V. Vega

Tuning the magnetic anisotropy of Co–Ni nanowires: comparison between single nanowires and nanowire arrays in hard-anodic aluminum oxide membranes

Co(x)Ni(1-x) alloy nanowires with varying Co content (0 ≤ x ≤ 0.95), having a diameter of 130 nm and length of around 20 μm, are synthesized by template-assisted electrodeposition into the nanopores of SiO(2) conformal coated hard-anodic aluminum oxide membranes. The magneto-structural properties of both single isolated nanowires and hexagonally ordered nanowire arrays of Co-Ni alloys are systematically studied by means of magneto-optical Kerr effect magnetometry and vibrating sample magnetometry, respectively, allowing us to compare different alloy compositions and to distinguish between the magnetostatic and magnetocrystalline contributions to the effective magnetic anisotropy for each system. The excellent tunable soft magnetic properties and magnetic bistability exhibited by low Co content Co-Ni nanowires indicate that they might become the material of choice for the development of nanostructured magnetic systems and devices as an alternative to Fe-Ni alloy based systems, being chemically more robust. Furthermore, Co contents higher than 51 at.% allow us to modify the magnetic behavior of Co-rich nanowires by developing well controlled magnetocrystalline anisotropy, which is desirable for data storage applications.

Influence of Anodic Conditions on Self-ordered Growth of Highly Aligned Titanium Oxide Nanopores

Self-aligned nanoporous TiO2templates synthesized via dc current electrochemical anodization have been carefully analyzed. The influence of environmental temperature during the anodization, ranging from 2 °C to ambient, on the structure and morphology of the nanoporous oxide formation has been investigated, as well as that of the HF electrolyte chemical composition, its concentration and their mixtures with other acids employed for the anodization. Arrays of self-assembled titania nanopores with inner pores diameter ranging between 50 and 100 nm, wall thickness around 20–60 nm and 300 nm in length, are grown in amorphous phase, vertical to the Ti substrate, parallel aligned to each other and uniformly disordering distributed over all the sample surface. Additional remarks about the photoluminiscence properties of the titania nanoporous templates and the magnetic behavior of the Ni filled nanoporous semiconductor Ti oxide template are also included.

Magneto-thermopower and magnetoresistance of single Co-Ni alloy nanowires

The magneto-thermopower is measured and correlated to the anisotropic magnetoresistance of Co-Ni alloyed nanowires with varying composition. The highest absolute and relative variation of the Seebeck coefficient in perpendicularly applied magnetic fields at room temperature is determined to be 1.5 μVK−1 for Co0.24Ni0.76 and 8.1% for Co0.39Ni0.61 nanowires. Power factors of 3.7 mW/mK2 have been achieved, which is competitive with common thermoelectric materials like Bi2Te3. For Co-Ni nanowires containing up to 39% Co, a linear relationship between the magnetic field dependent change of the Seebeck coefficient and the electrical conductivity is found.

Electroplating and magnetostructural characterization of multisegmented Co54Ni46/Co85Ni15 nanowires from single electrochemical bath in anodic alumina templates.

Highly hexagonally ordered hard anodic aluminum oxide membranes, which have been modified by a thin cover layer of SiO2 deposited by atomic layer deposition method, were used as templates for the synthesis of electrodeposited magnetic Co-Ni nanowire arrays having diameters of around 180 to 200 nm and made of tens of segments with alternating compositions of Co54Ni46 and Co85Ni15. Each Co-Ni single segment has a mean length of around 290 nm for the Co54Ni46 alloy, whereas the length of the Co85Ni15 segments was around 430 nm. The composition and crystalline structure of each Co-Ni nanowire segment were determined by transmission electron microscopy and selected area electron diffraction techniques. The employed single-bath electrochemical nanowire growth method allows for tuning both the composition and crystalline structure of each individual Co-Ni segment. The room temperature magnetic behavior of the multisegmented Co-Ni nanowire arrays is also studied and correlated with their structural and morphological properties.

