To save content items to your account,
please confirm that you agree to abide by our usage policies.
If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account.
Find out more about saving content to .
To save content items to your Kindle, first ensure no-reply@cambridge.org
is added to your Approved Personal Document E-mail List under your Personal Document Settings
on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part
of your Kindle email address below.
Find out more about saving to your Kindle.
Note you can select to save to either the @free.kindle.com or @kindle.com variations.
‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi.
‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.
Vanadium oxides are strongly correlated electron systems that are interesting both from a fundamental scientific point of view and for possible future applications including memory and sensors. In this contribution, we report on the epitaxial growth of V2O3 thin films on c-Al2O3 (0001) with molecular beam epitaxy and atomic oxygen. We studied the influence of deposition rate and substrate temperature on the structural properties and the metal-insulator transition.
In this paper we show that a flash lamp can be employed to induce controlled lateral solidification of a-Si thin films. Specifically, a dual xenon-arc-lamp-based system was utilized to induce location-controlled complete melting by shaping the incident beam using a contact mask. The resulting laterally solidified microstructure consisted of exceptionally long grains (~10s to ~100s of μm) that were relatively free of intragrain-defects. With further development and optimization, the approach may lead to cost-effective/high-throughput processes and systems that can capture and enhance the advantages of laser-based/melt-mediated crystallization techniques.
One of the main driving force for the development of advanced structural materials is weight saving especially in the transportation industry in order to reduce CO2 emission. The utilization of gamma aluminides, as good candidates for aerospace applications, is strongly related to the development of a cost-effective and robust processing route, as far as possible. It is well established that the processing route, i.e. cast, wrought or PM, has a dramatic effect on the microstructure and texture of gamma-TiAl alloys. Therefore, significant microstructural variations through post-heat treatments coupled with compositional modifications can only guarantee a proper balance of desired properties. However, a number of metallurgical factors during the processing steps can contribute to some scattering in properties. This review will highlight several critical process variables in terms of the resulting g-TiAl microstructures. Of primary importance is the as-cast texture which is difficult to control and may contribute to prefer some alternative processing routes to ensure a better repeatability in mechanical results. Some innovative processing techniques for controlling the structure will then be presented. The main point which will be discussed in this paper is whether an approach leading to a robust process would not be at the expense of the high performance of the structural material.
A three-dimensional (3D) carbon nanotube (CNT) network computational model was developed to investigate the electrical conductivity and current flow in polymer composites with randomly dispersed CNTs. A search algorithm was developed to determine conductive paths for 3D CNT arrangements and to account for electron tunneling effects. Tunneled currents were obtained as a function of tunneling distance and matrix material. Several possible CNT conductive paths were obtained and finite-element representative volume elements (RVEs) were then used to predict current densities in different CNT arrangements. The predictions indicate that random CNT arrangements can be optimized for current transport.
In this contribution we report on the dynamics of the phase evolution in electrochemically deposited Sn thin films on copper coated substrates studied by in-situ X-ray diffraction (XRD) and Focused Ion Beam Microscopy (FIB). The data obtained is used to extract fundamental parameters such as the activation energy and the rate constant of the reaction. Results indicate that the formation of intermetallic phases in these thin layers, in which the grain size exceeds the layer thickness, is not limited by diffusion but rather by reaction kinetics.
We present here new information on the effect of irradiation temperature on the strength and mechanical anisotropy of Zr-2.5%Nb CANDU pressure tube material. Polished samples aligned normal to the transverse (TN), axial (AN) and radial (RN) directions of the pressure tube were irradiated at 300°C with 8.5 MeV Zr+ ions to assess the effect of concurrent thermal annealing of the irradiation damage. Constant-load micro-indentation creep tests were performed at 25°C at indentation depths from 0.1 to 2.0 μm on the ion irradiated samples.
The increase in the initial indentation stress with increasing levels of Zr+ ion irradiation at 300°C was lower than that reported earlier for similar samples exposed to Zr+ irradiation at 25°C. While the anisotropy of the indentation stress decreased significantly with Zr+ ion irradiation, the level of the decrease was reduced when the irradiation was performed at 300oC compared to 25oC. The apparent activation energy ΔG0 of the obstacles that limit the rate of dislocation glide during indentation creep did not change with indentation direction but did increase with increasing levels of Zr+ ion damage. The values of ΔG0 were, again, lower for samples that were irradiated at 300°C than for those irradiated at 25oC.
The observed differences in the magnitude of, and the anisotropy of, the initial indentation stress and also the decrease in the apparent activation energy of the indentation creep process of Zr-2.5%Nb samples irradiated with Zr+ ions at 300oC compared to those irradiated at 25oC indicate the effect that concurrent thermal annealing has on the accumulation of irradiation damage. The effect of irradiation temperature on reducing the degree of, and the strength of, irradiation induced crystallographic damage must therefore be considered when predicting the strength and thermal creep behaviour of irradiated nuclear materials.
