Ag nanoparticles exhibit various colors depending on their localized surface plasmon resonance (LSPR). Based on this phenomenon, Ag deposition-based electrochromic devices can represent various optical states in a single device such as the three primary colors (cyan, magenta, and yellow), silver mirror, black and transparent. Bcl-2 inhibitor clinical trial A control of the morphology of Ag nanoparticles can lead to dramatic changes in color, as their size and shape influence the LSPR band. In this research, we focused on the diffusion rate of Ag+ ions when Ag nanoparticles are electrochemically deposited. Consequently, well-isolated Ag nanoparticles were obtained due to the slow growth rate by using an electrolyte with a low concentration of Ag+ ions, resulting in an improvement in the color quality of cyan and magenta. Additionally, spherical Ag nanoparticles were deposited in the same device by optimizing their voltage application conditions, which represented yellow and green colors. In particular, green coloration is a unique phenomenon because it can appear by the combination of two absorption peaks of LSPR. As a result of investigating the finite-difference time-domain method, it was observed that the LSPR band in the long wavelength region was originated from the effects of the connection between Ag particles.The charge reduction of multiply charged macromolecular ions via recombination with small ions in the gas phase is commonly employed to modulate the charge on macromolecules prior to mass spectrometric and mobility analyses. We employ a recently developed continuum-Molecular Dynamics (MD) calculation approach to determine the recombination rate coefficient of multiply charged (1 to 7 excess positive charged) polyethylene glycol ions (mass of 4600 Da) with smaller singly charged anions, modeled as NO2- ions. The continuum-MD approach accounts explicitly for the influence of the background gas on the recombination process, accounts explicitly for ion translational, vibrational, and rotational motion, and enables recombination rate coefficient calculation in nitrogen near atmospheric pressure, wherein neither low pressure nor high pressure recombination theories are strictly applicable. Continuum-MD simulations yield recombination rate coefficients near 3.9 × 10-14 m3 s-1 for singly charged ions, increasing to 3.0 × 10-11 m3 s-1 for the +7 ion. Pre-existing collision rate coefficient expressions for rigid ions are found to be within a factor of 2-5 of calculations for all charge states, but their use requires knowledge of an appropriate collision distance, which is not well-defined for flexible polymer ions. Continuum-MD-inferred rate coefficients are incorporated into a model of charge reduction, and the charge state distribution versus anion concentration determined with it is compared to charge reduction measurements made via atmospheric pressure differential mobility analysis. Good agreement is observed between simulations and experiments; although results are extremely sensitive to the recombination rate coefficients, experimental results are bound by models utilizing rates within a factor of 2 (0.5-2.0×) of the continuum-MD rates.Herein, triethoxysilane-derived SiOx is used as a robust adhesive anchor to bind Si nanoparticles (NPs) and carbon nanotubes (CNTs) to prepare a structurally reinforced Si/CNT microsphere composite. The chemical reaction between the silanol groups of triethoxysilane with the hydroxyl groups on the Si surface and acid-treated CNTs induce strong chemical bonds between the Si NPs and CNTs and among neighboring CNTs, facilitating electron-conduction pathways and structural integrity of the composite, even under severe stress/strain. Thus, the structurally reinforced Si/CNT/SiOx microsphere composite exhibits superior cyclability ∼88% of its initial capacity of 1112 mA h g-1 is retained after 100 cycles at 0.5 A g-1. Moreover, the Si/CNT/SiOx composite exhibits a negligible change in electrode thickness after 100 cycles. The stable electrochemical behavior and negligible change in the electrode thickness are attributed to the maintenance of the electron-conduction pathways and structural integrity of the Si/CNT/SiOx composite, enabled by the binding of neighboring CNTs with the SiOx anchor.A multifunctional molecular design of fluorescent discotic liquid crystal (DLC) consisting of a tetraphenylethylene core is reported, which is found to serve as an excellent solid-state emitter in OLED devices with EQE of 4.4% and tunable mechanochromism. X-ray diffraction studies unveiled that change in supramolecular self-assembly is the physical origin of mechanochromism. The luminescent DLC molecule has been shown to act as a highly selective probe for labelling acidic cellular compartments (such as lysosomes) in bio-imaging using HeLa cells.Herein, we present an approach for the analytical determination and quantification of semi-permanent hair dyes in wash water samples released during washing of dyed hair employing a liquid chromatography-tandem mass spectrometry-selected reaction monitoring (LC-MS/MS-SRM) method with electrospray ionization detection. Specifically, Basic Blue 99 (BB 99), Basic Brown 16 (BB 16), Basic Red 76 (BR 76), Basic Yellow 57 (BY 57) and Acid Violet 43 (AV 43) are hair dyes with properties known to be harmful to human health and the environment. The hair dyes are present in commercial formulation and are discharged into the effluents without fully effective treatment. The detection and quantification by the LC-MS/MS technique show a linear relationship for each studied hair dye in the concentration range from 1 to 200 ng mL-1 in aqueous solution. The limits of detection and quantification were found from 0.66 to 20 ng mL-1 and from 2.0 to 63 ng mL-1, respectively, values that are compatible with the level required in wash water analysis. The method was applied in samples collected from 5 successive washings of hair dyed with a commercial formulation using the established procedure. BB 99 and BY 57 dyes have lower fixation on the scalp and hair, showing 866 ng mL-1 and 145 ng mL-1 release on the first day of washing, respectively. The accumulation of dye and slow release after washing can lead to future problems for both the environment and living organisms.