Search

Krisen treten regelmäßig auf und betreffen aufgrund zunehmender Globalisierung immer mehr Unternehmen gleichzeitig. In diesem Beitrag wird ein Ansatz für ein dynamisches Prozessmanagement vorgestellt, welches die Fähigkeit der Früherkennung von Disruptionen und gleichzeitig auch Routine sowie Agilität im Normal- wie auch im Krisenmodus durchgängig unterstützt.

After the discovery of graphene, many other 2D materials have been predicted theoretically and successfully prepared. In this context, single-sheet black phosphorus - phosphorene - is emerging as a viable contender in the field of (2D) semiconductors. Phosphorene offers high carrier mobility and an anisotropic structure that gives rise to a modulation of physical and chemical properties. This opens the way to many novel and fascinating applications related to field-effect transistors and optoelectronic devices. In previous studies, a single layer of blue phosphorene intermixed with Au atoms was grown using purified black phosphorus as a precursor. Starting from the observation that phosphorus vapor mainly consists of P clusters, in this work we aimed at obtaining blue phosphorus using much less expensive purified red phosphorus as an evaporant. By means of microscopy, spectroscopy and diffraction experiments, we show that black or red phosphorus deposition on Au(111) substrates yields the same blue phosphorus film.

On-surface chemistry holds the potential for ultimate miniaturization of functional devices. Porphyrins are promising building-blocks in exploring advanced nanoarchitecture concepts. More stable molecular materials of practical interest with improved charge transfer properties can be achieved by covalently interconnecting molecular units. On-surface synthesis allows to construct extended covalent nanostructures at interfaces not conventionally available. Here, we address the synthesis and properties of covalent molecular network composed of interconnected constituents derived from halogenated nickel tetraphenylporphyrin on Au(111). We report that the π-extended two-dimensional material exhibits dispersive electronic features. Concomitantly, the functional Ni cores retain the same single-active site character of their single-molecule counterparts. This opens new pathways when exploiting the high robustness of transition metal cores provided by bottom-up constructed covalent nanomeshes.

Uncommon metal oxidation states in porphyrinoid cofactors are responsible for the activity of many enzymes. The F₄₃₀ and P450nor co-factors, with their reduced NiI- and FeIII-containing tetrapyrrolic cores, are prototypical examples of biological systems involved in methane formation and in the reduction of nitric oxide, respectively. Herein, using a comprehensive range of experimental and theoretical methods, we raise evidence that nickel tetraphenyl porphyrins deposited in vacuo on a copper surface are reactive towards nitric oxide disproportionation at room temperature. The interpretation of the measurements is far from being straightforward due to the high reactivity of the different nitrogen oxides species (eventually present in the residual gas background) and of the possible reaction intermediates. The picture is detailed in order to disentangle the challenging complexity of the system, where even a small fraction of contamination can change the scenario.

High-quality nitrogen-doped graphene on nickel is prepared by exploiting both the catalytic properties of nickel and the solubility of nitrogen atoms into its bulk. Following the standard chemical vapor deposition procedure, a previously nitrogen-doped nickel substrate is exposed to carbon-containing precursors so that nitrogen atoms, segregating to the surface, remain trapped in the growing graphene network. Morphological and chemical characterization by scanning tunneling microscopy and X-ray photoelectron spectroscopy demonstrates that the process yields a flat, wide, continuous nitrogen-doped graphene layer. Experimental results are combined with a thorough density functional theory investigation of possible structural models, to obtain a clear description at the atomic scale of the various configurations of the nitrogen atoms observed in the graphene mesh. This growth method is potentially scalable and suitable for the production of high-performance nano-devices with well-defined nitrogen centers, to be exploited as metal-free carbon-based catalysts in several applicative fields such as electrochemistry, energy storage, gas storage/sensing or wastewater treatment., 21 pages, including 4 figures, plus SI

