We present an overview of the Elettra-Sincrotrone Trieste research center, which hosts synchrotron and free-electron laser light sources. We review the current status, provide examples of recent achievements in basic and applied research and discuss the upgrade programs of the facility.

With size reduction of active elements in microelectronics to tens of nanometers and below, the effect of surface and interface properties on overall device performance becomes crucial. High resolution spectroscopic and imaging techniques provide a metrological route for characterization of these properties relevant to device diagnostics and failure analysis. With its roughly 100 nm spatial resolution, superior surface sensitivity, and approximately 200 meV spectral resolution, scanning photoelectron microscopy (SPEM) stands out as a comprehensive tool to access the surface/interface composition of nanodevices, as well to provide chemical state designations and materials property evolutions upon treatment by thermal, electrical, chemical, radiative and other stimuli. Here we present a SPEM-on-device setup that combines X-ray spectromicroscopy with advanced NIST microhotplate technology to demonstrate new combined analytical and electrical measurements capabilities of this metrology platform for operando nanodevice characterization. Using model integrated SnO2 nanowire (NW) chemiresistor devices, the chemically induced alterations in the chemical state of the nanowire surface are correlated to the observed conductance changes, thus directly testing the receptor and transduction mechanisms for SnO2 NW conductometric chemical sensors.

Solid-state batteries (SSB), characterized by solid-state electrolytes-in particular inorganic ones (ISSE)-are an ideal option for the safe implementation of metallic Li anodes. Even though SSBs with ISSEs have been extensively investigated over the last two decades, they still exhibit a series of technological drawbacks. In fact, mechano-chemical issues, mainly the stability of the electrolyte/anode interface, hinder their widespread application. The present investigation focusses on a thin-film LMO (Lithium-Manganese-Oxide)/LAGP (LiAlGe Phosphate)/Copper, anodeless Lithium-metal battery and explores the morphochemical evolution of the electrode/electrolyte interfaces with synchrotron-based Scanning Photoelectron Microscopy (SPEM) of intact pristine and cycled cells. Chemical images were acquired with submicrometer resolution, to highlight the coupled geometrical and chemical-state changes caused by electrochemical ageing. Geometrical changes of the electrolyte/cathode interface were induced by periodic volume changes, causing de-cohesion of the solid-solid contact, but no chemical-state changes accompany the cathodic damaging mode. Instead, shape changes of the electrolyte/anode region pinpoint the correlation between mechanical damaging with the decomposition of the LAGP ISSE, due to the reduction of Ge, triggered by the contact with elemental Li. The micro-spectroscopic approach adopted in this study enabled the assessment of the highly localized nature of the cathodic and anodic degradation modes in SSB devices and to single out the chemical and mechanical contributions.

The development of ultra-bright extreme ultraviolet (EUV) and X-ray free electron laser (FEL) sources has enabled the extension of wave-mixing approaches into the short wavelength regime. Such a class of experiments relies upon nonlinear interactions among multiple light pulses offering a unique tool for exploring the dynamics of ultrafast processes and correlations between selected excitations at relevant length and time scales adding elemental and site selectivity as well. Besides the availability of a suitable photon source, the implementation of wave mixing methodology requires efforts in developing the instrumental set-up. We have realized at the FERMI FEL two dedicated set-ups to handle multiple FEL beams with preselected parameters in a non-collinear fashion and control their interaction sequence at the target. These unique apparatuses, combined with the exceptional characteristics of the seeded FERMI FEL, have allowed us to make the first steps into this field and further advances are foreseen in the near future.

Sustainability, environmental and safety concerns raised by the increasing demand of batteries are driving research towards post-lithium technologies. Rechargeable Zn batteries are strong candidates, but still not practically viable, owing to the extensively studied, but poorly understood unstable behavior of Zn metal upon discharge-charge cycling. This limiting factor warrants more fundamental investigations and the present report provides the lacking molecular-level information on the Zn-based compounds forming at the electrode/electrolyte interface as a result of electrochemical cyclic in weakly acidic aqueous electrolyte. The results are obtained using ex situ X-ray absorption spectromicroscopy maps, modelled mathematically and complemented with cyclic voltammetry, symmetric-cell tests and electron microscopy. We have identified the role of the zincate precipitation resulting from local alkalinization during recharge, combined with additional zincate formation and decomposition to zinc oxide during discharge. The mathematical model allowed a transparent interpretation of morphochemical changes observed. The synergy of these processes leads to electrochemical localization effects, resulting in the formation of a complexly structured and low conductive ZnO-based template, that might play a role in driving shape changes.

