A study on carbon coating to silicon and electrochemical characteristics of Si-C/Li cells

The aim of this paper is to study the electrochemical behavior of Si-C material synthesized by heating a mixture of silicon and polyvinylidene fluoride (PVDF) in the ratios of 5, 20, and 50 wt%. The particle size of the synthesized material was found to be increased with increase in the PVDF ratio. The coexistence of silicon with carbon was confirmed from the XRD analysis. A field emission scanning electron microscope (FESEM) study performed with the material proved the improvement in coating efficiency with increase in the PVDF ratio. Coin cells of the type 2025 were made by using the synthesized material, and the electrochemical properties were studied. An electrode was prepared by using the developed Si-C material. Si-C|Li cells were made with this electrode. A charge|discharge test was performed for 20 cycles at 0.1 C hour rate. Initial charge and discharge capacities of Si-C material derived from 20 wt% of PVDF was found to be 1,830 and 526 mAh|g, respectively. Initial charge/discharge characteristics of the electrode were analyzed. The level of reversible specific capacity was about 216mAh/g at Si-C material derived from 20 wt% of PVDF, initial intercalation efficiency (IIE), intercalation efficiency at initial charge/discharge, was 68%. Surface irreversible specific capacity was 31 mAh/g, and average specific resistance was 2.6 ohm * g.     

Closed-loop identification of wafer temperature dynamics in a rapid thermal process

Single wafer rapid thermal processing (RTP) can be used for various wafer fabrication steps such as annealing, oxidation and chemical vapor deposition. A key issue in RTP is accurate temperature control, i.e., the wafer temperatures should be rapidly increased while maintaining uniformity of the temperature profile. A closed-loop identification method that suppresses RTP drift effects and maintains a linear operating region during identification tests is proposed. A simple graphical identification method that can be implemented on a field controller for autotuning and a nonlinear least squares method have been investigated. Both methods are tested with RTP equipment based on a design developed by Texas Instruments.     

Synthesis and evaluation of an intercalator-polyamide hairpin designed to target the inverted CCAAT box 2 in the topoisomerase IIalpha promoter

The synthesis and DNA-binding properties of a novel naphthalimide-polyamide hairpin (3) designed to target the inverted CCAAT box 2 (ICB2) site on the topoisomerase IIalpha (topoIIalpha) promoter are described. The polyamide component of 3 was derived from the minor-groove binder, 2, and tailored to bind to the 5'-TTGGT sequence found in and flanking ICB2. The propensity of mitonafide 4 to intercalate between G-C base pairs was exploited by the incorporation of a naphthalimide moiety at the N terminus of 2. Hybrid 3 targeted 5'-CGATTGGT and covered eight contiguous base pairs, which included the underlined ICB2 site. DNase I footprinting analysis with the topoIIalpha promoter sequence demonstrated that 3 bound selectively to the ICB2 and ICB3 sites. Thermal-denaturation studies confirmed these results, and the highest degree of stabilization was found for ICB2 and -3 in preference to ICB1 (4.1, 4.6, and 0.6 degrees C, respectively). CD studies confirmed minor-groove binding and suggested a 1:1 binding stoichiometry. Emission-titration experiments established intercalative binding. Surface plasmon resonance results showed strong binding to ICB2 (2.5x10(7) M(-1)) with no observable binding to ICB1. Furthermore, the binding constant of 3 to ICB2 was larger than that of the parent polyamide 2. The increased binding affinity was primarily due to a reduction in the dissociation-rate constant of the polyamide-DNA complex, which can be attributed to the N-terminal naphthalimide moiety. In addition, the binding site of 3 was larger than that of 2, which innately improved sequence selectivity. We conclude that the polyamide-naphthalimide 3 selectively binds to the ICB2 site by simultaneous intercalation and minor-groove binding, and warrants further investigation as a model compound for the regulation of topoIIalpha gene expression.     

Interfacial Peeling Moments and Shear Forces at Free Edges of Multilayers Subjected to Thermal Stresses

Stresses normal to interfaces, i.e., interfacial peeling stresses and interfacial shear stresses, exist locally at edges of multilayers because of both the thermal mismatch between layers and the free-edge effect. These peeling and shear stresses can result in modes I and II edge delamination, respectively. However, because of the complexity of the problem, exact closed-form solutions for these stresses are very difficult if not impossible to derive even for bilayered systems. Hence, instead of the detailed stress field at edges, both the interfacial peeling moment resulting from the localized peeling stresses and the interfacial shear force resulting from the localized shear stresses are analyzed here. Exact closed-form solutions for the peeling moment and the shear force at each interface in elastic multilayered systems are derived. To illustrate the application of present closed-form solutions, specific results are calculated for five-layered thermal barrier coating systems, and a finite-element analysis is also performed to confirm the analytical results.     

