Comparing carbon nanotubes and graphene nanoplatelets as reinforcements in polyamide 12 composites.

We investigate the influence of nanofillers including carbon nanotubes (CNTs) and graphene nanoplatelets on a thermoplastic engineering polymer, polyamide 12 (PA12). The comparison between these two important nanofillers as to how they influence the structure and properties of the polymer is systematically studied. The polymer-nanofiller composites were prepared using a twin-screw micro-extruder and the composite was thereafter hot pressed into thin films. The structure (using wide angle x-ray diffraction and differential scanning calorimetry) and properties (through tensile testing and conductivity measurement) of the thin films have been investigated. The composites incorporating surfactant showed the best CNT distribution and dispersion, causing an improvement of up to 80% in the toughness modulus over pure PA12. Electrical percolation could also be achieved at nanofiller concentrations of 1 to 2 wt%. In this study we observed that CNT fillers bring about more pronounced improvements in PA12 compared to graphene nanoplatelets, as far as mechanical and electrical properties are concerned.

Improvement of toughness and electrical properties of epoxy composites with carbon nanotubes prepared by industrially relevant processes.

The addition of carbon nanotubes (CNTs) to polymeric matrices or master batches has the potential to provide composites with novel properties. However, composites with a uniform dispersion of CNTs have proved to be difficult to manufacture, especially at an industrial scale. This paper reports on processing methods that overcome problems related to the control and reproducibility of dispersions. By using a high pressure homogenizer and a three-roll calendaring mill in combination, CNT reinforced epoxies were fabricated by mould casting with a well dispersed nanofiller content from 0.1 to 2 wt%. The influence of the nano-carbon reinforcements on toughness and electrical properties of the CNT/epoxies was studied. A substantial increase of all mechanical properties already appeared at the lowest CNT content of 0.1 wt%, but further raising the nanofiller concentration only led to moderate further changes. The most significant enhancement was obtained for fracture toughness, reaching up to 82%. The low percolation thresholds were confirmed by electrical conductivity measurements on the same composites yielding a threshold value of only about 0.01 wt%. As corroborated by a thorough microscopic analysis of the composites, mechanical and electrical enhancement points to the formation of an interconnected network of agglomerated CNTs.

Effect of coadsorbent on the photovoltaic performance of squaraine sensitized nanocrystalline solar cells.

The effect of chenodeoxycholic acid as the coadsorbent with a squaraine sensitizer on TiO(2) nanocrystalline solar cells was investigated, and it was found that the coadsorbent prevents the squaraine sensitizer from aggregating on the TiO(2) nanoparticles but reduces dye loading leading to an interdependent photovoltaic performance. Analysis of the absorption spectra, and incident monochromatic photon-to-current conversion efficiency data showed that the load of squaraine sensitizer as well as the appearance of H-aggregates is strongly dependent on the molar concentration of chenodeoxycholic acid coadsorbent. The open circuit voltage of the solar cells with chenodeoxycholic acid increases due to the enhanced electron lifetime in the TiO(2) nanoparticles coupled with the band edge shift of TiO(2) to negative potentials.

Efficient co-sensitization of nanocrystalline TiO(2) films by organic sensitizers.

Dye-sensitized solar cells based on co-sensitization of organic dyes having complementary spectral absorption in the visible region resulted in a panchromatic response, which exhibited 86% incident monochromatic photon-to-current conversion efficiency in the visible region; the optimized cell gave a short circuit current density of 15.5 mA cm(-2), an open circuit voltage of 685 mV and a fill factor of 0.70 corresponding to an overall conversion efficiency of 7.43% under solar simulated light irradiation of 100 mW cm(-2).

Transport and recombination in organic light-emitting diodes studied by electrically detected magnetic resonance.

We have used electrically detected magnetic resonance (EDMR) to study a series of multilayer organic devices based on aluminum (III) 8-hydroxyquinoline (Alq3). These devices were designed to identify the microscopic origin of different spin-dependent processes, i.e. hopping and exciton formation. The EDMR signal in organic light-emitting diodes (OLEDs) based on Alq3 is only observed when the device is electroluminescent and is assigned to spin-dependent exciton formation. It can be decomposed in at least two Gaussians: one with peak-to-peak line (deltaH(PP)) of 1.6 mT and another with deltaH(PP) of 2.0 to 3.4 mT, depending on bias and temperature. The g-factors of the two components are barely distinguishable and close to 2.003. The broad line is attributed to the resonance in Alq3 anions, while the other line is attributed to cationic states. These attributions are supported by line shape and its electrical-field dependence of unipolar Alq3-based diodes, where hopping process related to dication and dianion formation is observed. In these unipolar devices, it is shown that the signal coming from spin-dependent hopping occurs close to organic semiconductor/metal interfaces. The sign of the magnetic-resonance-induced conductivity change is dominated by charge injection rather than charge mobility. Our results indicate that the probability of singlet exciton formation in our OLEDs is smaller than 25%.