Notes

Subacute transversus myelitis being a specialized medical presentation involving neurobrucellosis.
Radio frequency (RF) magnetron sputtering allows the fabrication of TiO2 films with high purity, reliable control of film thickness, and uniform morphology. In the present study, the change in surface roughness upon heating two different thicknesses of RF sputter-deposited TiO2 films was investigated. As a measure of the process of the change in surface morphology, chemically -synthesised phosphine-protected Au9 clusters covered by a photodeposited CrOx layer were used as a probe. Subsequent to the deposition of the Au9 clusters and the CrOx layer, samples were heated to 200 ℃ to remove the triphenylphosphine ligands from the Au9 cluster. After heating, the thick TiO2 film was found to be mobile, in contrast to the thin TiO2 film. The influence of the mobility of the TiO2 films on the Au9 clusters was investigated with X-ray photoelectron spectroscopy. It was found that the high mobility of the thick TiO2 film after heating leads to a significant agglomeration of the Au9 clusters, even when protected by the CrOx layer. The thin TiO2 film has a much lower mobility when being heated, resulting in only minor agglomeration of the Au9 clusters covered with the CrOx layer.Efficient and low-cost degradation of ethylene has always been a difficult problem in the storage and transportation of fruits and vegetables. Although photocatalysis is considered to be a feasible and efficient solution for ethylene degradation, the low degradation ability of conventional catalysts for small non-polar molecules limits its application. TiO2 has the advantage of tunable microstructure, but it also has the defects of wide band gap and low utilization of sunlight. The surface plasmon resonance (SPR) effect of noble metals can effectively improve the visible light absorption range of catalysts, and the synergy of noble metals further enhances the photocatalytic ability. Herein, we developed a series of AuPt catalysts through the photo-deposition method. Benefited from the SPR effect and the synergy of Au and Pt, the efficiency of AuPt-TiO2 was 19.9, 4.64 and 2.42 times that of TiO2, Au-TiO2 and Pt-TiO2, and the photocatalytic degradation ability of AuPt-TiO2 was maintained in five cyclic stability tests. Meanwhile, the transient photocurrent spectra and PL spectra proved that the light absorption capacity and carrier separation efficiency of AuPt-TiO2 were enhanced. This work provides a new direction for enhancing non-polar small-molecule photodegradation of semiconductors.The Special Issue of Nanomaterials "Frontiers in Nanotoxicology" highlights the modern problems of nanotoxicology and nanobiomedicine, including the toxicity of metal-based, silicon-based, carbon-based, and other types of nanoparticles, occupational safety of nanoproduction workers, comprehensive assessment on new biomedical nanomaterials, improvement of nanotoxicology methods, as well as the current state and prospects of research in the fields of theoretical, experimental, and toxicological aspects of the prospective biomedical application of functionalized magnetic nanoparticles activated by a low-frequency non-heating alternating magnetic field, biomedical applications and the toxicity of graphene nanoribbons, and fetotoxicity of nanoparticles [...].With high safety and good flexibility, polymer-based composite solid electrolytes are considered to be promising electrolytes and are widely investigated in solid lithium batteries. However, the low conductivity and high interfacial impedance of polymer-based solid electrolytes hinder their industrial applications. Herein, a composite solid-state electrolyte containing graphene (PVDF-LATP-LiClO4-Graphene) with structurally stable and good electrochemical performance is explored and enables excellent electrochemical properties for lithium-ion batteries. The ionic conductivity of the composite electrolyte membrane containing 5 wt% graphene reaches 2.00 × 10-3 S cm-1 at 25 °C, which is higher than that of the composite electrolyte membrane without graphene (2.67 × 10-4 S cm-1). The electrochemical window of the composite electrolyte membrane containing 5 wt% graphene reaches 4.6 V, and its Li+ transference numbers reach 0.84. Assembling this electrolyte into the battery, the LFP/PVDF-LATP-LiClO4-Graphene /Li battery has a specific discharge capacity of 107 mAh g-1 at 0.2 C, and the capacity retention rate was 91.58% after 100 cycles, higher than that of the LiFePO4/PVDF-LATP-LiClO4/Li (LFP/PLL/Li) battery, being 94 mAh g-1 and 89.36%, respectively. This work provides a feasible solution for the potential application of composite solid electrolytes.In this research, the LiY zeolite was firstly synthesized by using NaY as the parent zeolite; thereafter, the LiYAg and NaYAg zeolites created for formaldehyde gas detection were prepared with further Ag+-Li+/Na+ exchange and a mild thermal treatment at 300 °C to promote the formation of luminescent Ag CLs. The spectra experimental results indicated that Ag CLs showed stronger and blue-shifted emissions in LiYAg compared with in NaYAg, and the emission intensity of Ag CLs in both zeolites monotonously decreased when exposed to increasing formaldehyde gas content. Moreover, the linear dependence of the Ag CLs' emission intensity variation on formaldehyde content indicated a reliable method for fast and sensitive formaldehyde detection. According to the XPS, UV-vis absorption, and N2 adsorption-desorption isotherm studies, the formaldehyde-gas-induced luminescence quenching of Ag CLs is due to the formation of Ag2O and Ag NPs, in which the higher content of Ag+/Ag0 redox couples in LiYAg and larger surface area of NaYAg benefit the precise detection of formaldehyde gas in low- and high-content