Ammonium vanadate with bronze structure (NH4V4O10) is a promising cathode material for zinc-ion batteries due to its high specific capacity and low cost. However, the extraction of $${\text{NH}}_{{4}}^{ + }$$ NH 4 + at a high voltage during charge/discharge processes leads to irreversible reaction and structure degradation. In this work, partial $${\text{NH}}_{{4}}^{ + }$$ NH 4 + ions were pre-removed from NH4V4O10 through heat treatment; NH4V4O10 nanosheets were directly grown on carbon cloth through hydrothermal method. Deficient NH4V4O10 (denoted as NVO), with enlarged interlayer spacing, facilitated fast zinc ions transport and high storage capacity and ensured the highly reversible electrochemical reaction and the good stability of layered structure. The NVO nanosheets delivered a high specific capacity of 457 mAh g−1 at a current density of 100 mA g−1 and a capacity retention of 81% over 1000 cycles at 2 A g−1. The initial Coulombic efficiency of NVO could reach up to 97% compared to 85% of NH4V4O10 and maintain almost 100% during cycling, indicating the high reaction reversibility in NVO electrode.

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The fast consumption of fossil energy accompanied by the ever-worsening environment urge the development of a clean and novel energy storage system. As one of the most promising candidates, the supercapacitor owns unique advantages, and numerous electrodes materials have been exploited. Hence, biomass-derived porous carbon materials (BDPCs), at low cost, abundant and sustainable, with adjustable dimension, superb electrical conductivity, satisfactory specific surface area (SSA) and superior electrochemical stability have been attracting intense attention and highly trusted to be a capable candidate for supercapacitors. This review will highlight the recent lab-scale methods for preparing BDPCs, and analyze their effects on BDPCs' microstructure, electrical conductivity, chemical composition and electrochemical properties. Future research trends in this field also will be provided.

Reproducibility in surface enhanced Raman scattering (SERS) measurements is a challenge. This work developed a facile way to make highly dispersed uniform silver nanoparticles (AgNPs) loaded in the agar/polyacrylonitrile (PAN) nanofibers by the coupling the electrospinning technology from metal complex-containing polymer solution and in situ photoreductive technique. Agar, as hydrophilic component, was introduced into the electrospinning solution considering that its abundant hydroxyl group sites could greatly improve the contents of silver ions in the polymers because of the rich silver ion chelated with the hydroxyl group, whereas hydrophilic agar was integrated with hydrophobic PAN by -OH···N≡C- hydrogen bonds as a bridge. Meanwhile, the in situ photoreductive reaction was made under different light irradiations such as desk lamp, 365 nm UV-lamp, and 254 nm UV-lamp. High yield of stable AgNPs with highly uniform and dispersion are available in the agar/PAN nanofibers after the in situ photoreductive reaction, supplying the possibility of reproducible SERS signals. To identify that concept of proof, a facile approach for the determination of malachite green (MG) in three environmental practical samples was demonstrated by using the composite nanofibrous material irradiated by 365 nm UV-lamp, giving the minimum detection concentration of MG as low as 0.1 μmol/L with a good linear response ranging from 0.1-100 μmol/L (R(2) = 0.9960).

In this study, we report a feasible strategy for fabricating high-dielectric-constant polymer composites for applications in energy storage devices and embedded capacitors. Hierarchical flower-like TiO2 particles were prepared via a facile solvothermal process and incorporated into the P(VDF-HFP) matrix. The temperature and frequency dependent dielectric properties of flower-like TiO2/P(VDF-HFP) composites as well as commercial TiO2/P(VDF-HFP) composites were investigated. The results reveal that the flower-like TiO2 particles are more effective in increasing the dielectric constant of P(VDF-HFP) when compared with commercial TiO2. Typically, the dielectric constant of the P(VDF-HFP) composite filled with 20 vol % flower-like TiO2 reaches 83.1 at 100 Hz, in contrast to 43.4 for the composite filled with 20 vol % commercial TiO2 and 11.3 for pristine P(VDF-HFP). Also, the flower-like TiO2-filled composites exhibit similar characteristic breakdown strengths to their commercial TiO2-filled counterparts. The significant improvement in the dielectric constant could be attributed to the enhancement of Maxwell-Wagner-Sillars polarization, which originates from the sophisticated morphology of flower-like TiO2 particles.