This work presents a basis of using the theory of nonlinear photoelasticity to guide the analysis of experiments.We introduce a facile method to generate aggregation-induced emission (AIE) properties in fused-ring electron acceptors through tetraphenylethylene decoration. Organic solar cells (OSCs) based on the AIE photovoltaic materials show decreased nonradiative energy loss during the energy conversion progress, with improvements in the open circuit voltage and device efficiency.Common in myopia and aging, vitreous opacities arise from clumped collagen fibers within the vitreous body that cast shadows on the retina, appearing as 'floaters’ to the patient. Vitreous opacities degrade contrast sensitivity function and can cause significant impairment in vision-related quality-of-life, representing an unmet and underestimated medical need. One therapeutic approach could be the use of versatile light-responsive nanostructures which (i) interfere with the formation of collagen fibers and/or (ii) destroy aggregates of vitreous collagen upon pulsed-laser irradiation at low fluences. In this work, the potential of positively and negatively charged carbon quantum dots (CQDs) to interfere with the aggregation of type I collagen is investigated. We demonstrate that fibrillation of collagen I is prevented most strongly by positively charged CQDs (CQDs-2) and that pulsed-laser illumination allowed to destroy type I collagen aggregates and vitreous opacities (as obtained from patients after vitrectomy) treated with CQDs-2.Herein, we describe the nonlinear processes for the formation of thin films of the PbS-CdS system using chemical bath deposition with a gradual change in the cadmium nitrate content in the reaction mixture. The morphology of films was studied via scanning electron microscopy and atomic force microscopy. The mechanism for the formation of thin-film compounds can be considered as cluster-particle aggregation (diffusion-limited aggregation). X-ray diffraction confirmed the formation of single-phase layers of substitutional B1-type CdxPb1-xS solid solutions (space group Fm3[combining macron]m) when the concentration of cadmium nitrate in the reaction bath increased up to [Cd(NO3)2] = 0.08 M. The maximum cadmium content in CdxPb1-xS solid solutions was determined to be x = 0.094. At the concentration of [Cd(NO3)2] = 0.10 M, a two-phase film was formed, where the film consisted of crystallites of cubic CdxPb1-xS with x = 0.071 (lower compared to the film obtained at [Cd(NO3)2] = 0.08 M) and fine-crystalline hexagon eV, whereas at the critical cadmium salt concentration (0.10 M), two crystalline phases with Eg equal to 0.73 and 2.47 eV were observed.Tris(dimethylsilyl)amine (TDMSA) is used in the presence of O2 and NH3 for the atmospheric pressure chemical vapor deposition (CVD) of conformal, corrosion barrier silicon oxynitride (SiOxNy) films at moderate temperature. Plausible decomposition pathways taking place during the process, as well as resulting gas-phase by-products, are investigated by an innovative methodology, coupling solid-state films characteristics with gas phase analysis. Liquid NMR, gas chromatography coupled with mass spectrometry (GC-MS) and electron spin resonance (ESR) allow probing stable compounds and radical intermediate species in the gas phase. At least fifteen by-products are identified, including silanols, siloxanes, disilazanes, silanamines, and mixed siloxane-silanamine molecules, in addition to more usual compounds such as water. The radical dimethylsilane, Me2HSi˙, is noted across all experiments, hinting at the decomposition of the TDMSA precursor. Deposition of SiOxNy films occurs even in the absence of NH3, demonstrating the judicious choice of the silanamine TDMSA as a dual source of nitrogen and silicon. Additionally, the presence of Si-H bonds in the precursor structure allows formation of SiOxNy films at temperatures lower than those required by other conventional silazane/silanamine precursors. Addition of NH3 in the inlet gas supply results in lower carbon impurities in the films. The identified by-products and formulated decomposition and gas-phase reactions provide stimulating insight and understanding of the deposition mechanism of SiOxNy films by CVD, offering possibilities for the investigation of representative chemical models and process simulation.Aqueous glycerol was used in this study as a liquid-phase hydrogen source for the hydrogenation of CO2. It was found that hydrogen could be efficiently evolved from aqueous glycerol upon highly dispersed Ru on layered double hydroxide (LDH), inducing the transformation of CO2 into formaldehyde under base-free conditions at low temperature.Hexagonal boron nitride (h-BN) nanostructures are well-known for their good chemical stability, thermal conductivity and high elastic modulus. BN can be used as a filler in hydrogels to significantly improve their mechanical and thermal properties, to reinforce their biocompatibility and to provide self-healing capacity. Moreover, in contrast with their carbon equivalents, BN nanocomposites are transparent and electrically insulating. Herein, we present an overview of BN-based nanocomposite hydrogels. First, the properties of h-BN are described, as well as common exfoliation and functionalization techniques employed to obtain BN nanosheets. Then, methods for preparing BN-nanocomposite hydrogels are explained, followed by a specific overview of the relationship between the composition and structure of the nanocomposites and the functional properties. Finally, the main properties of these materials are discussed in view of the thermal, mechanical, and self-healing properties, along with the potential applications in tissue engineering, thermal management, drug delivery and water treatment.Designing devices with excellent spin-polarized properties has been a challenge in physics and materials science. In this work, we report a theoretical investigation of the spin injection and spin-polarized transport properties of monolayer and