ranges, respectively. Furthermore, the blue-shifted peak position and widened FWHM of Ag CLs can also be used for the indication of formaldehyde gas and the detection limit of NaYAg and LiYAg, which both meet with the standards of the WHO and OSHA.This study aimed to develop novel bio-nanofluids using Solanum torvum extracts in synergy with nanoparticles of different chemical nature as a proposal sustainable for enhanced oil recovery (EOR) applications. For this, saponin-rich extracts (SRE) were obtained from Solanum torvum fruit using ultrasound-assisted and Soxhlet extraction. The results revealed that Soxhlet is more efficient for obtaining SRE from Solanum torvum and that degreasing does not generate additional yields. SRE was characterized by Fourier transformed infrared spectrophotometry, thermogravimetric analysis, hydrophilic-lipophilic balance, and critical micelle concentration analyses. Bio-nanofluids based on SiO2 (strong acid), ZrO2 (acid), Al2O3 (neutral), and MgO (basic) nanoparticles and SRE were designed to evaluate the effect of the chemical nature of the nanoparticles on the SRE performance. CT-707 cell line The results show that 100 mg L-1 MgO nanoparticles improved the interfacial tension up to 57% and the capillary number increased by two orders of magnitude using this bio-nanofluid. SRE solutions enhanced with MgO recovered about 21% more than the system in the absence of nanoparticles. The addition of MgO nanoparticles did not cause a loss of injectivity. This is the first study on the surface-active properties of Solanum torvum enhanced with nanomaterials as an environmentally friendly EOR process.A Lattice Boltzmann model is proposed, combining the theories of nucleation and crystal growth for the study of the laser-induced deposition in solution (LIDS). The conjugate heat transfer and the natural convection of the liquid precursor were simulated with the evolving interface of crystal growth. In turn, the morphology of the deposited materials was affected by multiple process parameters, including conditions of chemical precursor and the laser-induced heat and mass transfer. Simulation results indicated that the morphology of deposited materials was mostly affected by the initial concentration of the precursor solution. Specifically, the nonuniformity of thin films was caused by the convection induced by the pulsed-laser, and the surface roughness was due to the competition of local structures for the precursor supply. A relationship of process-condition-material was established, providing guidance of choosing various parameters in LIDS for a desirable morphology of deposited material, facilitating the capabilities of pulsed lasers in precise control in nanomanufacturing.Colloidal quantum dots (CQDs) as photodetector materials have attracted much attention in recent years due to their tunable energy bands, low cost, and solution processability. However, their intrinsically low carrier mobility and three-dimensional (3D) confinement of charges are unsuitable for use in fast-response and highly sensitive photodetectors, hence greatly restricting their application in many fields. Currently, 3D topological insulators, such as bismuth telluride (Bi2Te3), have been employed in high-speed broadband photodetectors due to their narrow bulk bandgap, high carrier mobility, and strong light absorption. In this work, the advantages of topological insulators and CQDs were realized by developing a hybrid Bi2Te3/PbS CQDs photodetector that exhibited a maximum responsivity and detectivity of 18 A/W and 2.1 × 1011 Jones, respectively, with a rise time of 128 μs at 660 nm light illumination. The results indicate that such a photodetector has potential application in the field of fast-response and large-scale integrated optoelectronic devices.As an n-type semiconductor material, tungsten oxide (WO3) has good application prospects in the field of gas sensing. Herein, using oxalic acid (OA), citric acid (CA) and tartaric acid (TA) as auxiliary agents, three homogeneous tungsten oxide nanosheets were prepared by the rapid microwave-assisted hydrothermal method. The potential exhaled gases of various diseases were screened for the gas sensitivity test. Compared with WO3-OA and WO3-TA, WO3-CA exhibits significant sensitivity to formaldehyde, acetone and various alkanes. Photoluminescence (PL) chromatography and photoelectric properties show that its excellent gas sensitivity is due to its abundant oxygen vacancies and high surface charge migration rate, which can provide more preferential reaction sites with gas molecules. The experiment is of great significance for the sensor selection of the large disease exhaled gas sensor array.Antireflection and light-trapping coatings are important parts of photovoltaic architectures, which enable the reduction of parasitic optical losses, and therefore increase the power conversion efficiency (PCE). Here, we propose a novel approach to enhance the efficiency of perovskite solar cells using a light-trapping electrode (LTE) with non-reciprocal optical transmission, consisting of a perforated metal film covered with a densely packed array of nanospheres. Our LTE combines charge collection and light trapping, and it can replace classical transparent conducting oxides (TCOs) such as ITO or FTO, providing better optical transmission and conductivity. One of the most promising applications of our original LTE is the optimization of efficient bifacial perovskite solar cells. We demonstrate that with our LTE, the short-circuit current density and fill factor are improved for both front and back illumination of the solar cells. Thus, we observe an 11% improvement in the light absorption for the monofacial PSCs, and a 15% for the bifacial PSCs.
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