RESUMO
Recently, scientists have been facing major obstacles in terms of improving the performances of dielectric materials for triboelectric nanogenerators. The triboelectric nanogenerator (TENG) is one of the first green energy technologies that can convert random mechanical kinetic energy into electricity. The surface charge density of TENGs is a critical factor speeding up their commercialization, so it is important to explore unique methods to increase the surface charge density. The key to obtaining a high-performance TENG is the preparation of dielectric materials with good mechanical properties, thermal stability and output performance. To solve the problem of the low output performance of PI-based triboelectric nanogenerators, we modified PI films by introducing nanomaterials and designed a new type of sandwich-shaped nanocomposite film. Herein, we used polyimide (PI) with ideal mechanical properties, excellent heat resistance and flexibility as the dielectric material, prepared an A-B-A sandwich structure with PI in the outer layer and modified a copper calcium titanate/polyimide (CCTO/PI) storage layer in the middle to improve the output of a TENG electrode. The doping amount of the CCTO was tailored. The results showed that at 8 wt% CCTO content, the electrical output performance was the highest, and the open-circuit voltage of CCTO/PI was 42 V. In the TENG, the open-circuit voltage, short-circuit current and transfer charge of the prepared sandwich-structured film were increased by 607%, 629% and 672% compared to the TENG with the PI thin film, respectively. This study presents a novel strategy of optimizing dielectric materials for triboelectric nano-generators and has great potential for the future development of high output-performance TENGs.
RESUMO
The widespread use of cross-linked polyethylene (XLPE) as insulation in cables may be attributed to its outstanding mechanical and dielectric properties. In order to quantitatively evaluate the insulation status of XLPE after thermal ageing, an accelerated thermal ageing experimental platform is established. Polarization and depolarization current (PDC) as well as elongation at break of XLPE insulation under different ageing durations are measured. XLPE insulation state is determined by the elongation at break retention rate (ER%). Based on the extended Debye model, the paper proposed the stable relaxation charge quantity and the dissipation factor at 0.1 Hz to evaluate the insulation state of XLPE. The results show that the ER% of XLPE insulation decreases with the growth of ageing degree. The polarization and depolarization current of XLPE insulation will increase obviously with thermal ageing. Conductivity and trap level density will also increase. The number of branches of the extended Debye model increases, and new polarization types appear. Stable relaxation charge quantity and dissipation factor at 0.1 Hz proposed in this paper have a good fitting relationship with ER% of XLPE insulation, which can evaluate the thermal ageing state of XLPE insulation effectively.
RESUMO
Polyaluminum chloride (PAC) is an inorganic polymer material that has the advantages of a simple preparation process and special electronic structure. It is considered to be the most efficient and widely used flocculation material for water treatment. In this work, PAC has been used as a Lewis acid catalyst in interdisciplinary fields because of its polynuclear Al-O cation structure. Further, its catalytic mechanism in green organic synthesis has been studied in detail by using the multicomponent Biginelli reaction as the probe. The effect of solvent on the self-assembly and aggregation process of PAC materials was investigated using optical microscopy, UV-Vis spectrophotometry, particle size analysis, XPS, IR, SEM and HR-TEM. The results show that the PAC materials have different morphological characteristics in different solvents. The Al-O-Al cations were transformed in the ethanol solvent to form new multi-nuclear cation aggregates Alb, which could be used as inorganic micro-nano reactors with unique synergistic catalysis in catalytic reactions. This is the first time the role of PAC in the Biginelli reaction has been analyzed with a liquid in situ infrared instrument, which provided favorable evidence for the speculated reaction mechanism. The PAC-ethanol system is, therefore, considered to be a green, efficient (best yield >99%), economic and recyclable catalyst for catalyzing organic synthesis reactions. The development and utilization of PAC materials in organic synthesis will bring new vitality to this cheap material, which is widely used in industries.
