Graphene composites (GCs) have attracted much attention recently. It is interesting to explore thermal properties of GCs in which graphene filler concentrations are tunable. Here, we use 3ω method to measure the thermal conductivity of GCs synthesized from reduced graphene oxide (RGO) dispersed in polystyrene. To avoid the detrimental effect of lithography processes to GCs, we have developed a novel method employing polyvinyl alcohol and poly(methyl methacrylate) (PMMA) as a holder film to transfer micrometer-sized metal heaters/sensors onto GC surface. Room temperature measurements of the thermal conductivity of GCs are performed. The thermal conductivity is enhanced by ∼ 35 % when adding 5 vol.% of RGO filler concentration. Our measurements will be helpful to probe and understand the thermal transport properties of graphene based composites.

We have analyzed the hopping movement of a new ionic solid electrolyte by calculating defect formation energies and activation barriers. The role of the lattice during diffusion was established. Thermodynamic properties were determined by means of first principles and phonon calculations at working temperatures. The new solid electrolyte, an antiperovskite, Li3-2xMxAO (in which M is a higher valent cation like Ca2+ or Mg2+ and A is a halide like Cl- or Br- or a mixture of halides), was studied either pure or doped. Moreover, we present experimental ionic conductivity data for these novel solid state ionic conductors for the doped and the pure solid electrolyte from room temperature and up to ∼253 °C. In this paper, we compare the ionic conductivity of the latter solid electrolyte with other fast ionic conductors.

In this paper, we present a work plan for the dissemination of refreshable, photoactuatable tactile displays to the visually impaired, serving both Lab-to-Market and Lab-to-Classroom initiatives. The work plan is designed in accordance with the logic model, which identifies an overlap amongst classroom, market, and laboratory. This overlap seems to nucleate when a technology in developmental phase is deployed in a classroom with high affinity to such technology. In this scheme, students are stakeholders whom help decide both content and applications to be included in the developing curriculum, and provide technology feedback, effectively leading to increased consumer acceptance. The identified Lab-to-Market-to-Classroom continuum could be the missing link where to nurture sustainable scientific, technological, and curricular development.

The evaluation of the redox conditions in the Swedish ILW-LLW repository, SFR-1, is of high relevance in the performance assessment. The SFR-1 repository contains heterogeneous types of wastes, of different activity levels and with different materials in the waste and in the matrices and packaging. Steel and concrete-based materials are ubiquitous in the repository. The assessment presented in this work is based on the evaluation of the redox conditions and of the reducing capacity in 15 individual and representative waste package types in SFR-1. A combination of the individual models is used to determine the redox evolution of the different vaults in the repository. The results of the model indicate that in the initial time after repository closure, O2 is consumed through degradation of organic matter and metal corrosion during the initial time after repository closure. Afterwards, the system is kept under reducing conditions for long time periods, and H2(g) is generated due to the anoxic corrosion of steel forming magnetite as main corrosion product. The time at which steel is depleted varies with the amount and characteristics of steel and ranges from 5,000 to over 60,000 years. After complete steel corrosion, the reducing capacity of the system is mainly given by magnetite. The calculated redox potential under the chemical conditions imposed by the massive amounts of cements in the repository is in the order of -0.75 V (at pH 12.5). In case of assuming that the Eh of the system is controlled by the interaction between Fe(III)/Magnetite as a result of groundwater/magnetite interactions, redox potentials in the range -0.7 to -0.01V are calculated, considering the uncertainty in the pH prevalent in the system If the absence of oxic disturbances the Eh of the repository system would be kept reducing. In the event of oxidising and diluted glacial meltwater intrusion, magnetite would gradually convert into Fe(III) oxides, buffering the redox potential of the system and preventing it from oxidation for long time periods.

