No Arabic abstract
We report the magnetic properties of magnetic nano-composite, consisting of different quantity of NiFe2O4 nanoparticles in polymer matrix. The nanoparticles exhibited a typical magnetization blocking, which is sensitive on the variation of magnetic field, mode of zero field cooled/field cooled experiments and particle quantity in the matrix. The samples with lower particle quantity showed an upturn of magnetization down to 5 K, whereas the blocking of magnetization dominates at lower temperatures as the particle quantity increases in the polymer. We examine such magnetic behaviour in terms of the competitive magnetic ordering between core and surface spins of nanoparticles, taking into account the effect of inter-particle (dipole-dipole) interactions on nanoparticle magnetic dynamics.
The nucleation and growth of CdS nanoparticles within a polymer matrix was followed by in-situ synchrotron X-ray diffraction. The nanoparticles form by effect of the thermolysis of thiolate precursors at temperatures between 200 and 300 Celsius degrees. Above 240 Celsius degrees the precursor decomposition is complete and CdS nanoparticles grow in the polymer matrix forming a nanocomposite with interesting optical properties. The nanoparticle structural properties (size and crystal structure) depend on the annealing temperature.(abridged version)
Polymer assisted spherical FeNi nanoparticles were prepared via wet chemical method using hydrazine as a reducing agent and polymers (PVP and PEG) as reducing and stabilizing agent. Structural studies performed using XRD and TEM shows uniform dispersion of fine FeNi nanocrystallites in nanocomposite particles. The size and thermal stability of FeNi nanoparticles prepared under same reaction condition was found to be dependent on the type and the molecular weight of the polymer used. However, the magnetic properties of nanocomposite particles were not influenced by the polymers. The study highlights subtle differences in using polymers during the synthesis of alloyed nanocomposite particles.
We provide a detailed insight into piezoelectric energy generation from arrays of polymer nanofibers. For sake of comparison, we firstly measure individual poly(vinylidenefluoride-co-trifluoroethylene) (P(VDF-TrFe)) fibers at well-defined levels of compressive stress. Under an applied load of 2 mN, single nanostructures generate a voltage of 0.45 mV. We show that under the same load conditions, fibers in dense arrays exhibit a voltage output higher by about two orders of magnitude. Numerical modelling studies demonstrate that the enhancement of the piezoelectric response is a general phenomenon associated to the electromechanical interaction among adjacent fibers, namely a cooperative effect depending on specific geometrical parameters. This establishes new design rules for next piezoelectric nano-generators and sensors.
Microparticles including paraffin are currently used for textiles coating in order to deaden thermal shocks. We will show that polymer nanoparticles embedded in those microsized capsules allow for decreasing the thermal conductivity of the coating and enhance the protection in the stationary regime. A reasonable volume fraction of polymer nanoparticles reduces the conductivity more than predicted by Maxwell mixing rules. Besides, measurements prove that the polymer nanoparticles do not affect the latent heat and even improve the phase change behaviour as well as the mechanical properties.
Molybdenum disulfide (MoS2) has been attracting extraordinary attention for its intriguing optical, electronic and mechanical properties. Here we demonstrate hybrid, organic-inorganic light-emitting nanofibers based on MoS2 nanoparticle dopants obtained through a simple and inexpensive sonication process in N-methyl-2-pyrrolidone and successfully encapsulated in polymer filaments. Defectiveness is found to be kept low, and stoichiometry preserved, by the implemented, gentle exfoliation method that allows the MoS2 nanoparticles to be produced. So-achieved hybrid fibers are smooth, uniform, flawless, and exhibit bright and continuous light emission. Moreover, they show significant capability of waveguiding self-emitted light along their longitudinal axis. These findings suggest the use of emissive MoS2 fibers enabled by gentle exfoliation methods as novel and highly promising optical material for building sensing surfaces and as components of photonic circuits.