Millimeter-wave thermal analysis instrumentation is being developed for characterization of high temperature materials required for diverse fuel and structural needs in extreme high temperature reactor environments. A two-receiver 137 GHz system with orthogonal polarizations for anisotropic properties resolution has been implemented at MIT and is being tested with graphite and silicon carbide specimens at temperatures up to 1300ºC. Real time measurement sensitivity to submillimeter surface displacement and simulated anisotropic surface emissivity is demonstrated.
An optical isolator with a TiO2/(CeY)3Fe5O12 guiding layer was studied. A nonreciprocal phase shift was calculated in the magneto-optic waveguide with the TiO2/(CeY)3Fe5O12 guiding layer at a wavelength of 1.55 μm. By employing a multimode interference coupler as coupling devices, the total device length of approximately 600 μm was achieved. An interferometric optical isolator with distinct layer structures, which could be operated in a unidirectional magnetic field, was also designed.
The molecular structure and dynamics of carbon nanostructures is much discussed throughout the literature, mostly from the theoretical side because of a lack of suitable experimental techniques to adequately engage the problem. A technique that has recently become available is low-voltage aberration-corrected transmission electron microscopy. It is a valuable tool with which to directly observe the atomic structure and dynamics of the specimen in situ. Time series aberration-corrected low-voltage transmission electron microscopy is used to study the dynamics of single-wall carbon nanotubes in situ. We confirm experimentally previous theoretical predictions for the agglomeration of adatoms forming protrusions and subsequent removal. A model is proposed how lattice reconstruction sites spread. In addition, the complete healing of a multi-vacancy consisting of ca. 20 missing atoms in a nanotube wall is followed.
MnO nanoparticles were surface modified using two different multifunctional polymers. By introducing a PEG group, the long term stability, MRI applicability and sterile filtration could be greatly improved. Furthermore, PEGylated MnO NPs were less toxic compared to non-PEGylated NPs. The results suggest that these nanoparticles are suitable for in vivo applications.
We propose a novel concept of optical detection of thermal neutrons in a passive device that exploits transmutation of Dy-164, a dominant, naturally occurring isotope of dysprosium, into a stable isotope of either holmium Ho-165 or erbium Er-166. Combination of the high thermal neutron capture cross section of ~2,650 barns and transmutation into two other lanthanides makes Dy-164 a very attractive alternative to traditional methods of neutron detection that will be completely insensitive to gamma irradiation, thus reducing greatly the likelihood of false alarms. The optically enabled neutron detection relies on significant differences in optical properties of Dy, Ho, and Er that are not sensitive to a particular isotope, but change considerably from one element to another. While the concept applies equally well to bulk materials and to nanocrystals, nanocrystalline approach is much more attractive due to its significantly lower cost, relative ease of colloidal synthesis of high quality nanocrystals (NCs), and superior optical and mechanical properties of NCs compared to their bulk counterparts. We report on colloidal synthesis of DyF3 NCs, both doped and undoped with Ho and co-doped with Ce and Eu to enhance their optical properties. We also report on DyF3:10%Ce and DyF3:10%Eu NCs irradiated with thermal neutrons from a Cf-252 source and their optical characterization.
The combination of dwindling oil reserves and growing concerns over carbon dioxide emissions and associated climate change is driving the urgent development of routes to utilize renewable feedstocks as sustainable sources of fuels. Catalysis has a rich history of facilitating energy efficient selective molecular transformations and contributes to 90% of chemical manufacturing processes and to more than 20% of all industrial products. In a post-petroleum era catalysis will be central to overcoming the engineering and scientific barriers to economically feasible routes to bio-fuels. This article will highlight some of the recent developments in the development of solid acid and base catalysts for the transesterification of oils to biodiesel. Particular attention will be paid to the challenges faced when developing new catalysts and importance of considering the design of pore architectures to improve in-pore diffusion of bulky substrates.
Graphene reveals many extraordinary properties including extremely high room temperature carrier mobility and intrinsic thermal conductivity. Understanding how to controllably modify graphene’s properties is essential for its proposed applications. Here we report on a method for tuning the electrical properties of graphene via electron beam irradiation. It was observed that single-layer graphene is highly susceptible to the low-energy electron beams. We demonstrated that by controlling the irradiation dose one can change, by desired amount, the carrier mobility, shift the charge neutrality point, increase the resistance at the minimum conduction point, induce the “transport gap” and achieve current saturation in graphene. The change in graphene properties is due to defect formation on the graphene surface and in the graphene lattice. The changes are reversible by annealing until some critical irradiation dose is reached.
