A facile and clean process for exfoliating MoS2 nanosheets assisted by a surface active agent in aqueous solution.

A facile, efficient and environmentally friendly process to exfoliate MoS2 is essentially critical to apply the obtained mono- and few-layer nanosheets in various electronic devices and sensors. Here we report a liquid phase exfoliation method for exfoliation of MoS2, which employs a surfactant of sodium dodecyl benzene sulfonate (SDBS) in water. The nonpolar benzene rings in SDBS can firmly bind to the MoS2 layer, facilitating the effective exfoliation of nanosheets in aqueous solution. It is found that the exfoliation efficiency and thickness of MoS2 nanosheets are related to the concentration of SDBS, and the mechanism was investigated. Defect free mono- and few-layer MoS2 nanosheets are obtained by controlling the amount of SDBS in solution, which exhibit stable dispersion in water over months, and it renders them as having great potential for solution-based device fabrication.

Polyimide Films Impregnated with Epoxy Resin Demonstrating Superior Self-Healing Properties for Thermally Stable Energy Storage Capacitors.

Metallized polymer films (MPFs) with superior self-healing properties are extremely attractive for application in energy storage capacitors. Self-healing behaviors allow MPFs to keep insulating between the local electrical breakdown region and the electrode, thereby reserving long-term operational viability of the capacitors. Polyimide (PI) is a type of well-developed polymer material with excellent mechanical and thermal stabilities, but it is deficient in intrinsic self-healing capabilities. This work reports a facile surface engineering strategy to endow metalized PI films with self-healing capabilities. By simple immersion of bare PI films in the solution of epoxy resin (ER) accompanied by curing of ER, PI films impregnated with ER (P-E films) not only show enhanced dielectric characteristics but also obtain excellent self-healing abilities upon multiple cycles of electrical breakdowns, even at a high temperature. For example, in comparison to bare PI films, PI films impregnated in ER solution with a solid content of 1 wt % (P-1%E) display improved initial Weibull breakdown strength (αb1 of 353.0 versus 310.9 kV/mm), maximum discharging energy density (Ud of 2.1836 versus 0.8254 J/cm3), and charging/discharging efficiency (η of 95.72 versus 55.19%) at 150 °C. After 5 breakdown cycles, P-1%E films could maintain a much higher breakdown strength (αb5 of 338.1 versus 21.3 kV/mm). When subjected to a constant electrical strength of 350 kV/mm at 150 °C, P-1%E films show merely <6% decline in both Ud and η values after 5 breakdown cycles. On the contrary, bare PI films would undergo dramatic performance decay after 1 or 2 breakdowns under similar conditions. In view of their outstanding self-healing properties at a high temperature, P-E films can serve as a promising candidate to fabricate thermally stable MPF capacitors for long-term operation.

ZnO-Decorated Carbon Nanotube Hybrids as Fillers Leading to Reversible Nonlinear I-V Behavior of Polymer Composites for Device Protection.

Overvoltage protection is becoming increasingly important because of miniaturization and multifunctionality of electronic devices. Flexible, easily processable materials with nonlinear and reversible I-V behavior are highly desired. In this study, hybrid nanoparticles of ZnO-decorated carbon nanotubes (CNT-ZnO) were synthesized via a sol-gel hydrothermal process employed in an epoxy matrix to prepare composites. Microstructure analysis demonstrated that ZnO nanoparticles were well-bonded to the surface of CNT. The CNT-ZnO/epoxy composites exhibited nonlinear I-V behavior under increasingly applied voltage with a nonlinear coefficient of 5.01 (10 wt % filler loading). More importantly, the composites possessed excellent reversibility from dielectric to conductor and vise versa in the recycling of increase and decrease of applied electric field, in contrast to the poor recoverability of pure CNT-filled epoxy. The mechanism of the nonlinear I-V behavior and reversibility was investigated and discussed. A simple circuit was fabricated, which verified well the protection function of the CNT-ZnO/polymer composites.

Nano Ag-deposited BaTiO3 hybrid particles as fillers for polymeric dielectric composites: toward high dielectric constant and suppressed loss.

Nano Ag-deposited BaTiO3 (BT-Ag) hybrid particles usable as fillers for flexible polymeric composites to obtain high dielectric constant, low conductivity, and low dielectric loss were developed. BT-Ag hybrid particles were synthesized via a seed-mediated growing process by a redox reaction between silver nitrate and ethylene glycol. Nano Ag particles with a size less than 20 nm were discretely grown on the surface of the 100 nm BaTiO3. The similar lattice spacing of the (1 1 1) planes of BT and Ag led to the hetero-epitaxial growth of Ag on the BT surface. The thickness of the coherent interface was about 3 nm. The adhesion of Ag to BT efficiently prevented the continuous contact between Ag particles in the polyvinylidene fluoride (PVDF) matrix and suppressed the formation of the conducting path in the composite. As a result, with a filler loading of 43.4 vol %, the composite exhibited a dielectric constant (Dk) value of 94.3 and dielectric loss (tan δ) of 0.06 at 1 kHz. An even higher Dk value of 160 at 1 kHz (16 times larger than that of PVDF) was obtained when the content of BT-Ag was further increased, with low conductivity (σ < 10(-5) S m(-1)) and low dielectric loss (tan δ = 0.11), demonstrating promising applications in the electronic devices.