bilayer phosphorene devices with Co electrodes. Based on the analysis of transmission coefficients, spin-polarized current, magnetoresistance (MR) (or tunnel MR) ratio and spin injection efficiency (SIE), both devices show superior spin-polarized transport properties. As phosphorene in the device is changed from monolayer to bilayer, the charge carrier type can be tuned from n-type to p-type. For the monolayer phosphorene device, the tunnel MR ratio reaches about 210% and the SIE is about 80.7% at zero bias. Notably, the SIE and tunnel MR ratio maintain almost constant values against bias voltage and gate voltage, which makes it suitable for magnetic sensors. As for the bilayer phosphorene device, it not only exhibits a considerable tunnel MR ratio, but also shows significantly enhanced conductance, beneficial to the sensitivity of spintronic devices. Further analysis shows that the improvement of conductance is attributed to the low barrier height between the bilayer phosphorene channel and Co electrodes. According to our results, the studied phosphorene devices with Co electrodes demonstrate superior spin injection and transport properties. We believe that these theoretical findings will be a strong asset for future experimental works in spintronics.The heterogeneous gold(i)-catalyzed oxidative ring expansion of alkynyl quinols has been achieved by using a benzyldiphenylphosphine-modified MCM-41-immobilized gold(i) complex [MCM-41-BnPh2P-AuNTf2] as the catalyst and 8-methylquinoline N-oxide as the oxidant under mild reaction conditions, yielding a variety of functionalized tropone derivatives in good to excellent yields. Extension of this methodology allows for facile construction of other seven- or six-membered ring systems including dibenzotropones, dibenzooxepines, phenanthrenes, and quinolin-2(1H)-ones. This new heterogeneous gold(i) complex can be readily recovered through a simple filtration process and recycled at least eight times without any apparent decrease in catalytic efficiency.The well-developed design strategy of molecular modification for assembling molecular ferroelectrics mainly focuses on the cations. Herein, by homochiral anionic modification of the non-ferroelectric (quinuclidinium)(HSO4), we designed high-temperature multiaxial organic enantiomeric ferroelectrics, (quinuclidinium)(l- and d-camphorsulfonate). This work paves a new road for precisely constructing excellent molecular ferroelectrics.It is currently technologically important to predict new two-dimensional (2D) ferromagnetic materials for next-generation information storage media. However, discovered 2D ferromagnetic materials are still rare. Here, we explored the fact that 2D transition metal borides are potential room-temperature 2D ferromagnetic materials. By performing first-principles calculations, we found that the CrB monolayer is a ferromagnetic (FM) metal, while the FeB monolayer is a typically antiferromagnetic (AFM) semiconductor. Interestingly, both CrB and FeB monolayers are FM metals with a moderate magnetic anisotropy energy by saturating with functional groups. Monte Carlo simulations show that the Curie temperature (Tc) of the CrB monolayer is about 520 K, which is further increased to 580 K and 570 K through -F and -OH chemical modification, while Tc is about 250 K, 275 K and 300 K for the FeBF, FeBO and FeBOH monolayer, respectively. Thus, the 2D transition metal borides have great potential applications in information storage devices.Ligand-protected metal nanoclusters controlled by atomic accuracy (i. e. atomically precise metal NCs) have recently attracted considerable attention as active sites in heterogeneous catalysts. Using these atomically precise metal NCs, it becomes possible to create novel heterogeneous catalysts based on a size-specific electronic/geometrical structure of metal NCs and understand the mechanism of the catalytic reaction easily. However, to create high-performance heterogeneous catalysts using atomically precise metal NCs, it is often necessary to remove the ligands from the metal NCs. This review summarizes previous studies on the creation of heterogeneous catalysts using atomically precise metal NCs while focusing on the calcination as a ligand-elimination method. Through this summary, we intend to share state-of-art techniques and knowledge on (1) experimental conditions suitable for creating high-performance heterogeneous catalysts (e.g., support type, metal NC type, ligand type, and calcination temperature), (2) the mechanism of calcination, and (3) the mechanism of catalytic reaction over the created heterogeneous catalyst. We also discuss (4) issues that should be addressed in the future toward the creation of high-performance heterogeneous catalysts using atomically precise metal NCs. The knowledge and issues described in this review are expected to lead to clear design guidelines for the creation of novel heterogeneous catalysts.Dee are a unique and rapidly growing part of the global snack food market and are recognised as having distinct sensory properties (taste and texture). In this study, the development of important volatile aroma compounds over storage was evaluated and their chemical origin explained. Sweet potatoes were batch fried in high oleic sunflower oil (HOSO) and subjected to accelerated shelf life testing. Headspace volatiles were analysed using SPME GC-MS and correlated with sensory perception. All the components (sweet potatoes, oil and β-carotene) showed significant degradation after 3 weeks of storage at accelerated conditions (equivalent to 12 weeks in real-time at 25 °C). Marker volatiles associated with lipid oxidation such as hexanal, octanal, pentanal were identified, in addition to norisoprenoids from β-carotene degradation such as β-ionon, 5,6-epoxy-β-ionone, dihydroactinidiolide (DHA) and β-cyclocitral. The most prominent marker of lipid oxidation (hexanal) rapidly increased at week 1, whereas the carotene degradation makers did not rapidly increase until week 3 suggesting a delayed response.