In this work we report on opportunities for a colossal reduction in lattice thermal conductivity (LTC) of graded micro-nanoporous structures with inhomogeneous porosity which leads to the considerable improvement in thermoelectric figure of merit ZT. We employ the effective medium theory to calculate the LTC of a porous media with hole pores of variable radius and show that porous materials with inhomogeneous porosity are expected to have stronger reduction (about 30 times!) in thermal conductivity than those with pores of equal sizes. Such a reduction is caused by enhanced scattering of thermal phonons with the pore boundaries. We have studied the variations of the LTC as a function of porosity, pore sizes, geometry and the number of pore groups with different sizes. Our theoretical results show excellent agreement with experimental data.

This paper describes an alternate two-step metallization scheme for porous dielectrics. The patterned dielectric surface is first treated in a plasma etch chamber where the dielectric surface is coated with a very thin carbon-based film. This is followed by electroless copper deposition. The plasma post-etch treatment (PET) film seals the pores of the dielectric, minimizes dielectric damage, and functionalizes the dielectric to enable electroless plating.

We use data over an extended Q range from 0.01 to 100Å-1 from the recently commissioned NIMROD instrument at the ISIS pulsed neutron source to develop a multi-scale inverse modeling procedure which will provide insight in to the phase transformations of polymer systems. The first level of our procedure is atomistic and we use internal coordinates (bond length, bond angles and torsion angles) to define the polymer chain in full atomistic detail. Values were assigned to each internal coordinate within the chain using a stochastic Monte Carlo method in which the probabilities were drawn from distributions representing the possible range of values. Using this approach, random chain configurations could be rapidly built and the intrachain structure factor calculated utilizing a small set of parameters and compared with the experimental function. Parameters representing the probability distribution functions were systematically varied using a grid search to find the values which gave the best fit to the structure factor for Q > 3Å-1 in order to determine the details of the chain conformation in the molten phase. This process was repeated for data over the same extended Q range obtained at lower temperatures where the polymer was expected to crystallize. Polymers crystallize via chainfolded thin lamellae crystals. Such crystals give rise to an intense peak at Q ∼ 0.03Å-1. This scattering can be calculated using a lamellar stack model, coarse-grained from the single chain structure. We describe this approach using data obtained on the crystallization from the melt phase of perdeuterated polymers. The objective here is to follow the three key length scales; the chain folded lamellar thickness of ∼ 10nm, the crystal unit cell ∼ 1nm and the detail of the chain conformation is ∼ 0.1nm.

We have proposed new magnetic memories using parallel-aligned nanowires without mechanical moving parts, in order to achieve the ultra high transfer rate of more than 144 Gbps for Super Hi-Vision TV. In the magnetic memory using nanowires, the data are stored as the magnetic domains with up or down magnetization in magnetic nanowires, and the domains are shifted quite faster by applying optimum current along the nanowire direction for data writing and reading purpose. Since the electric circuits and the insulation space between the neighbor nanowires are necessary for moving the magnetic domain walls, the areal recording density is essentially reduced as compared with that of conventional hard disk drives. In this study, in order to increase the areal recording density of magnetic nanowire memory, we have tried to act one magnetic nanowire as the virtual multiple data tracks. The shallow scratched trench was introduced using scanning probe microscopy along the length direction on the surface of a single nanowire to form multiple internal tracks, and we have succeeded in realizing a couple of virtual tracks states.

In this paper we demonstrate that graphene is one of the best materials for new types of terahertz lasers as optical and/or injection pumping of graphene can exhibit negative-dynamic conductivity in the terahertz spectral range. We analyze the formation of nonequilibrium states in optically pumped graphene layers and in forward-biased graphene structures with lateral p-i-n junctions and consider the conditions of population inversion and lasing. The latter provides a significant advantage of the injection pumping in realization of graphene terahertz lasers. We benchmark graphene as a prospective material for injection-type terahertz lasers.

