Microbial fuel cells - Applications for generation of electrical power and beyond.

A Microbial Fuel Cell is a bioelectrochemical device that exploits metabolic activities of living microorganisms for generation of electric current. The usefulness and unique and exclusive architecture of this device has received wide attention recently of engineers and researchers of various disciplines such as microbiologists, chemical engineers, biotechnologists, environment engineers and mechanical engineers, and the subject of MFCs has thereby progressed as a well-developed technology. Sustained innovations and continuous development efforts have established the usefulness of MFCs towards many specialized and value-added applications beyond electricity generation, such as wastewater treatment and implantable body devices.

Spin interactions in mineral libethenite series: evolution of low-dimensional magnetism.

Interesting magnetic properties and spin-exchange interactions along various possible pathways in the half-integral spin quantum magnetic tetramer system: A(2)PO(4)OH (A=Co, Cu) are investigated. Interplay of structural distortion and the magnetic properties with the evolution of localized band structure explain the gradual transition from a three-dimensional antiferromagnet to a low-dimensional frustrated magnetic system along the series. A detailed study of the exchange mechanism in this system explores various possibilities of complex magnetic interaction.

Slow magnetic relaxations in manganese(III) tetra(meta-fluorophenyl)porphyrin-tetracyanoethenide. Comparison with the relative single chain magnet ortho compound.

Mn(III) tetra(meta-fluorophenyl)porphyrin-tetracyanoethenide coordination polymer (abbreviated meta-F) was synthesized and crystallographically and magnetically characterized. The compound crystallizes in the space group C2/c with four equivalent molecules in the unit cell arranged along two symmetry related nonparallel linear chain directions. Magnetic properties were studied by SQUID dc magnetization and ac susceptibility techniques and high field-high frequency electron spin resonance (HF-ESR).

Charge transport in ultrathin iron-phthalocyanine thin films under high electric fields.

The temperature dependent current-voltage (J-V) characteristics of 20 nm thick iron-phthalocyanine films are investigated in the temperature range of 300-30 K, and in the bias range of ±200 V. In the temperature range of 300-100 K, the charge transport is governed by bulk-limited processes with a bias dependent crossover from Ohmic (J∼V) to exponentially distributed shallow trap mediated space-charge-limited conduction (J∼V(α), α ≥ 2) to space-charge-limited conduction with field enhanced mobility (lnμ∼E(1/2)). However, at temperatures less than 100 K, the charge transport is electrode-limited, and undergoes a bias dependent transition from Schottky (lnJ∼V(1/2)) to multistep tunneling.

Room temperature ppb level Cl2 sensing using sulphonated copper phthalocyanine films.

We present room temperature chemiresistive gas sensing characteristics of drop casted sulphonated copper phthalocyanine (CuTsPc) films. It has been demonstrated that these films are highly selective to Cl(2) and the sensitivity in the 5-2000 ppb range varies linearly between 65 and 625%. However, for concentrations >or=2000 ppb, the response becomes irreversible, which is found to be due to the chemical bond formation between Cl(2) and SO(3)Na group of CuTsPc films.

Structural disorder in alkaline earth metal doped Ba(x)Mn[Fe(CN)6](2(x+1)/3)·zH2O molecular magnets: a reverse Monte Carlo study.

We report a detailed structural disorder study of the Ba(x)Mn[Fe(CN)(6)](2(x+1)/3)·zH(2)O (x = 0 and 0.3) molecular magnets by carrying out Reverse Monte Carlo (RMC) simulations of neutron diffraction data. Both samples have also been investigated using X-ray diffraction, infrared spectroscopy and dc magnetization techniques.

Effectiveness of two different HDR brachytherapy regimens with the same BED value in cervical cancer.

Purpose: To analyze the effectiveness of biologically effective dose (BED) in two different regimens of HDR brachytherapy keeping the same total BED to point A and to compare the relationship of overall treatment time in terms of local control and bladder and rectal complications.

Material And Methods: The study included two groups comprising a total of 90 cervical cancer patients who underwent external beam radiotherapy (EBRT) followed by HDR intracavitary brachytherapy (ICBT). EBRT treatment was delivered by a Co-60 teletherapy unit to a prescribed dose of 45 Gy with 1.

Application of aligned ZnO nanowires/nanobelts as a room temperature NO gas sensor.

