Bacterial DNA recognition by SERS active plasma-coupled nanogold

It is shown that surface-enhanced Raman spectroscopy (SERS) can identify bacteria based on their genomic DNA composition, acting as a “sample-distinguishing marker”. Successful spectral differentiation of bacterial species was accomplished with nanogold aggregates synthesized through single-step plasma reduction of the ionic gold-containing vapored precursor. A high enhancement factor (EF = 10$^7$) in truncated coupled plasmonic particulates allowed SERS-probing at nanogram sample quantities. Simulations confirmed the occurrence of the strongest electric field confinement within nanometric gaps between gold dimers/chains from where the molecular fingerprints of bacterial DNA fragments gained photon scattering enhancement. The most prominent Raman modes linked to fundamental base-pair molecular vibrations were deconvoluted and used to proceed with nitrogenous base content estimation. The genomic composition (percentage of guanine-cytosine and adenine-thymine) was successfully validated by third-generation sequencing using nanopore technology, further proving that the SERS technique can be employed to swiftly specify bioentities by the discriminative principal-component statistical approach

Phase detection and modulation improvement for active load modulation during continuous transmission

The paper covers one of the communication technologies used in wireless sensor networks. We have presented improvements in existing radio frequency identification (RFID) systems to address the problem of the phase selection in active load modulation (ALM). The phase selection affects the interoperability of communication devices and has to be addressed in the design phase of a new tag. A novel transmission method is presented to make the phase selection irrelevant for device interoperability. A second solution is shown to improve the existing system synchronization, which allows operation with arbitrary selected phase. A mathematical analysis of signals present on the antenna was used together with the reference reader model to perform an analysis of proposed improvements. We proved that the proposed transmission method is less affected by phase selection. Furthermore, we demonstrated that existing system improvement allows synchronization and operation at an arbitrarily selected phase despite the continuous transmission and large signal-to-interference ratio

Integrative computational modeling to unravel novel potential biomarkers in hepatocellular carcinoma

Hepatocellular carcinoma (HCC) is a major health problem around the world. The management of this disease is complicated by the lack of noninvasive diagnostic tools and the few treatment options available. Better clinical outcomes can be achieved if HCC is detected early, but unfortunately, clinical signs appear when the disease is in its late stages. We aim to identify novel genes that can be targeted for the diagnosis and therapy of HCC. We performed a meta-analysis of transcriptomics data to identify differentially expressed genes and applied network analysis to identify hub genes. Fatty acid metabolism, complement and coagulation cascade, chemical carcinogenesis and retinol metabolism were identified as key pathways in HCC. Furthermore, we integrated transcriptomics data into a reference human genome-scale metabolic model to identify key reactions and subsystems relevant in HCC. We conclude that fatty acid activation, purine metabolism, vitamin D, and E metabolism are key processes in the development of HCC and therefore need to be further explored for the development of new therapies. We provide the first evidence that GABRP, HBG1 and DAK (TKFC) genes are important in HCC in humans and warrant further studies

Photocatalytic nano-composite architectural lime mortar for degradation of urban pollutants under solar and visible (interior) light

Recent advances in nano-technology and nano-additives can give enhanced properties to natural hydraulic lime (NHL), creating a multifunctional material. We have prepared a novel nanocomposite, made of a commercial mortar with 1 wt% and 5 wt% added titania nanoparticles (NPs). These TiO2 NPs are themselves doped with 1 mol% silver, to give the material enhanced photocatalytic and antimicrobial properties. The Ag-doped TiO2 NPs were made from a simple, costs effective, aqueous green nanosynthesis process, and the end material only contains 0.01–0.05% Ag. As this mortar is intended to both combat atmospheric pollution, and create more durable/lower maintenance building façades (plastering and finishing) by limiting attack from microorganisms and pollutants, its photocatalytic anti-pollution activity under solar and visible (no UV) light for nitrous oxide (NOx) and volatile organic compound (VOC) removal was studied. The addition of dopants did not significantly alter the physical properties or curing of the mortar, while it showed excellent photocatalytic activity under sunlight, The mortars with only 1 and 5 wt% additives degraded 10.6% and 21% NOx after 45 mins, respectively, comparing well to a value of 50% for a pure TiO2/Ag+ sample. They also degraded VOCs under visible light, of the kind used for lighting inside buildings, with no UV component. As the NPs are contained in the whole of the mortar layer, not just as a coating, if the surface is chipped or damaged this mortar will not loose its photocatalytic capabilities

Hydrothermal Synthesis of Rare-Earth Modified Titania: Influence on Phase Composition, Optical Properties, and Photocatalytic Activity

