Jianmin Gu

Controllable synthesis of nickel bicarbonate nanocrystals with high homogeneity for a high-performance supercapacitor

The electrochemical performance of supercapacitors might be associated with the homogeneous structure of the electrode materials. However, the relationship between the degree of uniformity for the electrode materials and the electrochemical performance of the supercapacitor is not clear. Herein, we synthesize two types of nickel bicarbonate nanocrystals with different degrees of uniformity to investigate this relationship. As the electroactive material, the nickel bicarbonate nanocrystals with a homogeneous structure could provide a larger space and offer more exposed atoms for the electrochemical reaction than the nanocrystals with a heterogeneous structure. The homogeneous nickel bicarbonate nanocrystals exhibit better electrochemical performance and show excellent specific capacitance (1596 F g-1 at 2 A g-1 and 1260 F g-1 at 30 A g-1), which is approximately twice that of the heterogeneous nickel bicarbonate nanocrystals. The cycling stability for the homogeneity (∼80%) is higher than the inhomogeneity (∼61%) at a high current density of 5 A g-1.

Controlled Self-Assembly of Low-Dimensional Alq3 Nanostructures from 1D Nanowires to 2D Plates via Intermolecular Interactions

Due to the intense influence of the shape and size of the photon building blocks on the limitation and guidance of optical waves, an important strategy is the fabrication of different structures. Herein, organic semiconductor tris-(8-hydroxyquinoline)aluminium (Alq3) nanostructures with controllable morphology, ranging from one-dimensional nanowires to two-dimensional plates, have been prepared through altering intermolecular interactions with employing the anti-solvent diffusion cooperate with solvent-volatilization induced self-assembly method. The morphologies of the formed nanostructures, which are closely related to the stacking modes of the molecules, can be exactly controlled by altering the polarity of anti-solvents that can influence various intermolecular interactions. The synthesis strategy reported here can potentially be extended to other functional organic nanomaterials.Graphical Abstract

Homoleptic cyclometalated iridium(III) complex nanowires electrogenerated chemiluminescence sensors for high-performance discrimination of proline enantiomers based on the difference of electron-transfer capability

Chiral molecules can generally exhibit different physiological and biological activities, thus triggering wide interest in chiral discrimination. Herein, we demonstrate a sensitive homoleptic cyclometalated iridium(III) complexes nanowires (Ir(piq)3 NWs) electrogenerated chemiluminescence (ECL) sensor for high-performance discrimination of chiral molecules based on the difference in electron-transfer ability between different radicals. The developed Ir(piq)3 NWs/ITO sensor exhibits high ECL signal and satisfying stability without the presence of co-reactant based on hot electron-induced ECL, which would spur its further application in detecting proline enantiomers. Obvious difference on the ECL intensity towards L-Pro and D-Pro is observed under the presence of high concentration of proline enantiomers, which attributes to the different electron-transfer capability between Ir+(piq)3 and L-pro•/D-pro•. In order to attain high-performance discrimination, we construct the Ir(piq)3 NWs/TPrA sensor to achieve chiral discrimination for trace amounts of proline enantiomers (1.0 × 10-9 M), which attributes to the strong molecular interactions enhanced by introduction of active radical TPrA•.

Evaluation of antibiotic oxytetracycline removal in water using a gas phase dielectric barrier discharge plasma

Degradation of oxytetracycline (OTC), a primary member of antibiotics in water, was performed by a gas phase dielectric barrier discharge (GPDBD) plasma reactor. The influences of operation conditions including applied voltages, air bubbling rates, initial OTC concentrations and initial pH values on OTC abatement were investigated respectively. The results showed that the decontamination process can be fitted by first order kinetics, and the removal ratio and rate were affected obviously by those parameters. After 20 min of discharge treatment, approximately 93.4% of OTC was removed under the experimental conditions: applied voltage of 7.5 kV, air flow rate of 1.0 L/min, initial OTC concentration of 100 mg/L, and initial pH of 5.0. In addition, TOC and COD removal efficiency reached 43.0% and 73.7% at the original pH 9.3, respectively. Furthermore, the amounts of hydrogen peroxide and ozone in aqueous were quantitatively measured to evaluate their roles during antibiotic removal, and the main function of hydroxyl radicals was demonstrated by the radicals scavenger test. At last, the analyses of UV-Vis spectra and HPLC-MS were employed to study the OTC elimination mechanism, and the possible decomposition pathway was proposed based on the speculated intermediates.