Gas sensing properties of devices fabricated using ZnO nanowires/nanobelts (NS) aligned between two electrodes using dielectrophoresis technique were investigated. ZnO nanostructures were synthesized by carbothermal method. The devices were characterized as gas sensors and showed high sensitivity for detection of NO gas at room temperature.

Electrical characterization of self-assembled monolayers of alkyltrichlorosilanes on native oxide of silicon.

The octadecyltrichlorosilane (C18), dodecyltrichlorosilane (C12) and octyltrichlorosilane (C8) monolayers have been deposited on the native oxide of silicon by self-assembly technique. The morphology of the monolayers studied by atomic force microscopy revealed an average roughness of approximately 1.0 A.

Temperature dependent current-voltage characteristics of iron-phthalocyanine thin films.

The current-voltage (I-V) characteristics of the crystalline alpha-phase iron phthalocyanine (FePc) thin films grown by molecular beam epitaxy have been investigated by using a planar geometry in which the metal electrodes are separated by 15 microm. By carrying out the room temperature I-V measurements on vacuum annealed (200 degrees C for 30 min under 10(-6) torr) FePc thin films under vacuum and after exposing them to the air, we demonstrate that the hysteresis in FePc films is intimately related to the filling and de-filling of surface traps created by chemisorbed oxygen. The presence of chemisorbed oxygen has been confirmed by the X-ray photoelectron spectroscopy.

Chlorine gas sensors using one-dimensional tellurium nanostructures.

Tellurium nanotubes have been grown by physical vapor deposition under inert environment at atmospheric pressure as well as under vacuum conditions. Different techniques such as scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD) and optical absorption have been utilized for characterization of grown structures. Films prepared using both types of tellurium nanotubes were characterized for sensitivity to oxidizing and reducing gases and it was found that the relative response to gases depends on the microstructure.

Microscopic understanding of negative magnetization in Cu, Mn, and Fe based Prussian blue analogues.

A crossover of the field-cooled magnetization from positive to negative has been observed below the magnetic ordering temperature (17.9 K) in a multimetal Prussian Blue analogue (PBA), Cu_{0.73}Mn_{0.

DNA-templated assemblies of nickel hexacyanoferrate crystals.

We report here the synthesis of nickel hexacyanoferrate (NiHCF) crystals using calf thymus DNA (CT-DNA) as a template. The double-stranded CT-DNA has been used as a template to self-assemble NiHCF crystals and to produce aggregates having different morphologies at different temperatures. The guided self-assembly behavior of DNA was studied at different temperatures by scanning electron microscopy.

Electrostatic ion trap and Fourier transform measurements for high-resolution mass spectrometry.

We report on the development of an electrostatic ion trap for high-resolution mass spectrometry. The trap works on purely electrostatic fields and hence trapping and storing of ions is not mass restrictive, unlike other techniques based on Penning, Paul, or radio frequency quadrupole ion traps. It allows simultaneous trapping and studying of multiple mass species over a large mass range.

Self assembled monolayers on silicon for molecular electronics.

We present an overview of various aspects of the self-assembly of organic monolayers on silicon substrates for molecular electronics applications. Different chemical strategies employed for grafting the self-assembled monolayers (SAMs) of alkanes having different chain lengths on native oxide of Si or on bare Si have been reviewed. The utility of different characterization techniques in determination of the thickness, molecular ordering and orientation, surface coverage, growth kinetics and chemical composition of the SAMs has been discussed by choosing appropriate examples.

Improved performance of polyaniline-uricase biosensor.

Uricase has been covalently immobilized using glutaraldehyde as cross-linker onto electrochemically synthesized polyaniline (PANI) films. These PANI-uricase electrodes have been characterized using spectroscopic, cyclic voltammetry and impedance measurements. The morphology and covalent linkage of uricase lead to high enzyme loading and better shelf life.

Growth of highly oriented crystalline polyaniline films by self-organization.

Silicon substrates with (100) orientation were modified with amino-silane self-assembled monolayer (SAM) to provide amino (NH(2)) moieties at the substrate surface. Self-organization of polyaniline during chemical polymerization, on this modified surface, leads to the growth of highly oriented films at the substrate-polymer interface. The morphology studied using scanning electron microscopy and atomic force microscopy revealed the formation of polymer film with well faceted pyramidal crystallites.

Polymer-surfactant layered heterostructures by electropolymerization of phenosafranine in Langmuir-Blodgett films.

