Novel preparation and high electrical performance effect of Mn-doped ultra-high surface area activated carbon (USAC) as an additive for Ni hybrid capacitors

This paper reports the synthesis of various molar concentrations of manganese (Mn)-doped Ultra-High Surface area Activated Carbon (USAC) additives and their efficient use as cathode materials for supercapacitors. We synthesized the nanoparticles via a novel and facile dip-coating process and characterized them in detail by various analytical techniques. The SEM, EDAX, and XPS results showed that the Mn ions were successfully substituted on the USAC additives’ layered structure without any structural changes. The long cyclic stability of the as-prepared Mn-doped USAC additives was tested as a cathode material for supercapacitors at different current densities. The detailed experimental results showed that the Mn dopant content crucially determines the electrochemical performances of the USAC additives. Electrochemical measurements showed that the MnCEP-S600HTT with 0.10 mol% molar concentration of Mn dopant gives the best cycling performances. It delivers a discharge capacity of 262.9 mAh g^?1 after 100 cycles. Further increasing the current density to 1000 mA g^?1 allowed it to still maintain 253.6 mAh g^?1 after 200 cycles. We confirmed that the structure of Mn-doped USAC additives is an important pole to improve the structural stability and electrochemical properties.     

Direct electrochemistry of laccase immobilized on au nanoparticles encapsulated-dendrimer bonded conducting polymer: application for a catechin sensor

The direct electrochemistry of laccase was promoted by Au nanoparticle (AuNP)-encapsulated dendrimers (Den), which was applied for the detection of catechin. To increase the electrical properties, AuNPs were captured in the interiors of the dendrimer (Den-AuNPs) as opposed to attachment at the periphery of dendrimer. To prepare Den-AuNPs, the Au(III) ions were first coordinated in the interior of dendrimer with nitrogen ligands and then reduced to form AuNPs. The size of AuNPs encapsulated within the interior of the dendrimer was determined to be 1.7 +/- 0.4 nm. AuNPs-encapsulated dendrimers were then used to covalently immobilize laccase (PDATT/ Den(AuNPs)/laccase) through the formation of amide bonds between carboxylic acid groups of the dendrimer and the amine groups of laccase. Each layer of the PDATT/Den(AuNPs)/laccase probe was characterized using CV, EIS, QCM, XPS, SEM, and TEM. The PDATT/Den(AuNPs)/laccase probe displayed a well-defined direct electron-transfer (DET) process of laccase. The quasi-reversible redox peak of the Cu redox center of the laccase molecule was observed at -0.03/+0.13 V vs Ag/AgCl, and the electron-transfer rate constant was determined to be 1.28 s (-1). A catechin biosensor based on the electrocatalytic process by direct electrochemistry of laccase was developed. The linear range and the detection limit in the catechin analysis were determined to be 0.1-10 and 0.05 +/- 0.003 microM, respectively. Interference effects from various phenolic and polyphenolic compounds were also studied, and the general applicability of the biosensor was evaluated by selective analysis of real samples of catechin.     

J resistance behavior in functionally graded materials using cohesive zone and modified boundary layer models

This paper describes elastic–plastic crack growth resistance simulation in a ceramic/metal functionally graded material (FGM) under mode I loading conditions using cohesive zone and modified boundary layer (MBL) models. For this purpose, we first explore the applicability of two existing, phenomenological cohesive zone models for FGMs. Based on these investigations, we propose a new cohesive zone model. Then, we perform crack growth simulations for TiB/Ti FGM SE(B) and SE(T) specimens using the three cohesive zone models mentioned above. The crack growth resistance of the FGM is characterized by the J-integral. These results show that the two existing cohesive zone models overestimate the actual J value, whereas the model proposed in the present study closely captures the actual fracture and crack growth behaviors of the FGM. Finally, the cohesive zone models are employed in conjunction with the MBL model. The two existing cohesive zone models fail to produce the desired K–T stress field for the MBL model. On the other hand, the proposed cohesive zone model yields the desired K–T stress field for the MBL model, and thus yields J _R curves that match the ones obtained from the SE(B) and SE(T) specimens. These results verify the application of the MBL model to simulate crack growth resistance in FGMs.     

Direct analysis of trace phenolics with a microchip: in-channel sample preconcentration, separation, and electrochemical detection

A micrototal analytical method assembling in-channel preconcentration, separation, and electrochemical detection steps has been developed for trace phenolic compounds. A micellar electrokinetic chromatography separation technique was coupled with two preconcentration steps of field-amplified sample stacking (FASS) and field-amplified sample injection (FASI). An amperometric detection method with a cellulose-dsDNA-modified, screen-printed carbon electrode was applied to detect preconcentrated and separated species at the end of the channel. The microchip was composed of three parallel channels: first, two are for the sample preconcentration using FASS and FASI methods, and the third one is for the separation and electrochemical detection. The modification of the electrode surface improved the detection performance by enhancing the signal-to-noise characteristic without surface fouling of the electrode. The method was examined for the analysis of eight phenolic compounds. Experimental parameters affecting the analytical performance of the method were assessed and optimized. The preconcentration factor was increased by about 5200-fold as compared with a simple capillary zone electrophoretic analysis using the same channel. Reproducible response was observed during multiple injections of samples with a RSD of <8.0%. The calibration plots were shown to be linear (with the correlation coefficient between 0.9913 and 0.9982) over the range of 0.4-600 nM. The sensitivity was between 0.17 +/- 0.001 and 0.48 +/- 0.006 nA/nM, with the detection limit of approximately 100 to approximately 150 pM based on S/N = 3. The applicability of the method to the direct analysis of trace phenolic compounds in water samples was successfully demonstrated.     