An effective method to probe local magnetostatic properties in a nanometric FePd antidot array

A simple method to quantitatively characterize the local magnetic behaviour of a patterned nanostructure, like a ferromagnetic thin film of antidot arrays, is proposed. The first-order reversal curve (FORC) analysis, coupled with simulations using physically meaningful hysterons, allows us to obtain a quantitative and physically related description of the interaction field and each magnetization reversal process. The hysterons system is built from previously known hypotheses on the magnetic behaviour of the sample. This method was successfully applied to a highly hexagonal ordered FePd antidot array with nanometric dimensions. We achieved a complete characterization of the two different magnetization reversal mechanisms in function of the in-plane applied field angle. For a narrow range of high fields, the magnetization initiates rotating reversibly around the pores, while at lower fields, domain walls are nucleated and propagated. This in-plane magnetization reversal mechanism, partly reversible and partly irreversible, is the only angularly dependent one. While going away from the easy axis, its reversible proportion increases, as well as its switching field distribution. Finally, the results indicate that the high surface roughness between adjacent holes of the antidot thin film induces a parallel interaction field. The proposed method demonstrates its ability also to be applied to characterizing patterned nanostructures with rather complex magnetization reversal processes.

Changes in Morphology and Ionic Transport Induced by ALD SiO2 Coating of Nanoporous Alumina Membranes

Nanoporous anodic alumina membranes (NPAMs) were produced by the two-step anodization method in sulphuric, oxalic and phosphoric acidic electrolytes displaying a hexagonally ordered spatial arrangement of pores with well controlled nanopore size distribution and low porosity. Some selected NPAMs were further modified by conformal coating their surface and inner pore walls with a thin layer of SiO2 by means of atomic layer deposition (ALD), which reduces both the pore radii and porosity but it also seems to affect to the electric fixed charge on the membranes surface. A comparative study about the influence of silica modification of NPAMs surfaces on the ionic transport through the nanoporous membranes has been performed by measuring membrane potentials and electrochemical impedance spectroscopy with NaCl solutions. According to these results, a direct correlation between the membrane effective fixed charge and the NaCl diffusion coefficient can be established. The coating with a SiO2 thin layer causes a reduction of 75% in the positive effective fixed charge of the NPAMs independently of their pore radii and the increase in counterion transport (cation transport number and diffusion coefficient) even through constrained nanopores, which can be of interest in several applications (microfluidics, drug delivery, nanofilter devices, etc.). Moreover, slight changes in the membrane/solution interface due to the SiO2 cover layer are also indicated.

Magnetothermopower and magnetoresistance of single Co-Ni/Cu multilayered nanowires

The magnetothermopower and the magnetoresistance of single Co-Ni/Cu multilayered nanowires with various thicknesses of the Cu spacer are investigated. Both kinds of measurement are performed as a function of temperature (50–325 K) and under applied magnetic fields perpendicular to the nanowire axis, with magnitudes up to −15% at room temperature. A linear relation between thermopower S and electrical conductivity σ of the nanowires is found, with the magnetic field as an implicit variable. Combining the linear behavior of the S vs σ relation and the Mott formula, the energy derivative of the resistivity is determined. In order to extract the true nanowire materials parameters from the measured thermopower, a simple model based on the Mott formula is employed to distinguish the individual thermopower contributions of the sample. By assuming that the nondiffusive thermopower contributions of the nanowire can be neglected, it is found that the magnetic-field-induced changes of thermopower and resistivity are equivalent. The emphasis in the present paper is on the comparison of the magnetoresistance and magnetothermopower results and it is found that the same correlation is valid between the two sets of data for all samples, irrespective of the relative importance of the giant magnetoresistance or anisotropic magnetoresistance contributions in the various individual nanowires.

