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High-quality graphene is highly enviable material due to its seminal role amongst several areas in modern technology including its role as nanocarrier for site selective drug grafting and delivery applications. Here, we report a facile, cost-effective and single-step method to produce high-quality graphene through customised electrochemical exfoliation of graphite anode in alkaline electrolyte medium. The quality of graphene sheets (GS) were investigated by Raman, TEM/HRTEM, AFM, and FTIR techniques. The high quality as well as excellent Π-Π stacking nature of the honeycomb lattice of graphene was confirmed by measuring the quenching capability through photo-luminescence spectroscopy using organic dyes. A plausible mechanism for the graphite exfoliation has been given where evolution of high density of oxygen molecules exerts large force on the graphitic layers leads to exfoliation and consequent synthesis of graphene. Furthermore, to explore the application of the graphene sheets so synthesized, we carried out studies which may make them as suitable carriers for drug delivery. For this, graphene sheets were functionalized with L-cysteine and attached with the drugs Amphotericin-B (AmB) and Tamoxifen citrate (TMX). The conjugation of drugs with L-cysteine functionalized graphene has been confirmed through FTIR and Raman spectroscopic techniques. The drug loading efficiency of FGS for AmB and TMX was 75.00% and 94.31%, respectively. The present formulation of drugs (AmB and TMX) conjugated with graphene is suitable for the targeted drug delivery as it will enhance the efficacy and reduce cytotoxicity associated with drug.

The present report describes the catalytic activity of mechanically activated nano quasicrystalline Al65Cu20Fe15 and related nano crystalline Al50Cu28Fe22 for the synthesis of carbon nanotubes (CNTs). CNTs are synthesized by catalytic decomposition of ethanol through nano quasicrystalline Al65Cu20Fe15 and related crystalline Al50Cu28Fe22 alloys as a catalyst. The synthesized multi-walled CNTs exhibits tube diameter ranging from 5 to 25 nm. The synthesized CNTs are characterized by scanning and transmission electron microscopy. It is found that Al65Cu20Fe15 nanoquasicystal shows better catalytic behaviour as compared to nano-crystalline Al50Cu28Fe22 alloys for decomposition of ethanol during the synthesis of multi-walled CNTs.

The present paper explores the enhancement in hydrogen sorption behavior of MgH2 with TiO2 nanoparticles. The catalytic effect of TiO2 nanoparticles with different sizes (7, 25, 50, 100 and 250 nm) were used for improving the sorption characteristics of MgH2. The MgH2 catalyzed with 50 nm of TiO2 exhibited the optimum catalytic effect for hydrogen sorption behavior. The desorption temperature of MgH2 catalyzed through 50 nm TiO2 was found to be 310 degrees C. This is 80 degrees C lower as compared to MgH2 having a desorption temperature of 390 degrees C. It was noticed that the dehydrogenated MgH2 catalyzed with 50 nm TiO2 reabsorbed 5.1 wt% of H2 within 6 minutes at temperature and pressure of 250 degrees C and 50 atm, respectively. The 50 nm TiO2 catalyst lowered the absorption activation energy of MgH2 from - 92 to - 52.7 kJ mol(-1).

Copper nanoparticles have been synthesized by anodic oxidation through a simple electrolysis process employing de-oxy ribonucleic acid (DNA) as electrolyte. Platinum was taken as cathode and copper as anode. The applied voltage was 4 V and the electrolysis was performed for duration of 1 h. The copper nanoparticles were prepared in situ from the electron beam irradiation on residues of electrolyte consisting of DNA and copper particles: DNA (Cu) complexes. The size of the nanoparticles ranges between 5-50 nm. A tentative explanation has been given for the formation of copper nanoparticles.

The macroscopic coaxial carbon cylinders (dia. approximately 0.5 cm with varying lengths approximately 2-5 cm) consisting of aligned carbon nanotube (CNT) stacks have been prepared by spray pyrolysis of benzene-ferrocene solution in argon atmosphere at approximately 850 degrees C-900 degrees C temperature. The coaxial carbon cylinders of CNT stacks have been formed directly inside the quartz tube. We attempted to prepare superimposed multi carbon cylinder configurations, each consisting of ordered and aligned CNTs stacked over each other. For this, we have terminated the spray of precursor after run of about 25 minutes, for a short interval (approximately 5 min), and then the solution was sprayed again over the already deposited hot CNT stack. Gross structural characterization of CNTs was done through X-ray diffraction technique (XRD). Microstructural characterizations of as prepared coaxial carbon cylinders with CNT stacks were done by scanning electron microscopic (SEM) techniques. SEM studies show that the CNTs are well aligned along the periphery of the cross section of coaxial carbon cylinder, each consisting of CNTs of the type described in the above. Comparisons have been made between the present macroscopic coaxial carbon cylinders with CNT stacks studied earlier by several other workers. Plausible explanation for the synthesis of CNT stacks will be put forward.