The availability of sub 100 fs short and highly intense free-electron laser (FEL) pulses allows for new insights in laser-induced ultrafast demagnetization (LID) of ferromagnetic thin films on nanometer length scales. We designed a pair of in-vacuum Helmholtz coils, providing pulsed magnetic fields up to µ 0 H z = ±45 mT, for time-resolved experiments at FEL sources in transmission geometry. We report on the implementation of the Helmholtz coils in an optical-pump–resonant-magnetic-scattering (tr-XRMS) experiment at the FEL FERMI (Elettra, Trieste) to study LID in different magnetic domain networks. We discuss the limitations for multi-shot measurements, that rely on the full reversibility of the demagnetization process in-between two pump–probe events, and emphasize the importance of reference–pump–probe schemes, especially in tr-XRMS experiments that employ external H z fields.

Batteries with inorganic solid-state electrolytes (ISSE) are attracting notable interest for next-generation systems implementing Lithium (Li) metal anodes, in view of achieving higher energy densities combined with superior safety. Notwithstanding extensive research and development work, this technology is not yet ready for industrial implementation, one of the key challenges being the stability of ISSEs, chiefly at the anodic interface. This work attacks this issue for the specific case of the LAGP/Li (Lithium Aluminium Germanium Phosphate/Lithium) interface with a micro-spectroscopic approach centred on post mortem Scanning Transmission X-ray Microscopy (STXM) of intact LMO/LAGP/Li thin-film batteries, microfabricated in discharged state. Pristine and cycled cells were mapped to pinpoint morphochemical changes, induced by electrochemical ageing. The evidenced shape changes, corresponding to mechanical damaging of the solid/solid electrodic interfaces correlate with LAGP decomposition at the anode, leading to reduction of Ge, whereas the chemical state at the cathodic interface is preserved. Thanks to its submicron spacial resolution, the STXM at the Ge L-edge and O K-edge spectra allowed to assess the highly localized nature of the chemical transformation of LAGP and its correlation with the formation of Li outgrowth features.

Abstract Ultrashort and intense extreme ultraviolet (XUV) and X-ray pulses readily available at free-electron lasers (FELs) enable studying non-linear light−matter interactions on femtosecond timescales. Here, we report on the non-linear fluence dependence of magnetic scattering of Co/Pt multilayers, using FERMI FEL’s 70-fs-long single and double XUV pulses, the latter with a temporal separation of 200 fs, with a photon energy slightly detuned to the Co M2,3 absorption edge. We observe a quenching in magnetic scattering that sets-in already in the non-destructive fluence regime of a few mJ/cm² typically used for FEL-probe experiments on magnetic materials. Calculations of the transient electronic structure in tandem with a phenomenological modeling of the experimental data by means of ultrafast demagnetization unambiguously show that XUV-radiation-induced demagnetization is the dominant mechanism for the quenching in the investigated fluence regime of <50 mJ/cm², while light-induced changes of the electronic core levels are predicted to additionally occur at higher fluences. The modeling of the data further indicates that the demagnetization proceeds on the sub-20-fs timescale. This ultrashort timescale is consistent with non-coherent models for ultrafast demagnetization, considering the sub-femtosecond lifetime of hot electrons with energies of a few 10 eV generated by the XUV radiation.

The corrosion control of WC-Co type hardmetals is steadily gaining momentum for novel crucial applications in the Oil & Gas and food industries. The corrosion rate of the Co-based binder, and the extent to which coupling to WC speeds it up, are strongly influenced by alloying. In this paper, we investigate the impact of Cr on the corrosion-product film formation of Co- and CoNi based hardmetal binders in acidic, neutral and alkaline aqueous solutions. We centred our study on the role of Cr in driving the distribution of oxidized Co and Ni at the micrometre scale, thanks to synchrotron-based soft-X ray microspectroscopy. We have investigated morphochemical distributions for the following grades: Co96Cr4, Co48Ni48Cr4, Co50Cr50. Chemical-state mapping has been complemented by electrochemical measurements and metallographic observations. Amounts of Cr and Ni of ca. 50% notably increase the corrosion resistance in all ambients, with a stronger beneficial effect of the former element. 4% addition of Cr results in slight positive effects, with the exception of the CoNi system in alkaline ambient, that, together with Co50Cr50, outperforms the other grades. In all investigated alloy-ambient combinations, a continuous oxidized metal film grows, onto which micrometric island form of shape and dimensions that depend on the specific grade and aggressive conditions. Quantitative descriptors of chemical-state maps and their theoretical interpretation in terms of electrochemical phase-formation by oxy-hydroxide precipitation, allow to correlate the island patterns with the degree of pseudopassivation.

Adding submicrometer lateral resolution to the analytic capabilities of photoelectron spectroscopy was a milestone that opened up new opportunities to access lateral fluctuations in the chemical composition and electronic and magnetic structure of surfaces and interfaces and to explore exotic properties of nanostructured matter. To achieve a high spatial resolution while preserving the spectral resolution of this technique requires the very intense photon flux that has become available with the advent of third-generation synchrotron storage rings. The high spatial resolution of x-ray photoelectron microscopes, operated at synchrotron facilities, is achieved by either: (i) magnifying the image of the irradiated surface area using a suitable electron optical imaging system; or (ii) demagnifying the incident photon beam using x-ray photon optics. The contrast mechanisms in both instruments are based on photon absorption and the photon-induced electron emission is used to obtain spectroscopic information encoding the composition and electronic structure of the sample under investigation. This paper offers a brief overview of the history, operational principles and potential of scanning photoelectron microscopes where the imaging is performed by scanning the sample with respect to the focused beam.