The capability to display images containing chemical, magnetic, and structural information and to perform spectroscopy and diffraction from a μm-sized area makes cathode lens electron microscopy one of the most used and reliable techniques to analyze surfaces at the mesoscale. Thanks to its versatility, LEEMlow-energyelectron microscopy (LEEM)/PEEM systems are currently employed to study model systems in the fields of nanotechnology, nanomagnetism, material science, catalysis, energy storage, thin films, and 2-D (two-dimensional) materials. In this chapter, we will present a brief but complete review of this class of instruments. After a historical digression in the introductory section, we will first show the basic operating principles of a simple setup and then the elements that can be added to improve performance. Later, two sections will be dedicated to LEEM and PEEMphotoelectronemission microscopy (PEEM), respectively. In both cases, a theoretical discussion on the contrast mechanisms will prelude to a showcase of the operating modes of the instrument, with clear examples that will show the best performance available today. Finally, a brief discussion about the future developments of cathode lens electron microscopy will close the chapter.

High-quality nitrogen-doped graphene on nickel is prepared by exploiting both the catalytic properties of nickel and the solubility of nitrogen atoms into its bulk. Following the standard chemical vapor deposition procedure, a previously nitrogen-doped nickel substrate is exposed to carbon-containing precursors so that nitrogen atoms, segregating to the surface, remain trapped in the growing graphene network. Morphological and chemical characterization by scanning tunneling microscopy and X-ray photoelectron spectroscopy demonstrates that the process yields a flat, wide, continuous nitrogen-doped graphene layer. Experimental results are combined with a thorough density functional theory investigation of possible structural models, to obtain a clear description at the atomic scale of the various configurations of the nitrogen atoms observed in the graphene mesh. This growth method is potentially scalable and suitable for the production of high-performance nano-devices with well-defined nitrogen centers, to be exploited as metal-free carbon-based catalysts in several applicative fields such as electrochemistry, energy storage, gas storage/sensing or wastewater treatment.

The capability to display images containing chemical, magnetic and structural information and to perform spectroscopy and diffraction from a {\mu}m-sized area makes cathode lens electron microscopy one of the most used and reliable techniques to analyze surfaces at the mesoscale. Thanks to its versatility, LEEM/PEEM systems are currently employed to study model systems in the fields of nanotechnology, nanomagnetism, material science, catalysis, energy storage, thin films and 2D materials. In the following chapter, we will present a brief but complete review of this class of instruments. After an historical digression in the introducing section, we will show first the basic operating principles of a simple setup and then the elements that can be added to improve the performances. Later, two sections will be dedicated to LEEM and PEEM respectively. In both cases, a theoretical discussion on the contrast mechanisms will prelude to a showcase of the operating modes of the instrument, with clear examples that will show the best performances available nowadays. Finally, a brief discussion about the future developments of cathode lens electron microscopy will close the chapter.

PurposeThis paper aims to study the extent of the transformation of European manufacturing companies towards the factory of the future (FoF) and related concepts, e.g. Industry 4.0 and digitalisation.Design/methodology/approachA qualitative survey design was used to investigate the areas, patterns and elements for implementing FoF. A total of 92 responses from manufacturing firms of Alpine regions were collected and analysed, followed by in-depth interviews with a subset of respondents to identify common challenges, drivers and opportunities for the transformation.FindingsManufacturing companies are gaining awareness on their needs and gaps in the FoF path, the implications on business strategy and the rates of innovation and technology adoption. Nevertheless, they still need to shape their organisational structures (e.g. from highly centralised to more collaborative ones) and nurture their managerial capabilities in operations and supply chain management, and customer relationships, only partially based on FoF technologies.Research limitations/implicationsThis study aims to contribute to recent literature and practice of FoF (and related concepts) by depicting a picture of the possible areas of intervention, main issues and gaps (especially in terms of skills, supply chain and customer relationships) of manufacturing companies in their digital transformation. The qualitative research design and its scope represent the main limitations.Originality/valueThis paper provides a systemic overview for FoF by encompassing the technological, strategic, managerial and organisational perspectives of digitalisation in manufacturing and integrating the insights from a multi-sectorial and multi-dimensional analysis.