In order to expand the use of titania indoor as well as to increase its overall performance, narrowing the band gap is one of the possibilities to achieve this. Modifying with rare earths (REs) has been relatively unexplored, especially the modification of rutile with rare earth cations. The aim of this study was to find the influence of the modification of TiO2 with rare earths on its structural, optical, morphological, and photocatalytic properties. Titania was synthesized using TiOSO4 as the source of titanium via hydrothermal synthesis procedure at low temperature (200 °C) and modified with selected rare earth elements, namely, Ce, La, and Gd. Structural properties of samples were determined by X-ray powder diffraction (XRD), and the phase ratio was calculated using the Rietveld method. Optical properties were analyzed by ultraviolet and visible light (UV-Vis) spectroscopy. Field emission scanning electron microscope (FE-SEM) was used to determine the morphological properties of samples and to estimate the size of primary crystals. X-ray photoelectron spectroscopy (XPS) was used to determine the chemical bonding properties of samples. Photocatalytic activity of the prepared photocatalysts as well as the titania available on the market (P25) was measured in three different setups, assessing volatile organic compound (VOC) degradation, NOx abatement, and water purification. It was found out that modification with rare earth elements slows down the transformation of anatase and brookite to rutile. Whereas the unmodified sample was composed of only rutile, La- and Gd-modified samples contained anatase and rutile, and Ce-modified samples consisted of anatase, brookite, and rutile. Modification with rare earth metals has turned out to be detrimental to photocatalytic activity. In all cases, pure TiO2 outperformed the modified samples. Cerium-modified TiO2 was the least active sample, despite having a light absorption tail up to 585 nm wavelength. La- and Gd-modified samples did not show a significant shift in light absorption when compared to the pure TiO2 sample. The reason for the lower activity of modified samples was attributed to a greater Ti3+/Ti4+ ratio and a large amount of hydroxyl oxygen found in pure TiO2. All the modified samples had a smaller Ti3+/Ti4+ ratio and less hydroxyl oxygen

TiO2 photocatalyst with single and dual noble metal co-catalysts for efficient water splitting and organic compound removal

International audiencePhotocatalysts can be used both for air cleaning and solar energy harvesting through water splitting. However, pure TiO2 photocatalysts are often inefficient and therefore co-catalysts are needed to improve the yield. To achieve this goal, we prepared TiO2 and deposited Pt, Ir and Ru co-catalysts on its surface. Two base TiO2 nanoparticles were used: P25 and rutile TiO2 synthesized via hydrothermal method. Co-catalysts were deposited by wet impregnation technique using single element and a combination of two elements (Pt and Ir or Pt and Ru), followed by annealing in either air or H2/Ar. Annealing in reducing atmosphere increased the photocatalytic activity of oxidation of isopropanol compared to annealing in air. We demonstrated a clear influence of the co-catalysts on the photocatalytic degradation of isopropanol and on electrochemical water-splitting reaction. The platinum-containing samples showed the best HER activity

Impact of Rutile Fraction on TiO2 Visible-Light Absorption and Visible-Light-Induced Photocatalytic Activity

Titanium dioxide is by far the most utilised semiconductor material for photocatalytic applications. Still, it is transparent to visible-light. Recently, it has been proved that a type-II band alignment for the rutile−anatase mixture would improve its visible-light absorption.In this research paper we thoroughly characterised the real crystalline and amorphous phases of synthesised titanias – thermally treated at different temperatures to get distinct ratios of anatase-rutile-amorphous fraction – as well as that of three commercially available photocatalytic nano-TiO2. The structural characterisation was done via advanced X-ray diffraction method, namely the Rietveld-RIR method, to attain a full quantitative phase analysis of the specimens. The microstructure was also investigated via an advanced X-ray method, the whole powder pattern modelling. These methods were validated combining advanced aberration-corrected scanning transmission microscopy and high-resolution electron energy-loss spectroscopy. The photocatalytic activity was assessed in the liquid- and gas-solid phase (employing rhodamine B and 4-chlorophenol, and isopropanol, respectively, as the organic substances to degrade) using a light source irradiating exclusively in the visible-range.Optical spectroscopy showed that even a small fraction of rutile (2 wt%) is able to shift to lower energies the apparent optical band gap of an anatase-rutile mixed phase. But is this enough to attain a real photocatalytic activity promoted by merely visible-light?We tried to give a reply to that question.Photocatalytic activity results in the liquid-solid phase showed that a high surface hydroxylation led to specimen with superior visible light-induced catalytic activity (i.e. dye and ligand-to-metal charge transfer complexes sensitisation effects). That is: not photocatalysis sensu-strictu.On the other hand, the gas-solid phase results showed that a higher amount of the rutile fraction (around 10 wt%), together with less recombination of the charge carriers, were more effective for an actual photocatalytic oxidation of isopropanol.</div

A comparative study of TiO2 preparation method on their photocatalytic activity for CO2 reduction

In this work, we aimed to correlate the structural properties of different TiO2 with their photocatalytic performance and selectivity during CO2 photocatalytic reduction at different pH. We prepared two types of TiO2 photocatalysts and characterized them in detail using X-ray powder diffraction, field emission scanning electron microscope, nitrogen adsorption, UV-Vis spectroscopy, photoelectrochemical measurements and X-ray photoelectron spectroscopy techniques. The prepared photocatalysts demonstrated significantly higher selectivity to CO2 reduction (CH4 and CO yields), than a commercial P25. Among them, the photocatalysts TiSG, which had the lowest portion of hydroxyl oxygen species, had the highest photoreduction efficiency. Therefore, the key factors in photocatalytic CO2 reduction with TiO2 are not only the phase composition but also the portion of different types of surface oxygen species, which strongly affects their efficiency and selectivity. Another objective was to investigate the effect of pH on the efficiency and especially the selectivity of photocatalytic CO2 reduction. While methane is mainly formed in basic environments, carbon monoxide is formed in more acidic environments. Also, hydrogen production is twice as high in more acidic environment compared to the basic environment.Web of Science413art. no. 11394