Search

With the emergence of stretchable/wearable devices, functions, such as sensing, energy storage/harvesting, and electrical conduction, should ideally be carried out by a single material, while retaining its ability to withstand large elastic deformations, to create compact, functionally-integrated and autonomous systems. A new class of trimodal, stretchable yarn-based transducer formed by coating commercially available Lycra® yarns with PEDOT:PSS is presented. The material developed can sense strain (first mode), and temperature (second mode) and can power itself thermoelectrically (third mode), eliminating the need for an external power-supply. The yarns were extensively characterized and obtained an ultrahigh (gauge factor ∼3.6 × 105, at 10–20% strain) and tunable (up to about 2 orders of magnitude) strain sensitivity together with a very high strain-at-break point (up to ∼1000%). These PEDOT:PSS-Lycra yarns also exhibited stable thermoelectric behavior (Seebeck coefficient of 15 μV K−1), which was exploited both for temperature sensing and self-powering (∼0.5 μW, for a 10-couple module at ΔT ∼ 95 K). The produced material has potential to be interfaced with microcontroller-based systems to create internet-enabled, internet-of-things type devices in a variety of form factors.

Ferromagnetically filled graphitic-carbon foams are a new class of materials characterized by an open-cell structure continuously filled with ferromagnetic crystals. Targeted design for applications requires knowledge of the magnetic ordering and the interaction between magnetic moments in the filling and those due to the spin of the delocalized π-electrons which contribute to thermal and electrical conduction in the graphitic carbon. Magnetometry together with electron spin resonance, thermoelectric, and calorimetric measurements on iron-filled carbon foam reveal ferromagnetic responses at room temperature with a transition to antiferromagnetic behavior in some fraction of the filling at 130 K. This observation is consistent with the α-Fe (bcc) to γ-Fe (fcc) transition at this temperature predicted by others. Seebeck coefficient measurements revealed a behavior typical of unmodified graphitic carbon indicating the absence of any interaction between the magnetic moments of the filling and the conduction electrons in the graphitic carbon.

Hybrid organic–inorganic perovskites have generated considerable research interest in the field of optoelectronic devices. However, there have been significantly fewer reports of their thermoelectric properties despite some promising early results. In this article, we investigate the thermoelectric properties of bismuth-doped CH3NH3PbBr3 (MAPbBr3) single crystals. The high-quality Bi-doped crystals were synthesized by inverse temperature crystallization and it was found that Bi substitutes onto the B-site of the ABX3 perovskite lattice of MAPbBr3 crystals with very little distortion of the crystal structure. Bi doping does not significantly alter the thermal conductivity but dramatically enhances the electrical conductivity of MAPbBr3, increasing the charge carrier density by more than three orders of magnitude. We obtained a negative Seebeck coefficient of −378 μV K−1 for 15% (x = 0.15) Bi-doped MAPb(1−x)BixBr3 confirming n-type doping and also measured the figure of merit, ZT. This work highlights routes towards controlled substitutional doping of halide perovskites to optimise them for thermoelectric applications.

Thermoelectric energy conversion within a homogeneous conductor is governed by the charge carrier mobility and the density of electronic states, intrinsic trades-off limit efficiency. Heterogeneous conduction created by the spatial variation of disorder is considered undesirable because it is conceptually difficult and not easily reproduced. However, could it be the basis for unique, exploitable thermoelectric effects? Here we show that the heterogeneous conduction typically found in conducting polymer films can result in thermoelectricity governed by only quantum mechanical tunneling of charge carriers through nanoscale Coulomb barriers at order-disorder boundaries. We conclude this to be the basis of a new category of thermoelectric system centered on heterogeneous conductors or conducting networks. We show that thermoelectricity of this origin can be engineered without doping or intrinsic trades-off. Our findings point to a wide range of alternatives to the doped inorganic semiconductor paradigm.

