Surface Engineering of Anodic WO3 Layers by In Situ Doping for Light-Assisted Water Splitting.

This study presents a novel approach to fabricating anodic Co-F-WO3 layers via a single-step electrochemical synthesis, utilizing cobalt fluoride as a dopant source in the electrolyte. The proposed in situ doping technique capitalizes on the high electronegativity of fluorine, ensuring the stability of CoF2 throughout the synthesis process. The nanoporous layer formation, resulting from anodic oxide dissolution in the presence of fluoride ions, is expected to facilitate the effective incorporation of cobalt compounds into the film. The research explores the impact of dopant concentration in the electrolyte, conducting a comprehensive characterization of the resulting materials, including morphology, composition, optical, electrochemical, and photoelectrochemical properties. The successful doping of WO3 was confirmed by energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), Raman spectroscopy, photoluminescence measurements, X-ray photoelectron spectroscopy (XPS), and Mott-Schottky analysis. Optical studies reveal lower absorption in Co-doped materials, with a slight shift in band gap energies. Photoelectrochemical (PEC) analysis demonstrates improved PEC activity for Co-doped layers, with the observed shift in photocurrent onset potential attributed to both cobalt and fluoride ions catalytic effects. The study includes an in-depth discussion of the observed phenomena and their implications for applications in solar water splitting, emphasizing the potential of the anodic Co-F-WO3 layers as efficient photoelectrodes. In addition, the research presents a comprehensive exploration of the electrochemical synthesis and characterization of anodic Co-F-WO3, emphasizing their photocatalytic properties for the oxygen evolution reaction (OER). It was found that Co-doped WO3 materials exhibited higher PEC activity, with a maximum 5-fold enhancement compared to pristine materials. Furthermore, the studies demonstrated that these photoanodes can be effectively reused for PEC water-splitting experiments.

Human erythrocytes under stress. Spectroscopic fingerprints of known oxidative mechanisms and beyond.

In this work, we investigated the oxidative stress-related biochemical alterations in red blood cells (RBCs) and their membranes with the use of spectroscopic techniques. We aimed to show their great advantage for the in situ detection of lipid classes and secondary structures of proteins without the need for their extraction in the cellular environment. The exposition of the cells to peroxides, t-butyl hydroperoxide (tBOOH) or hydrogen peroxide (H2O2) led to different degradation processes encompassing the changes in the composition of membranes and structural modifications of hemoglobin (Hb). Our results indicated that tBOOH is generally a stronger oxidizing agent than H2O2 and this observation was congruent with the activity of superoxide and glutathione peroxidase. ATR-FTIR and Raman spectroscopies of membranes revealed that tBOOH caused primarily the partial loss and peroxidation of the lipids resulting in loss of the integrity of membranes. In turn, both peroxides induced several kinds of damage in the protein layer, including the partial decrease of their content and irreversible aggregation of spectrin, ankyrin, and membrane-bound globin. These changes were especially pronounced on the membrane surface where stress conditions induced the formation of ß-sheets and intramolecular aggregates, particularly for tBOOH. Interestingly, nano-FTIR spectroscopy revealed the lipid peroxidative damage on the membrane surface in both cases. As far as hemoglobin was concerned, tBOOH and H2O2 caused the increase of the oxyhemoglobin species and conformational alterations of its polypeptide chain into ß-sheets. Our findings confirm that applied spectroscopies effectively track the oxidative changes occurring in the structural components of red blood cells and the simplicity of conducting measurements and sample preparation can be readily applied to pharmacological and clinical studies.

Photoelectrochemical Performance of Nanotubular Fe2O3-TiO2 Electrodes under Solar Radiation.

Fe2O3-TiO2 materials were obtained by the cathodic electrochemical deposition of Fe on anodic TiO2 at different deposition times (5-180 s), followed by annealing at 450 °C. The effect of the hematite content on the photoelectrochemical (PEC) activity of the received materials was studied. The synthesized electrodes were characterized by field emission scanning electron microscopy (FE-SEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), Raman spectroscopy, diffuse reflectance spectroscopy (DRS), Mott-Schottky analysis, and PEC measurements. It was shown that the amount of deposited iron (ca. 0.5 at.%-30 at.%) and, consequently, hematite after a final annealing increased with the extension of deposition time and directly affected the semiconducting properties of the hybrid material. It was observed that the flat band potential shifted towards more positive values, facilitating photoelectrochemical water oxidation. In addition, the optical band gap decreased from 3.18 eV to 2.77 eV, which resulted in enhanced PEC visible-light response. Moreover, the Fe2O3-TiO2 electrodes were sensitive to the addition of glucose, which indicates that such materials may be considered as potential PEC sensors for the detection of glucose.

