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The magnetic proximity effect in top and bottom Pt layers induced by Co in Ta/Pt/Co/Pt multilayers has been studied by interface sensitive, element specific x-ray resonant magnetic reflectivity. The asymmetry ratio for circularly polarized x-rays of left and right helicity has been measured at the Pt $L_3$ absorption edge (11567 eV) with an in-plane magnetic field ($\pm158$ mT) to verify its magnetic origin. The proximity-induced magnetic moment in the bottom Pt layer decreases with the thickness of the Ta buffer layer. Grazing incidence x-ray diffraction has been carried out to show that the Ta buffer layer induces the growth of Pt(011) rather than Pt(111) which in turn reduces the induced moment. A detailed density functional theory study shows that an adjacent Co layer induces more magnetic moment in Pt(111) than in Pt(011). The manipulation of the magnetism in Pt by the insertion of a Ta buffer layer provides a new way of controlling the magnetic proximity effect which is of huge importance in spin-transport experiments across similar kind of interfaces., 7 pages, 9 figures

Tailoring the optical and electronic properties of nanostructured polymer-metal composites demonstrates great potential for efficient fabrication of modern organic optical and electronic devices such as flexible sensors, transistors, diodes, or photovoltaics. Self-assembled polymer-metal nanocomposites offer an excellent perspective for creating hierarchical nanostructures on macroscopic scales by simple bottom-up processes. We investigate the growth processes of nanogranular silver (Ag) layers on diblock copolymer thin film templates during sputter deposition. The Ag growth is strongly driven by self-assembly and selective wetting on the lamella structure of polystyrene

We report synchrotron-based small-angle X-ray scattering experiments on a template-grown porous silica matrix (Santa Barbara Amorphous-15) upon in situ sorption of fluorinated pentane C5F12 along with volumetric gas sorption isotherm measurements. Within the mean-field model of Saam and Cole for vapor condensation in cylindrical pores, a nitrogen and C5F12 sorption isotherm is well described by a bimodal pore radius distribution dominated by meso- and micropores with 3.4 and 1.6 nm mean radius, respectively. In the scattering experiments, two different periodicities become evident. One of them (d1 = 11.5 nm) reflects the next nearest neighbor distance in a 2D-hexagonal lattice of tubular mesopores. A second periodicity (d2 = 11.4 nm) found during in situ sorption and freezing experiments is traced back to a superstructure along the cylindrical mesopores. It is compatible with periodic pore corrugations found in electron tomograms of empty SBA-15 by Gommes et al. ( Chem. Mater. 2009, 21, 1311 - 1317). A Rayleigh-Plateau instability occurring at the cylindrical blockcopolymer micelles characteristic of the SBA-15 templating process quantitatively accounts for the superstructure and thus the spatial periodicity of the pore wall corrugation. The consequences of this peculiar morphological feature on the spatial arrangement of C5F12, in particular the formation of periodically arranged nanobubbles (or voids) upon adsorption, desorption, and freezing of liquids, are discussed in terms of capillary bridge formation and cavitation in tubular but periodically corrugated pores.

The progress of organic electronics demands an increased participation of nanotechnology, and it has already been shown that the presence of metallic nanoparticles and/or nanostructured thin films can enhance the device performance. Nevertheless, to gain control over the device final performance, it is crucial to achieve a profound understanding of the nanostructure development and assembly. We investigate the growth kinetics of silver (Ag) on a tris(8-hydroxyquinolinato)aluminum (Alq3) thin film via sputter deposition. The increase of the average electron density of the Ag nanostructured film is observed to follow a sigmoidal shape development as a function of the deposited Ag thickness, as a consequence of dominant island-mediated growth. The nanoclustered film is percolated at around a thickness of 5.0 ± 0.1 nm. At this film thickness the effective film density is about 50%. Moreover, our simulation results indicate that the shape of the nanoclusters changes from truncated spheres to cylinders upon sur...

In this work, formation of self-organized Si nanostructures induced by pure Fe incorporation during normal incidence low-energy (1keV) Ar $$^+$$ ion bombardment is presented. It has been observed that the incorporation of Fe affects the evolution of the surface topography. The addition of Fe generates pronounced nanopatterns, such as dots, ripples and combinations of dots and ripples. The orientation of the ripple wave vector of the patterns formed is found to be in a direction normal to the Fe flow. The nanoripples with wavelength of the order of 39 nm produced is expected to be the lowest wavelength of the patterns reported on ion-beam-eroded structures under the incorporation of metallic impurities as per our knowledge. From the AFM and GISAXS analysis, it has been confirmed that the ripples formed are asymmetric in nature. The effect of the concentration of the Fe on morphological transition of the patterns has been studied using Rutherford backscattering measurements.

Long-range ordered nanostructures are prepared in the poly(styrene)-block-poly(E >-caprolactone) diblock copolymer thin films using micromolding. We evaluated the change in crystallinity based on grazing-incidence X-ray diffraction and proved that the crystallinity increased with the decrease of the mold size. This means that ordered nanostructures with atomic length scale order can be adjusted by tuning the mesoscale confinement. The inherent mechanism was the cooperation of geometric confinement, microphase structure and surface-induced ordering of PS-b-PCL in the melt, which paved the way for the subsequent crystal growth. These findings establish a route to promote the cost-effective nanofabrication by combining the mature microfabrication technique with the emerging directed self-assembly of block copolymers.

Carbon nanotube “forests” show great promise in a variety of applications, from supercapacitors to fuel cells, but the realization of such materials for functional devices relies on a better control over processing routes such that targeted structures and associated properties can be reproducibly obtained. The orientation distribution of the nanotubes is a critical structural property affecting both electrical and mechanical response, yet it remains a challenging characteristic to quantify. Small-angle X-ray scattering (SAXS) is a technique well suited to investigate the vertical alignment of nanotubes. Here we show that the orientation distribution obtained from SAXS is not satisfactorily represented by the normal distribution or the Lorentzian, which have been used until now. Instead, an excellent agreement between model and data is found with the generalized normal distribution (GND). Such quantification of the carbon nanotube alignment can be used as direct input in simulations for optimizing structur...