A simple wet chemical method involving only sonication in aqueous GdCl3 solution was used for surface functionalization of iron-filled multiwalled carbon nanotubes with gadolinium. Functional groups on the sidewalls produced by the sonication provide active nucleation sites for the loading of Gd3+ ions. Characterization by EPR, EELS, and HRTEM confirmed the presence of Gd3+ ions on the sidewall surface. The room temperature ferromagnetic properties of the encapsulated iron nanowire, saturation magnetization of 40 emu/g and coercivity 600 Oe, were maintained after surface functionalization. Heating functionality in an alternating applied magnetic field was quantified through the measurement of specific absorption rate: 50 W/gFe at magnetic field strength 8 kA/m and frequency of 696 kHz. These results point to candidacy for dual-functioning MRI imaging and magnetic hyperthermia structures for cancer therapy.

Boundary layer chemical vapour synthesis is a new technique that exploits random fluctuations in the viscous boundary layer between a laminar flow of pyrolysed metallocene vapour and a rough substrate to yield ferromagnetically filled radial-carbon-nanotube structures departing from a core agglomeration of spherical nanocrystals individually encapsulated by graphitic shells. The fluctuations create the thermodynamic conditions for the formation of the central agglomeration in the vapour which subsequently defines the spherically symmetric diffusion gradient that initiates the radial growth. The radial growth is driven by the supply of vapour feedstock by local diffusion gradients created by endothermic graphitic-carbon formation at the vapour-facing tips of the individual nanotubes and is halted by contact with the isothermal substrate. The radial structures are the dominant product and the reaction conditions are self-sustaining. Ferrocene pyrolysis yields three common components in the nanowire encapsulated by multiwall carbon nanotubes, Fe3C, α-Fe, and γ-Fe. Magnetic tuning in this system can be achieved through the magnetocrystalline and shape anisotropies of the encapsulated nanowire. Here we demonstrate proof that alloying of the encapsulated nanowire is an additional approach to tuning of the magnetic properties of these structures by synthesis of radial-carbon-nanotube structures with γ-FeNi encapsulated nanowires.

Ultra-high molecular weight polyethylene/multi-wall carbon nanotube (UHMW-PE/MWNT) composites have been prepared by a novel approach which involves the use of a mixture of solvents during the gelation process. By combining one of the best known organic solvents for nanotubes, N,N-dimethylformamide (DMF) with xylene and use this mixed-solvent in the gelation/crystallisation process for UHMW-PE/MWNT composite fabrication, an attempt is made to improve the dispersion of carbon nanotubes in UHMW-PE. The obtained films were drawn to obtain highly oriented tapes, which were characterized in terms of electrical and mechanical properties. The conductivity of the drawn tapes is maintained at 10−4 S/m at draw ratio 30, two orders of magnitude higher than the minimum level required to provide electrostatic discharge. Although the mechanical properties are compromised by use of DMF and MWNTs, the Young’s modulus still remains at 25 GPa, in comparison with 35 GPa for pure UHMW-PE tape at draw ratio 30.

This research concerns the effect of conductive network formation in a polymer melt on the conductivity of multi-walled carbon nanotube/thermoplastic polyurethane composite systems. An extremely low percolation threshold of 0.13 wt.% was achieved in hot-pressed composite film samples, whereas a much higher CNT concentration (3-4 wt.%) is needed to form a conductive network in extruded composite strands. This is explained in terms of the dynamic percolation behaviour of the CNT network in the polymer melt. The temperature and CNT concentration needed for dynamic percolation to take effect were studied by the conductivity versus temperature behaviour of extruded strands, in an attempt to optimise the processing conditions. © 2008 Elsevier Ltd. All rights reserved.

The development of new flexible and stretchable sensors addresses the demands of upcoming application fields like internet-of-things, soft robotics, and health/structure monitoring. However, finding a reliable and robust power source to operate these devices, particularly in off-the-grid, maintenance-free applications, still poses a great challenge. The exploitation of ubiquitous temperature gradients, as the source of energy, can become a practical solution, since the recent discovery of the outstanding thermoelectric properties of a conductive polymer, poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS). Unfortunately the use of PEDOT:PSS is currently constrained by its brittleness and limited processability. Herein, PEDOT:PSS is blended with a commercial elastomeric polyurethane (Lycra), to obtain tough and processable self-standing films. A remarkable strain-at-break of ≈700% is achieved for blends with 90 wt% Lycra, after ethylene glycol treatment, without affecting the Seebeck voltage. For the first time the viability of these novel blends as stretchable self-powered sensors is demonstrated.

