Impact of electrically formed interfacial layer and improved memory characteristics of IrOx/high-κx/W structures containing AlOx,GdOx, HfOx,and TaOx switching materials

Improved switching characteristics were obtained from high-κ oxides AlO_x, GdO_x, HfO_x, and TaO_x in IrO_x/high-κ_x/W structures because of a layer that formed at the IrO_x/high-κ_x interface under external positive bias. The surface roughness and morphology of the bottom electrode in these devices were observed by atomic force microscopy. Device size was investigated using high-resolution transmission electron microscopy. More than 100 repeatable consecutive switching cycles were observed for positive-formatted memory devices compared with that of the negative-formatted devices (only five unstable cycles) because it contained an electrically formed interfacial layer that controlled ‘SET/RESET’ current overshoot. This phenomenon was independent of the switching material in the device. The electrically formed oxygen-rich interfacial layer at the IrO_x/high-κ_x interface improved switching in both via-hole and cross-point structures. The switching mechanism was attributed to filamentary conduction and oxygen ion migration. Using the positive-formatted design approach, cross-point memory in an IrO_x/AlO_x/W structure was fabricated. This cross-point memory exhibited forming-free, uniform switching for >1,000 consecutive dc cycles with a small voltage/current operation of ±2 V/200 μA and high yield of >95% switchable with a large resistance ratio of >100. These properties make this cross-point memory particularly promising for high-density applications. Furthermore, this memory device also showed multilevel capability with a switching current as low as 10 μA and a RESET current of 137 μA, good pulse read endurance of each level (>10⁵ cycles), and data retention of >10⁴ s at a low current compliance of 50 μA at 85°C. Our improvement of the switching characteristics of this resistive memory device will aid in the design of memory stacks for practical applications.     

Solubilities of Carbon Dioxide in Polyethylene Glycol Ethers

New extensive data are reported for the solubility of carbon dioxide in fourteen physical solvents, and compared to two other solvents widely used in industry (selexol® and sulfolane). The solubility data are expressed by Henry's law constants and have been measured at 25 °C, 40 °C and 60 °C, using an Autoclave cell. The study concludes that polyethylene glycol dimethyl ethers, and mixtures of these solvents are the best solvents for CO₂ removal.     

A Novel Approach to Model Threshold Voltage and Subthreshold Current of Graded-Doped Junctionless-Gate-All-Around (GD-JL-GAA) MOSFETs

Silicon - This present article interprets the analytical models of central channel potential, the threshold voltage, and subthreshold current for Graded-Doped Junctionless-Gate-All-Around...     

Martian regolith—Ti6Al4V composites via additive manufacturing

In order to investigate the in-space in situ resource utilization, directed energy deposition (DED)-based additive manufacturing (AM) has been utilized to process Martian regolith—Ti6Al4V (Ti64) composites. Here we investigated the processability of depositing 5, 10, and 100 wt% of Martian regolith premixed with Ti6Al4V using laser-based DED, analyzing the printed structure via X-ray diffraction, Vicker's microhardness, scanning electron microscopic imaging, and wear characteristics utilizing an abrasive water jet cutter to simulate abrasive environments on the Martian surface. The results indicate that the surface roughness and hardness of the composites increase with respect to the Martian regolith’ weight percentage due to in situ ceramic reinforcement. For instance, i5-wt% addition of Martian regolith increased the Vicker's microhardness from 366 ± 6 HV_0.2 for as-printed Ti64 to 730 ± 27 HV_0.2 while maintaining similar abrasive wear performance as Ti6Al4V. The results point toward laser-based AM for fabricating Ti64—Martian regolith composites with comparable properties. The study also reveals promising results in limiting the mass burden for future space missions, resulting in cheaper and easier launches.     

Filler Wetting in Miscible ESBR/SSBR Blends and Its Effect on Mechanical Properties

The selective wetting behavior of silica in emulsion styrene butadiene rubber (ESBR)/solution styrene butadiene rubber (SSBR) blends is characterized by the wetting concept, which is further developed for filled blends based on miscible rubbers. It is found that not only the chemical rubber–filler affinity but also the topology of the filler surface significantly influences the selective filler wetting in rubber blends. The nanopore structure of the silica surface has been recognized as the main reason for the difference in the wetting behavior of the branched ESBR molecules and linear SSBR molecules. However, the effect of nanopore structure becomes more significant in the presence of silane. It is discussed that the adsorption of silane on silica surface constricts the nanopore to some extent that hinders effectively the space filling of the nanopores by the branched ESBR molecules but not by the linear SSBR molecules. As a result, in silanized ESBR/SSBR blends the dominant wetting of silica surface by the tightly bonded layer of SSBR molecules causes a low‐energy dissipation in the rubber–filler interphase. That imparts the low rolling resistance to the blends similar to that of a silica‐filled SSBR compound, while the ESBR‐rich matrix warrants the good tensile behavior, i.e., good abrasion and wear resistance of the blends.

