O. Volobujeva

Nanoporous carbon-based electrodes for high strain ionomeric bending actuators

Ionic polymer metal composites (IPMCs) are electroactive material devices that bend at low applied voltage (1–4 V). Inversely, a voltage is generated when the materials are deformed, which makes them useful both as sensors and actuators. In this paper, we propose two new highly porous carbon materials as electrodes for IPMC actuators, generating a high specific area, and compare their electromechanical performance with recently reported RuO2 electrodes and conventional IPMCs. Using a direct assembly process (DAP), we synthesize ionic liquid (Emi-Tf) actuators with either carbide-derived carbon (CDC) or coconut-shell-based activated carbon-based electrodes. The carbon electrodes were applied onto ionic liquid-swollen Nafion membranes using a direct assembly process. The study demonstrates that actuators based on carbon electrodes derived from TiC have the greatest peak-to-peak strain output, reaching up to 20.4 me (equivalent to>2%) at a 2 V actuation signal, exceeding that of the RuO2 electrodes by more than 100%. The electrodes synthesized from TiC-derived carbon also exhibit significantly higher maximum strain rate. The differences between the materials are discussed in terms of molecular interactions and mechanisms upon actuation in the different electrodes.

ZnO Nanorods via Spray Deposition of Solutions Containing Zinc Chloride and Thiocarbamide

In this work we present the results on formation of ZnO nanorods prepared by spray of aqueous solutions containing ZnCl2and thiocarbamide (tu) at different molar ratios. It has been observed that addition of thiocarbamide into the spray solution has great impact on the size, shape and phase composition of the ZnO crystals. Obtained layers were characterized by scanning electron microscopy (SEM) equipped with energy selected backscattered electron detection system (ESB), X-ray diffraction (XRD) and photoluminescence spectroscopy (PL). Small addition of thiocarbamide into ZnCl2solution (ZnCl2:tu = 1:0.25) supports development of significantly thinner ZnO nanorods with higher aspect ratio compared to those obtained from ZnCl2solution. Diameter of ZnO rods decreases from 270 to 100 nm and aspect ratio increases from ∼2.5 to 12 spraying ZnCl2and ZnCl2:tu solutions, respectively. According to XRD, well crystallized (002) orientated pure wurtzite ZnO crystals have been formed. However, tiny ‘spot’—like formations of ZnS were detected on the side planes of hexagonal rods prepared from the thiocarbamide containing solutions. Being adsorbed on the side facets of the crystals ZnS inhibits width growth and promotes longitudinalc-axis growth.

Gel-forming structures and stages of red algal galactans of different sulfation levels

Sol-gel transition processes of algal galactans were studied using cryofixation method in combination with freeze-drying and scanning electron microscopy (SEM) techniques. The structures formed in successive stages of gelling process upon cooling were rapidly frozen at defined temperature points and viewed by SEM. It was established that in the case of both types of gelling galactans investigated, a fine honeycomb-like network exists for a wide range of solution temperatures. The formation and structure of this network depends on the structural type, gelling stage, and concentration of the galactan in solution. The honeycomb suprastructures exist also in carrageenan and agarose sols (at temperatures considerably exceeding the gelling temperatures). An additional helical network formed showed different behaviour in the case of carrageenan and agar-type polysaccharides. In the gel-formation process, tightening of the network takes place in both types of galactan gels; the honeycomb structures persist in carrageenan (furcellaran) but not in agarose gels.

Polydopamine as an adhesive coating for open tubular capillary electrochromatography

Polydopamine (PolyD) coating was used as an adhesive layer in the preparation of biological stationary phases for open tubular capillary electrochromatography (OT‐CEC). The influence of coating solution freshness, coating time, temperature and dopamine hydrochloride concentration on the PolyD layer formation was studied. The performance of the polyD coating was monitored by measuring the electro‐osmotic flow in coated capillaries. Following polyD coating of the capillary, secondary layer material (e.g. cell membrane solutions, phospholipid mixtures or mitochondria) was inserted into the capillary for at least 1 h. The performance of these double‐coated capillaries (a polyD layer+a biological material layer) was compared with capillaries containing the respective biological material directly attached to the capillary wall. The study reveals that the presence of polyD layer in fused silica capillaries improves the performance of lipid and membrane fragment coatings in capillaries. At the same time, the thickness of the polyD layer does not have marked impact on the secondary coatings. Analysis with test analytes demonstrated that double‐coated capillaries can be applied to study membrane–drug interactions.

