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The magnetization behavior of nanowires embedded in an array is influenced by the sum of the dipolar fields produced by all surrounding nanowires. These magnetostatic interactions largely modify the array properties and thus complicate the reconstruction of the ensemble averaged behavior of the individual nanowires, such as the intrinsic switching field distribution. Simply correcting the shearing of the hysteresis in a mean-field approach does not account for the locally fluctuating demagnetizing field, which originates from the individual magnetization configuration in the close surrounding of each nanowire. We present an in-field Magnetic Force Microscopy study of electrochemically produced Co48Fe52 nanowires, in which the influence of the magnetic nearest neighbor configuration on the switching behavior of the individual embedded nanowires is clearly detected. Based on this finding, a statistical evaluation method of nearest neighbor histograms is proposed, which potentially allows to judge the strength of the local magnetostatic interactions against the magnitude of the intrinsic switching field distribution. [ABSTRACT FROM AUTHOR]

The influence of a magnetic field yielding high magnetic flux densities and high flux density gradients on the free corrosion behavior of iron in a low concentrated acidic solution with and without chloride ions is studied by long time exposure experiments and electrochemical impedance spectroscopy (EIS). A decrease of the corrosion rate in electrode surface regions of high magnetic flux density is detected. This decrease of the dissolution rate is significantly stronger in the presence of chloride ions. The observed effects are discussed on the basis of the magnetically induced forces acting on the ions present in the solution, the surface coverage fraction of adsorbed species, and the stability of these adsorbed species. [ABSTRACT FROM AUTHOR]

A modified glassy carbon electrode was prepared through electropolymerization of caffeic acid in the presence of either carbon nanotubes or nano-carbon drop cast onto the electrode surface. The voltammetric behaviour of the electrode was characterized using the ortho-quinone moiety on the caffeic acid unit and the surface loading optimized for current response. The nanocomposite mediated electrode was used for the sensitive detection of glutathione at concentrations as low as 500 nM. [ABSTRACT FROM AUTHOR]

We report the detection and characterisation of polymer nanoparticles using electrochemistry using poly( N-vinylcarbazole) nanoparticles (PVK NPs) as a model system. These were synthesised using the reprecipitation method. The number of electrons ( n=2) transferred per PVK monomer was characterised by drop-casting method. Sticking and sensing experiments were then conducted, which involve PVK nanoparticle immobilisation on the electrode surface and subsequent oxidative sensing, to enable rapid detection of polymer nanoparticles in aqueous solution. It is shown for the first time, that using this 'stick and sense' method, polymer nanoparticles in aqueous solution can be immobilised, preconcentrated and quantified. [ABSTRACT FROM AUTHOR]

The relative influence of the Lorentz force and magnetic gradient force on micro-structured copper deposition is studied with simple magnetic elements consisting of cylindrical permanent magnets placed closely behind the surface of the cathode. Analytical findings and numerical simulations reveal that for magnets of small diameter the magnetic gradient force dominates. In experiments, it is found that the thickness of the deposited copper layer increases in the vicinity of the magnets. The combined analysis of simulations and experiments shows that this enhancement of mass transfer results from a local convection towards the electrode, which is forced by the magnetic gradient force. Finally, a more general case with electrically inert paramagnetic ions is discussed, where an inverse structuring effect can be expected. [ABSTRACT FROM AUTHOR]

In-situ velocity measurements were performed during potentiostatic Cu electrodeposition in different magnetic gradient fields (⊽B). Astigmatism Particle Tracking Velocimetry was used to enable three-dimensional measurements of al three velocity components in a large part of the cell volume. A complex three-dimensional fluid flow was observed. Thus, the magnetic field gradient force (F⊽B) driven electrode-normal convection during deposition in high ⊽B was experimentally proven and the interplay of F⊽B and the Lorentz force could be analysed for different ⊽B-setups. Moreover, in-situ measurements of the ion concentration during deposition and dissolution of Cu in a magnetic gradient field were performed by Mach-Zehnder interferometry. [ABSTRACT FROM AUTHOR]

Vanadium redox flow battery (VRFB) electrodes face challenges related to their long-term operation. We investigated different electrode treatments mimicking the aging processes during operation, including thermal activation, aging, soaking, and storing. Several characterization techniques were used to deepen the understanding of the treatment of carbon felts. Synchrotron X-ray imaging, electrochemical impedance spectroscopy (EIS) with the distribution of relaxation times analysis, and dynamic vapor sorption (DVS) revealed differences between the wettability of felts. The bulk saturation after electrolyte injection into the carbon felts significantly differed from 8 % to 96 %. DVS revealed differences in the sorption/desorption behavior of carbon felt ranging from a slight change of 0.8 wt % to over 100 wt %. Additionally, the interactions between the water vapor and the sample change from type V to type H2. After treatment, morphology changes were observed by atomic force microscopy and scanning electron microscopy. Cyclic voltammetry and EIS were used to probe the electrochemical performance, revealing different catalytic activities and transport-related impedances for the treated samples. These investigations are crucial for understanding the effects of treatments on the performance and optimizing materials for long-term operation., (© 2023 The Authors. ChemSusChem published by Wiley-VCH GmbH.)