     

Elastic Constants of Erbia Single Crystals

The elastic properties of single-crystalline erbia (Er₂O₃) at room temperature have been investigated using resonant ultrasound spectroscopy. The three independent stiffness constants of anisotropic Er₂O₃ cubic type-C crystals have been measured. The values of the stiffness constants were c ₁₁= 256.4 GPa, c ₁₂= 146.8 GPa, and c ₄₄= 75.2 GPa. From the stiffness constants, the estimated values for dense polycrystalline erbia for Young's modulus, the shear modulus, the bulk modulus, and Poisson's ratio at room temperature were 179 GPa, 67 GPa, 183.3 GPa, and 0.337, respectively. The value of Young's modulus is a minimum along [001] and a maximum along [111]. The value of the shear modulus is independent of the direction in the (001) and (111) planes, whereas it decreases in (11¯0) from 75 GPa along [001] to 55 GPa along [110].     

Cavitation Erosion Characteristics of Nitrocarburized and HPDL-Treated Martensitic Stainless Steels

This article deals with plasma ion-nitrocarburising and high power diode laser (HPDL) surface treatment of 13Cr4Ni and X10CrNiMoV1222 martensitic stainless steels to enhance their cavitation erosion resistance. These steels are commonly used in hydro turbines and boiler feed pumps. These treated steels have been evaluated for cavitation erosion resistance and it has been observed that the plasma ion-nitrocarburising process has significantly enhanced the cavitation erosion resistance as compared to untreated steel whereas HPDL-treated steels have shown marginal improvement. This is due to formation of high hardness nitrides during nitrocarburising and formation of moderate hardness martensitic phase due to rapid heating and cooling rates involved in HPDL treatment. The cavitation erosion and micro-hardness data of plasma ion-nitrocarburized as well as HPDL-treated steel samples and their comparison with hard deposits such as stellite and HVOF coating form the main part of the article.     

Calibration of a hexapod machine tool using a redundant leg

Parallel configurations are recently being applied to the machine tool with the hopes of greater rigidity, stability, and accuracy than conventional multi-axis structures allow. However, the many calibration methods presently available for serial machine tools are not applicable to hexapod type structures. A calibration method is presented that uses a ball–bar or other simple length measuring device to act as an ‘extra leg,’ allowing calibration of the hexapod's true kinematic parameters. This method utilizes a total least squares minimization, does not require any special hexapod configuration or difficult six degree of freedom pose measurements, and is effective with as few as one additional length sensor. Selection of calibration pose sets is briefly discussed, as well as the influence of measurement noise on calibration accuracy. Simulations show the potential for this algorithm to significantly reduce errors to the point where machining errors are within 5–10 times the measurement errors.     

Blends of polypropylene and ethylene octene comonomer with conducting fillers: Influence of state of dispersion of conducting fillers on electrical conductivity

Blends of polypropylene/ethylene octene comonomer (PP/EOC) with conducting fillers viz., carbon black (CB) and multiwall carbon nanotubes (MWNT) were prepared using melt mixing technique with varying filler concentration and blend compositions. Thermo gravimetric analysis studies indicated that presence of filler enhanced the thermal stability of PP/EOC blends. Morphological analysis revealed the formation of matrix‐dispersed droplet and co‐continuous type of morphology depending on the blend compositions. Significant reduction in droplet size and finer ligament thickness in co‐continuous structure were observed in the blends with filler due to compatibilization action. Fillers were found to be aggregated in the EOC phase irrespective of blends compositions and could be related to the affinity of the fillers toward EOC phase. The electrical conductivity of PP/EOC blends with CB and MWNT was found to be highest for 80/20 composition and decreased as EOC content increased. The percolation threshold of CB was between 10 and 15 wt% for the 80/20 and 70/30 blends whereas it was 15–20 wt% for blends with EOC content higher than 30 wt%. The percolation threshold was 2–3 wt% MWNT for PP/EOC blends. This was attributed to the aggregated filler network preferentially in the EOC phase. The melt‐rheological behavior of PP/EOC blends was significantly influenced in presence of both the fillers. POLYM. ENG. SCI., 2009. © 2009 Society of Plastics Engineers