Many applications of molecular layers deposited on metal surfaces, ranging from single-atom catalysis to on-surface magnetochemistry and biosensing, rely on the use of thermal cycles to regenerate the pristine properties of the system. Thus, understanding the microscopic origin behind the thermal stability of organic/metal interfaces is fundamental for engineering reliable organic-based devices. Here, we study nickel porphyrin molecules on a copper surface as an archetypal system containing a metal center whose oxidation state can be controlled through the interaction with the metal substrate. We demonstrate that the strong molecule-surface interaction, followed by charge transfer at the interface, plays a fundamental role in the thermal stability of the layer by rigidly anchoring the porphyrin to the substrate. Upon thermal treatment, the molecules undergo an irreversible transition at 420 K, which is associated with an increase of the charge transfer from the substrate, mostly localized on the phenyl substituents, and a downward tilting of the latters without any chemical modification. This journal is

The irradiation with photons or electrons can dramatically influence the chemical stability of a molecule, either free or adsorbed on a surface, inducing its fragmentation or desorption. We revisit here the exostimulated dissociation of CO, a prototypical case, choosing hcp thin cobalt films as model support. Intense, microfocused soft X-rays or electron beams are used to locally stimulate CO dissociation. Fast-XPS gives direct access to the adsorbates' chemical state and coverage during irradiation, enabling the kinetics of the process to be monitored in real time. The energy-dependent cross sections for photon and electron stimulated molecular dissociation and desorption are estimated for a fixed initial CO coverage of 1 / 3 ML. In the soft X-ray regime, the desorption channel always prevails over dissociation and is significantly enhanced above the O K edge. The relative dissociation probability increases steadily with increasing photon energy, reaching 30% at 780 eV. Furthermore, we show that low energy electrons in the range 50 to 200 eV dissociate CO more efficiently than X-rays. The prolonged irradiation of the Co surface in CO ambient is found to produce a continuous increase of the carbon coverage, initially promoting the formation of carbides and subsequently accumulating sp 2 carbon on the surface. Far from being a detrimental effect, the CO stimulated dissociation can be exploited to lithographically graft carbon-rich microscopic patterns on Co, with resolution well into the nanometer scale. A brief thermal treatment following irradiation results in the formation of a graphitic carbon overlayer, which effectively protects Co from oxidation upon exposure to ambient conditions, preserving its out-of-plane magnetic anisotropy and domain configuration.

We report on the proof of principle of a scalable method for writing the magnetic state by electron-stimulated molecular dissociative adsorption on ultrathin Co on Re(0001). Intense microfocused low-energy electron beams are used to promote the formation of surface carbides and graphitic carbon through the fragmentation of carbon monoxide. Upon annealing at the CO desorption temperature, carbon persists in the irradiated areas, whereas the clean surface is recovered elsewhere, giving origin to chemical patterns with nanometer-sharp edges. The accumulation of carbon is found to induce an in-plane to out-of-plane spin reorientation transition in Co, manifested by the appearance of striped magnetic domains. Irradiation at doses in excess of 1000 L of CO followed by ultrahigh vacuum annealing at 380 °C determines the formation of a graphitic overlayer in the irradiated areas, under which Co exhibits out-of-plane magnetic anisotropy. Domains with opposite magnetization are separated here by chiral Neél walls. Our fabrication protocol adds lateral control to spin reorientation transitions, permitting to tune the magnetic anisotropy within arbitrary regions of mesoscopic size. We envisage applications in the nano-engineering of graphene-spaced stacks exhibiting the desired magnetic state and properties.

