Search Results (12)

Our paper introduces a simulation-based framework designed to interpret differential phase contrast (DPC) magnetic imaging within the transmission electron microscope (TEM). We investigate patterned magnetic membranes, particularly focusing on nano-patterned Co₇₀Fe₃₀ thin-film membranes fabricated via focused ion beam (FIB) milling. Our direct magnetic imaging reveals regular magnetic domain patterns in these carefully prepared systems. Notably, the observed magnetic structure aligns precisely with micromagnetic simulations based on the dimensions of the underlying nanostructures. This agreement emphasizes the usefulness of micromagnetic simulations, not only for the interpretation of DPC data, but also for the prediction of possible microstructures in magnetic sensor systems with nano-patterns. Full article

The practical significance of ferroelectric domains and various domain boundaries has been growing steadily in recent years. In this work, various domain structures were written with an electron beam through a thin aluminum film on a −Z cut of bulk lithium niobate. The use of relatively low accelerating voltages (5 and 10 kV) and the grounding of the surface metallization made it possible to write periodic structures (1D and 2D) on large areas with domain sizes ≤1 μm. Selective domain etching and AFM in contact mode were used to observe various domain shapes obtained in the experiments. An unusual feature of the submicron-sized domains was needle-like vertices. Importantly, the vertices of the domains were deepened relative to the irradiated surface. It was found that the size and proximity of the irradiated regions to each other in the patterns used can significantly change the upper part of the domains. The experimental data were analyzed and discussed taking into account the computer simulation of the spatial field distribution of injected electron beam charges. The obtained results contribute to the development of controlled writing of submicron-sized domain structures using an electron beam. Full article

Acid rain is a major problem for animals, plants, buildings, and also for the top glass of photovoltaic (PV) solar panels and greenhouses. Air pollutants such as NOx, NH₃, and H₂S can mix with water in the atmosphere to form acid rain. It was discovered that atmospheric water vapor adsorbed on the surface of glass can also lead to corrosion of the glass surface. The purpose of this work is to obtain a protective film for glasses used in different domains such as solar cells, windows, stained glass windows from historical buildings, etc. Thin film deposited on glass must be protective against acid rain, transparent in the visible domain with a band gap up to 3.2 eV, and have a vitreous structure (glass). Electron beam (e-gun) technology is a deposition technique for producing high-purity and dense coatings in a short time. It is well known that Ta₂O₅ is an oxide with anticorrosive properties, but it is expensive and cannot form glass by itself. ZnO is an oxide known as a glass former, exhibiting good optical properties. In this paper, a thin film obtained by the deposition of ZnO and Ta₂O₅ on a glass substrate using e-gun technology are studied. The simulated acid rain effect on the structure, morphology, and optical properties of thin films are studied after a 65% nitric acid attack on the surface. The X-ray diffraction (XRD) pattern shows the vitreous state of the thin film with a composition 50%ZnO 50%Ta₂O₅ before and after the acid attack. The morphology, composition, and thickness of the film are investigated using scanning electron microscopy with energy dispersive spectroscopy (SEM/EDS) and profilometry. Full article

Patterned elements of permalloy (Py) with a thickness as large as 300 nm have been defined by electron beam lithography on X-ray-transparent 50 nm thick membranes in order to characterize their magnetic structure via Magnetic Transmission X-ray Microscopy (MTXM). To avoid the situation where the fragility of the membranes causes them to break during the lithography process, it has been found that the spin coating of the resist must be applied in two steps. The MTXM results show that our samples have a central domain wall, as well as other types of domain walls, if the nanostructures are wide enough. Full article

