A SiO nanoparticle decorated polypropylene (PP) separator (PP-SiO) has been prepared by simply immersing the PP separator in the hydrolysis solution of tetraethyl orthosilicate (TEOS) with the assistance of Tween-80. After decoration, the thermal stability and the electrolyte wettability of the PP-SiO separator are obviously improved. When the PP-SiO separator is used for lithium-sulfur (Li-S) batteries, the cyclic stability and rate capability of the batteries are greatly enhanced. The capacity retention ratio of the Li-S battery configured with the PP-SiO separator is 64% after 200 cycles at 0.2 C, which is much higher than that configured with the PP separator (45%). Moreover, the rate capacity of the Li-S batteries using the PP-SiO separator reaches 956.3, 691.5, 621, and 567.6 mAh g at the current density of 0.2, 0.5, 1, and 2 C, respectively. The reason could be ascribed to that the polar silica coating not only alleviates the shuttle effect but also facilitates Li-ion migration.

No abstract

Herein, we reported the fabrication of conjugated microporous polymer (CMP) films based on three thiophene derivatives using a one-step templateless electropolymerization in dichloromethane without any surfactants. The formation of hydrophilic or hydrophobic films with specific morphology is a comprehensive result of the polymerization sites in each monomer, the polymerization rate, and the gas bubble produced in situ during the polymerization process, which can be easily controlled by the experimental conditions, such as electropolymerization method, electrolyte, and "trace water" existed in the organic solvent. Moreover, the electrochemical reduction of metronidazole as a prototypical nitro-analyte at CMP-modified glassy carbon (GC) electrode shows remarkably increased current response compared to nonmodified GC electrode. The process is demonstrated to be typical adsorption-controlled, and the hydrophobic surface of the electrode coating film is more favorable to the absorption and thus reduction of metronidazole. This work provides a new perspective and a breakthrough point for the application of CMPs in the electrochemical sensors.

Single-emulsion toluene oil droplets (femtoliter) containing a hydrophobic redox probe that are dispersed in water stochastically collide with an ultramicroelectrode (UME). The fast-scan cyclic voltammetry (FSCV) or Fourier-transformed sinusoidal voltammetry (FTSV) is applied: the UME was scanned with a fast, repetitive triangular, or sinusoidal potential, and its current in time/frequency domains were monitored. The electron transfer at the UME/oil interface is coupled with ion transfer at the oil/water interface. Thus, the obtained transient voltammograms of a myriad of ions were used to estimate thermodynamics of ion transfer at the toluene/water interface. Additionally, the single-droplet voltammogram combined with finite element simulations reveal the droplet's size and shape distributions. Four collision mechanisms with new physical insights were also uncovered via comprehensive analysis of phase angle in the frequency domain, time domain FSCVs, and finite element simulations.

No abstract