The phase-field crystal (PFC) method has emerged as a promising technique to simulate the evolution of crystalline patterns with atomistic resolution on mesoscopic time scales. We use a 2D PFC model based on Elder et al. [Phy. Rev. B 75, 064107 (2007)] to perform a systematic analysis of a liquid-solid interface for a binary alloy system. We propose the method of determining interfacial energies for a curved liquid-solid interface by stabilizing the circular solid seed in the surrounding liquid phase and the liquid droplet in the solid phase for various seed sizes in a finite system. We also investigate the impact of model parameters on the resulting interface energies. The interface energies are computed with various system sizes in order to study the system size effects. In particular, we compare the simulation results in the form of the interface energy as a function of radius with the existing theories.

The deformation behavior of two of the five Fe-Zn intermetallic phases (Γ, Γ1, δ1k, δ1p and ζ), which are formed in the coating layer of galvannealed steel, has been investigated through uniaxial compression tests for single-phase polycrystalline micropillars. The ζ phase is ductile to some extent while the Γ1 phase is brittle. These results are consistent with the Peierls stress estimated from the crystal structures by assuming the primitive Peierls-Nabarro model.

Light-Emitting Electrochemical Cells (LECs) consist of solution processable ionic light-emitting materials and use air stable electrodes. Their operational mechanism relies on both ionic and electronic conduction. The dynamic behavior is primarily determined by the ionic conductivity. Here, we demonstrate that with increasing temperature the LECs turn-on faster yet without decreasing the efficiency. This is due to the activation energy of ionic transport and the temperature independent photoluminescence quantum yields.

The use of a continuous flow non-thermal plasma reactor for the formation of silicon nanoparticles has attracted great interest because of the advantageous properties of the process [1]. Despite the short residence time in the plasma (around 10 milliseconds), a significant fraction of the precursor, silane, is converted and collected in the form of nanopowder. The structure of the produced powder can be tuned between amorphous and crystalline by adjusting the power of the radio-frequency excitation source, with higher power leading to the formation of crystalline particles. Numerical modeling suggests that higher excitation power results in a higher plasma density, which in turn increases the nanoparticle heating rate due to the interaction between ions, free radicals and the nanopowder suspended in the plasma [2]. While the experimental evidence suggests that plasma heating may be responsible for the formation of crystalline powder, an understanding of the mechanism that leads to the crystallization of the powder while in the plasma is lacking. In this work, we present an experimental investigation on the crystallization kinetic of plasma-produced amorphous powder. Silicon nanoparticles are nucleated and grown using a non-thermal plasma reactor similar to the one described in [1], but operated at low power to give amorphous nanoparticles in a 3-10 nm size range. The particles are then extracted from the reactor using an orifice and aerodynamically dragged into a low pressure reactor placed in a tube furnace capable of reaching temperatures up to 1000°C. Raman and TEM have been used to monitor the crystalline fraction of the material as a function of the residence time and temperature. It is expected that for a residence time in the annealing region of approximately ∼300 milliseconds, a temperature of at least 750 °C is needed to observe the onset of crystallization. A range of crystalline percentages can be observed from 750 °C to 830 °C. A discussion of particle growth and particle interaction, based on experimental evidence, will be presented with its relation to the overall effect on crystallization. Further data analysis allows extrapolating the crystallization rate for the case of this simple, purely thermal system. We conclude that thermal effects alone are not sufficient to explain the formation of crystalline powder in non-thermal plasma reactors.

Technetium-99, a β-emitting radioactive fission product of 235U, formed in nuclear reactors, presents a major challenge to nuclear waste disposal strategies. Its long half-life (2.1 x 105 years) and high solubility under oxic conditions as the pertechnetate anion [Tc(VII)O4] is particularly problematic for long-term disposal of radioactive waste in geological repositories. In this study, we demonstrate a novel technique for quantifying the transport and immobilisation of technetium-99m, a γ-emitting metastable isomer of technetium-99 commonly used in medical imaging. A standard medical gamma camera was used for non-invasive quantitative imaging of technetium-99m during co-advection through quartz sand and various cementitious materials commonly used in nuclear waste disposal strategies. Spatial moments analysis of the resulting 99mTc plume provided information about the relative changes in mass distribution of the radionuclide in the various test materials. 99mTc advected through quartz sand demonstrated typical conservative behaviour, while transport through the cementitious materials produced a significant reduction in radionuclide centre of mass transport velocity over time. Gamma camera imaging has proven an effective tool for helping to understand the factors which control the migration of radionuclides for surface, near-surface and deep geological disposal of nuclear waste.