In the present study, attempts have been made to synthesize the nano-crystalline (Co, Ni)Al2 O4 spinel powders by ball milling and subsequent annealing. An alloy of Al70Co15Ni15, exhibitingthe formation of a complex intermetallic compound known as decagonal quasicrystal is selected as the starting material for mechanical milling. It is interesting to note that this alloy is close to the stoichiometry of aluminum and transition metal atoms required to form the aluminate spinel. The milling was carried out in an attritor mill at 400 rpm for 40 hours with ball to powder ratio of 20 : 1 in hexane medium. Subsequent to this annealing was performed in an air ambience for 10, 20, and 40 h at 600°C in side the furnace in order to oxidize the decagonal phase and finally to form the spinel structure. The X-ray diffraction (XRD) and transmission electron microscopy (TEM) confirmed the formation of nano-sized decagonal phase after milling and then (Co, Ni)Al2O4 spinel type phase after annealing. The XRD studies reveal the lattice parameter to be 8.075 Å and the lattice strain as 0.6%. The XRD and TEM explorations of spinel phase indicate the average grain size to be ∼40 nm.

We have investigated the effect of ferrocene concentration on the synthesis of carbon-nitrogen (C-N) nanotubes. The bamboo-shaped carbon-nitrogen nanotubes were synthesized by spray pyrolysis of Fe(C5H5)2 and CH3CN solution using argon as a carrier gas at the optimum temperature of approximately 900 degrees C. The effect of ferrocene concentration on the length and concentration of nitrogen in nanotubes was studied. Micro-structural features of the nanotubes were monitored employing scanning and transmission electron microscopic techniques. SEM studies reveal that with decreasing ferrocene concentration from 25 mg ml(-1) to 5 mg ml(-1), the length of the nanotubes vary from 80 microm to 430 microm. A feasible growth model has been described and discussed. X-ray photoelectron spectroscopic studies have confirmed the formation of nitrogen-doped carbon nanotubes. These studies reveal that the nitrogen concentration in the nanotubes decreases with the increase of ferrocene concentration. The present synthesis route also provides means of producing carbon nanotubes with different concentrations of nitrogen.

We report the formation of germanium nanoparticles and threadlike nanostructures by the process of thermal vapor deposition. Germanium was thermally evaporated and condensed on graphite substrates under varied ambient helium pressures of 100, 200, 300, and 400 torr. The deposited films were characterized through transmission electron microscopy. These investigations revealed the occurrence of germanium particles. The size of these particles varied inversely with ambient pressure. Whereas for an ambient pressure of 100 torr the average particle size was approximately 0.3-0.5 micron, for 400 torr the average size was approximately 30-60 nm. At high He pressure (e.g., approximately 400 torr), the nanoparticles that formed when annealed for 30 min at 200 degrees C in vacuum adopted threadlike nanostructures. A qualitative explanation has been put forward for the formation of germanium particles and variation of size of these particles with helium pressure in terms of condensation, collision, and coalescence.

We report the formation of bamboo-shaped carbon-nitrogen nanotubes by employing a simple, one-step and economically viable spray pyrolysis technique using new precursor; acetonitrile and ferrocene solution. By varying the concentration of ferrocene with respect to acetonitrile, it has been found that the optimum concentration of ferrocene in acetonitrile is 5 mg/ml. The special feature of the as-synthesized bamboo-shaped carbon-nitrogen nanotubes bundles is that they are produced in a high yield (1.25 gms/run). They also have long linear extents (approximately 430 microm) and are very clean. The average composition of carbon-nitrogen nanotubes comes out to be C26N.

Multi-walled carbon nanotubes (MWNTs)-polyacrylamide (PAM) composites have been prepared using as purified, with ball milling and functionalized MWNTs by solution cast technique and characterized through scanning electron microscopy (SEM) and transmission electron microscopy (TEM). A comparative study has been made on the electrical property of these MWNTs-PAM composites with different MWNTs loadings. It has been shown that the ball milling and functionalization of MWNTs improves the dispersion of MWNTs into the polymer matrix. As the MWNTs loading increases from 0 to 40 wt% electrical conductivity of composite film increases by approximately 7 orders of magnitude whereas the electrical conductivity of functionalized composite film increases only approximately 4 orders of magnitude with respect to the pure PAM film. A model based on power law percolation for the electronic behavior of above composite has been developed and shows good agreement with the experimental data.

We report the Synthesis of different CuO (ellipsoid, ribbon and sheet like) nanostructures in a solution phase with high yield at low cost bysimple reduction of aqueous solution of copper nitrate with alkaline solution of sodium hydroxide (NaOH). The morphology of the synthesized nanostructures is significantly influenced by the feedingconcentration of alkaline NaOH solution. Cu(OH)2 nanomaterials can be readily obtained by the reduction of Cu(NO3)2 solution with NaOH solution and these synthesized materials obtained atdifferent molar concentration of NaOH solution get transformed into different nanostructures ofCuO by subsequent heat treatment at 80 degrees C for half an hour. Nanoellipsoid, nanoribbon and nanosheet like structures were obtained after heating the copper nitrate solution reduced with 0.25 M, 0.50 M, 0.75 M and 1 M concentrated NaOH solution respectively. Optical absorption spectra and corresponding band gap calculation showed that these nanomaterials have higher band gap than their bulk materials.

In the present work, aligned TiO2 nanotubes have been synthesized by a simple method of electrochemical anodization of high purity, well cleaned, etched and ultrasonicated Ti-sheet (Purity approximately 99.99%) in a fluoride mediated electrolytic media consisting of a solution of 0.14 M NaF and a solution of 0.5 M/1.0 M H3PO4. Studies on the effects of anodization voltage, time and electrolyte concentration on the formation of TiO2 nanotubes have been carried out. The TiO2 nanotube arrays have been synthesized at applied anodization voltages of approximately 10 V and approximately 20 V. The anodization was carried out for 1 hour and 2 hours at each applied voltage. Structural/microstructural characterizations of TiO2 nanotubes have been carried out through scanning electron microscopy (SEM) and transmission electron microscopy (TEM). SEM images of TiO, nanotubes showed interesting features relating to morphology, the pore size (diameter of the tubes) and the lengths of the tube. TEM investigations revealed that the as synthesized nanotubes are amorphous in nature and on electron beam annealing, these transformed to crystalline phases (rutile and brookite). The optical characterizations through UV-Visible spectroscopy exhibited that the band gap are approximately 3.03 eV and approximately 2.87 eV for tubes synthesized at applied anodization voltages of approximately 10 V and approximately 20 V respectively. A tentative mechanism for the growth of TiO2 nanotube has been put forward.

We report the Synthesis of different metal oxide (Cu2O, SnO2, Fe3O4 and PbO2) nanostructures by simple electrolysis based oxidation of metals (Cu, Sn, Fe and Pb). We have utilized the two electrode set up for the electrolysis and used different metal electrodes as anode and platinum as cathode. The synthesized nanomaterials were delaminated in the electrolyte. The microstructural characterization of synthesized materials in electrolytes after electrolysis at different electrode potentials revealed that the nanostructures strongly depend on the applied voltage between the electrodes. Various nanostructures (nanothreads, nanowires, nanocubes, nanotetrapods and hexagons-like) of metal oxides have been synthesized by this method. In case of copper electrode we have found nanothreads and nanowires of cuprous oxide. Tin electrode resulted nanothreads, nanotetrapod and nanocube like structures of tin oxide. Iron electrode resulted, nanowire like structures of iron oxide and lead sheet transformed into hexagon like and six petals like structures of lead oxide.