Among lithium battery cathode materials, Li_1.2Ni_0.13Mn_0.54Co_0.13O₂ (LR-NMC) has a high theoretical capacity, but suffers from voltage and capacity fade during cycling. This is partially ascribed to transition metal cation migration, which involves the local transformation of the honeycomb layered structure to spinel-like nano-domains. Determination of the honeycomb layered/spinel phase ratio from powder X-ray diffraction data is hindered by the nanoscale of the functional material and the domains, diverse types of twinning, stacking faults, and the possible presence of the rock salt phase. Determining the phase ratio from transmission electron microscopy imaging can only be done for thin regions near the surfaces of the crystals, and the intense beam that is needed for imaging induces the same transformation to spinel as cycling does. In this article, it is demonstrated that the low electron dose sufficient for electron diffraction allows the collection of data without inducing a phase transformation. Using calculated electron diffraction patterns, we demonstrate that it is possible to determine the volume ratio of the different phases in the particles using a pair-wise comparison of the intensities of the reflections. Using this method, the volume ratio of spinel structure to honeycomb layered structure is determined for a submicron sized crystal from experimental three-dimensional electron diffraction (3D ED) and precession electron diffraction (PED) data. Both twinning and the possible presence of the rock salt phase are taken into account. After 150 charge–discharge cycles, 4% of the volume in LR-NMC particles was transformed irreversibly from the honeycomb layered structure to the spinel structure. The proposed method would be applicable to other multi-phase materials as well. Full article

Hierarchical micro/-nanostructures were produced on polycarbonate polymer surfaces by employing a two-step UV-laser processing strategy based on the combination of Direct Laser Interference Patterning (DLIP) of gratings and pillars on the microscale (3 ns, 266 nm, 2 kHz) and subsequently superimposing Laser-induced Periodic Surface Structures (LIPSS; 7–10 ps, 350 nm, 100 kHz) which adds nanoscale surface features. Particular emphasis was laid on the influence of the direction of the laser beam polarization on the morphology of resulting hierarchical surfaces. Scanning electron and atomic force microscopy methods were used for the characterization of the hybrid surface structures. Finite-difference time-domain (FDTD) calculations of the laser intensity distribution on the DLIP structures allowed to address the specific polarization dependence of the LIPSS formation observed in the second processing step. Complementary chemical analyzes by micro-Raman spectroscopy and attenuated total reflection Fourier-transform infrared spectroscopy provided in-depth information on the chemical and structural material modifications and material degradation imposed by the laser processing. It was found that when the linear laser polarization was set perpendicular to the DLIP ridges, LIPSS could be formed on top of various DLIP structures. FDTD calculations showed enhanced optical intensity at the topographic maxima, which can explain the dependency of the morphology of LIPSS on the polarization with respect to the orientation of the DLIP structures. It was also found that the degradation of the polymer was enhanced for increasing accumulated fluence levels. Full article

Directed self-assembly (DSA) was investigated on self-assembled monolayers (SAMs) chemically modified by electron beam (EB) irradiation, which is composed of 6-(4-nitrophenoxy) hexane-1-thiol (NPHT). Irradiating a NPHT by EB could successfully induce the orientation and selective patterning of block copolymer domains. We clarified that spatially-selective lamellar orientations of polystyrene-block-poly(methyl methacrylate) (PS-b-PMMA) could be achieved by a change of an underlying SAM. The change of an underlying SAM is composed of the transition of an NO₂ group to an NH₂ group, which is induced by EB. The modification in the polarity of different regions of the SAM with EB lithography controlled the lamellar orientation of PS-b-PMMA. The reduction of the NPHT SAM plays an important role in the orientation of block copolymer. This method might significantly simplify block copolymer DSA processes when it is compared to the conventional DSA process. By investigating the lamellae orientation with EB, it is clarified that only suitable annealing temperatures and irradiation doses lead to the vertical orientation. We also fabricated pre-patterned Si substrates by EB lithographic patterning and reactive ion etching (RIE). DSA onto such pre-patterned Si substrates was proven to be successful for subdivision of the lithographic patterns into line and space patterns. Full article

