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Due to growing concerns about environmental pollution from plastic waste, plastic recycling research is gaining momentum. Traditional methods, such as incorporating inorganic particles, increasing cross-linking density with peroxides, and blending with silicone monomers, often improve mechanical properties but reduce flexibility for specific performance requirements. This study focuses on synthesizing silica nanoparticles with vinyl functional groups and evaluating their mechanical performance when used in recycled plastics. Silica precursors, namely sodium silicate and vinyltrimethoxysilane (VTMS), combined with a surfactant, were employed to create pores, increasing silica's surface area. The early-stage introduction of vinyl functional groups prevented the typical post-synthesis reduction in surface area. Porous silica was produced in varying quantities of VTMS, and the synthesized porous silica nanomaterials were incorporated into recycled polyethylene to induce cross-linking. Despite a decrease in surface area with increasing VTMS content, a significant surface area of 883 m2/g was achieved. In conclusion, porous silica with the right amount of vinyl content exhibited improved mechanical performance, including increased tensile strength, compared to conventional porous silica. This study shows that synthesized porous silica with integrated vinyl functional groups effectively enhances the performance of recycled plastics. [ABSTRACT FROM AUTHOR]

The biodegradable electronics are on the rise, not just due to their role in medical implants, but also because of their eco‐friendly attributes. A variety of methods, including transfer printing, have been employed to integrate inorganic electronics onto biodegradable polymer substrates. However, the use of expensive materials, multiple intermediary steps, and labor‐intensive procedures can undermine their environment‐friendly benefits. Here, a straightforward yet efficient fabrication method is introduced for creating high‐performance biodegradable electronic devices. This method leverages the controlled adhesion between the biodegradable device and substrate using self‐assembled monolayers of octadecyltrichlorosilane. Mechanical and thermal analyses based on scratch tests and time‐domain thermoreflectance quantify the adhesion by adjusting the packing density of octadecyltrichlorosilane. Controlled adhesion allows the photolithography process without delamination while facilitating easy delamination during transfer printing. The authors demonstrate the direct fabrication of electronics consisted of inorganic materials (Mg, Zn, SiO2, Si nanomembrane) on wafers and transfer‐printing onto polymer substrates via a single transfer step. This streamlined approach enables wafer‐scale fabrication of biodegradable electronics, highlighting its potential for mass manufacturing. Pilot conceptual demonstration of mass‐produced edible hydration sensors and their application in salivation measurement through in vivo model show the potential capability of proposed fabrication method in the use of practical level. [ABSTRACT FROM AUTHOR]

Double buffer layers composed of (AlxGa1−x)2O3/Ga2O3 structures were employed to grow a Sn-doped α-Ga2O3 epitaxial thin film on a sapphire substrate using mist chemical vapor deposition. The insertion of double buffer layers improved the crystal quality of the upper-grown Sn-doped α-Ga2O3 thin films by blocking dislocation generated by the substrates. Rapid thermal annealing was conducted for the double buffer layers at phase transition temperatures of 700–800 °C. The slight mixing of κ and β phases further improved the crystallinity of the grown Sn-Ga2O3 thin film through local lateral overgrowth. The electron mobility of the Sn-Ga2O3 thin films was also significantly improved due to the smoothened interface and the diffusion of Al. Therefore, rapid thermal annealing with the double buffer layer proved advantageous in achieving strong electrical properties for Ga2O3 semiconductor devices within a shorter processing time. [ABSTRACT FROM AUTHOR]

To adsorb and remove formaldehyde, which is a harmful volatile organic chemical (VOC) detected indoors, an alkylamine was introduced into the substrate as a formaldehyde adsorbent. In this study, Tetraethylenepentaamine (TEPA) was introduced into the mesoporous silica using the amine impregnation method. Since the impregnated alkylamine can block the pores of the silica substrate, the pore size and pore volume are very important factors for its use as a substrate for an adsorbent. Focusing on the substrate's pore properties, Santa Barbara Amorphous-15 (SBA-15) was chosen as a conventional one-dimensional pore-structured mesoporous silica, and dendritic mesoporous silica (DMS) as a three-dimensional pore-structured mesoporous silica. To 1 g each of silica substrate DMS and SBA-15, 0, 0.5, 1.5, and 2.5 g of TEPA were introduced. A fixed concentration and amount of formaldehyde gas was flowed through the adsorbent and then the adsorbent was changed to the 2,4-Dinitrophenylhydrazine (2,4-DNPH) cartridge to adsorb the remaining formaldehyde. According to the methods recommended by the World Health Organization (WHO) and National Institute for Occupational Safety & Health (NIOSH), the formaldehyde captured by 2,4-DNPH was analyzed using high-performance liquid chromatography (HPLC). A comparison of DMS and SBA-15 in the amine impregnation method shows that not only surface area, but also large pore size and high pore volume, contribute to the formaldehyde adsorption ability. [ABSTRACT FROM AUTHOR]

Previous research has shown that the majority of 8-year-old children share valuable resources equally with others, whereas 4-year-olds are more likely to favor themselves in their sharing allocations. In this study, we examine whether these patterns of sharing behavior are affected by the needs of the recipient or by the recipient's previous moral or immoral actions. One-hundred and sixty 4- and 8-year-old children had the opportunity to share stickers with hypothetical recipients who were assigned varying characteristics. For both age groups, sharing increased when recipients were needy (i.e., feels sad or has few toys) and morally deserving (i.e., shares with other children and does not push). The differentiation of sharing based on recipient characteristics increased between 4 and 8 years of age, with 8-year-olds also demonstrating decreased sharing when recipients were morally undeserving (i.e., pushes other children and does not share). Our findings provide evidence that children show increased sharing with recipients who are morally deserving and those who demonstrate need. This suggests that children indirectly reciprocate others' past moral behavior and behave more altruistically towards those with higher need.