Trilayer Composite System Based on SiO2, Thiol-Ene, and PEDOT:PSS. Focus on Stability after Thermal Treatment and Solar Irradiance

The trilayer composite was fabricated by combining functional layers of fumed SiO2, thiol-ene, and poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) (PEDOT-PSS). Optical, scratch-healing, non-wetting, and electrical stability was investigated at different instances of time after thermal and solar irradiance treatment. The trilayer composite was found to be optically stable and highly transparent for visible light after thermal and irradiance treatment for 25 h. Both treatment processes had a minor effect on the shape-memory assisted scratch-healing performance of the trilayer composite. Thermal treatment and solar irradiance did not affect the superhydrophobic properties (contact angle 170 ± 1°) of the trilayer composite. The sheet resistance increased from 90 ± 3 Ω/square (initial) to 109 ± 3 Ω/square (thermal) and 149 ± 3 Ω/square (irradiance) after 25 h of treatment, which was considered as not significant change.

Determination of Two Differently Manufactured Silicon Dioxide Nanoparticles by Cloud Point Extraction Approach in Intestinal Cells, Intestinal Barriers and Tissues

Food additive amorphous silicon dioxide (SiO2) particles are manufactured by two different methods—precipitated and fumed procedures—which can induce different physicochemical properties and biological fates. In this study, precipitated and fumed SiO2 particles were characterized in terms of constituent particle size, hydrodynamic diameter, zeta potential, surface area, and solubility. Their fates in intestinal cells, intestinal barriers, and tissues after oral administration in rats were determined by optimizing Triton X-114-based cloud point extraction (CPE). The results demonstrate that the constituent particle sizes of precipitated and fumed SiO2 particles were similar, but their aggregate states differed from biofluid types, which also affect dissolution properties. Significantly higher cellular uptake, intestinal transport amount, and tissue accumulation of precipitated SiO2 than of fumed SiO2 was found. The intracellular fates of both types of particles in intestinal cells were primarily particle forms, but slowly decomposed into ions during intestinal transport and after distribution in the liver, and completely dissolved in the bloodstream and kidneys. These findings will provide crucial information for understanding and predicting the potential toxicity of food additive SiO2 after oral intake.

A facile preparation of PEO–LiClO4–fumed SiO2 composite solid-state electrolyte with improved electrochemical performance for lithium-metal batteries

PEO–LiClO4–fumed SiO2 composite solid-state electrolyte is successfully fabricated with superior 3 migration capacity to Li+ and improved electrochemical performance for lithium-metal battery by a 4 facile preparation process.

Fumed SiO2-H2SO4-PVA Gel Electrolyte CO Electrochemical Gas Sensor

The conventional CO electrochemical gas sensor uses aqueous H2SO4 solution as electrolyte, with inevitable problems, such as the drying and leakage of electrolyte. Thus, research on new alternative electrolytes is an attractive field in electrochemical gas sensors. In this paper, the application of a new fumed SiO2 gel electrolyte was studied in electrochemical gas sensors. The effects of fumed SiO2 and H2SO4 contents on the performance of the CO gas sensor were investigated. The results showed that the optimized composition of the SiO2 gel electrolyte was 4.8% SiO2, 38% H2SO4, and 0.005% polyvinyl alcohol (PVA). Compared with aqueous H2SO4, the gel electrolyte had better water retention ability. The signal current of the sensor was proportional to the CO concentration. The sensitivity to CO was 78.6 nA/ppm, and the response and recovery times were 31 and 38 s, respectively. The detection limit was 2 ppm. The linear range was from 2 to 500 ppm. The gel electrolyte CO sensor possesses equivalent performance to that with aqueous electrolyte.

SiO2-Based Nanostructured Superhydrophobic Film with High Optical Transmittance

Superhydrophobic and transparent films would be very useful in optoelectronic applications where non-wetting is desired. Herein, hexamethyldisilazane was used for functionalization of fumed SiO2 nanoparticles via silylation derivatization reaction. Modified fumed SiO2 nanoparticle dispersion was used for fabrication of SiO2-based nanostructured film via drop-casting method. This film exhibited a combination of high optical transmittance in the visible spectrum portion and superhydrophobicity (163° ± 1° and hysteresis as low as ~2°). This was possible to achieve due to the submicrometer-scale roughness (Rq = 252.7 nm) and branched network structure of the film surface with convenient surface chemistry of hydrophobic methyl groups. The method reported herein is not complicated, allows for obtaining large quantities of modified SiO2 nanoparticle dispersions and can be used in combination with other deposition methods.

Highly Dispersed Co Nanoparticles Prepared by an Improved Method for Plasma-Driven NH3 Decomposition to Produce H2

Previous studies reveal that combining non-thermal plasma with cheap metal catalysts achieved a significant synergy of enhancing performance of NH3 decomposition, and this synergy strongly depended on the properties of the catalyst used. In this study, techniques of vacuum-freeze drying and plasma calcination were employed to improve the conventional preparation method of catalyst, aiming to enhance the activity of plasma-catalytic NH3 decomposition. Compared with the activity of the catalyst prepared by a conventional method, the conversion of NH3 significantly increased by 47% when Co/fumed SiO2 was prepared by the improved method, and the energy efficiency of H2 production increased from 2.3 to 5.7 mol(kW·h)−1 as well. So far, the highest energy efficiency of H2 formation of 15.9 mol(kW·h)−1 was achieved on improved prepared Co/fumed SiO2 with 98.0% ammonia conversion at the optimal conditions. The improved preparation method enables cobalt species to be highly dispersed on fumed SiO2 support, which creates more active sites. Besides, interaction of Co with fumed SiO2 and acidity of the catalyst were strengthened according to results of H2-TPR and NH3-probe experiments, respectively. These results demonstrate that employing vacuum-freeze drying and plasma calcination during catalyst preparation is an effective approach to manipulate the properties of catalyst, and enables the catalyst to display high activity towards plasma-catalytic NH3 decomposition to produce H2.