An early detection of prostate cancer drug in water to prevent loss of biodiversity

Hexamethyldisiloxane (HMDSO) based films containing silicon monoxide (SiO) were obtained by a plasma process. The HMDSO hybrid films were prepared on the substrates by evaporating SiO during HMDSO plasma polymerization in rf discharge. SiO was evaporated by heating in rf plasma consisting of HMDSO and oxygen at a pressure of the order of 10-4 Torr. The structures of the HMDSO hybrid films thus obtained were analyzed by fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS) spectra. The structures of the HMDSO hybrid films containing SiO were also analyzed by FTIR. The ratio of Si/C in the hybrid films formed under the HMDSO monomer gas pressure at 7×10-4 Torr were found to be about 1.5 by XPS spectra. The HMDSO hybrid films were found to be pinhole free, and exhibited the characteristics of electrical insulators.

The chemisorbed structure for an aromatic molecule on a silicon surface plays an important part in promoting the development of organic semiconductor material science. The carbon K-shell x-ray photoelectron spectroscopy (XPS) and the x-ray absorption near-edge structure (XANES) spectra of the interfacial structure of an s-triazine molecule adsorbed on Si(100) surface have been performed by the first principles, and the landscape of the s-triazine molecule on Si(100) surface has been described in detail. Both the XPS and XANES spectra have shown their dependence on different structures for the pristine s-triazine molecule and its several possible adsorbed configurations. By comparison with the XPS spectra, the XANES spectra display the strongest structural dependency of all of the studied systems and thus could be well applied to identify the chemisorbed s-triazine derivatives. The exploration of spectral components originated from non-equivalent carbons in disparate local environments has also been implemented for both the XPS and XANES spectra of s-triazine adsorbed configurations.

Boosting Electrocatalytic CO ₂ Reduction with Conjugated Bimetallic Co/Zn Polyphthalocyanine Frameworks

Plasma treatment of paper for protein immobilization on paper-based chemiluminescence immunodevice

In this work, a collimated helium beam was used to activate a thiol-poly(ethylene glycol) (SH-PEG) monolayer on gold to selectively capture proteins in the exposed regions. Protein patterns were formed at high throughput by exposing a stencil mask placed in proximity to the PEG-coated surface to a broad beam of helium particles, followed by incubation in a protein solution. Attenuated Total Reflectance–Fourier Transform Infrared Spectroscopy (ATR–FTIR) spectra showed that SH-PEG molecules remain attached to gold after exposure to beam doses of 1.5–60 µC/cm2 and incubation in PBS buffer for one hour, as evidenced by the presence of characteristic ether and methoxy peaks at 1120 cm−1 and 2870 cm−1, respectively. X-ray Photoelectron Spectroscopy (XPS) spectra showed that increasing beam doses destroy ether (C–O) bonds in PEG molecules as evidenced by the decrease in carbon C1s peak at 286.6 eV and increased alkyl (C–C) signal at 284.6 eV. XPS spectra also demonstrated protein capture on beam-exposed PEG regions through the appearance of a nitrogen N1s peak at 400 eV and carbon C1s peak at 288 eV binding energies, while the unexposed PEG areas remained protein-free. The characteristic activities of avidin and horseradish peroxidase were preserved after attachment on beam-exposed regions. Protein patterns created using a 35 µm mesh mask were visualized by localized formation of insoluble diformazan precipitates by alkaline phosphatase conversion of its substrate bromochloroindoyl phosphate-nitroblue tetrazolium (BCIP-NBT) and by avidin binding of biotinylated antibodies conjugated on 100 nm gold nanoparticles (AuNP). Patterns created using a mask with smaller 300 nm openings were detected by specific binding of 40 nm AuNP probes and by localized HRP-mediated deposition of silver nanoparticles. Corresponding BSA-passivated negative controls showed very few bound AuNP probes and little to no enzymatic formation of diformazan precipitates or silver nanoparticles.