In situ synchrotron-based techniques are starting to be intensively exploited to investigate a range of electrochemical systems; in particular, X-ray photoelectron spectroscopy (XPS), owing to its utmost surface sensitivity and photon-in/electron-out nature, has been recognized as a powerful tool to achieve insight into phenomena occurring at the electrode surface and at the electrode/electrolyte interface of solid oxide–based electrochemical devices, in the presence of a reactive gas and under applied electrochemical polarization. Conventional XPS exhibits the key limitation of extensive space averaging that results in missing important details of the morphochemical structure of the materials forming the electrochemical device, that, instead, have a notable impact on electrocatalytic performance and durability. For this reason, combining the analytical power of XPS with space-resolution capability can provide unique and practically useful insight for the understanding and improvement of electrochemical devices. In this chapter, we focus on in situ XPS microspectroscopy, enabling elemental and chemical state mapping with high spatial resolution under electrochemical operating conditions. Specifically, we describe our recent work on a range of solid oxide fuel cell materials and configurations, performed with reactive gases and gas mixtures both in high-vacuum and near-ambient pressure conditions This chapter includes on the one hand details of instrumental solutions regarding cell engineering, gas feed modes, and pressure management, and on the other hand, a representative selection of the kind of electrochemical information that can be drawn from photoelectron microspectroscopy.

The microstructure and physicochemical properties of the surface of rapidly solidified Al–Cr alloys containing 1 and 3 at % of chromium are studied by means of photoelectron microscopy using synchrotron radiation, scanning probe microscopy, and the sessile-drop technique. We find that the surface oxide-hydroxide layer of foils has a heterogeneous structure with highly dispersed chromium inclusions (possibly clusters). Chromium and aluminum are predominantly in a metallic state in chromium-enriched regions of the foil surface. We find that the equilibrium contact angle of wetting of the samples with water depends on their morphology and the concentration of chromium in the alloys. The wettability is mainly determined by the chemical composition of the surface of foils and to a lesser extent its roughness. A decrease from poor to low water wettability of rapidly solidified Al–Cr alloys with an increase in the chromium concentration up to 3 at % is due to the aggregation of chromium inclusions.

Lithium fluoride (LiF) films and crystals are versatile X-ray imaging detectors based on the optical reading of visible photoluminescence from radiationinduced electronic defects. Distinctive features of these detectors are their high spatial resolution across a large field of view, wide dynamic range and insensitivity to ambient light. These peculiarities of LiF detectors appear to be promising for monitoring the spatial intensity distribution of ultra-short, ultra-high pulses of the EUV-X-ray Free Electron Laser (XFEL) and could be exploited for coherent diffraction imaging experiments.

Implementation of in-situ and operando experimental set-ups for bridging the pressure gap in characterization techniques based on monitoring of photoelectron emission has made significant achievements at several beamlines at Elettra synchrotron facility. These set-ups are now operational and have been successfully used to address unsolved issues exploring events occurring at solid-gas, solid-liquid and solid-solid interfaces of functional materials. The sections in the article communicate the research opportunities offered by the current set-ups at APE, BACH, ESCAmicroscopy and Nanospectroscopy beamlines and outline the next steps to overcome the present limits.

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Understanding and controlling the thermal transport at nanoscale is a key ingredient for the development of future nanoelectronical devices. In this study of thin silicon carbide (SiC) membrane we demonstrate the potential of free electron laser extreme ultraviolet (EUV) transient grating (TG) technique as contactless probe for thermoelastic response at length scales of 84 nm, where the Fourier heat diffusion law is no longer valid. The results have revealed that the mechanical behavior of the system can be fully described in the framework of Lamb waves. Moreover, by use of a bidimensional spatial detector to measure the TG signal, a new feature is the observed, time dependence in the emission angle of the transient diffraction, correlated to the transient grating signal intensity.

The rapid development of extreme ultraviolet (EUV) and x-ray ultrafast coherent light sources such as free electron lasers (FELs) has triggered the extension of wave-mixing techniques to short wavelengths. This class of experiments, based on the interaction of matter with multiple light pulses through the Nth order susceptibility, holds the promise of combining intrinsic ultrafast time resolution and background-free signal detection with nanometer spatial resolution and chemical specificity. A successful approach in this direction has been the combination of the unique characteristics of the seeded FEL FERMI with dedicated four-wave-mixing (FWM) setups, which leads to the demonstration of EUV-based transient grating (TG) spectroscopy. In this perspective paper, we discuss how the TG approach can be extended toward more general FWM spectroscopies by exploring the intrinsic multiparameter nature of nonlinear processes, which derives from the ability of controlling the properties of each field independently.