Lateral quantum confinement is of great interest in tuning the electronic properties of graphene-based nanostructures, making them suitable for technological applications. In principle, these properties might be controlled through the edge topology: for example, zigzag nanoribbons are predicted to have spin-polarized edge states. The practical realization of these structures is of utmost importance in fully harnessing the electronic properties of graphene. Here, the formation of regular, 1.4 nm wide ribbon-like graphene structures with zigzag edges are reported, showing 1D electronic states. It is found that these “pseudo-ribbons” embedded in single-layer graphene supported on Ni(100) can spontaneously form upon carbon segregation underneath 1D graphene moiré domains, extending hundreds of nanometers in length. On the basis of both microscopy/spectroscopy/diffraction experiments and theoretical simulations, it is shown that these structures, even though seamlessly incorporated in a matrix of strongly interacting graphene, exhibit electronic properties closely resembling those of zigzag nanoribbons.

We have studied the epitaxial growth of thin layers of vanadium and vanadium oxide on a Rh(110) surface with low-energy electron diffraction (LEED), low-energy electron microscopy (LEEM), Auger electron spectroscopy (AES), and X-ray photoelectron spectroscopy (XPS). Up to six monolayers of V/VOx were deposited with temperatures varying between 370 and 770 K. For V deposition, (1 × n) and (n × 1) overlayers with n = 2 and 4 are observed. For the deposition of 3 MLE of VOx, a (12 × 1) structure is obtained as a stable structure. XPS of V 2p3/2 reveals the simultaneous presence of an oxidic and a metallic or strongly reduced (V2+) V component.

A major obstacle for the implementation of redox-based memristive memory or logic technology is the large cycle-to-cycle and device-to-device variability. Here, we use spectromicroscopic photoemission threshold analysis and operando XAS analysis to experimentally investigate the microscopic origin of the variability. We find that some devices exhibit variations in the shape of the conductive filament or in the oxygen vacancy distribution at and around the filament. In other cases, even the location of the active filament changes from one cycle to the next. We propose that both effects originate from the coexistence of multiple (sub)filaments and that the active, current-carrying filament may change from cycle to cycle. These findings account for the observed variability in device performance and represent the scientific basis, rather than prior purely empirical engineering approaches, for developing stable memristive devices.

Interest in resolving the mechanisms behind ceria’s activity has been intense due to the numerous industrial applications including those in heterogeneous catalysis. In this work, we study the reduction and reoxidation of ultrathin CeO2(111) nanoislands on Rh(111) and Pt(111) substrates, so-called inverse model catalysts, with a combination of real and reciprocal space techniques based on X-ray photoemission electron microscopy (XPEEM) and low energy electron microscopy. Soft X-ray microfocused illumination was employed to reduce the ceria islands, which we are able to control by varying the oxygen partial pressure within the measurement chamber. Low energy electron diffraction measurements of the irradiated ceria films demonstrate the formation of an ordered array of oxygen vacancies leading to a (√7 × √7)R19.1° superstructure attributed to the ι-phase (Ce7O12)(111). Resonant photoelectron spectroscopy provides the required high sensitivity to detect small changes in Ce3+ concentration. The high spatial ...

Magnetic skyrmions are chiral spin structures with a whirling configuration. Their topological properties, nanometer size and the fact that they can be moved by small current densities have opened a new paradigm for the manipulation of magnetisation at the nanoscale. To date, chiral skyrmion structures have been experimentally demonstrated only in bulk materials and in epitaxial ultrathin films and under external magnetic field or at low temperature. Here, we report on the observation of stable skyrmions in sputtered ultrathin Pt/Co/MgO nanostructures, at room temperature and zero applied magnetic field. We use high lateral resolution X-ray magnetic circular dichroism microscopy to image their chiral N\'eel internal structure which we explain as due to the large strength of the Dzyaloshinskii-Moriya interaction as revealed by spin wave spectroscopy measurements. Our results are substantiated by micromagnetic simulations and numerical models, which allow the identification of the physical mechanisms governing the size and stability of the skyrmions., Comment: Submitted version. Extended version to appear in Nature Nanotechnology

