Activity

248 W*m-1*K-1 for 2.5 wt% addition of PANI. The key factor is that the stability of the sample is improved for MoS2/ PANI nanocomposites than pristine MoS2. Our work paved a new approach to improve TE performance by preparing TE MoS2 material through simple chemical route.This work presents solution- and solid-state evidence of the enhancement of J-like aggregation of a cationic polythiophene (CPT) with isothiouronium functionalities (PT1), caused by a decrease in the polarity and hydrogen-bonding (H-bonding) capacity of the solvent, generated by using a 5050 v/v 1,4-dioxane-water mixture (W-DI) instead of water. In solution, the presence of 1,4-dioxane (DI) seems to generate selective solvation, tuning the energy transfer within PT1 from inter-chain into intra-chain, enhancing J-like aggregation. On the other hand, during the casting process, the presence of DI directs the interaction with solid-substrates, generating an increase in the solid-state fluorescence, modifying the morphology from one similar to ballistic-aggregation (BA) into one similar to attachment limited aggregation (ALA), DI also modifies the SFE by increasing slightly its polar contribution (γSp) and decreasing the dispersive one (γSd). These results can be explained to be caused by a “coating” effect in prsly.

Effective interactions of thermoresponsive microgels are known to be influenced by their volume phase transition. These soft colloids behave as repulsive spheres in the swollen state but show strong attraction in the collapsed state. We hypothesize that this transition in microgel interactions is governed by the interplay between surface tension and bulk elasticity.

Using dissipative particle dynamics, we modeled the interactions between two coarse-grained microgel particles having a lower critical solution temperature around 32°C, which are suspended in an explicit solvent. GSK923295 supplier of mean force between microgels with different crosslinking densities were systematically characterized in the temperature range of 12-58°C across the volume phase transition from steered molecular dynamics simulation trajectories.

The detailed dynamics of interaction is uncovered for microgels in different states. The simulations reveal the formation of capillary bridges between collapsed microgels at high temperaturmicrogels.Highly active electrocatalysts for electrochemical oxygen reduction reaction (ORR) were prepared by high-temperature pyrolysis from 5-methylresorcinol, Co and/or Fe salts and dicyandiamide, which acts simultaneously as a precursor for reactive carbonitride template and a nitrogen source. The electrocatalytic activity of the catalysts for ORR in alkaline solution was studied using the rotating disc electrode (RDE) method. The bimetallic catalyst containing iron and cobalt (FeCoNC-at) showed excellent stability and remarkable ORR performance, comparable to that of commercial Pt/C (20 wt%). The superior activity was attributed to high surface metal and nitrogen contents. The FeCoNC-at catalyst was further tested in anion exchange membrane fuel cell (AEMFC) with poly-(hexamethyl-p-terphenylbenzimidazolium) (HMT-PMBI) membrane, where a high value of peak power density (Pmax = 415 mW cm-2) was achieved.Insightful understanding of size-dependent optical signatures and precise regularity of nanosensors is critical for developing applications of plasmonic sensing. This work presents a systematic study on localized surface plasmon resonance (LSPR)-based nanosensors of plasmonic silver nanocubes (AgNCs) with the edge lengths of 59.84 ± 7.97 nm (no. 1 AgNCs), 75.70 ± 9.05 nm (no. 2 AgNCs) and 110.32 ± 14.63 nm (no. 3 AgNCs), respectively. The effects of different sizes on the scattering signatures and refractive index (RI) sensitivities of AgNCs were in situ determined using the multi-model co-localization approach of single AgNC by dark-field microscope (DFM), LSPR spectroscopy and scanning electron microscopy (SEM). The scattering light colour of single AgNC took place bathochromic shift from monocolour to multicolour with the growth of edge length of single AgNC. The LSPR scattering spectra of no. 1 and 2 AgNCs exhibited singlet and singlet with the shoulder peak from quadrupolar resonance mode, respectively. Compared with the scattering signatures of no. 1 and 2 AgNCs, the interesting LSPR effect of plasmon line shape with two distinct peaks was observed on single no. 3 AgNC. In situ studies on the scattering spectral response of single AgNC to the ambient solvents and probing the small-molecule adsorbates on the surface of single silver nanocube reveal that no. 2 AgNC is more suitable as nanosensor due to strong regularity and higher sensitivity. The mechanism involved in optical signatures was elaborated clearly by combining with the experiments and theoretical simulation.Although the theoretical energy density of lithium-oxygen batteries is extremely high, pulverization of lithium metal anode obviously influences batteries cycling performance. In this work, the cathode was coated with a membrane to protect the lithium anode from moisture attacking and avoid the pulverization. The membrane is composed of polyethylene oxide and poly tetra fluoroethylene, which improves the cycle life of the lithium-oxygen batteries cycles to 230 times, with a limited specific capacity of 1000 mAh·g-1, at a current density of 100 mA·g-1. Furthermore, the batteries perform stable charge and discharge cycles for 55 times in the air atmosphere, with the relative humidity greater than 50%. #link# It demonstrates this strategy provides a new direction for the development of high-performance lithium-oxygen batteries.In this work, we present the process to provide anodic alumina nanotubes with magnetic responsivity based on magnetic nanoparticles. We demonstrate the possibility to cause the motion of these composite nanotubes under magnetic field, providing them with guided mobility. The obtained magnetic anodic alumina nanotubes are completely characterized and their potential to undergo selective and effective functionalization, and stimuli-responsive load release is demonstrated. For this purpose, protease-triggered release of fluorescent molecules loaded inside the magnetic anodic alumina nanotubes (MAANTs) by selective functionalization is performed. The inner walls of the MAANTs were selectively covered with protein padding of albumin-fluorescein isothiocyanate conjugate (FITC-BSA) through means of silanization. Protein functionalization was designed to undergo proteolytic hydrolysis in presence of cathepsin B- protease highly expressed during growth and initial stages of tumor metastasis – in order to cleave peptide bond of albumin and release fluorescent fragments of the protein.