Electrodeposited carbon nanotube thin films

A successful attempt to grow carbon nanotubes (CNTs) by electrodeposition technique for the first time is reported here. Carbon nanotubes were grown on Si (001) substrate using acetonitrile (1% v/v) and water as electrolyte at an applied d.c. potential ∼20 V. The films were characterized by X-ray Diffraction (XRD), Scanning Electron Microscope (SEM), Raman, optical absorbance, Fourier Transform Infra Red spectroscopy (FTIR) and Electron Spin Resonance (ESR) measurements. The effect of magnetic field on the growth of nanotubes was studied critically. It was found that the presence of magnetic field during electro-deposition played a crucial role on the growth of carbon nanotubes and hence the electronic properties. Photoluminescence (PL) studies indicated band edge luminescence ∼0.72-0.83 eV. Field emission studies indicated lower turn-on voltage and higher current density for films deposited with magnetic field.     

Design of Smart Door Closer System with Image Classification over WLAN

Wireless Personal Communications - A dual purpose system is presented in this paper which serves not only as a door closer, but is equally effective for surveillance purposes. The currently...     

Grafting. III. Copolymerization of methyl methacrylate and methacrylic acid

The method of graft copolymerization of methyl methacrylate on halogen-containing polymer has been utilized for grafting of methyl methacrylate–methacrylic acid monomer pair onto poly(vinyl chloride) and chlorinated rubber. Substantial grafting could be obtained by using the method reported earlier. However, the compositions of the grafted chains are found to deviate appreciably from the compositions calculated from r₁ and r₂ values reported in literature. The reactivity ratios for this pair of monomers have been therefore evaluated using azobisisobutyronitrile and n-butane thiol–dimethyl sulfoxide as initiators. The anomalies of the grafted chain compositions have been discussed and an explanation presented on preferential solvation.     

5G-ZOOM-Game: small cell zooming using weighted majority cooperative game for energy efficient 5G mobile network

Wireless Networks - The rapid escalation of user traffic and service innovation has made the deployment of small cell base stations essential for eventually decreasing energy consumption in future...     

Hot-electron transport in In0.53Ga0.47As

A set of physical constants for In_0.53Ga_0.47As as required for transport calculations is obtained by reviewing the literature. Velocities for fields up to 100 kV/cm, calculated by the Monte Carlo method using these constants, are presented for the temperatures of 95 and 300 K. The calculated values are found to be in good agreement with the available experimental results.     

Electrochemical Impedance Spectroscopic Analysis of Sensitization-Based Solar Cells

Electrochemical impedance spectroscopy (EIS) is a very powerful tool for elucidation of charge transfer and transport processes in sensitization-based solar cells (e.g., dye-sensitized solar cells [DSSCs], quantum dot-sensitized solar cells [QDSSCs], and perovskite solar cells [PSCs]). EIS measures the electrochemical response to small amplitude AC signals over a wide range of frequencies. Analysis of the EIS response provides information about the corresponding parameters of the cells. Here, we review the fundamentals of EIS, charge transport kinetic processes, and equivalent circuit models of sensitization-based solar cells and use these concepts to explain the EIS spectra of DSSCs, QDSSCs, and PSCs. This review will be very useful for understanding the fundamental charge transfer and transport processes in different sensitization-based solar cells and the use of an equivalent circuit model to interpret the observed charge transfer and reactions.     

Studies on IPNS based on nitrile rubber and polyalkyl methacrylates

Sequential interpenetrating polymer networks (IPNs) based on nitrile rubber and various types of polyalkyl methacrylates such as poly(n-butyl methacrylate), poly(ethyl methacrylate), and poly(methyl methacrylate) were synthesized. The compositions of the IPNs could be varied by varying the reaction parameters such as swelling time and concentration of crosslinker. The tensile properties of the IPNs show that with increase in bulkiness of the ester group of the acrylates the tensile strength decreases, whereas elongation at break increases because of decreased stiffness of the acrylate phase. The dynamic modulus and loss tangent of the IPNs also show similar trend because of the above reason. All the IPNs were also tested for dynamic properties under multifrequency mode, and with the help of the WLF equation, the behavior of these IPNs in the frequency range of 1–10⁵ Hz were evaluated. The results showed reasonably high tan δ with good storage modulus in the entire frequency range for all the IPNs. © 1997 John Wiley & Sons, Inc. J Appl Polm Sci 65:549–554, 1997     

Half-of-the-sites reactivity of F235C {lambda}-repressor: implications for the structure of the whole repressor

A site-directed mutation, F235C, was created at the penultimateresidue of the -repressor. Measurement of dimer–monomerdissociation constant suggested that dimer–monomer dissociationof the mutant repressor is similar to that of the wild-type.Affinity towards a single operator O_R1 is also similar to thatof the wild-type repressor. The mutant repressor gene in a multi-copyplasmid confers immunity towards infection by a cI^- lambda phage,suggesting preservation of functional integrity. Far-UV circulardichroism spectra show no major change in the secondary structure.Fluorescence quenching experiments, however, suggest increasedexposure of some tryptophan residues. The urea denaturationprofile indicates decreased stability of a part of the C-terminaldomain. Under non-denaturing conditions, cysteine-235 showshalf-of-the-sites reactivity, i.e. on average only one out oftwo cysteine-235 residues in the dimer shows reactivity towardssulfhydryl reagents. Fluorescence energy transfer between randomlylabeled donor and acceptor fluorescent probes indicates thatonly one sulfhydryl per dimer is reactive, suggesting true half-of-the-sitesreactivity. The structural role of the C-terminal tail in thewhole repressor dimer is discussed.     

Studies on semi‐interpenetrating polymer network based on nitrile rubber and poly(methyl methacrylate)

Sequential interpenetrating polymer networks (IPNs) based on nitrile rubber and poly(methyl methacrylate) (PMMA) were synthesized. IPN compositions were varied by varying the swelling time. Two methods were adopted for making IPNs. The first method is “single‐step IPN” (SIPN) and the second method is “multistep IPN” (MIPN). The compositions were fixed around 90, 80, 70, 60 and 50% of NBR. In SIPN mode, swelling in monomer and subsequent curing was done once. In MIPN mode, swelling in monomer and curing was repeatedly done. Tensile strength of IPNs was found to increase with PMMA content, MIPN showing higher strength compared to SIPN. Dynamic modulus showed a similar trend. The tan δ value was found to decrease with PMMA content. At 62/38 nitrile rubber (NBR)/PMMA, MIPN composition isolated tan δ peaks appeared near glass transition temperatures of NBR and PMMA, respectively. Scanning electron micrograph showed phase‐separated morphology at the same MIPN composition. Solvent resistance increased with IPN formation maintaining higher resistance for MIPN compared to SIPN. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 354–360, 2004     

Molecular modeling guided isotope separation of gadolinium with strong cation exchange resin using displacement chromatography

Molecular modeling was carried out using DFT to identify the suitable displacing agent for carrying out Gd isotope separation using displacement chromatography. EDTA was identified as the best eluting agent among EDTA, malic acid and citric acid. Displacement chromatography of Gd adsorption band in cation exchange resin was performed to observe the isotope effects in the Gd ion exchange processes involving complex forming reagent – EDTA. The heavier isotope of ¹⁶⁰Gd was found to be enriched at the front boundary of Gd adsorption band, while the lighter isotopes of ¹⁵⁵Gd and ¹⁵⁷Gd were enriched at the rear boundary.