Langmuir-Blodgett (LB) films of the water-soluble dye phenosafranine (PS) have been prepared by its adsorption from aqueous dye solution to an arachidic acid (AA) monolayer at the air-water interface. Atomic force microscopy (AFM) images of the LB films revealed the effect of change in pH of deposition on the degree of complexation of AA with the PS dye. Well-defined circular islands and holes were observed which disappeared with the increase in pH.

Sodium chloride and ethanol induced sphere to rod transition of triblock copolymer micelles.

Dynamic light scattering (DLS), small-angle neutron scattering (SANS), and viscosity studies have been carried out to examine the influence of NaCl and ethanol on the structure of triblock copolymer [(EO)20(PO)70(EO)20] (EO = ethylene oxide; PO = propylene oxide) micelles in aqueous medium. The studies show that while the pure triblock copolymer solutions do not show any significant growth of the micelles on approaching the cloud point, the presence of a small amount of ethanol (5-10%) induces a sphere to rod shape transition of micelles at high temperatures. Interestingly, this ethanol induced sphere to rod transition of micelles can be brought down to room temperature (25 degrees C) with the addition of NaCl.

Time response and stability of porous silicon capacitive immunosensors.

The time response of affinity sensors made with nanostructured materials is a topic of considerable interest, since affinity sensors made with nanostructured materials provide greater sensitivities than corresponding planar crystalline devices but at the cost of stability and drift. We present a study of the time response of capacitive immunosensors made using porous silicon and ultrathin room temperature anodic oxide. It was found that sensor drift can be substantial but can be reduced by subjecting the capacitive immunosensor in buffer to an anodic bias that is larger than the bias at which sensor capacitance is measured.

Polyaniline nanoparticles prepared in rodlike micelles.

The effect of aniline hydrochloride (AHC) on the size and shape of sodium dodecyl sulfate (SDS) micelles has been investigated by dynamic light scattering. A monotonic decrease in the diffusion coefficient of the micelles was observed with an increase in AHC at fixed SDS concentration. This was ascribed to prolate ellipsoidal growth of the micelles due to decrease of the effective headgroup area/molecule by adsorption of AHC on SDS micelles.

SOM assembly of hydroxynaphthoquinone and its oxime: polymorphic X-ray structures and EPR studies.

Investigation on solvent-induced polymorphism in X-ray structures of 2-hydroxy-1,4-naphthoquinone (Lawsone) 1, is carried out. In protic methanol, 1 crystallizes in monoclinic space group P2(1)/c (1a) comprising of 2D hydrogen bonded network via cyclic dimers. In aprotic solvent such as acetone on the other hand, 1 exhibits orthorhombic space group Pna 2(1) (1b) and emerges with 1D catemeric chain.

Structure, insertion electrochemistry, and magnetic properties of a new type of substitutional solid solutions of copper, nickel, and iron hexacyanoferrates/hexacyanocobaltates.

Substitutional solid solutions of metal hexacyanometalates in which low-spin iron(III) and cobalt(III) ions populate the carbon-coordinated sites were synthesized and studied by powder diffraction including Rietveld refinement, cyclic voltammetry of immobilized microparticles, diffuse reflection vis-spectrometry, and magnetization techniques. The continuous solid solution series of potassium copper(II), potassium nickel(II), and iron(III) [(hexacyanoferrate(III))(1-x)(hexacyanocobaltate(III))(x)] show that the substitution of low-spin iron(III) by cobalt(III) in the hexacyanometalate units more strongly affects the formal potentials of the nitrogen-coordinated copper(II) and high-spin iron(III) ions than those of the remaining low-spin iron(III) ions. In the case of copper(II) and iron(III) [(hexacyanoferrate(III))(1-x)(hexacyanocobaltate(III))(x)] the peak currents decrease much more than can be explained by stoichiometry, indicating that the charge propagation is slowed by the substitution of low-spin iron(III) by cobalt(III).

A Three-Dimensional Ferrimagnet with a High Magnetic Transition Temperature (T ) of 53 K Based on a Chiral Molecule.

The transparent, double bridged-(R)-spiral three-dimensional polymeric complex K [Cr(CN) ][Mn(S)-pn](S)-pnH ((S)-pn=(S)-1,2-diaminopropane) has been synthesized and characterized (see X-ray structure; Cr: brown, Mn: red, C: gray, N: blue, K: green). Magnetic measurements on the complex show that the Mn and Cr ions interact ferrimagnetically and magnetic transition occurs at 53 K (Curie temperature).