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Combining the quantum optical properties of single-photon emitters with the strong near-field interactions available in nanophotonic and plasmonic systems is a powerful way of creating quantum manipulation and metrological functionalities. The ability to actively and dynamically modulate emitter-environment interactions is of particular interest in this regard. While thermal, mechanical and optical modulation have been demonstrated, electrical modulation has remained an outstanding challenge. Here we realize fast, all-electrical modulation of the near-field interactions between a nanolayer of erbium emitters and graphene, by in-situ tuning the Fermi energy of graphene. We demonstrate strong interactions with a >1,000-fold increased decay rate for 25% of the emitters, and electrically modulate these interactions with frequencies up to 300 kHz - orders of magnitude faster than the emitters radiative decay (100 Hz). This constitutes an enabling platform for integrated quantum technologies, opening routes to quantum entanglement generation by collective plasmon emission or photon emission with controlled waveform., Comment: to be published in Nat Commun

Protection of silver mirror stacks from environmental degradation before launching is crucial for space applications. Hereby, we report a comparative study of the advanced protection of silver mirror stacks for space telescopes provided by SiO2 and Al2O3 coatings in conditions of accelerated aging by sulfidation. The model silver stack samples were deposited by cathodic magnetron sputtering on a reference silica substrate for optical applications and a surface-pretreated SiC substrate. Accelerated aging was performed in dry and more severe wet conditions. Optical micrographic observations, surface and interface analysis by Time-of Flight Secondary Ion Mass Spectrometry (ToF-SIMS) and reflectivity measurements were combined to comparatively study the effects of degradation. The results show a lower kinetics of degradation by accelerated aging of the stacks protected by the alumina coating in comparable test conditions., Comment: JOURNAL OF MATERIALS SCIENCE \& TECHNOLOGY, 2020, Advanced Corrosion-Resistant Materials and Emerging Applications

Passivation mechanisms were investigated on (100)-oriented Fe-18Cr-13Ni surfaces with direct transfer between surface preparation and analysis by X-ray photoelectron spectroscopy and scanning tunneling microscopy and electrochemical characterization. Starting from oxide-free surfaces, pre-oxidation at saturation under ultra-low pressure (ULP) oxygen markedly promotes the oxide film Cr(III) enrichment and hinders/delays subsequent iron oxidation in water-containing environment. Exposure to sulfuric acid at open circuit potential causes preferential dissolution of oxidized iron species. Anodic passivation forces oxide film re-growth, Cr(III) dehydroxylation and further enrichment. ULP pre-oxidation promotes Cr(III) hydroxide formation at open circuit potential, compactness of the nanogranular oxide film and corrosion protection.

Electrochemical polarization measurements were combined with surface analysis by Time of Flight Secondary Ion Mass Spectroscopy (ToF-SIMS), X-Ray Photoelectron Spectroscopy (XPS) and Atomic Force Microscopy (AFM) to study the alterations of the passive film on 316L austenitic stainless steel induced by the presence of chlorides in sulfuric acid electrolyte. The work was performed at a stage of initiation of localized corrosion preceding metastable pitting at the micrometer scale as verified by current transient analysis and AFM. The results show that Cl-ions enter the bilayer structure of the surface oxide already formed in the native oxide-covered initial surface state at concentrations below the detection limit of XPS (< 0.5 at%), mostly in the hydroxide outer layer where Fe(III) and Mo(IV,VI) species are concentrated but barely in the oxide inner layer enriched in Cr(III). Their main effect is to produce a less resistive passive state by poisoning dehydroxylation and further Cr(III) and Mo(IV,VI) enrichments obtained in the absence of chlorides. This detrimental effect can be suppressed by pre-passivation in a Cl-free electrolyte, which blocks the entry of chlorides in the passive film, including in the outer exchange layer, and enables the beneficial aging-induced variations of the composition to take place despite the presence of chlorides in the environment.