Metadislocations are highly complex and pivotal defects mediating plastic deformation in complex metallic alloys. Here, we review recent results on the structure of metadislocations in the phases T-Al-Mn-Pd, T-Al-Mn-Fe and o-Al13Co4. In these materials, metadislocation motion is of particular interest as it takes place by pure glide in contrast to most other complex metallic alloys. Recently, novel metadislocations were found in the T-phase [1]. They have Burgers vectors ${\rm{\vec b}} = \pm \tau ^{ - n} c\left( {\matrix{ 0 & 0 & 1 \cr } } \right)$ (n = 2, 3, 4) and are associated to two, four and six planar defects, respectively. The type of planar defect depends on the deformation geometry. Metadislocation glide creates (1 0 0) stacking faults and climb creates (0 0 1) phason planes. Metadislocation glide was observed in the o-Al13Co4 phase, as well [2]. The close structural relation of metadislocations in the phases T-Al-Mn-Pd, T-Al-Mn-Fe, Al13Co4 and ε6-Al-Pd-Mn is discussed.

The present work reports the covalent functionalization of single-walled carbon nanotubes (SWCNTs) by ferrocene derivatives with polyethyleneglycol linkers. A very clean initial sample was chosen to avoid any residual catalyst and carbon impurities. Functionalized SWCNTs (f-CNTs) are deposited on the surface of a glassy carbon electrode (GCE) and this modified electrode is used for oxidizing the cofactor NADH (dihydronicotinamide adenine dinucleotide) in the presence of diaphorase. A clear electrocatalytic effect is evidenced, which can only be attributed to the f-CNTs.

Thin films of nanocrystalline ceria on a Si substrate have been irradiated with 3 MeV Au+ ions to fluences of up to 1x1016 ions cm-2, at temperatures ranging between 160 to 400 K. During the irradiation, a band of contrast is observed to form at the thin film/substrate interface. Analysis by scanning transmission electron microscopy in conjunction with energy dispersive and electron energy loss spectroscopy techniques revealed that this band of contrast was a cerium silicate amorphous phase, with an approximate Ce:Si:O ratio of 1:1:3.

Magnetite (Fe3O4) formation within Magnetospirillum magneticum strain AMB-1 occurs under the influence of the Mms6 protein. It is hypothesised that if key iron binding sites within the C-terminus of the Mms6 protein are substituted for alanine, the protein’s overall iron binding ability is diminished. In this study, an atomistic model of Mms6-driven magnetite formation was developed and the attachment of series amino acid repeats (alanine-alanine, alanine-glutamic acid & glutamic acid-glutamic acid) to the {100} & {111} magnetite surfaces were investigated. Our results suggest the substitution of glutamic acid for alanine residues significantly reduces iron binding affinity of the system, thus confirming the hypothesis. In addition, it is shown that the surface of preferable attachment is the {111} magnetite surface.

We report for the first time the a-Si:H/μc-Si:H/μc-Si:H triple-junction solar cells fabricated on W-textured ZnO having a very high haze value which can improve light scattering effect. For further enhancement of light confinement effects, p-type a-SiOx:H and μc-SiOx:H as wide-gap window-layers, n-type μc-SiOx:H as intermediate layers and a back reflector were employed in these solar cells too. From theoretical analysis, we have found an advantage of a-Si:H/μc-Si:H/μc-Si:H structure for an application to low-concentration photovoltaics. For the fabricated solar cells, a conversion efficiency of 8.86% at 1 sun and and 9.86% under 7.2 suns, and a total photocurrent from each subcell of 24.1 mA/cm2 were achieved although there was still a current mismatch among component subcells.