Polymerized ionic liquids (PolyILs) are promising candidates for a broad range of technologies. However, the relatively low conductivity of PolyILs at room temperature has strongly limited their applications. In this work, we provide new insights into the roles of various microscopic parameters controlling ion transport in these polymers, which are crucial for their rational design and practical applications. Using broadband dielectric spectroscopy and neutron and light scattering techniques, we found a clear connection between the activation energy for conductivity, fast dynamics, and high-frequency shear modulus in PolyILs at their glass transition temperature (Tg). In particular, our analysis reveals a correlation between conductivity and the amplitude of fast picosecond fluctuations at Tg, suggesting the possible involvement of fast dynamics in lowering the energy barrier for ion conductivity. We also demonstrate that both the activation energy for ion transport and the amplitude of the fast fluctuations depend on the high-frequency shear moduli of PolyILs, thus identifying a practically important parameter for tuning conductivity. The parameters recognized in this work and their connection to the ionic conductivity of PolyILs set the stage for a deeper understanding of the mechanism of ion transport in PolyILs in the glassy state.Polystyrene beads are often used as test particles in aerosol science. Here, a contact-less technique is reported for determining the refractive index of a solid aerosol particle as a function of wavelength and temperature (20-234 °C) simultaneously. Polystyrene beads with a diameter of 2 μm were optically trapped in air in the central orifice of a ceramic heating element, and Mie spectroscopy was used to determine the radius and refractive index (to precisions of 0.8 nm and 0.0014) of eight beads as a function of heating and cooling. Refractive index, n, as a function of wavelength, λ (0.480-0.650 μm), and temperature, T, in centigrade, was found to be n = 1.5753 - (1.7336 × 10-4)T + (9.733 × 10-3)λ-2 in the temperature range 20 less then T less then 100 °C and n = 1.5877 - (2.9739 × 10-4)T + (9.733 × 10-3)λ-2 in the temperature range 100 less then T less then 234 °C. The technique represents a step change in measuring the refractive index of materials across an extended range of temperature and wavelength in an absolute manner and with high precision.Herein, we reported a simple microwave-assisted method for synthesizing uniform CsPbBr3 and Cs4PbBr6 perovskite nanocrystals (PeNCs). The phase structure, photoluminescence (PL) emission, and quantum yield (QY) of CsPbBr3 PeNCs can be tuned by changing the radiation time and power of the microwave. The optimized CsPbBr3 PeNCs showed a high PLQY of up to 87%. The transformation from green-luminescent three-dimensional (3D) CsPbBr3 PeNCs to nonluminescent zero-dimensional (0D) Cs4PbBr6 PeNCs was easily realized by adjusting the amount of oleamine (OAm) and oleic acid (OA), and the changes in morphology and phase structure during the transformation process were studied by a microwave-assisted technique. Meanwhile, the optical properties of Cs4PbBr6 PeNCs were revealed by monitoring the changes in absorption and emission spectra.  https://www.selleckchem.com/products/Mycophenolic-acid(Mycophenolate).html  Furthermore, through first-principles calculations based on density functional theory (DFT), the luminescene origination of as-prepared PeNCs was further explained. In this work, we controlled the phase transition from CsPbBr3 to Cs4PbBr6 through a simple method, which provides a strategy for other types of perovskite phase transitions.Chemical and colloidal stability in complex aqueous media are among the main challenges preventing nanoparticles from successfully entering into the biomedical field. Small core-shell upconversion nanoparticles (UCNPs) NaYF4Yb,Er@NaYF4 of 12 nm in diameter with a high surface-to-volume ratio are utilized to demonstrate that self-assembling phospholipid bilayers (PLMs) have several benefits compared to common ligand-exchange and ligand-addition particle coatings such as poly(acrylic acid) and amphiphilic polymers. An efficient hydrophobic barrier against water quenching and toward particle disintegration is formed by PLM. Particles with this functionalization have a higher upconversion luminescence in aqueous media in contrast to common surface ligands. They attract with better colloidal stability in phosphate buffer, in a wide pH range, in high ionic solutions, and in complex cell media, as is required for biological applications. Moreover, kidney cells (NRK) are not affected by these stable PLM-coated UCNPs as first cell viability tests reveal.In vitro drug release systems have recently received tremendous attention because they allow noninvasive, convenient, and prolonged administration of pharmacological agents. On-demand epidermal drug release systems can improve treatment efficiency, prevent multidrug resistance, and minimize drug toxicity to healthy cells. In addition, real-time monitoring of drug content is also essential for guiding the determination of drug dosage and replacing drug carriers in time. Therefore, it is important to integrate the above properties in one ideal epidermal patch. Herein, photonic crystals (PCs) based on Fe3O4@C nanoparticles were introduced into drug-loaded poly(N-isopropylacrylamide-co-acrylic acid) (P(NIPAM-AAc)) hydrogel-functionalized textiles. Drug loading and release depended on the expansion and contraction of the hydrogels. The lower critical solution temperature (LCST) of the hydrogels was adjusted to 40 °C, which is higher than the skin temperature, by varying the content of hydrophilic comonomer acrylic acid (AAc) to store the drug at room temperature, and on-demand release was achieved by mild thermal stimulation. Moreover, the lattice spacing (d) of PCs varied with the expansion and contraction of the hydrogels, which can cause the color of P(NIPAM-AAc) hydrogel-functionalized textiles to change. These synchronous thermoresponsive chromic drug uptake and release behaviors provided an effective method for visual and real-time monitoring of drug content. Furthermore, in view of the poor mechanical properties of hydrogel wound dressings, textile matrices were composited to prevent holistic breaking during the stretching process. Biological experiments proved that the drug-loaded P(NIPAM-AAc) hydrogel-functionalized textiles had good antibacterial properties and wound-healing effects.