Derivation of new energy-loss functions as applied to analysis of Si 2p XPS spectra

Highly Dispersive Metal Atoms Anchored on Carbon Matrix Obtained by Direct Rapid Pyrolysis of Metal Complexes

Dual-Resistance of Ion Migration and Moisture Erosion via Hydrolytic Crosslinking of Siloxane Functionalized Poly(Ionic Liquids) for Efficient and Stable Perovskite Solar Cells

Compared with traditional quantum dots, carbon quantum dots (CQDs) have aroused tremendous research interest among scientists as new fluorescent carbon nanomaterials due to their unique properties (easy surface functionalization, good biocompatibility, and low toxicity). The nitrogen-doped carbon quantum dots (NCDs) was synthesized with one-step hydrothermal treatment with citric acid as carbon source, and ammonia as nitrogen source. The obtained NCDs exhibited excellent water-solubility and high stability. High-resolution Transmission electron microscopy (HRTEM) image showed that the diameter of particles was about 3nm. Fourier transform infrared (FIIR) and X-ray photoelectron spectroscopy (XPS) spectra analysis demonstrated that the NCDs are functionalized with hydroxyl, amino, carbonyl, and carboxylic acid groups, which indicated NCDs has better water-solubility. It was further demonstrated that such NCDs can serve as effective fluorescent sensing platform for Hg2+ ions detection with sensitivity and selectivity. In a PBS butter solution (0.1 mol·L-1 pH 7.0), the fluorescence quenching ratio (F/F0) indicated linear responses with Hg2+ concentration ranging from 0.001 to 0.1 μmol·L-1, with the detection limit of 2.1 nmol·L-1. The fluorescence technique was superior in terms of sensitivity, selectivity and simplicity. It was successfully applied to determination of Hg2+ in samples.

Important mechanisms that lead to features, often complex, in X-ray photoelectron spectroscopy (XPS) spectra are defined and described. It is shown that there is much information in an XPS spectrum that can be obtained by examining these features rather than examining only the shifts of main peaks between different materials. These mechanisms are presented with a focus on describing the underlying chemical and physical phenomena responsible for features of the XPS and on showing how these XPS features can be related to the properties and electronic structure of the material studied. While it is necessary to consider certain quantum mechanical rules, the mathematical formalism is not discussed. However, a general awareness of multiplet splittings, which are a result of angular momentum coupling combined with ligand field and spin–orbit splittings, and of covalent mixings in the metal–ligand bond of oxides is essential to properly interpret the significance of XPS features. A conceptual framework of shake excitation from bonding to anti-bonding orbitals is introduced to provide an understanding of the significance of XPS satellites. While the coupling of theory and measurement is required to extract quantitative information from XPS, it may be possible to obtain useful qualitative information directly from features of the XPS spectra provided that one takes into account more than only shifts of the XPS binding energies. A correct analysis of XPS features may require a careful treatment of many-body effects that distribute intensity over many individual, unresolved final states.

Effects of Coster–Kronig fluctuation and decay on X-ray photoelectron spectroscopy spectra

ABSTRACTThe surface chemistry of silica glass implanted with N+ or P+ ions has been studied. The X-ray photoelectron spectroscopy (XPS) spectra of N(1s) for silica glass implanted with N+ shows the possibility of the formation of oxynitride glass. For the first time, the effect of the implantation of N+ and additional Si+ on the surface chemistry of silica glass has been studied and found to be significant in increasing the nitrogen concentration in the silica glass. The peak concentration of N increases several times, and does not change even if the sample is annealed at 900°C. The XPS spectra of P(2p) for silica glass implanted with P+ ions shows two interactions, both P-O and P-P. Therefore, the XPS spectra shows the possibility for the formation of phosphosilicate glass using P+ implantation into silica glass.

Surface treatment with Fenton for separation of acrylonitrile-butadiene-styrene and polyvinylchloride waste plastics by flotation

CuCo2O4 photocatalyst for bifunctional applications: Toxic dye degradation and antimicrobial activity

Highly efficient uranium (VI) capture from aqueous solution by means of a hydroxyapatite-biochar nanocomposite: Adsorption behavior and mechanism