It is shown that on Pt(111) it is possible to prepare hexagonal boron nitride (h-BN) and graphene (G) in-plane heterojunctions from a single molecular precursor, by thermal decomposition of dimethylamine borane (DMAB). Photoemission, near-edge X-ray absorption spectroscopy, low energy electron microscopy, and temperature programmed desorption measurements indicate that the layer fully covers the Pt(111) surface. Evidence of in-plane layer continuity and weak interaction with Pt substrate has been established. The findings demonstrate that dehydrogenation and pyrolitic decomposition of DMAB is an efficient and easy method for obtaining a continuous almost freestanding layer mostly made of G, h-BN with only a low percentage (h-BN or boron carbonitride, BCN at the boundaries) in the same 2D sheet on a metal substrate, such as Pt(111), paving the way for the advancement of next-generation G-like-based electronics and novel spintronic devices.

This study analyses the effects and dynamics behind a new type of innovation policy for Small and Medium Enterprises (SMEs): innovation vouchers. This policy is aimed at encouraging SMEs to collaborate with universities and with organisations offering Knowledge Intensive Services. Despite its innovativeness and growing diffusion, the innovation voucher has received only limited attention in the literature. After reviewing the literature on R&D collaborations and innovation vouchers, the article conducts in-depth analysis on two innovation voucher programs in the Lombardy region (Italy). The analysis is based on seven case studies of SMEs that have benefitted from this policy. The results highlight how innovation vouchers have influenced the development of innovation projects and technological collaboration in SMEs. The article concludes with discussion on the effectiveness of the voucher policy, its limitations and policy implications.

We report the imaging of magnetic domains in ferromagnetic CoNiB nanotubes with very long aspect ratio, fabricated by electroless plating. While axial magnetization is expected for long tubes made of soft magnetic materials, we evidence series of azimuthal domains. We tentatively explain these by the interplay of anisotropic strain and/or grain size, with magneto-elasticity and/or anisotropic interfacial magnetic anisotropy. This material could be interesting for dense data storage, as well as curvature-induced magnetic phenomena such as the non-reciprocity of spin-wave propagation., Comment: Focus only on azimuthal domains, information on domain walls (part of v1) removed - title, abstract and discussion changed accordingly, tubular racetracks scheme removed; new references, figures. Submission to SciPost (reformatted, new abstract, DOI added to references). Enhanced discussion of anisotropy, disagreement of synchrotron data and magnetometry rectified, new MOKE data added

International audience; Cylindrical nanowires made of soft magnetic materials, in contrast to thin strips, may host domain walls of two distinct topologies. Unexpectedly, we evidence experimentally the dynamic transformation of topology upon wall motion above a field threshold. Micromagnetic simulations highlight the underlying precessional dynamics for one way of the transformation, involving the nucleation of a Bloch-point singularity, however, fail to reproduce the reverse process. This rare discrepancy between micromagnetic simulations and experiments raises fascinating questions in material and computer science.

We report on the effect of the lateral confinement and a perpendicular magnetic field on isolated room-temperature magnetic skyrmions in sputtered Pt/Co/MgO nanotracks and nanodots. We show that the skyrmions size can be easily tuned by playing on the lateral dimensions of the nanostructures and by using external magnetic field amplitudes of a few mT, which allow to reach sub-100 nm diameters. Our XMCD-PEEM observations also highlight the important role of the pinning on the skyrmions size and stability under an out-of-plane magnetic field. Micromagnetic simulations reveal that the effect of local pinning can be well accounted for by considering the thin film grain structure with local anisotropy variations and reproduce well the dependence of the skyrmion diameter on the magnetic field and the geometry., Comment: 17 pages, 4 figures

Metal nanostructures confined between sp2 hybridized 2D materials and solid supports are attracting attention for their potential application in new nanotechnologies. Model studies under well-defined conditions are valuable for understanding the fundamental aspects of the phenomena under 2D covers. In this work we investigate the intercalation of iron atoms through a single layer of mixed graphene and hexagonal boron nitride on Pt(111) using a combination of spectroscopic and microscopic techniques. Thermally activated diffusion of iron proceeds preferentially under graphene and only partially under hexagonal boron nitride areas. When oxygen is coadsorbed with iron, the intercalation rate is higher, and formation of B2O3 and oxygenated B-C species is observed. Our results suggest the possibility of confining ferromagnetic layers under heterostructures of graphene and hexagonal boron nitride with potential technological implications in the fields of spintronics, magnetic data storage or chemistry under 2D covers. © 2018 Elsevier Ltd