Fabrication of nanoparticle arrays on a substrate is one of the most concerned aspects for manipulating assembly of nanoparticles and preparing functional nanocomposites. Here, we studied in situ the assembly kinetics of polystyrene nanocolloids by using grazing incidence small-angle X-ray scattering. The structure formation of the nanoparticle film is monitored during air-brush spraying, which provides a rapid and scalable preparation. By optimizing the substrate temperature, the dispersion of the nanocolloids can be tailored to prepare monolayer film. The success of the monolayer preparations is attributed to the fast solvent evaporation which inhibits the aggregation of the nanocolloids. The present study may open a new avenue for the manufacture-friendly preparation of well-dispersed nanoparticle thin films., S.Y. acknowledges the kind financial support from Knut and Alice Wallenberg Foundation.

A detailed mechanism of the nanoripple pattern formation on Si substrates generated by the simultaneous incorporation of pure Fe impurities at low energy (1 keV) ion beam erosion has been studied. To understand and clarify the mechanism of the pattern formation, a comparative analysis of the samples prepared for various ion fluence values using two complimentary methods for nanostructure analysis, atomic force microscopy, and grazing incidence small angle x-ray scattering has been done. We observed that phase separation of the metal silicide formed during the erosion does not precede the ripple formation. It rather concurrently develops along with the ripple structure. Our work is able to differentiate among various models existing in the literature and provides an insight into the mechanism of pattern formation under ion beam erosion with impurity incorporation.

The fabrication of substrates for Surface Enhanced Raman Scattering (SERS) applications matching the needs for high sensitive and reproducible sensors remains a major scientific and technological issue. We correlate the morphological parameters of silver (Ag) nanostructured thin films prepared by sputter deposition on flat silicon (Si) substrates with their SERS activity. A maximum enhancement of the SERS signal has been found at the Ag percolation threshold, leading to the detection of thiophenol, a non-resonant Raman probe, at concentrations as low as 10-10M, which corresponds to enhancement factors higher than 7 orders of magnitude. To gain full control over the developed nanostructure, we employed the combination of in-situ time-resolved microfocus Grazing Incidence Small Angle X-ray Scattering with sputter deposition. This enables to achieve a deepened understanding of the different growth regimes of Ag. Thereby an improved tailoring of the thin film nanostructure for SERS applications can be realized. © 2014 AIP Publishing LLC.

Recent simulations of vertically aligned carbon nanotube arrays have shown that the shape of the orientation distribution of nanotubes within the array has a drastic effect on the electrical properties of the array. Orienting of shape-anisotropic objects can be carried out in several different ways such as shearing, magnetically steering, or by vibrating the objects. Nevertheless, perfect orientation is difficult if not impossible to achieve. In the case of the growth of carbon nanotube arrays, self-confinement can occur affecting the resultant orientation distribution. Yet so far the shape of the orientation distribution has not been quantified in great detail and it has been mostly assumed to be Gaussian or Lorentzian. In the present work, multi-walled carbon nanotube arrays were grown via aerosol-assisted chemical vapour deposition with iron catalyst and investigated using small-angle X-ray scattering, a method perfectly suited to characterizing the orientation of carbon nanotubes. Using a microfocused X-ray beam of 24 μm x 17 μm in size at beamline P03 of the PETRA III synchrotron storage ring in Hamburg, we determined the orientation distribution of the vertically aligned carbon nanotubes along the film height. Remarkably, the packing density of the carbon nanotubes seems to correlate not only with the width of the distribution but also its shape. The shape of the orientation distribution was then compared to that from different oriented systems. These findings indicate that by using alignment methods that are based on steric interaction between particles, such as shearing or self-confinement during particle growth, the system will reach an alignment with an orientation distribution closer to the Laplace distribution than to the normal distribution. Such a finding has profound implications for simulation studies of mechanical, electrical and other properties of many hierarchical materials.

Electronic excitation mediated energy loss by 120 MeV Au9+ swift heavy ions (SHIs) results in significant structural modifications of FeCo nanoparticles embedded in thin SiO2 matrix. The variations in local atomic structure and particle size/shape at different irradiation fluences are probed by extended x-ray absorption fine structure spectroscopy (EXAFS) and grazing incidence small angle x-ray scattering (GISAXS). The crystallinity and ordering of the films are found to first decrease and then increase with fluence. The observed alterations in co-ordination number of Fe/Co from EXAFS are correlated primarily with particle size modifications due to a transient thermal spike generated in the embedded nanoparticles by SHIs. The role of hydrogen desorption from nanoparticles is also highlighted.

The field emission (FE) properties of nickel nanoparticles embedded in thin silica matrix irradiated with 100 MeV Au+7 ions at various fluences are studied here. A large increase in FE current density is observed in the irradiated films as compared to their as deposited counterpart. The dependence of FE properties on irradiation fluence is correlated with surface roughness, density of states of valence band and size distribution of nanoparticles as examined with atomic force microscope, X-ray photoelectron spectroscopy, and grazing incidence small angle x-ray scattering. A current density as high as 0.48 mA/cm2 at an applied field 15 V/μm has been found for the first time for planar field emitters in the film irradiated with fluence of 5.0 × 1013 ions/cm2. This significant enhancement in the current density is attributed to an optimized size distribution along with highest surface roughness of the same. This new member of field emission family meets most of the requirements of cold cathodes for vacuum micro/nanoelectronic devices.