Unveiling the Hard Anodization Regime of Aluminum: Insight into Nanopores Self-Organization and Growth Mechanism

Pores growth mechanism and their self-ordering conditions are investigated for nanoporous alumina membranes synthesized by hard anodization (HA) of Al in a broad range of anodic conditions, covering oxalic acid electrolytes with concentrations from 0.300 M down to 0.075 M and potentiostatic anodization voltages between 120 and 225 V. The use of linear sweep voltammetry (LSV) and scanning and transmission electron microscopy, together with image analysis techniques allow one to characterize the intrinsic nature of the HA regime. HA of aluminum is explained on the basis of a phenomenological model taking into account the role of oxalate ions and their limited diffusion through alumina nanochannels from a bulk electrolyte. The depletion of oxalate ions at the bottom of the pores causes an increased growth of the alumina barrier layer at the oxide/electrolyte interface. Furthermore, an innovative method has been developed for the determination of the HA conditions leading to self-ordered pore growth in any given electrolyte, thus allowing one to extend the available range of interpore distances of the highly ordered hexagonal pore arrangement in a wide range of 240-507 nm, while keeping small pore diameters of 50-60 nm.

Pulsed Radiofrequency Glow Discharge Time-of-Flight Mass Spectrometry for Nanostructured Materials Characterization

Progress in the development of advanced materials strongly depends on continued efforts to miniaturizing their structures; thus, a great variety of nanostructured materials are being developed nowadays. Metallic nanowires are among the most attractive nanometer-sized materials because of their unique properties that may lead to applications as interconnectors in nanoelectronic, magnetic, chemical or biological sensors, and biotechnological labels among others. A simple method to develop self-ordered arrays of metallic nanowires is based on the use of nanoporous anodic alumina (NAA) and self-assembled nanotubular titanium dioxide membranes as templates. The chemical characterization of nanostructured materials is a key aspect for the synthesis optimization and the quality control of the manufacturing process. In this work, the analytical potential of pulsed radiofrequency glow discharge with detection by time-of-flight mass spectrometry (pulsed rf-GD-TOFMS) is investigated for depth profile analysis of self-assembled metallic nanostructures. Two types of nanostructured materials were successfully studied: self-assembled NAA templates filled with arrays of single metallic nanowires of Ni as well as arrays of multilayered Au/FeNi/Au and Au/Ni nanowires and nanotubular titanium dioxide templates filled with Ni nanowires, proving that pulsed rf-GD-TOFMS allows for fast and reliable depth profile analysis as well as for the detection of contaminants introduced during the synthesis process. Moreover, ion signal ratios between elemental and molecular species (e.g., (27)Al(+)/(16)O(+) and (27)Al(+)/(32)O(2)(+)) were utilized to obtain valuable information about the filling process and the presence of possible leaks in the system.

Ionic transport across tailored nanoporous anodic alumina membranes

Highly ordered Nanoporous Alumina Membranes (NPAMs) with a precise control of the pore size and different porosity but thickness around 63 μm were fabricated by the two-step anodization process using different acidic aqueous solutions, oxalic (Al-Ox), sulfuric (Al-Sf), and phosphoric (Al-Ph) acids, respectively. The pore size was controlled by properly changing the anodization voltage and the electrochemical bath conditions, obtaining the following average pores diameter values, d(p), as determined by scanning electron micrographic analysis: Al-Ox (d(p)=46±2 nm), Al-Sf (d(p)=27±2 nm), and Al-Ph (d(p)=240±20 nm). A pore increasing of around 5% for samples Al-Ox and Al-Sf was obtained after membranes immersion in 5 wt.% phosphoric acid for a certain etching time. Electrochemical characterization of NPAMs was performed with the samples in contact with NaCl solutions at different electrolyte concentrations. Ionic transport numbers and effective membrane fixed charge were determined from membrane potential measurements, which clearly show the significant influence of the pore diameter on ions transport. Moreover, frictional and electrical effects on mass transfer parameters (salt and ions diffusion coefficients) into the pores of alumina membranes were also evaluated from these results.