Piezoelectric Multilayer Ceramic/Polymer Composite Transducer with 2–2 Connectivity

A multilayer piezoelectric ceramic/polymer composite with 2–2 connectivity was fabricated by thermoplastic green machining after co-extrusion. The multilayer ceramic body was composed of piezoelectrically active lead zirconate titanate (PZN)–lead zinc niobate (PZN)-lead zirconate titanate (PZT) layers and electrically conducting PZN–PZT/Ag layers. After co-extruding the thermoplastic body, which consisted of five piezoelectric layers interspersed with four conducting layers, it was computer numeric-controlled machined to create periodic channels within it. Following binder burnout and sintering, an 18 vol% array of 190 μm thin PZT slabs with a channel size of 880 μm was fabricated. The channels were filled with epoxy in order to fabricate a PZN–PZT/epoxy composite with 2–2 connectivity. The piezoelectric coefficient (effective d ₃₃) and hydrostatic figure of merit ( d _h× g _h) of the PZN–PZT/epoxy composite were 1200 pC/N and 20 130 × 10⁻¹⁵ m²/N, respectively. These excellent piezoelectric characteristics as well as the relatively simple fabrication procedure will contribute in widening the application range of the piezoelectric transducers.     

Synthesis and structural properties of lithium titanium oxide powder

Recently, lithium titanium oxide material has gained renewed interest in electrodes for lithium ion rechargeable batteries. We investigated the influence of excess Li on the structural characteristics of lithium titanium oxide synthesized by the conventional powder calcination method, considering the potential for mass production. The lithium excess ratio is controlled by using different weight of Li₂CO₃ powder during calcination. X-ray diffraction (XRD) measurement for the synthesized powder showed that the lithium titanium oxide material with excess lithium content had a spinel crystal structure as well as a different crystal one. In addition, high resolution transmission electron microscopy (HRTEM) and field emission scanning electron microscopy (FESEM) measurement revealed that the lithium titanium oxide powders with a lithium excess ratio of 5–20% exhibited a two phase formation. Inductively coupled plasma — atomic emission spectrometer (ICP-AES) and energy dispersive x-ray spectroscopy (EDX) measurements were used to analyze composition of the lithium titanium oxide powder. These results suggested that the conventional calcination method, considering the potential for mass production, formed two phases according to the Li excess amount in initial raw materials.     

Sulfate attack monitored by microCT and EDXRD: Influence of cement type, water-to-cement ratio, and aggregate

X-ray microtomography (microCT) and spatially resolved energy dispersive X-ray diffraction (EDXRD) were used in combination to non-destructively monitor the physical and chemical manifestations of damage in Portland cement paste samples subjected to severe sodium sulfate attack. Additional measurements of expansion and compressive strength were made on complementary mortar and cement paste specimens. Specifically, the influences of cement type (ASTM Types I and V), water-to-cement ratio (0.485 and 0.435), and the presence of aggregate on the rate and forms of damage were examined. As expected, Type V cement samples exhibited less cracking and expansion than the Type I cement samples. EDXRD indicated an anticorrelation between ettringite and gypsum in the near-surface region for Type V samples, which may be associated with crack formation. An unanticipated result for Type I cement pastes was that cracking was apparent at earlier exposure times and progressed more rapidly for samples with w / c of 0.435, than for those with w / c of 0.485. Possible mechanisms for this behavior are proposed. The presence of aggregate particles resulted in a more rapid rate of cracking, as compared to the corresponding cement paste sample.     

A new testing configuration for shrinkage cracking of shotcrete and fiber reinforced shotcrete

Shotcrete and fiber reinforced shotcrete are commonly employed to produce layers or linings with large surface area versus volume ratios. Restrained shrinkage cracking is hence an important concern. The common test set-up used for shrinkage cracking of concrete, with a ring specimen cast around a stiff steel form, is not applicable to shotcrete. A new testing configuration, consisting of a shotcrete specimen bonded to a steel I-section and angles, is therefore proposed. In this investigation, a finite element analysis was first performed to identify member sizes that provide a good compromise between the effectiveness of constraint and weight of steel members. Restrained shrinkage tests using this new configuration were performed for plain and fiber reinforced shotcrete. Despite the simplifying assumptions in the finite element analysis, the predicted degree of restraint is in reasonable agreement with test results. From the results, the proposed set-up is shown to be a practical and viable approach for investigating the shrinkage cracking behavior of shotcrete and fiber reinforced shotcrete.     

Numerical analysis of galvanic corrosion of Zn/Fe interface beneath a thin electrolyte

A numerical analysis of galvanic corrosion of a Zn/Fe interface beneath a thin layer electrolyte is presented. Specifically, a circular defect, where the zinc coating has been removed, is considered. It is assumed that both oxygen reduction and iron oxidation can occur on the Fe surface, while only zinc oxidation occurs on the Zn surface. The importance of electrolyte thickness and conductivity and defect radius is considered. It is assumed that the iron and zinc oxidation rates are described by a Tafel relationship. If the kinetic parameters of the oxidation reactions are known, the cathodic protection of Fe is a function of a Wagner number, the ratio of the electrolyte thickness to the defect radius, and the ratio of the radius of the defect to the outer radius of the zinc layer.