Molecular Precursor-Driven Synthesis of Copper Telluride Nanostructures for LIB Anode Application.

Copper tellurides have garnered substantial interest for their applicability as an electrocatalyst for water splitting, battery anodes and photodetectors, etc. Moreover, synthesis of phase pure metal tellurides using the multi-source precursor method is challenging. Therefore, a facile synthesis protocol for copper tellurides is anticipated. The current study involves a simplistic single source molecular precursor pathway for the synthesis of orthorhombic-Cu2.86Te2 nano blocks and -Cu31Te24 faceted nanocrystals employing the [Cu{TeC5H3(Me-5)N}]4 cluster in thermolysis and pyrolysis, respectively. The pristine nanostructures were carefully characterized by powder X-ray diffraction, energy-dispersive X-ray spectroscopy, electron microscopic techniques (scanning electron microscopy and transmission electron microscopy), and diffuse reflectance spectroscopy to know the crystal structure, phase purity, elemental composition, distribution of elements, morphology, and optical band gap. These measurements suggests that the reaction conditions fetch nanostructures of different sizes, crystal structures, morphologies, and band gaps. As prepared nanostructures were evaluated for lithium-ion batteries (LIBs) anode material. The cells fabricated with orthorhombic Cu2.86Te2 and orthorhombic Cu31Te24 nanostructures deliver capacities of 68 and 118 mA h/g after 100 cycles. The LIB anode made up of Cu31Te24 faceted nanocrystals exhibited good cyclability and mechanical stability.

Preparation and structure of uranium-incorporated Gd2Zr2O7 compounds and their thermodynamic stabilities under oxidizing and reducing conditions.

Gd2Zr2O7 is being contemplated as a futuristic matrix for the incorporation of high-level radioactive nuclear waste. This compound has the unique ability to incorporate several fission products and heavy metal ions like uranium and thorium into its lattice sites without undergoing structural changes. X-ray diffraction analyses of Gd2-xUxZr2O7+δ samples indicate that the parent compound can incorporate a substantial amount of uranium, both under oxidizing and reducing conditions. The oxidation state of these samples was investigated by X-ray photoelectron spectroscopy. The thermodynamic stability of uranium-substituted Gd2Zr2O7 is an important parameter that will govern the long-term storage of uranium and minor actinides in this matrix. High-temperature calorimetry has been used to investigate the stability of the Gd2-xUxZr2O7+δ (0.00 ≤ x ≤ 0.15) compositions. The standard molar free energy of the formation of Gd2-xUxZr2O7+δ (0.00 ≤ x ≤ 0.15) compositions has been estimated. From the free energy of formation data, the sample corresponding to x = 0.15 was found to be most stable in the Gd2-xUxZr2O7+δ (0.00 ≤ x ≤ 0.15) series. The relative stabilities of U(4+) and U(6+) substituted gadolinium zirconate have been discussed on the basis of the charge on the uranium ion and the incorporation of corresponding extra oxygen atoms into the lattice for charge compensation.

Enhanced magneto-dielectric coupling in multiferroic Fe and Gd codoped PbTiO3 nanorods synthesized via microwave assisted technique.

The quest for new multiferroic materials is on the rise due to their potential application in spintronics and futuristic multiple state memory devices. Here we report the microwave synthesis of iron/gadolinium co-doped PbTiO3 nanorods, which display multiferroic behavior. Both the undoped and doped PbTiO3 samples have been characterized using powder X-ray diffraction, energy dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS) techniques. The morphology of the samples has been studied using transmission electron microscopy (TEM) and high resolution transmission electron microscopy (HRTEM), which confirmed the formation of nanorods. The substitution of Fe ions for Ti and Gd ions for Pb enhances the ferromagnetic and ferroelectric properties of this system. The reasons for this observation have been explored in detail. The ferroelectric, magnetic and magneto-capacitive measurements at room temperature substantiate the multiferroic nature of the codoped samples with significant magnetoelectric coupling observed in case of nano PbTiO3:Gd(3+)(0.5%):Fe(3+)(5%).

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.