The characteristics of electron-beam domain writing (EBDW) on the polar and nonpolar surfaces of the field-cooled (FC) and zero-field cooled (ZFC) Sr_0.61Ba_0.39Nb₂O₆ (SBN) crystals are presented in the range of accelerating voltage U from 10 to 25 kV. The exposure characteristics of the domain diameter d and length L_d (when writing on the polar and nonpolar surfaces, respectively) were measured. With increasing exposure time, d tends to a saturation value, whereas L_d grows linearly, the frontal velocity V_f being of 40 μm/s. At U = 25 kV the achieved d and L_d are of 7 and 40 µm, respectively. The observed peculiar features of EBDW—specifically the domain widening with exposure times and the effect of the polarization state of the crystal on the domain stability—are accounted for by the relaxor features inherent to this material. The effects of electron-beam (EB) irradiation on the local hysteresis loops is evidence of a domain fixation. Full article

Metal nanoparticles (NP) in minerals are an emerging field of research. Development of advanced analytical techniques such as Z-contrast imaging and mapping using high-angle annular dark field scanning transmission electron microscopy (HAADF STEM) allows unparalleled insights at the nanoscale. Moreover, the technique provides a link between micron-scale textures and chemical patterns if the sample is extracted in situ from a location of petrogenetic interest. Here we use HAADF STEM imaging and energy-dispersive X-ray spectrometry (EDX) mapping/spot analysis on focused ion beam prepared foils to characterise atypical Cu-As-zoned and weave-twinned hematite from the Olympic Dam deposit, South Australia. We aim to determine the role of solid-solution versus the presence of discrete included NPs in the observed zoning and to understand Cu-As-enrichment processes. Relative to the grain surface, the Cu-As bands extend in depth as (sub)vertical trails of opposite orientation, with Si-bearing hematite NP inclusions on one side and coarser cavities (up to hundreds of nm) on the other. The latter host Cu and Cu-As NPs, contain mappable K, Cl, and C, and display internal voids with rounded morphologies. Aside from STEM-EDX mapping, the agglomeration of native copper NPs was also assessed by high-resolution imaging. Collectively, such characteristics, corroborated with the geometrical outlines and negative crystal shapes of the cavities, infer that these are opened fluid inclusions with NPs attached to inclusion walls. Hematite along the trails features distinct nanoscale domains with lattice defects (twins, 2-fold superstructuring) relative to hematite outside the trails, indicating this is a nanoprecipitate formed during replacement processes, i.e., coupled dissolution and reprecipitation reactions (CDRR). Transient porosity intrinsically developed during CDRR can trap fluids and metals. Needle-shaped and platelet Cu-As NPs are also observed along (sub)horizontal bands along which Si, Al and K is traceable along the margins. The same signature is depicted along nm-wide planes crosscutting at 60° and offsetting (012)-twins in weave-twinned hematite. High-resolution imaging shows linear and planar defects, kink deformation along the twin planes, misorientation and lattice dilation around duplexes of Si-Al-K-planes. Such defects are evidence of strain, induced during fluid percolation along channels that become wider and host sericite platelets, as well as Cl-K-bearing inclusions, comparable with those from the Cu-As-zoned hematite, although without metal NPs. The Cu-As-bands mapped in hematite correspond to discrete NPs formed during interaction with fluids that changed in composition from alkali-silicic to Cl- and metal-bearing brines, and to fluid rates that evolved from slow infiltration to erratic inflow controlled by fault-valve mechanism pumping. This explains the presence of Cu-As NPs hosted either along Si-Al-K-planes (fluid supersaturation), or in fluid inclusions (phase separation during depressurisation) as well as the common signatures observed in hematite with variable degrees of fluid-mineral interaction. The invoked fluids are typical of hydrolytic alteration and the fluid pumping mechanism is feasible via fault (re)activation. Using a nanoscale approach, we show that fluid-mineral interaction can be fingerprinted at the (atomic) scale at which element exchange occurs. Full article

