Graphene Oxide-Assisted Morphology and Structure of Electrodeposited ZnO Nanostructures.

In this paper, ZnO electrodeposition was studied with the presence of graphene oxide (GO) exploited as a possible structure-directing agent. The effect of deposition potential and duration on the morphology and structure of ZnO was analyzed. The morphology and structure of the hybrids was analyzed by Raman spectroscopy, X-ray diffraction (XRD), and Scanning Electron Microscopy (SEM). The Raman results indicate a successful modification of ZnO with GO sheets and a hybridization threshold of 10 mg L-1 by the evolution of the defect related band of ZnO at 580 cm-1. The morphology results show that a low GO content only slightly influences the morphology and orientation of ZnO nanostructures while a high content as 10 mg L-1 changes the morphology in nanoplates and growth orientation to lateral. The results show that while GO participated in the deposition reaction, it has a two-fold role, also by structure-controlling ZnO, indicating that the approach is valid for the use of GO as a structure-directing agent for the fabrication of ZnO nanostructures by electrodeposition with varying morphologies and orientations.

The CeFe11Ti permanent magnet: a closer look at the microstructure of the compound.

High-performance permanent magnets (PM) are compounds with outstanding intrinsic magnetic properties. Most PMs are obtained from a favorable combination of rare earth metals (RE = Nd, Pr, Ce) with transition metals (TM = Fe, Co). Amongst them, CeFe11Ti claims considerable attention due to its large Curie temperature, saturation magnetization, and significant magnetocrystalline anisotropic energy. CeFe11Ti has several potential applications, in particular, in the development of electric motors for future automatic electrification. In this work, we shed some light on the mictrostructure of this compound by performing periodic hybrid-exchange density functional theory (DFT) calculations. We use a combined approach of atom-centered local orbitals, plane waves and full-potential linear muffin-tin orbital (LMTO) for our computations. The electronic configuration of the atoms involved in different steps of formation of the crystal structure of CeFe11Ti gives an explanation on the effect of Ce and Ti on its magnetic properties. While Ti stabilizes the structure, atomic orbitals of Ce hybridizes with Fe atomic orbitals to a significant extent and alters the electronic bands. Our calculations confirm a valence of 3+ for Ce, which has been deemed crucial to obtain a large magnetocrystalline anisotropy. In addition, we analyze several spin configurations, with the ferromagnetic configuration being most stable. We compare and contrast our data to those available and provide an insight for further development of optimized high-performance PMs. Moreover, we compute the Magnetocrystalline Anisotropy of this compound by means of two approaches: the Force Theorem and a full-potential LMTO method.

Seed layer technique for high quality epitaxial manganite films.

We introduce an innovative approach to the simultaneous control of growth mode and magnetotransport properties of manganite thin films, based on an easy-to-implement film/substrate interface engineering. The deposition of a manganite seed layer and the optimization of the substrate temperature allows a persistent bi-dimensional epitaxy and robust ferromagnetic properties at the same time. Structural measurements confirm that in such interface-engineered films, the optimal properties are related to improved epitaxy. A new growth scenario is envisaged, compatible with a shift from heteroepitaxy towards pseudo-homoepitaxy. Relevant growth parameters such as formation energy, roughening temperature, strain profile and chemical states are derived.

Surface nanostructures in manganite films.

Ultrathin manganite films are widely used as active electrodes in organic spintronic devices. In this study, a scanning tunnelling microscopy (STM) investigation with atomic resolution revealed previously unknown surface features consisting of small non-stoichiometric islands. Based upon this evidence, a new mechanism for the growth of these complex materials is proposed. It is suggested that the non-stoichiometric islands result from nucleation centres that are below the critical threshold size required for stoichiometric crystalline growth. These islands represent a kinetic intermediate of single-layer growth regardless of the film thickness, and should be considered and possibly controlled in manganite thin-film applications.

Mechanical properties of low-density polyethylene filled by graphite nanoplatelets.

The mechanical properties of GNP/LDPE nanocomposites (graphite nanoplatelets/low density polyethylene) have been investigated, in order to establish the effect of nanoscale reinforcement within the polymer matrix. Results show that the presence of the filler does not involve a change in the microscopic structure of the polymer. However, on a macroscopic scale, GNPs limit the mobility of the polymer chains, resulting in an increase in stiffness for the final composite. Orientation of GNPs within the LDPE matrix is also an important issue that affects mechanical properties and it has been evaluated by testing nanocomposites made by different manufacturing techniques (compression moulding and blown extrusion). The comparison between the experimental data and the Halpin-Tsai model shows that the orientation of GNPs due to the extrusion process leads to values of tensile modulus higher than that obtained with the randomly oriented disposition resulting from the compression moulding technique.

Electrodeposition efficiency of Co and Cu in the fabrication of multilayer nanowires by polymeric track-etched templates.

Co/Cu-multilayer nanowires can be exploited to develop magnetoresistive sensors. One of the easiest methods for their production is filling nanoporous templates by pulsed-electrodeposition (PED) from a single bath. Multiple parameters effecting the growth of these nano-objects must be controlled to tailor their properties. In this study, the deposition efficiency of Co/Cu-multilayer nanowires produced in nanoporous-polymeric membranes is assessed, and the influence of the space confinement produced by the nanopores themselves on the continuous and pulsed-electrodeposition is evaluated. The growth dependence on some of the most significant process parameters has been investigated. It is shown here that, for each species, when depositing Co and Cu separately, a decrease of current efficiency is observed when the charge density is increased and the pore diameter is reduced; on the contrary, in the Co/Cu-PED, changing the degree of polarization for each deposition step of the different metals results in a sensible reduction of this effect.