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MAXPEEM, a dedicated photoemission electron microscopy beamline at MAX IV Laboratory, houses a state-of-the-art aberration-corrected spectroscopic photoemission and low-energy electron microscope (AC-SPELEEM). This powerful instrument offers a wide range of complementary techniques providing structural, chemical and magnetic sensitivities with a single-digit nanometre spatial resolution. The beamline can deliver a high photon flux of ≥1015 photons s−1 (0.1% bandwidth)−1 in the range 30–1200 eV with full control of the polarization from an elliptically polarized undulator. The microscope has several features which make it unique from similar instruments. The X-rays from the synchrotron pass through the first beam separator and impinge the surface at normal incidence. The microscope is equipped with an energy analyzer and an aberration corrector which improves both the resolution and the transmission compared with standard microscopes. A new fiber-coupled CMOS camera features an improved modulation transfer function, dynamic range and signal-to-noise ratio compared with the traditional MCP-CCD detection system.

Abstract The widely used stainless steels and their deformed variants are anticorrosive in ambient conditions due to passivation layers composed of chromium oxides. Conventionally, corrosion and erosion of the steels are attributed to the breakdown of such layers but seldomly to the origin that depends on surface heterogeneity at the microscopic level. In this work, the nanometer-scaled chemical heterogeneity at the surface unveiled via spectro-microscopy and chemometric analysis unexpectedly dominates the breakdown and corrosion behavior of the cold-rolled Ce-modified 2507 super-duplex stainless steels (SDSS) over its hot-deformed counterpart. Though relatively uniformly covered by a native Cr2O3 layer revealed by X-ray photoemission electron microscopy, the cold-rolled SDSS behaved poorly in passivity because of locally distributed Fe3+ rich nano-islands over the Fe/Cr oxide layer. This atomic-level knowledge provides a deep understanding of corrosion of stainless steel and is expected to benefit corrosion controls of similar high-alloyed metals.

Despite the common challenge of investigating non-metallic inclusions within ultra-high-strength-steel (UHSS) at sub-micrometer scale via conventional methods, probing nitride inclusions at elevated temperatures is vital for guiding steel’ performance. Herein, an in-situ spectro-microscopic determination using advanced Synchrotron X-ray absorption spectroscopy (XAS) coupled with photoelectron emission microscopy (PEEM) is employed to explore the local structure and electronic properties of selective h-boron nitride (h-BN) containing inclusions (A1 and A2) embedded within steel matrix. While the variation in the relative intensity of π∗/σ∗ excitonic peaks at spatially different locations refers to the polarization and or thickness effects. Several minute features observed in the 192–195 eV energy range show oxygen (O) substituted nitrogen (N) defects (ON,2N,3N), which are more dominant in A2 inclusion. The observed dominance further explains the relatively high intense π∗ peak in A2 due to increased localization. Weak shoulder on the left side of π∗ peak in both room and high-temperature XAS spectra is ascribed to the interaction between h-BN and the local environment, such as Ca-based inclusion or steel matrix. Defects are commonly found in h-BN, and precise identification of the same is vital as they affect the overall physical, chemical, and mechanical properties. Moreover, significant changes in high-temperature B K-edge XAS spectra, such as relative intensity of π∗/σ∗ excitonic peaks at the same location and reduced intensity of defects, suggest the adjusting nature of BN inclusion, complicating their precise prediction and control towards clean steel production.

Abstract The weak dielectric screening in 2D semiconducting transition metal dichalcogenides give rise to strongly bound quasiparticles, which provides a platform to investigate the diverse excitonic phenomena and correlated physics. However, how to effectively control these quasiparticles is still a challenge for their applications in optoelectronic and valleytronic devices. Herein, by means of fabricating monolayer WSe2 and transition metal oxide (TMO) heterostructures, polaronic trion, that is a trion dressed with soft rotational optical (RO) phonons, is realized due to the strong interfacial coupling. This Fröhlich bound state of trion dramatically increases the trion binding energy (BE) from room temperature to 65 meV at 80 K in WSe2/LaAlO3 (LAO). However, the increase of the trion BE for WSe2/SrTiO3 (STO) occurs below the phase transition temperature. This work expands the possibilities of the TMDs/TMOs heterostructures and promotes the development of 2D van der Waals materials for quasiparticle‐based devices.

Dimensionality of a material is a critical parameter to control its electronic properties. Here, the authors report that 2D gold transforms from a semiconductor, with valence band maximum 50 meV below the Fermi level, into a metal by tuning the number of layers from 1 to 2 in between graphene and SiC.

Owing to long spin lifetime and diffusion length, graphene holds promise for spintronics, yet it does not possess intrinsic magnetic properties. Here, the authors observe experimentally a large, positive magnetoresistance at graphene nanodomain boundaries.