Scheelite (CaWO₄) and powellite (CaMoO₄) are isostructural minerals considered as a non-ideal solid solution series. Micron- to nanoscale investigation of a specimen of skarnoid from Zhibula, Gangdese Belt, Tibet, China, was carried out to assess the identity of the phases within a broad scheelite-powellite (Sch-Pow) compositional range, and to place additional constraints on redox changes during ore formation. An electron probe microanalysis shows that Mo-rich domains within complex oscillatory-zoned single crystals, and as thin sliver-like domains, have a compositional range from 20 mol.% to 80 mol.% Pow. These occur within a matrix of unzoned, close-to-end-member scheelite aggregates (87 mol.%–95 mol.% Sch). Laser-ablation inductively coupled plasma mass spectrometry spot analysis and element mapping reveal systematic partitioning behaviour of trace elements in skarn minerals (grossular₅₀, diopside₈₀, anorthite, and retrograde clinozoisite) and scheelite-powellite aggregates. The Mo-rich domains feature higher concentrations of As, Nb, and light rare earth elements LREE, whereas W-rich domains are comparatively enriched in Y and Sr. Transmission electron microscopy (TEM) was carried out on focused-ion-beam-prepared foils extracted in situ from domains with oscillatory zoning occurring as slivers of 20 mol.%–40 mol.% Pow and 48 mol.%–80 mol.% Pow composition within an unzoned low-Mo matrix (20 mol.% Pow). Electron diffractions, high-angular annular dark field (HAADF) scanning-TEM (STEM) imaging, and energy-dispersive spectroscopy STEM mapping show chemical oscillatory zoning with interfaces that have continuity in crystal orientation throughout each defined structure, zoned grain or sliver. Non-linear thermodynamics likely govern the patterning and presence of compositionally and texturally distinct domains, in agreement with a non-ideal solid solution. We show that the sharpest compositional contrasts are also recognisable by variation in growth direction. Atomic-scale resolution imaging and STEM simulation confirm the presence of scheelite-powellite within the analysed range (20 mol.%–80 mol.% Pow). Xenotime-(Y) inclusions occur as nm-wide needles with epitaxial orientation to the host scheelite-powellite matrix throughout both types of patterns, but no discrete Mo- or W-bearing inclusions are observed. The observed geochemical and petrographic features can be reconciled with a redox model involving prograde deposition of a scheelite+molybdenite assemblage (reduced), followed by interaction with low-T fluids, leading to molybdenite dissolution and reprecipitation of Mo as powellite-rich domains (retrograde stage, oxidised). The observation of nanoscale inclusions of xenotime-(Y) within scheelite carries implications for the meaningful interpretation of petrogenesis based on rare earth element (REE) concentrations and fractionation patterns. This research demonstrates that HAADF-STEM is a versatile technique to address issues of solid solution and compositional heterogeneity. Full article

We demonstrate the application of confocal Raman microscopy (CRM) for nondestructive imaging of ferroelectric domains both at the surface and in the bulk of lead magnesium niobate-lead titanate (PMN-PT) ferroelectric single crystals. The studied model periodical domain structure was created at a [001] cut of tetragonal-phase PMN-PT crystal by the electron beam patterning technique. It was shown that the surface CRM domain image coincides in details with the image obtained by piezoresponse force microscopy. Full article

Graphene grown on C-face SiC substrates using two procedures, high and low growth temperature and different ambients, was investigated using Low Energy Electron Microscopy (LEEM), X-ray Photo Electron Electron Microscopy (XPEEM), selected area Low Energy Electron Diffraction (μ-LEED) and selected area Photo Electron Spectroscopy (μ-PES). Both types of samples showed formation of μm-sized grains of graphene. The sharp (1 × 1) μ-LEED pattern and six Dirac cones observed in constant energy photoelectron angular distribution patterns from a grain showed that adjacent layers are not rotated relative to each other, but that adjacent grains in general have different azimuthal orientations. Diffraction spots from the SiC substrate appeared in μ-LEED patterns collected at higher energies, showing that the rotation angle between graphene and SiC varied. C 1s spectra collected did not show any hint of a carbon interface layer. A hydrogen treatment applied was found to have a detrimental effect on the graphene quality for both types of samples, since the graphene domain/grain size was drastically reduced. From hydrogen treated samples, μ-LEED showed at first a clear (1 × 1) pattern, but within minutes, a pattern containing strong superstructure spots, indicating the presence of twisted graphene layers. The LEED electron beam was found to induce local desorption of hydrogen. Heating a hydrogenated C-face graphene sample did not restore the quality of the original as-grown sample. Full article