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The high rate performance of a battery requires the anode to be conductive not just ionically but also electronically. This criterion has significantly stimulated the study on 3D porous topological metals composed of nonmetal atoms with a light mass. BTK inhibitor chemical structure Many carbon-based 3D topological metals for batteries have been reported, while similar work for 3D boron remains missing. Here, we report the first study of a 3D boron topological metal as an anode material for Li or Na ions. Based on systematic calculations, we found that the reported 3D topological metal H-boron composed of B4 cluster shows a low mass density (0.91 g/cm3) with multiple adsorption sites for Li and Na ions due to the electron-deficient feature of boron, leading to an ultrahigh specific capacity of 930 mAh/g for Li and Na ions with a small migration barrier of 0.15 and 0.22 eV, respectively, and small volume changes of 0.6% and 9.8%. These intriguing features demonstrate that B-based 3D topological quantum porous materials are worthy of further study for batteries.We developed a new transition-metal-free intermolecular Claisen rearrangement process to introduce allyl and allenyl groups into the α position of tertiary amides. In this transformation, amides were activated by trifluoromethanesulfonic anhydride to produce the keteniminium ion intermediates that exhibit strong electrophilic activity. This atom-economical process delivers α position-modified amides under mild conditions in moderate to good yields and showcases a broad substrate compatibility.This first asymmetric total synthesis of (+)-srilankenyne (1), a halogenated C15 tetrahydropyran acetogenin isolated from Aplysia oculifera, features a sequence-sensitive process guided by conformational analysis to solve the challenging problem of introducing halogens. A competing semipinacol rearrangement during the installation of C(12)-bromide was suppressed by our A1,3 strain-controlled bromination protocol with support from X-ray crystallographic and computational studies. The C(10)-chloride was then placed by the Nakata chloromesylate-mediated chlorination.Liquid evaporation and the associated vapor transport in micro/nanopores are ubiquitous in nature and play an important role in industrial applications. Accurate modeling of the liquid evaporation process in nanopores is critical to achieving a better design of devices for enhanced evaporation. Although having high impact on evaporation rate, vapor transport resistance in micro/nanopores remains incompletely understood. In this study, we proposed a new model which, for the first time, considered vapor transport in finite-length pores under various Knudsen regimes and then coupled the transport resistance to liquid evaporation. Direct Simulation Monte Carlo and laboratory experiments were conducted to provide validation for our model. The model successfully predicts the variation of pore transmissivity with Knudsen number and nanopore size, which cannot be revealed by prior theories. The relative error of model-predicted evaporation rate was within 1% in L/r = 0 cases and within 3.5% in L/r > 0 cases. Our model is featured by its applicability under the entire range of Knudsen numbers. The evaporation of various types of liquids in arbitrarily sized pores can be modeled using a universal relation.Thiol ligands bound to the metallic core of nanoparticles determine their interactions with the environment and self-assembly. Recent studies suggest that equilibrium between bound and free thiols alters the ligand coverage of the core. Here, X-ray scattering and MD simulations investigate water-supported monolayers of gold-core nanoparticles as a function of the core-ligand coverage that is varied in experiments by adjusting the concentration of total thiols (sum of free and bound thiols). Simulations demonstrate that the presence of free thiols produces a nearly symmetrical coating of ligands on the core. X-ray measurements show that above a critical value of core-ligand coverage the nanoparticle core rises above the water surface, the edge-to-edge distance between neighboring nanoparticles increases, and the nanoparticle coverage of the surface decreases. These results demonstrate the important role of free thiols they regulate the organization of bound thiols on the core and the interactions of nanoparticles with their surroundings.Lanthanide-doped nanoparticles have great potential for energy conversion applications, as their optical properties can be precisely controlled by varying the doping composition, concentration, and surface structures, as well as through plasmonic coupling. In this Perspective we highlight recent advances in upconversion emission modulation enabled by coupling upconversion nanoparticles with well-defined plasmonic nanostructures. We emphasize fundamental understanding of luminescence enhancement, monochromatic emission amplification, lifetime tuning, and polarization control at nanoscale. The interplay between localized surface plasmons and absorbed photons at the plasmonic metal-lanthanide interface substantially enriches the interpretation of plasmon-coupled nonlinear photophysical processes. These studies will enable novel functional nanomaterials or nanostructures to be designed for a multitude of technological applications, including biomedicine, lasing, optogenetics, super-resolution imaging, photovoltaics, and photocatalysis.In this work, the effects of polarization of confining charged planar dielectric surfaces on induced electroosmotic flow are investigated. To this end, we use dissipative particle dynamics to model solvent and ionic particles together with a modified Ewald sum method to model electrostatic interactions and surfaces polarization. A relevant difference between counterions number density profiles, velocity profiles, and volumetric flow rates obtained with and without surface polarization for moderate and high electrostatic coupling parameters is observed. For low coupling parameters, the effect is negligible. An increase of almost 500% in volumetric flow rate for moderate/high electrostatic coupling and surface separation is found when polarizable surfaces are considered. The most important result is that the increase in electrostatic coupling substantially increases the electroosmotic flow in all studied range of separations when the dielectric constant of electrolytes is much higher than the dielectric constant of confining walls.
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