization process of Li2MnSiO4 is not directly connected with lithium ions deintercalation but with additional electrochemical reactions running in the working cell.

Tuning of the Seebeck Coefficient and the Electrical and Thermal Conductivity of Hybrid Materials Based on Polypyrrole and Bismuth Nanowires

The growing demand for clean energy catalyzes the development of new devices capable of generating electricity from renewable energy resources. One of the possible approaches focuses on the use of thermoelectric materials (TE), which may utilize waste heat, water, and solar thermal energy to generate electrical power. An improvement of the performance of such devices may be achieved through the development of composites made of an organic matrix filled with nanostructured thermoelectric materials working in a synergetic way. The first step towards such designs requires a better understanding of the fundamental interactions between available materials. In this paper, this matter is investigated and the questions regarding the change of electrical and thermal properties of nanocomposites based on low-conductive polypyrrole enriched with bismuth nanowires of well-defined geometry and morphology is answered. It is clearly demonstrated that the electrical conductivity and the Seebeck coefficient may be tuned either simultaneously or separately within particular Bi NWs content ranges, and that both parameters may be increased at the same time.

Charge transfer tuning in TiO2 hybrid nanostructures with acceptor–acceptor systems

An interesting interplay between two different modifiers and the surface of titanium dioxide leads to a significant change in the photoelectrochemical properties of the designed hybrid materials. The semiconductor is photosensitized by one of the counterparts and exhibits the photoelectrochemical photocurrent switching effect due to interactions with graphene oxide – the second modifier mediates charge transfer processes in the system, allowing us to design the materials response at the molecular level. Based on the selection of molecular counterpart we may affect the behaviour of hybrids upon light irradiation in a different manner, which may be useful for the applications in photovoltaics, optoelectronics and photocatalysis. Here we focus particularly on the nanocomposites made of titanium dioxide with graphene oxide combined with either 2,3,5,6-tetrachlorobenzoquinone or 2,3-dichloro-5,6-dihydroxybenzoquinone – for these two materials we observed a major change in the charge transfer processes occurring in the system.

Study on Stability and Electrochemical Properties of Nano-LiMn1.9Ni0.1O3.99S0.01-Based Li-Ion Batteries with Liquid Electrolyte Containing LiPF6

Herein, we report on the stability and electrochemical properties of nanosized Ni and S doped lithium manganese oxide spinel LiMn1.9Ni0.1O3.99S0.01, LMN1OS in relation to the most commonly used electrolyte solution containing LiPF6 salt. The influence of electrochemical reaction in the presence of selected electrolyte on the LMN1OS electrode chemistry was examined. The changes in the structure, surface morphology, and composition of the LMN1OS cathode after 30 cycles of galvanostatic charging/discharging were determined. In addition, thermal stability and reactivity of the LMN1OS material towards the electrolyte system were verified. Performed studies revealed that no degradative effects, resulting from the interaction between the spinel electrode and liquid electrolyte, occur during electrochemical cycling. The LMN1OS electrode versus LiPF6-based electrolyte has been indicated as an efficient and electrochemically stable system, exhibiting high capacity, good rate capability, and excellent coulombic efficiency. The improved stability and electrochemical performance of the LMN1OS cathode material originate from the synergetic substitution of LiMn2O4 spinel with Ni and S.