The durability of passivable metals and alloys is often limited by the stability of the surface oxide film, the passive film, providing self-protection against corrosion in aggressive environments. Improving this stability requires to develop a deeper understanding of the surface structure and initial surface reactivity at the nanometric or atomic scale. In this work we applied scanning tunneling microscopy to unravel the surface structure of a model stainless steel surface in the metallic state and its local modifications induced by initial reaction in dioxygen gas. The results show a rich and complex structure of the oxide-free surface with reconstructed atomic lattice and self-organized lines of surface vacancies at equilibrium. New insight is brought into the mechanisms of initial oxidation at steps and vacancy injection on terraces leading to Cr-rich oxide nuclei and locally Cr-depleted terraces, impacting the subsequent mechanism of chromium enrichment essential to the stability of the surface oxide., Comment: 17 pages, 3 figures

Time of Flight Secondary Ion Mass Spectroscopy, X-Ray Photoelectron Spectroscopy, in situ Photo-Current Spectroscopy and electrochemical analysis were combined to characterize the physicochemical alterations induced by electrochemical passivation of the surface oxide film providing corrosion resistance to 316L stainless steel. The as-prepared surface is covered by a ~2 nm thick, mixed (Cr(III)-Fe(III)) and bi-layered hydroxylated oxide. The inner layer is highly enriched in Cr(III) and the outer layer less so. Molybdenum is concentrated, mostly as Mo(VI), in the outer layer. Nickel is only present at trace level. These inner and outer layers have band gap values of 3.0 and 2.6-2.7 eV, respectively, and the oxide film would behave as an insulator. Electrochemical passivation in sulfuric acid solution causes the preferential dissolution of Fe(III) resulting in the thickness decrease of the outer layer and its increased enrichment in Cr(III) and Mo(IV-VI). The further Cr(III) enrichment of the inner layer causes loss of photoactivity and improved corrosion protection with the anodic shift of the corrosion potential and the increase of the polarization resistance by a factor of ~4. Aging in the passive state promotes the Cr enrichment in the inner barrier layer of the passive film., Comment: 27 pages, 4 tables, 14 figures

The initiation of intergranular corrosion at various types of grain boundaries (GBs) was studied at the nanometer scale on microcrystalline copper in 1 mM HCl aqueous solution. In situ Electrochemical Scanning Tunneling Microscopy (ECSTM) and Electron Back-Scatter Diffraction analysis of the same local microstructural region were combined using an innovative methodology including micro marking performed with the STM tip. The results demonstrate that electrochemically-induced intergranular dissolution, at the surface termination of GBs, is dependent on the grain boundary character. It is found that random high angle boundaries as well as sigma9 coincidence site lattice (CSL) boundaries are susceptible to nanoscale initiation of intergranular corrosion while for sigma3 CSL boundaries the behavior is dependent on the deviation angle of the GB plane from the exact orientation. For the sigma3 twins, a transition from resistance to susceptibility occurs between 1{\deg} and 1.7{\deg} of deviation as a result of the increase of the density of steps (i.e. misorientation dislocations) in the coincidence boundary plane. The work emphasizes the precision needed in the design of the grain boundary network in applications where intergranular corrosion or its initiation must be controlled at the nanoscale., Comment: 25 pages, 1 Table, 6 Figures

Oxide passive films are a key for the durability of metals and alloys components as well as a central issue in corrosion science and engineering. Herein, we discuss current developments of the nanometer and sub-nanometer scale knowledge of the barrier properties and adsorption properties of passive oxide films brought by recent model experimental and theoretical investigations. The discussed aspects include (i) the chromium enrichment and its homogeneity at the nanoscale in passive films formed on Cr-bearing alloys such as stainless steel, (ii) the corrosion properties of grain boundaries in early intergranular corrosion before penetration and propagation in the grain boundary network, and (iii) the interaction of organic inhibitor molecules with incompletely passivated metallic surfaces. In all three cases, key issues are highlighted and future developments that we consider as most relevant are identified., Comment: Current Opinion in Solid State and Materials Science, Elsevier, final accepted preprint