Annealing effect for SnS thin films prepared by high-vacuum evaporation

Thin films of SnS are deposited onto molybdenum-coated soda lime glass substrates using the high-vacuum evaporation technique at a substrate temperature of 300 °C. The as-deposited SnS layers are then annealed in three different media: (1) H2S, (2) argon, and (3) vacuum, for different periods and temperatures to study the changes in the microstructural properties of the layers and to prepare single-phase SnS photoabsorber films. It is found that annealing the layers in H2S at 400 °C changes the stoichiometry of the as-deposited SnS films and leads to the formation of a dominant SnS2 phase. Annealing in an argon atmosphere for 1 h, however, causes no deviations in the composition of the SnS films, though the surface morphology of the annealed SnS layers changes significantly as a result of a 2 h annealing process. The crystalline structure, surface morphology, and photosensitivity of the as-deposited SnS films improves significantly as the result of annealing in vacuum, and the vacuum-annealed films are fo...

Chemical etching of Cu 2 ZnSn(S,Se) 4 monograin powder

Cu2ZnSn(S,Se)4 (CZTS,Se) monograin powders were synthesized in the liquid phase of molten KI as flux material from binary compounds in evacuated quartz ampoules. Monograin powders were subjected to various chemical treatments with several etchants (HCl, KCN, NH4OH and Br in methanol (Br2-MeOH)) to modify the crystal surface. Polarographic analyses of leaching solutions showed that Sn and Se were removed preferably by HCl etching. Treatment with 10% KCN dissolved mainly Cu, Sn and chalcogen, and ammonia solution removed selectively Cu and chalcogen in an approximate ratio of 1∶2. From XPS measurements we found that after etching with 1% Br2-MeOH the material surfaces were Sn-rich. The prepared monograin powders were used as absorber materials in monograin layer solar cells: ZnO/CdS/CZT(S,Se)/graphite. A combination of chemical treatments before the deposition of CdS led to the best parameters of Cu2ZnSn(S,Se)4 monograin layer solar cells. The here achieved efficiencies of solar cells were above 4%.

Organic acid catalyzed synthesis of 5-methylresorcinol based organic aerogels in acetonitrile

A method of preparing 5-methylresorcinol and formaldehyde based organic aerogels in non-aqueous media with a benzoic acid derivative as a catalyst is being proposed in this paper. Here acetonitrile is used as a solvent that allows direct drying with carbon dioxide over the supercritical state without the need for a solvent exchange. The acidic properties of 2,6-dihydroxy-4-methyl benzoic acid promote the reaction of sol–gel polymerization, and at the same time it takes part in the reaction as a co-monomer and influences the nanostructure of the material. The evolution of the polymer was monitored using nuclear magnetic resonance spectroscopy and the structure of the resulting organic aerogels depending on the molar ratio of 5-methylresorcinol to 2,6-dihydroxy-4-methyl benzoic acid was studied by nitrogen adsorption–desorption measurements, scanning electron microscopy and infrared spectrometry.

CZTS Monograin Powders and Thin Films

This paper reviews results of studies on different materials and technologies for polycrystalline solar cells conducted at Tallinn University of Technology. Structural properties and defect structure of kesterite CZTS compounds (Cu2ZnSnSe4, Cu2ZnSn(SSe)4) were studied. Influence of selenization parameters of a Zn-Cu-Sn stacked layer on the CZTS layer growth and on the morphology, distribution of elements was analyzed. All the results obtained have been used to optimize the technology of producing solar cell structures in different designs. Cu2ZnSnSe4 and, Cu2ZnSn(SSe)4 based monograin layer solar cells were developed.

SEM analysis and selenization of Cu-Zn-Sn sequential films produced by evaporation of metals

The formation of Cu2SnZnSe4 thin films in the selenization of different sequential metallic and alloy films is investigated. It is shown that the main process of low temperature selenization (up to 300degC) is the formation of different binary copper selenides on the layer surface. High temperature selenization (over 400degC) leads to the formation of Cu2ZnSnSe4 phase with some excess of a separate ZnSe phase. The content of ZnSe diminishes with the rise of the selenization temperature, but the selenized films stayed always multiphased. The size of the formed Cu2ZnSnSe4 crystals is controlled by the composition of the precursor.

Carrier collection losses in interface passivated amorphous silicon thin-film solar cells

In silicon thin-film solar cells the interface between the i- and p-layer is the most critical. In the case of back diffusion of photogenerated minority carriers to the i/p-interface, recombination occurs mainly on the defect states at the interface. To suppress this effect and to reduce recombination losses, hydrogen plasma treatment (HPT) is usually applied. As an alternative to using state of the art HPT we apply an argon plasma treatment (APT) before the p-layer deposition in n-i-p solar cells. To study the effect of APT, several investigations were applied to compare the results with HPT and no plasma treatment at the interface. Carrier collection losses in resulting solar cells were examined with spectral response measurements with and without bias voltage. To investigate single layers, surface photovoltage and X-ray photoelectron spectroscopy (XPS) measurements were conducted. The results with APT at the i/p-interface show a beneficial contribution to the carrier collection compared with HPT and no plasma treatment. Therefore, it can be concluded that APT reduces the recombination centers at the interface. Further, we demonstrate that carrier collection losses of thin-film solar cells are significantly lower with APT.