The distribution of ultrathin layers of vanadium oxide on Rh(110) (theta(V)

Interaction with the substrate strongly affects the electronic/chemical properties of supported graphene. So far, graphene grown by chemical vapor deposition (CVD) on catalytic single crystal transition metal surfaces - mostly 3-fold close-packed - has mainly been studied. Herein, we investigated CVD graphene on a polycrystalline nickel (Ni) substrate, focusing in particular on (100) micrograins and comparing the observed behavior with that on single crystal Ni(100) substrate. The symmetry-mismatch leads to moiré superstructures with stripe-like or rhombic-network morphology, which were characterized by atomically-resolved scanning tunneling microscopy (STM). Density functional theory (DFT) simulations shed light on spatial corrugation and interfacial interactions: depending on the misorientation angle, graphene is either alternately physi- and chemisorbed or uniformly chemisorbed, the interaction being modulated by the (sub)nanometer-sized moiré superstructures. Ni(100) micrograins appear to be a promising substrate to finely tailor the electronic properties of graphene at the nanoscale, with relevant perspective applications in electronics and catalysis. Fil: Zou, Zhiyu. The Abdus Salam. International Centre for Theoretical Physics; Italia Fil: Carnevali, Virginia. Università degli Studi di Trieste; Italia Fil: Jugovac, Matteo. Università degli Studi di Trieste; Italia. Helmholtz Gemeinschaft. Forschungszentrum Jülich; Alemania. The Abdus Salam. International Centre for Theoretical Physics; Italia Fil: Patera, Laerte L.. Helmholtz Gemeinschaft. Forschungszentrum Jülich; Alemania. Vienna University of Technology; Austria Fil: Sala, Alessandro. Università degli Studi di Trieste; Italia Fil: Panighel, Mirco. Helmholtz Gemeinschaft. Forschungszentrum Jülich; Alemania. Università degli Studi di Trieste; Italia Fil: Cepek, Cinzia. Università degli Studi di Trieste; Italia Fil: Soldano, Germán. Helmholtz Gemeinschaft. Forschungszentrum Jülich; Alemania Fil: Mariscal, Marcelo. Università degli Studi di Trieste; Italia Fil: Peressi, Maria. Universitat Regensburg; Alemania Fil: Comelli, Giovanni. Laboratorio Nazionale Tasc; Fil: Africh, Cristina. Università degli Studi di Trieste; Italia

We provide direct evidence that irradiation of a graphene membrane on Ir with low-energy Ar ions induces formation of solid noble-gas nanobubbles. Their size can be controlled by thermal treatment, reaching tens of nanometers laterally and height of 1.5 nm upon annealing at 1080 °C. Ab initio calculations show that Ar nanobubbles are subject to pressures reaching tens of GPa, their formation being driven by minimization of the energy cost of film distortion and loss of adhesion.

Nature Nanotechnology 11, 449–454 (2016); published online 25 January 2016; corrected after print 18 July 2017 In the version of this Article originally published, the Dzyaloshinskii–Moriya interaction parameter, D, should have been multiplied by √3. The vertical scale of Fig. 2 has been updated accordingly as has the following sentence concerning D values: “For 5 monolayers (ML) of Co, equivalent to a total Co thickness of 1 nm, the ab initio calculations predict = 4.