Thermo-responsive actuation (thermomechanical effects) based on nematic liquid crystal elastomers (LCEs) have become a research priority in the preparation of soft actuators. Nematic LCEs combine the anisotropic features of liquid crystal phases with the rubber elasticity of polymer network. When heated at nematic to isotropic phase transition temperature (N-to-I temp.), a uniaxial thermomechanical deformation of LCEs will undergo at nearly constant volume due to a change of LC director order. Recently, an array of the micro-sized LCE pillars related to such thermomechanical effects have been successfully constructed through a soft lithography technology (i.e., replica molding). The prepared LCE pillars are mono-dispersive and micro-sized. They also possess N-to-I temp. higher than 100°C, largely limiting the available application. By contrast, the present study will report a hexagonal array of nano-sized thermo-responsive pillar actuators that are able to contract and expand in response to temperature changes around a lower N-to-I temp. is manufactured via using reactive rod-like liquid crystal and ultraviolet nanoimprinting technology. According to atomic force microscope (AFM) observation, a hexagonal array of pillars can be easily constructed by nanoimprinting and a responsive surface with a thermo-stimuli-driven roughness change is achieved. The room-temperature AFM scans quantitatively represent the single pillar shows a diameter of ca. 270 nm and 140 nm in depth, and the pitch meaning the averaged inter-pillar distance is measured as ca. 425 nm, thus lying in a nano-sized range. Furthermore, temperature-variable AFM is also utilized to demonstrate the pillar behaves as a thermally-stimulated nano-sized actuator. In our case, when heated above N-to-I phase transition temperature (ca. 65°C), it is clearly observed that the pillar diameter is expanded in the order of over 12-15 % and then reversibly contracted in response to temperature drop.
Shape control of nanocrystals has become an indispensable part in material research, such as developing new battery raw materials and synthesizing high activity catalysts. In this work, one-dimensional LiV3O8 nanorods have been fabricated by high temperature solid-state reaction using V2O5 nanowires as precursors obtained via a hydrothermal method. The as-prepared LiV3O8 nanorods were characterized by x-ray diffraction, transmission electron microscopy, scanning electron microscopy, and galvanostatic tests, compared with LiV3O8 samples synthesized by the traditional one-step solid-state method. The results show that LiV3O8 nanorods exhibited better electrochemical performance than those synthesized by the traditional method, indicating that a different shape will lead to huge distinctions in electrochemical properties. This work demonstrates that Li-insertion/deintercalation dynamics might be crystal morphology-sensitive.
In this report, we present a hot-injection strategy for the synthesis of CuInS2 (CIS) nanocrystals with hexagonal, pyramidal and nanorod shapes. For that purpose copper (I) and indium (III) acetates were dissolved in oleylamine as a high-boiling solvent. Tert-dodecanethiol (t-DDT) was used as a sulfur source. It was mixed with 1-dodecanothiol (1-DDT) and injected at a high temperature. The presence of the second dodecanethiol was necessary to control the growth of the synthesized nanocrystals. We observed a strong influence of the t-DDT amount on the morphology of the CIS nanocrystals. By the variation of the injected solution uniform CIS nanorods with different aspect ratio and size were obtained.
Mo3Ru5MPd (M = Ru, Rh, Pd) as the simulated materials for the undissolved residue in the nuclear fuel reprocessing were prepared by arc melting method. The physical properties and oxidation behavior of the alloys were evaluated from viewpoint of the safety and economy in the reprocessing. The electrical resistivity, ρ, of Mo3Ru5RhPd was shown to be 0.8 μΩm at room temperature. On the other hand, the ρ values of samples without Rh were marked at 0.4 μΩm. The thermal properties of the each sample had the different thermal transfer characteristics. In particular, although the thermal conductivities of Mo3Ru5RhPd and Mo3Ru5Pd2 samples show almost the same value, the lattice thermal conductivities of both samples showed different values. Oxidation behavior was analyzed using the thermogravity(TG) and differential thermal analyses(DTA). The TG curve of each sample by oxidation showed different results. These results indicate that the simulated materials of the alloys without Rh: Mo-Ru-Pd were not appropriate to simulate the thermophysical characteristics of the typical simulated materials with undissolved residue Mo-Ru-Rh-Pd alloys. Therefore, in the spent nuclear fuel reprocessing, the mock test of reprocessing without to use Rh is difficult to carry out.
Strain engineering in composition-controlled Si-Si/Ge nanocluster multilayers with high germanium content (~ 50%) is achieved by varying thicknesses of Si/SiGe layers and studied by low temperature photoluminescence (PL) measurements. The PL spectra show reduction in strained silicon energy bandgap and a splitting presumably associated with partial removal of heavy hole-light hole degeneracy in SiGe valence band. Time-resolved PL measurements performed under different excitation wavelengths show dramatically different PL lifetimes, ranging from ~ 2 μs to 10 ns and an unusually high PL quantum efficiency. The results are explained by using the Si/SiGe interface recombination model, which is supported by ultra-high resolution transmission and analytical electron microscopy measurements.