Ta2O5-Incorporated WO3 nanocomposite film for improved electrochromic performance in an acidic condition

We report electrochromic and electrochemical properties of a WO3-Ta2O5 nanocomposite electrode that was fabricated from co-sputtering. Transmission electron microscopy (TEM) images of the WO3-Ta20 nanocomposite electrode revealed that morphology of the WO3 film was changed by incorporation of Ta2O5 nanoparticles, and their chemical states were confirmed to be W6+ and Ta5+ oxides from X-ray photoelectron spectroscopy (XPS). The introduction of Ta2O5 to the WO3 film played a role in alleviating surface roughness increase during continuous potential cycling; whereas the surface roughness of the WO3 film was increased from ca. 3.0 nm to ca. 13.4 nm after 400 cycles, the roughness increase on the WO3-Ta2O5 was significantly reduced to 4.2 nm after 400 cycles, as investigated by atomic force microscopy (AFM). This improvement of the stability by adding Ta2O5 may be responsible for the enhanced electrochemical and optical properties over long-term cycling with the WO3-Ta2O5 nanocomposite electrode.     

Thermal conductivity and mechanical properties of various cross-section types carbon fiber-reinforced composites

In this work, to study the characteristics of carbon fiber-reinforced composites with different fiber cross-section types, such as round, C, and hollow-shape, the thermal conductivity and mechanical properties were investigated and compared. The thermal conductivity was measured by means of steady-state method to the parallel and perpendicular direction of reinforcing fibers. The mechanical properties were evaluated by a variety of test methods i.e., flexural, interlaminar shear strength, and impact strength. As a result, it was found that the thermal conductivity was greatly depended on the cross-section type of the reinforcing fibers, as well as, the reinforcing orientation. Especially, the anisotropy factor (k _///k ) and the thermal diffusivity factor (_///) of C and hollow-type carbon fiber-reinforced composites showed about two times higher values than those of round-type one. Also, the mechanical results showed that C and hollow-type carbon fibers-reinforced composites had higher values than those of round-type one in all mechanical tested. These results were probably due to the basic properties of non-circular (C and hollow-type) carbon fiber which can improve interfacial binding forces and widen interfacial contact area between reinforcement and matrix, resulting in effectively transferring the applied stress.     

Acicular ferrite microstructure in titanium bearing low carbon steels

Abstract

Different microstructures having acicular ferrite as the major phase but with various types and amounts of microphases were obtained by applying different cooling processes to C–Mn steels containing fine non-metallic inclusions. Optical and electron microscopy were carried out to identify the various microphases in the acicular ferrite microstructure, and their mechanical properties were measured and compared to study the effect of the microphases on the microstructure–properties relationship in C–Mn wrought steels. The existence and increase of the fraction of small isolated martensite between the acicular ferrite laths were found to play an important role in determining the tensile strength and low temperature impact toughness of the steels. However, the elongation and room temperature impact toughness were rather insensitive to the microphases. This may be attributed to the uniform distribution and isolation of relatively small martensite due to the fine interlocking character of the acicular ferrite microstructure.     

Doping and electrical characteristics of in-situ heavily B-doped Si1−x−yGexCy films epitaxially grown using ultraclean LPCVD

Doping and electrical characteristics of in-situ heavily B-doped Si_1−x−yGe_xC_y (0.22<x<0.6, 0<y<0.02) films epitaxially grown on Si(100) were investigated. The epitaxial growth was carried out at 550°C in a SiH₄–GeH₄–CH₃SiH₃–B₂H₆–H₂ gas mixture using an ultraclean hot-wall low-pressure chemical vapor deposition (LPCVD) system. It was found that the deposition rate increased with increasing GeH₄ partial pressure, and only at high GeH₄ partial pressure did it decrease with increasing B₂H₆ as well as CH₃SiH₃ partial pressures. With the B₂H₆ addition, the Ge and C fractions scarcely changed and the B concentration (C_B) increased proportionally. The C fraction increased proportionally with increasing CH₃SiH₃ partial pressures. These results can be explained by the modified Langmuir-type adsorption and reaction scheme. In B-doped Si_1−x−yGe_xC_y with y=0.0054 or below, the carrier concentration was nearly equal to C_B up to approximately 2×10²⁰ cm⁻³ and was saturated at approximately 5×10²⁰ cm⁻³, regardless of the Ge fraction. The B-doped Si_1−x−yGe_xC_y with high Ge and C fractions contained some electrically inactive B even at the lower C_B region. Resistivity measurements show that the existence of C in the film enhances alloy scattering. The discrepancy between the observed lattice constant and the calculated value at the higher Ge and C fraction suggests that the B and C atoms exist at the interstitial site more preferentially.