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Micron-sized alginate hydrogel beads are extensively employed as an encapsulation medium for biochemical and biomedical applications. Here we report on the microfluidic assisted fabrication of calcium alginate (Ca-alginate) beads by on-chip picoinjection of aqueous calcium chloride (CaCl2) in emulsified aqueous sodium alginate (Na-alginate) droplets or by picoinjection of Na-alginate solution in emulsified aqueous CaCl2 droplets. There is no added chelator to reduce the Ca activity in either of the two strategies. The two fabrication strategies are implemented using a flow-focusing and picoinjection modules in a single PDMS chip. Aqueous alginate solution was emulsified and infused with CaCl2 solution as the squeezed droplet pass the picoinjection channel; consequently, monodisperse, spherical, and structurally homogeneous Ca-alginate beads were obtained. check details Monodisperse alginate microgel populations with a mean diameter in the range of 8 to 28 μm and standard deviation less than 1 μm were successfully generated using microfluidic channels with various dimensions and controlling the flow parameters. Monodisperse but also non-spherical particles with diameters 6 to 15 μm were also fabricated when picoinjecting Na-alginate solution in emulsified aqueous CaCl2 droplets. The Ca-alginate microbeads fabricated with tailormade size in the range from sub-cellular and upwards were in both strategies realized without any use of chelators or change in pH conditions, which is considered a significant advantage for further exploitation as encapsulation process for improved enzymatic activity and cell viability.Photoelasticity often refers to the birefringence effect of materials induced by elastic deformation. Recently, many experiments on the photoelasticity of soft materials have been reported. However, the experimental results are mainly qualitative observations and lack any theoretical analysis. In this paper, we revisit Treloar's and Arruda's models of nonlinear photoelasticity for rubber-like materials. Both models establish the intrinsic relationship between stretch and birefringence, based on the statistics of chain polarizability and a network theory. We discuss the difference of the two models and build an experimental setup to measure the birefringence of PDMS samples as a function of stress/stretch. We vary the curing ratio of PDMS to study the effect of chain density on birefringence and compare with Treloar's theory. We further use experimental data of double-network hydrogels in the literature to compare with theory and find that when the deformation is large compared with the limiting stretch of the material, Arruda's model fits the experimental data much better than Treloar's model. 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.