NEMO is a ubiquitin-binding protein which regulates canonical NF-κB pathway activation in innate immune signaling, cell death regulation and host-pathogen interactions. Here we identify an NF-κB-independent function of NEMO in proteostasis regulation by promoting autophagosomal clearance of protein aggregates. NEMO-deficient cells accumulate misfolded proteins upon proteotoxic stress and are vulnerable to proteostasis challenges. Moreover, a patient with a mutation in the NEMO-encoding IKBKG gene resulting in defective binding of NEMO to linear ubiquitin chains, developed a widespread mixed brain proteinopathy, including α-synuclein, tau and TDP-43 pathology. NEMO amplifies linear ubiquitylation at α-synuclein aggregates and promotes the local concentration of p62 into foci. In vitro, NEMO lowers the threshold concentrations required for ubiquitin-dependent phase transition of p62. In summary, NEMO reshapes the aggregate surface for efficient autophagosomal clearance by providing a mobile phase at the aggregate interphase favoring co-condensation with p62., (© 2023. The Author(s).)

To date the electroactive species of selective aldehyde oxidation to carboxylates at gold electrodes is usually assumed to be the diolate. It forms with high concentration only in very alkaline electrolytes, when OH - binds to the carbonyl carbon atom. Accordingly, the electrochemical upgrading of biomass-derived aldehydes to carboxylates is believed to be limited to very alkaline electrolytes at many electrode materials. However, OH - -induced aldehyde decomposition in these electrolytes prevents application of electrochemical aldehyde oxidation for the sustainable upgrading of biomass to value-added chemicals at industrial scale. Here, we demonstrate the successful oxidation of aliphatic aldehydes at a rotating gold electrode at pH 12, where only 1 % of the aldehyde resides as the diolate species. This concentration is too small to account for the observed current, which shows that also other aldehyde species (i. e., the geminal diol and the non-hydrated aldehyde) are electroactive. This insight allows developing strategies to omit aldehyde decomposition while achieving high current densities for the selective aldehyde oxidation, making its future industrial application viable., (© 2023 The Authors. ChemSusChem published by Wiley-VCH GmbH.)

Small perturbations in the structure of materials significantly affect their properties. One example is single wall carbon nanotubes (SWCNTs), which exhibit chirality-dependent near-infrared (NIR) fluorescence. They can be modified with quantum defects through the reaction with diazonium salts, and the number or distribution of these defects determines their photophysics. However, the presence of multiple chiralities in typical SWCNT samples complicates the identification of defect-related emission features. Here, we show that quantum defects do not affect aqueous two-phase extraction (ATPE) of different SWCNT chiralities into different phases, which suggests low numbers of defects. For bulk samples, the bandgap emission (E 11 ) of monochiral (6,5)-SWCNTs decreases, and the defect-related emission feature (E 11 *) increases with diazonium salt concentration and represents a proxy for the defect number. The high purity of monochiral samples from ATPE allows us to image NIR fluorescence contributions (E 11 = 986 nm and E 11 * = 1140 nm) on the single SWCNT level. Interestingly, we observe a stochastic (Poisson) distribution of quantum defects. SWCNTs have most likely one to three defects (for low to high (bulk) quantum defect densities). Additionally, we verify this number by following single reaction events that appear as discrete steps in the temporal fluorescence traces. We thereby count single reactions via NIR imaging and demonstrate that stochasticity plays a crucial role in the optical properties of SWCNTs. These results show that there can be a large discrepancy between ensemble and single particle experiments/properties of nanomaterials.

Fluorophores that emit light in the near infrared (NIR) are advantageous in photonics and imaging due to minimal light scattering, absorption, phototoxicity and autofluorescence in this spectral region. The layered silicate Egyptian blue (CaCuSi 4 O 10 ) emits as a bulk material bright and stable fluorescence in the NIR and is a promising NIR fluorescent material for (bio)photonics. Here, we demonstrate a surfactant-based (mild) exfoliation procedure to produce nanosheets (EB-NS) of high monodispersity, heights down to 1 nm and diameters <20 nm in large quantities. The approach combines planetary ball milling, surfactant assisted bath sonication and centrifugation steps. It avoids the impurities that are typical for the harsh conditions of tip-sonication. Several solvents and surfactants were tested and we found the highest yield for sodium dodecyl benzyl sulfate (SDBS) and water. The NIR fluorescence emission ( λ em ≈ 930-940 nm) is not affected by this procedure, is extremely stable and is not affected by quenchers. This enables the use of EB-NS for macroscopic patterning/barcoding of materials in the NIR. In summary, we present a simple and mild route to NIR fluorescent nanosheets that promise high potential as NIR fluorophores for optical applications., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

The role of β-CoOOH crystallographic orientations in catalytic activity for the oxygen evolution reaction (OER) remains elusive. We combine correlative electron backscatter diffraction/scanning electrochemical cell microscopy with X-ray photoelectron spectroscopy, transmission electron microscopy, and atom probe tomography to establish the structure-activity relationships of various faceted β-CoOOH formed on a Co microelectrode under OER conditions. We reveal that ≈6 nm β-CoOOH(01 1 ‾ ${\bar{1}}$ 0), grown on [ 1 ‾ 2 1 ‾ ${\bar{1}2\bar{1}}$ 0]-oriented Co, exhibits higher OER activity than ≈3 nm β-CoOOH(10 1 ‾ ${\bar{1}}$ 3) or ≈6 nm β-CoOOH(0006) formed on [02 2 ‾ 1 ] ${\bar{2}1]}$ - and [0001]-oriented Co, respectively. This arises from higher amounts of incorporated hydroxyl ions and more easily reducible Co III -O sites present in β-CoOOH(01 1 ‾ ${\bar{1}}$ 0) than those in the latter two oxyhydroxide facets. Our correlative multimodal approach shows great promise in linking local activity with atomic-scale details of structure, thickness and composition of active species, which opens opportunities to design pre-catalysts with preferred defects that promote the formation of the most active OER species., (© 2023 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH.)