A facile chemical vapor deposition-based method for the texturing of substrate-supported iron-filled multiwalled carbon nanotube arrays is reported. The method is based on the interplay of temperature gradients and modulated vapor flow that produces annular height variation and a vertical-array-to-spherulitic morphological transformation in experimental conditions, which result in uniform, close-packed arrays of constant height in an unmodulated vapor flow. These observations are proposed to result from creation of stationary cells of feedstock vapor above the growth front.

Times Cited: 0 Ewels, Chris/A-1543-2012; Khare, varsha/A-1676-2010; Santa-Cruz, Petrus/C-7413-2011; Bikkarolla, Santosh Kumar/ Ewels, Chris/0000-0001-5530-9601; Santa-Cruz, Petrus/0000-0003-2475-7764; Bikkarolla, Santosh Kumar/0000-0001-5715-0323 0 1364-5498

Structures comprising single-crystal, iron-carbon-based nanowires encapsulated by multiwall carbon nanotubes self-organize on inert substrates exposed to the products of ferrocene pyrolysis at high temperature. The most commonly observed encapsulated phases are Fe3C, α-Fe, and γ-Fe. The observation of anomalously long-period lattice spacings in these nanowires has caused confusion since reflections from lattice spacings of ≥0.4 nm are kinematically forbidden for Fe3C, most of the rarely observed, less stable carbides, α-Fe, and γ-Fe. Through high-resolution electron microscopy, selective area electron diffraction, and electron energy loss spectroscopy we demonstrate that the observed long-period lattice spacings of 0.49, 0.66, and 0.44 nm correspond to reflections from the (100), (010), and (001) planes of orthorhombic Fe3C (space group Pnma). Observation of these forbidden reflections results from dynamic scattering of the incident beam as first observed in bulk Fe3C crystals. With small amounts of beam tilt these reflections can have significant intensities for crystals containing glide planes such as Fe3C with space groups Pnma or Pbmn.

The discovery of carbon nanotubes in 1991 spurred an enormous worldwide research effort spanning the physical, chemical, and life sciences. This review will attempt to convey to the reader the unique physical attributes of carbon nanotubes and the range of possible applications.

Field emission properties of B-doped carbon nanotubes are investigated from both theoretical and experimental standpoints. Using tight-binding and ab initio calculations, it is observed that B-saturating tip edges of carbon nanotubes induce the presence of large peaks within the local density of states (LDOS) located in an energy region close to the Fermi level (Ef). These localized states suggest a field emission enhancement for the B-doped tubes. In addition, ab initio theoretical results indicate that the work function for B-doped tubes is 1.7 eV lower when compared to pure carbon-terminated nanotubes. Experimentally, it is found that B-doped tubes, which are produced by arc discharge techniques and contain B mainly at the tips, exhibit stable electron field emission at lower turn-on voltages (1.4 V/mum) when compared to pure single- and multiwalled carbon nanotubes (2.8 and 3.0 V/mum, respectively) measured under the same conditions. We strongly believe our results will bring new insights in the fabrication of stable field emission sources.

A modified cathodic arc technique has been used to deposit carbon nitride thin films directly on n+ Si substrates. Transmission Electron Microscopy showed that clusters of fullerene-like nanoparticles are embedded in the deposited material. Field emission in vacuum from as-grown films starts at an electric field strength of 3.8 V/micron. When the films were etched in an HF:NH4F solution for ten minutes, the threshold field decreased to 2.6 V/micron. The role of the carbon nanoparticles in the field emission process and the influence of the chemical etching treatment are discussed., Comment: 22 pages, 8 figures, submitted to J. Vac. Sc. Techn. B

Corrected values for the coefficients G0 and T0 in Table 2 as well as the corrected value for the parameter T0 in Eq. (3) are given for the paper by Morgan et al. [Phys. Status Solidi A 205, No. 6, 1394–1398 (2008)]. (© 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim)