Mg doped Li2FeSiO4/C nanocomposites synthesized by the solvothermal method for lithium ion batteries.

A series of porous Li2Fe1-xMgxSiO4/C (x = 0, 0.01, 0.02, 0.04) nanocomposites (LFS/C, 1Mg-LFS/C, 2Mg-LFS and 4Mg-LFS/C) have been synthesized via a solvo-thermal method using the Pluronic P123 polymer as an in situ carbon source. Rietveld refinement of the X-ray diffraction data of Li2Fe1-xMgxSiO4/C composites confirms the formation of the monoclinic P21 structure of Li2FeSiO4. The addition of Mg facilitates the growth of impurity-free Li2FeSiO4 with increased crystallinity and particle size. Despite having the same percentage of carbon content (∼15 wt%) in all the samples, the 1Mg-LFS/C nanocomposite delivered the highest initial discharge capacity of 278 mA h g-1 (∼84% of the theoretical capacity) at the C/30 rate and also exhibited the best rate capability and cycle stability (94% retention after 100 charge-discharge cycles at 1C). This is attributed to its large surface area with a narrow pore size distribution and a lower charge transfer resistance with enhanced Li-ion diffusion coefficient compared to other nanocomposites.

Bifunctional Li and Co Doped ZnO Nanostructures Synthesized by Solvothermal Method: Stabilizer Controlled Shape and Size Tuning.

1D nanostructures of ZnO, Zn0.95Co0.05O and Zn0.85Co0.05Li0.10 were synthesized by a solvothermal chemical method with and without using oleic acid as a stabilizer. We report a very interesting observation of both room temperature ferromagnetism and photoluminescence properties along with development of different morphological transformation of these nanostructures on doping Co and Li in ZnO in the presence and absence of oleic acid. Zn0.95Co0.05O sample prepared in the presence of oleic acid showed increased saturation magnetization value (~ 4.1 emu/g and) compared to Zn0.95Co0.05O prepared without oleic acid (~ 1.1 emu/g). In both the cases it is observed that Li incorporation further enhances the room temperature ferromagnetic (RTFM) behavior and saturation magnetization values (~ 6 emu/g) of luminescent Zn0.95Co0.05 nanostructures. These results are significant, as the luminescent 1 D RTFM materials will have implications in photo magnetic devices like magneto-optical switches and sensors.

Fabrication of flexible and self-standing inorganic-organic three phase magneto-dielectric PVDF based multiferroic nanocomposite films through a small loading of graphene oxide (GO) and Fe3O4 nanoparticles.

Flexible inorganic-organic magneto-electric (ME) nanocomposite films (PVDF, PVDF-GO, PVDF-Fe3O4 and PVDF-GO-Fe3O4), composed of well-dispersed graphene oxide (GO 5 wt%) and magnetic Fe3O4 nanoparticles (5 wt%) embedded into a poly(vinylidene-fluoride) (PVDF) matrix, have been prepared by a solvent casting route. The magnetic, ferroelectric, dielectric, magneto-dielectric (MD) coupling and structural properties of these films have been systematically investigated. Magnetic (Ms = 2.21 emu g(-1)) and ferroelectric (P = 0.065 µC cm(-2)) composite films of PVDF-GO-Fe3O4 (PVDF loaded with 5% GO and 5% Fe3O4) with an MD coupling of 0.02% at room temperature (RT) showed a three times higher dielectric constant than that of the pure PVDF film, with a dielectric loss as low as 0.6. However, the PVDF-Fe3O4 film, which exhibited improved magnetic (Ms = 2.5 emu g(-1)) and MD coupling (0.04%) properties at RT with a lower dielectric loss (0.3), exhibited decreased ferroelectric properties (P = 0.06 µC cm(-2)) and dielectric constant compared to the PVDF-GO-Fe3O4 film. MD coupling measurements carried out as a function of temperature on the multi-functional PVDF-GO-Fe3O4 film showed a systematic increase in MD values up to 100 K and a decrease thereafter. The observed magnetic, ferroelectric, dielectric, MD coupling and structural properties of the nanocomposite films are attributed to the homogeneous dispersion and good alignment of Fe3O4 nanoparticles and GO in the PVDF matrix along with a partial conversion of nonpolar α-phase PVDF to polar ß-phase. The above multi-functionality of the composite films of PVDF-Fe3O4 and PVDF-GO-Fe3O4 paves the way for their application in smart multiferroic devices.

Disorder-induced room temperature ferromagnetism in glassy chromites.

We report an unusual robust ferromagnetic order above room temperature upon amorphization of perovskite [YCrO3] in pulsed laser deposited thin films. This is contrary to the usual expected formation of a spin glass magnetic state in the resulting disordered structure. To understand the underlying physics of this phenomenon, we combine advanced spectroscopic techniques and first-principles calculations. We find that the observed order-disorder transformation is accompanied by an insulator-metal transition arising from a wide distribution of Cr-O-Cr bond angles and the consequent metallization through free carriers. Similar results also found in YbCrO3-films suggest that the observed phenomenon is more general and should, in principle, apply to a wider range of oxide systems. The ability to tailor ferromagnetic order above room temperature in oxide materials opens up many possibilities for novel technological applications of this counter intuitive effect.

Inorganic-organic Ag-rhodamine 6G hybrid nanorods: "turn on" fluorescent sensors for highly selective detection of Pb2+ ions in aqueous solution.

Lead metal ions are of great concern and the monitoring of their concentration in the environment has become extremely important. In the present study, a new inorganic-organic hybrid assay of Ag nanorods (AgNR)-Rhodamine 6G (R6G) was developed for the sensitive and selective determination of Pb(2+) ions in aqueous solutions. To the best of our knowledge there is almost no literature on the use of silver nanorod sensors for determination of lead ions in aqueous solutions. The sensor is developed by the coating of R6G on the surface of AgNRs. The sensing is based on the photoluminescence of R6G. The sensor was rapid as the measurements were carried out within 3 min of addition of the test solution to the AgNR-R6G hybrid. Moreover, the system showed excellent stability at tested concentration levels of Pb(2+) ions. The naked eye detection of the colour was possible with 1 mg L(-1) of Pb(2+) ions. The present method has a detection limit of 50 µg L(-1) of Pb(2+) (for a signal/noise (S/N) ratio > 3). The selectivity toward Pb(2+) ions against other metal ions was improved using chelating agents. The proposed method was validated by analysis using different techniques.

Rare examples of fluoride-based multiferroic materials in Mn-substituted BaMgF4 systems: experimental and theoretical studies.

A series of Mn-substituted BaMgF(4) samples have been synthesized by a hydrothermal route. X-ray diffraction study reveals that the products are monophasic in nature. Scanning electron microscopy (SEM) and energy-dispersive spectrometry (EDS) studies were carried out to investigate the morphology and stoichiometry for these compounds. X-ray photoelectron spectroscoy (XPS) and electron spin resonance (ESR) studies were done to confirm the oxidation state of dopant ion. Room temperature ferromagnetism was observed on Mn substitution at the Mg site in BaMgF(4) samples. The saturation magnetization increases initially, shows a peaking effect, and then decreases with further increase in Mn concentration in BaMg(1-x)Mn(x)F(4) (0.0 ≤ x ≤ 0.15). However, ferroelectricity was found to decrease with an increase in Mn concentration in the series of investigated BaMg(1-x)Mn(x)F(4) (0.0 ≤ x ≤ 0.15) samples. First-principle calculations, using the projector augmented wave potentials on Mn-substituted BaMgF(4), confirmed the decrease in magnetic moment with an increase in Mn content beyond certain concentration. These samples exhibit very weak magnetocapacitive coupling, which can be attributed to the very small magnetic signal observed in these samples.

Experimental and theoretical investigations on magnetic behavior of (Al,Co) co-doped ZnO nanoparticles.

We present the structural and magnetic properties of Zn(0.95-x)Co(0.05)Al(x)O (x = 0.0 to 0.1) nanoparticles, synthesized by a novel sol-gel route followed by pyrolysis. Powder X-ray diffraction data confirms the formation of a single phase wurtzite type ZnO structure for all the compositions. The Zn(0.95)Co(0.05)O nanoparticles show diamagnetic behavior at room temperature. However, when Al is co-doped with Co with x = 0.0 to 0.10 in Zn(0.95-x)Co(0.05)Al(x)O, a systematic increase in ferromagnetic moment is observed up to x = 0.07 at 300 K. Above x = 0.07 (e.g. for x = 0.10) a drastic decrease in ferromagnetic nature is observed which is concomitant with the segregation of poorly crystalline Al rich ZnO phase as evidenced from TEM studies. Theoretical studies using density functional calculations on Zn(0.95-x)Co(0.05)Al(x)O suggest that the partial occupancy of S2 states leads to an increased double exchange interaction favoring the ferromagnetic ground states. Such ferromagnetic interactions are favorable beyond a threshold limit. At a high level doping of Al, the exchange splitting is reduced, which suppresses the ferromagnetic ordering.

Effect of doping on the morphology and multiferroic properties of BiFeO3 nanorods.

In this study we report the synthesis of BiFeO(3) nanorods using a sonochemical technique. The nanorods had a diameter of 20-50 nm, a length of 100-500 nm and exhibit aspect ratios in the range of 5-10. However, after doping, the TEM images of Bi(0.9)Ba(0.1)Fe(0.9)Mn(0.1)O(3) and Bi(0.9)Ca(0.1)Fe(0.9)Cr(0.1)O(3) samples show that the aspect ratios of both the double doped samples have reduced considerably, while retaining the crystallinity of the particles. BiFeO(3) nanorods show a weak ferromagnetic order at room temperature, which is quite different from the linear M-H relationship reported for bulk BiFeO(3). The saturation magnetization of these BiFeO(3) nanostructures has been found to increase on doping with various metal ions (Ba(2+), Ca(2+), Mn(2+), Cr(3+)), reaching a maximum value of 1.35 emu g(-1) for the Bi(0.9)Ba(0.1)Fe(0.9)Mn(0.1)O(3) nanostructures. However, saturation of electric polarization was observed only in case of the Bi(0.9)Ca(0.1)Fe(0.9)Cr(0.1)O(3) nanostructures.

Enhanced hydrogen generation by particles during sonochemical decomposition of water.

A novel effect of any oxide particle/intermetallics enhancing hydrogen generation from water as compared to water alone when subjected to ultrasonic irradiation is reported here. Addition of methanol to water or decrease in particle size also improved the hydrogen yield. Hydrogen generation from water was further enhanced by the presence of both methanol and particles in water.