This work reports an electronic and micro-structural study of an appealing system for optoelectronics: tungsten disulfide (WS2) on epitaxial graphene (EG) on SiC(0001). The WS2 is grown via chemical vapor deposition (CVD) onto the EG. Low-energy electron diffraction (LEED) measurements assign the zero-degree orientation as the preferential azimuthal alignment for WS2/EG. The valence-band (VB) structure emerging from this alignment is investigated by means of photoelectron spectroscopy measurements, with both high space and energy resolution. We find that the spin–orbit splitting of monolayer WS2 on graphene is of 462 meV, larger than what is reported to date for other substrates. We determine the value of the work function for the WS2/EG to be 4.5 ± 0.1 eV. A large shift of the WS2 VB maximum is observed as well, due to the lowering of the WS2 work function caused by the donor-like interfacial states of EG. Density functional theory (DFT) calculations carried out on a coincidence supercell confirm the experimental band structure to an excellent degree. X-ray photoemission electron microscopy (XPEEM) measurements performed on single WS2 crystals confirm the van der Waals nature of the interface coupling between the two layers. In virtue of its band alignment and large spin–orbit splitting, this system gains strong appeal for optical spin-injection experiments and opto-spintronic applications in general.

The implementation of imaging techniques with low-energy electrons at synchrotron laboratories allowed for significant advancement in the field of spectromicroscopy. The spectroscopic photoemission and low energy electron microscope, SPELEEM, is a notable example. We summarize the multitechnique capabilities of the SPELEEM instrument, reporting on the instrumental aspects and the latest developments on the technical side. We briefly review applications, which are grouped into two main scientific fields. The first one covers different aspects of graphene physics. In particular, we highlight the recent work on graphene/Ir(100). Here, SPELEEM was employed to monitor the changes in the electronic structure that occur for different film morphologies and during the intercalation of Au. The Au monolayer, which creeps under graphene from the film edges, efficiently decouples the graphene from the substrate lowering the Dirac energy from 0.42 eV to 0.1 eV. The second field combines magnetism studies at the mesoscopic length scale with self-organized systems featuring ordered nanostructures. This example highlights the possibility to monitor growth processes in real time and combine chemical characterization with X-ray magnetic circular dichroism–photoemission electron microscopy (XMCD–PEEM) magnetic imaging by using the variable photon polarization and energy available at the synchrotron source.

The reversible transformations of thin magnetite (Fe3O4) and hematite (α-Fe2O3) films grown on Pt(111) and Ag(111) single crystals as support have been investigated by a combined low energy electro...

The positive effect of double aberration correction in x-ray induced Photoelectron Emission Microscopy (XPEEM) has been successfully demonstrated for both, the lateral resolution and the transmission, using the Au 4f XPS peak for element specific imaging at a kinetic energy of 113 eV. The lateral resolution is improved by a factor of four, compared to a non-corrected system, whereas the transmission is enhanced by a factor of 5 at a moderate resolution of 80 nm. With an optimized system setting, a lateral resolution of 18 nm could be achieved, which is up to now the best value reported for energy filtered XPEEM imaging. However, the absolute resolution does not yet reach the theoretical limit of 2 nm, which is due to space charge limitation. This occurs along the entire optical axis up to the contrast aperture. In XPEEM the pulsed time structure of the exciting soft x-ray light source causes a short and highly intense electron pulse, which results in an image blurring. In contrast, the imaging with elastically reflected electrons in the low energy electron microscopy (LEEM) mode yields a resolution clearly below 5 nm. Technical solutions to reduce the space charge effect in an aberration-corrected spectro-microscope are discussed.

Combining low energy electron microscopy (LEEM) with low energy electron diffraction (LEED) and x-ray photoemission electron microscopy (XPEEM), we studied the phase transformations between Fe3O4, γ-Fe2O3, and α-Fe2O3, grown as 10 nm thin oxide films on Pt(111) and Ag(111) single crystals. These transformations occur as moving reaction fronts in most cases, the shapes and velocities of which show strong dependences on temperature and oxygen pressure, but also on defects like step bunches of the supporting substrate and domain boundaries in the initial oxide film. While the non-uniform moving fronts make quantitative analysis difficult, we have extracted approximate values for the average front velocities. We discuss these as well as the qualitative information on the non-uniform fronts in terms of the known geometric situations and the likely motional steps.