On the Effect of pH,Temperature, and Surfactant Structure on Bovine Serum Albumin–Cationic/Anionic/Nonionic Surfactants Interactions in Cacodylate Buffer–Fluorescence Quenching Studies Supported by UV Spectrophotometry and CD Spectroscopy

Due to the fact that surfactant molecules are known to alter the structure (and consequently the function) of a protein, protein–surfactant interactions are very important in the biological, pharmaceutical, and cosmetic industries. Although there are numerous studies on the interactions of albumins with surfactants, the investigations are often performed at fixed environmental conditions and limited to separate surface-active agents and consequently do not present an appropriate comparison between their different types and structures. In the present paper, the interactions between selected cationic, anionic, and nonionic surfactants, namely hexadecylpyridinium chloride (CPC), hexadecyltrimethylammonium bromide (CTAB), sodium dodecyl sulfate (SDS), polyethylene glycol sorbitan monolaurate, monopalmitate, and monooleate (TWEEN 20, TWEEN 40, and TWEEN 80, respectively) with bovine serum albumin (BSA) were studied qualitatively and quantitatively in an aqueous solution (10 mM cacodylate buffer; pH 5.0 and 7.0) by steady-state fluorescence spectroscopy supported by UV spectrophotometry and CD spectroscopy. Since in the case of all studied systems, the fluorescence intensity of BSA decreased regularly and significantly under the action of the surfactants added, the fluorescence quenching mechanism was analyzed thoroughly with the use of the Stern–Volmer equation (and its modification) and attributed to the formation of BSA–surfactant complexes. The binding efficiency and mode of interactions were evaluated among others by the determination, comparison, and discussion of the values of binding (association) constants of the newly formed complexes and the corresponding thermodynamic parameters (ΔG, ΔH, ΔS). Furthermore, the influence of the structure of the chosen surfactants (charge of hydrophilic head and length of hydrophobic chain) as well as different environmental conditions (pH, temperature) on the binding mode and the strength of the interaction has been investigated and elucidated.     

Residual stresses in epoxy systems by 3-D photoelastic method

The new 3-D photoelastic method was applied to the studies of residual stresses around spherical inclusion in polymeric matrices. Full stress tensor for several model samples was measured. The extent of significant stresses is not greater than three radii of an inclusion. It was found that the stress follows the 1/R³ rule at distances far from the inclusion, while in the narrow zone at the interface a plateau is observed. The level of stress ranges from few MPa up to the plastic yield of the polymeric matrix. The radial stress component is usually twice as large as the tangential stress component. Radial negative stress and tangential positive stresses are found in configuration with a hard inclusion, while radial positive stress and tangential negative stresses are in the systems with soft inclusion. The pressure in the matrix at points around inclusions calculated from the stress tensor is always near zero MPa, which indicates the action of purely deviatoric stresses in the matrix.     

Solvent‐Assisted Low‐Temperature Crystallization of SnO2 Electron‐Transfer Layer for High‐Efficiency Planar Perovskite Solar Cells

A high‐quality polycrystalline SnO₂ electron‐transfer layer is synthesized through an in situ, low‐temperature, and unique butanol–water solvent‐assisted process. By choosing a mixture of butanol and water as a solvent, the crystallinity is enhanced and the crystallization temperature is lowered to 130 °C, making the process fully compatible with flexible plastic substrates. The best solar cells fabricated using these layers achieve an efficiency of 20.52% (average 19.02%) which is among the best in the class of planar n–i–p‐type perovskite (MAPbI₃) solar cells. The strongly reduced crystallization temperature of the materials allows their use on a flexible substrate, with a resulting device efficiency of 18%.     

Organometallic Bonding in an Ullmann‐Type On‐Surface Chemical Reaction Studied by High‐Resolution Atomic Force Microscopy

The on‐surface Ullmann‐type chemical reaction synthesizes polymers by linking carbons of adjacent molecules on solid surfaces. Although an organometallic compound is recently identified as the reaction intermediate, little is known about the detailed structure of the bonded organometallic species and its influence on the molecule and the reaction. Herein atomic force microscopy at low temperature is used to study the reaction with 3,9‐diiododinaphtho[2,3‐b:2′,3′‐d]thiophene (I‐DNT‐VW), which is polymerized on Ag(111) in vacuum. Thermally sublimated I‐DNT‐VW picks up a Ag surface atom, forming a C? Ag bond at one end after removing an iodine. The C? Ag bond is usually short‐lived, and a C? Ag? C organometallic bond immediately forms with an adjacent molecule. The existence of the bonded Ag atoms strongly affects the bending angle and adsorption height of the molecular unit. Density functional theory calculations reveal the bending mechanism, which reveals that charge from the terminus of the molecule is transferred via the Ag atom into the organometallic bond and strengths the local adsorption to the substrate. Such deformations vanish when the Ag atoms are removed by annealing and C? C bonds are established.     

Dithizone modified gold nanoparticles films for potentiometric sensing

For the first time, application of a membrane composed of gold nanoparticles decorated with complexing ligand for potentiometric sensing is shown. Gold nanoparticles drop cast from a solution form a porous structure on a substrate electrode surface. Sample cations can penetrate the gold nanoparticles layer and interact with ligand acting as a charged ionophore, resulting in Nernstian potentiometric responses. Anchoring of complexing ligand on the gold surface abolishes the necessity of ionophore application. Moreover, it opens the possibility of preparation of potentiometric sensors using chelators of significantly different selectivity patterns further enhanced by the absence of polymeric membrane matrix. This was clearly seen, for example, for gold nanoparticles stabilizing the applied ligand-dithizone-thiol conformation leading to a high potentiometric selectivity toward copper ions, much higher than that of ionophores typically used to induce selectivity for polymeric ion-selective membranes.     

Durability and surface chemistry of horizontally aligned CNT films as electrodes upon electrolysis of acidic aqueous solution

We devised a simple and effective method of electrochemical functionalization of horizontally aligned CNT films in diluted HCl and H₂SO₄ solutions upon their electrolysis under a constant current mode. We were able to cause notable generation of carbon–oxygen and carbon–chlorine functional groups on the CNT film anodes as proven by EDX, XPS, and Raman spectroscopy. As a consequence, we observed significant changes of the morphology of the material under electron microscopy, what translated into improved compatibility of CNTs with hydrophilic media. In turn, application of CNT films as cathodes was found as a powerful tool for a thorough cleaning of the nanotubes. Finally, we demonstrated that by the selection of appropriate conditions, CNT films can act as easy-to-make and flexible electrodes with a high stability and performance superior to graphite for generation of non-oxidizing gases such as hydrogen from solution. CNT film electrodes are two orders of magnitude lighter and require much lower overpotential for faradaic splitting of water.     

A performance analysis of HICCUPS—a steganographic system for WLAN

The paper presents an analysis of performance features of the HICCUPS (HIdden Communication system for CorrUPted networkS) including the efficiency and the cost of the system in WLANs (Wireless Local Area Networks). The analysis relies on the original CSMA/CA (Carrier Sense Multiple Access with Collision Avoidance) 802.11 Markov chain-based model and proves that the HICCUPS is the efficient steganographic method with the reasonable cost.     

Untersuchungen der gerissenen Deckenplatten

The Investigation of Demage Monolith Ceiling Slab In recent years the monolith structures are cracked frequently, particularly in concrete walls and reinforced ceiling slab. Usually, the cracks are not the effect of the exterior loads. The reason of that situation lies in the material and in the processes, which occur in concrete during the bond. The paper presents this problem as an example of ceiling slab made of concrete with fly ashes. The large usefulness of nondestructive tests to diagnostics of damaged construction was underlined.