Dual-enhancement and dual-tag design for SERS-based sandwich immunoassays: evaluation of a metal-metal effect in 3D architecture.

The design of a sandwich-type SERS immunoassay (surface-enhanced Raman spectroscopy) is demonstrated operating in dual surface enhancement and dual-tag paradigm. The capture and detection antibodies are linked to two SERS-active substrates and form together the three-dimensional (3D) structure after specific binding to interleukin 6. A variety of metal combinations is tested (Au-Ag, Au-Au, and Ag-Ag), but an enhanced electromagnetic field is generated only due to coupling of Ag and Au nanoparticles with an Au hexagonal nanoarray. The amplified in that way Raman signals improve the limit of detection over 3 times in comparison to the assay with only one SERS-active substrate. It is also shown that the proper readout of the true-positive signal can be achieved in assays with two Raman tags, and this approach also improves LOD. For the optimal combination of the metal-metal junction and Raman tags, a linear relationship between the Raman signal and the concentration of IL-6 is obtained in the range 0-1000 pg⋅mL-1with LOD of 25.2 pg mL-1and RSD < 10%. The presented proof-of-concept of the SERS immunoassay with the dual-enhancement and dual-tag opens additional opportunities for engineering reliable SERS biosensing.

Response of physiological parameters in Dionaea muscipula J. Ellis teratomas transformed with rolB oncogene.

BACKGROUND: Plant transformation with rol oncogenes derived from wild strains of Rhizobium rhizogenes is a popular biotechnology tool. Transformation effects depend on the type of rol gene, expression level, and the number of gene copies incorporated into the plant's genomic DNA. Although rol oncogenes are known as inducers of plant secondary metabolism, little is known about the physiological response of plants subjected to transformation. RESULTS: In this study, the physiological consequences of rolB oncogene incorporation into the DNA of Dionaea muscipula J. Ellis was evaluated at the level of primary and secondary metabolism. Examination of the teratoma (transformed shoots) cultures of two different clones (K and L) showed two different strategies for dealing with the presence of the rolB gene. Clone K showed an increased ratio of free fatty acids to lipids, superoxide dismutase activity, synthesis of the oxidised form of glutathione, and total pool of glutathione and carotenoids, in comparison to non-transformed plants (control). Clone L was characterised by increased accumulation of malondialdehyde, proline, activity of superoxide dismutase and catalase, total pool of glutathione, ratio of reduced form of glutathione to oxidised form, and accumulation of selected phenolic acids. Moreover, clone L had an enhanced ratio of total triglycerides to lipids and accumulated saccharose, fructose, glucose, and tyrosine. CONCLUSIONS: This study showed that plant transformation with the rolB oncogene derived from R. rhizogenes induces a pleiotropic effect in plant tissue after transformation. Examination of D. muscipula plant in the context of transformation with wild strains of R. rhizogenes can be a new source of knowledge about primary and secondary metabolites in transgenic organisms.

Engineering a Poly(3,4-ethylenedioxythiophene):(Polystyrene Sulfonate) Surface Using Self-Assembling Molecules-A Chemical Library Approach.

The surface properties of poly(3,4-ethylenedioxythiophene):(polystyrene sulfonate) (PEDOT:PSS) affect the performance of many organic electronic devices. The work function determines the efficiency of the charge carrier transfer between PEDOT:PSS electrodes and the active layer of the device. The surface free energy affects phase separation in multicomponent blends that are typically used to fabricate active layers of organic light-emitting diodes and photovoltaic devices. Here, we present a method to prepare PEDOT:PSS films with a gradient work function and surface free energy. This modification was achieved by evaporation of trimethoxy(3,3,3-trifluoropropyl)silane in such a way that the degree of surface coverage of the molecules varied in the selected direction. Gradient films were used as electrodes to fabricate two-terminal PEDOT:PSS/poly(3-hexyl thiophene)/Au devices to rapidly screen for the influence of the modification on the performance of the prepared polymer diodes. Gradual changes in the morphology of the solution-cast model poly(3-butyl thiophene)/poly-bromostyrene films followed changes in the surface energy of the substrate.