A nano decagonal quasicrystalline phase in the Al70Cu10Co5Ni15 alloy has been synthesized by mechanical alloying of a mixture of elemental powders followed by annealing. A high-energy ball milling of the elemental mixture of Al, Cu, Co and Ni leads to the formation of B2 type quaternary intermetallic alloys. The X-ray diffraction and transmission electron microscopy techniques have been employed for characterization of the samples. It was observed that the dissolution of the individual elements into an alloy led to the formation of a nano B2 phase. This phase was found to be quite stable against milling and no other crystalline or amorphous phases could be detected. Milled powder after annealing at 700 degrees C for 60 h was found to transform to nano-decagonal phase. Attempts have been made to understand the evolution of the complex intermetallic nano phases and their relative stability during milling.

ZnO nanotetrapods and nanorods have been synthesized by a simple thermal evaporation of Zn powder (300 mesh, 99.99% purity) under simultaneous flow of oxygen and argon gases in two-zone furnace in two different temperature regions. These ZnO nanostructures have hexagonal structure, which grow along the [001] direction in the form of nanotetrapods (diameter approximately 60-150 nm, length approximately 1-4 microm) and nanorods (diameter approximately 30-60 nm, length approximately 2-5 microm). The morphologies of these ZnO nanostructures have been investigated by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). It has been found that growth parameters like temperature, gas flow rate etc., control the diameter of the nanotetrapods and nanorods. These novel structures of ZnO nanorods and nanotetrapods may be attractive for optical and other nanodevices.

This paper deals with the investigations on the nucleation and growth of Zinc Oxide (ZnO) nanostructures in a catalyst free synthesis. The ZnO nanostructures have been formed by evaporation of Zn (99.99%) in O2 and Ar atmosphere in single zone furnace under two temperature regions, region A (approximately 1173-1073 K) and region B (approximately 873-773 K). Through application of XRD and TEM techniques, it has been shown that first ZnO is formed which changes to ZnOx through creation of oxygen vacancies. The ZnOx acts as self-catalyst and leads to formation of various nanostructures. Those observed in the present investigation are nanotetrapods (1 D, diameter approximately 70-450 nm, length approximately 2-4.5 approximatelym) nanorods (1 D, diameter approximately 45-95 nm, length approximately 2.5-4.5 microm), nanoflowers(2D, central core diameter approximately 90-185 nm, length of petals/nanorod approximately 1.0-3.5 microm) and nanoparticles (3D, size approximately 0.85-2.5 microm). These nanostructures have been revealed by SEM explorations. Attempts have been made to explain the formation of the various nanostructures in terms of the creation and distribution of the ZnOx, the temperature as well as oxygenation conditions.

Carbon nanotubes play a fundamental role in the rapidly developing field of nanoscience and nanotechnology because of their unique properties and high potential applictions. In this article, the different synthesis method of CNTs are reviewed. From the industrial point of view, the chemical vapor depostion method has shown advantages over electric arc discharge and laser vaporization methods. Special CNTs configuration, such as nanocoils, nanohorns, bamboo-shaped CNTs and carbon cylinder made up from from CNTs are also discussed., Comment: 65 pages, 9 figures. To appear in JNN

We report the formation and characterization of copper nanostructures, nanotubules and nanothreads, which were obtained by electrical arc evaporation of Cu electrodes under varied conditions of He ambience. Electrical arc evaporation was done with approximately 10 V and (approximately 50-100 A) DC current. The current was used in a pulse mode. The evaporated material was condensed on a formvar-coated Cu grid mounted on a liquid N2-cooled specimen holder. Transmission electron microscopy was employed to characterize the condensed materials. These investigations revealed that the condensed materials consisted of the mentioned nanostructures. Nanotubes and nanothreads are formed for a He pressure in the chamber corresponding to approximately 140 and approximately 500 torr, respectively. Extensive electron microscopic investigations showed that the diameter of the nanotubes varied from approximately 5 nm to approximately 50 nm and their length from 2 microns to 3 microns.

Lanthanum carbide nanotubes have been synthesized by d.c. arc evaporation (approximately 20-30 V, approximately 200 Amp) of lanthanum metal (90 wt.%)-loaded graphite rod in a helium atmosphere (665 mbar). To explore the possibility of formation of lanthanum carbide nanotubes, the experiments were carried out with lanthanum metal in different concentrations (i.e., 30, 50, 70, and 90 wt.%) in the graphite rod. The as-synthesized samples were characterized by transmission electron microscopy and X-ray diffractometry. Lanthanum carbide nanotubes (LCNTs) with a diameter of approximately 65 to 95 nm and a length of approximately 0.2 to 1.5 microns were obtained in this study.