704 research outputs found

    Simultaneous interfacial reactivity and topography mapping with scanning ion conductance microscopy

    Get PDF
    Scanning ion conductance microscopy (SICM) is a powerful technique for imaging the topography of a wide range of materials and interfaces. In this report, we develop the use and scope of SICM, showing how it can be used for mapping spatial distributions of ionic fluxes due to (electro)chemical reactions occurring at interfaces. The basic idea is that there is a change of ion conductance inside a nanopipet probe when it approaches an active site, where the ionic composition is different to that in bulk solution, and this can be sensed via the current flow in the nanopipet with an applied bias. Careful tuning of the tip potential allows the current response to be sensitive to either topography or activity, if desired. Furthermore, the use of a distance modulation SICM scheme allows reasonably faithful probe positioning using the resulting ac response, irrespective of whether there is a reaction at the interface that changes the local ionic composition. Both strategies (distance modulation or tuned bias) allow simultaneous topography-activity mapping with a single channel probe. The application of SICM reaction imaging is demonstrated on several examples, including voltammetric mapping of electrocatalytic reactions on electrodes and high-speed electrochemical imaging at rates approaching 4 s per image frame. These two distinct approaches provide movies of electrochemical current as a function of potential with hundreds of frames (images) of surface reactivity, to reveal a wealth of spatially resolved information on potential- (and time) dependent electrochemical phenomena. The experimental studies are supported by detailed finite element method modeling that places the technique on a quantitative footing

    Nanoscale electrochemical mapping

    Get PDF
    Surfaces and interfaces, of both practical and fundamental interest, have long been recognized to be complex, yet while there are many microscopy and spectroscopy methods for imaging structure, topography and surface chemical composition at high spatial resolution, there are relatively few techniques for mapping associated chemical fluxes in the near-interface region. In this regard, scanning electrochemical probe microscopy (SEPM), which utilizes a small scale electrode probe as an imaging device, has had a unique place in the scanning probe microscopy (SPM) family of techniques, in being able to map chemical fluxes and interfacial reactivity. For a long time, techniques such as scanning electrochemical microscopy (SECM) were largely stuck at the micron –or larger –scale in terms of spatial resolution, but recent years have seen spectacular progress, such that a variety of different types of SEPM technique are now available and 10sof nm spatial resolution is becoming increasingly accessible. This step-change in capability is opening many new opportunities for the characterization of flux processes and interfacial activity in a whole raft of systems, including electrode surfaces, electromaterials, soft matter, living cells and tissues

    Synchronous electrical conductance‐ and electron tunnelling‐scanning electrochemical microscopy measurements

    Get PDF
    The requirement to separate topographical effects from surface electrochemistry information is a major limitation of scanning electrochemical microscopy (SECM). With many applications of SECM involving the study of (semi)conducting electrode surfaces, the hybridisation of SECM with scanning tunnelling microscopy (STM) or a surface conductance probe would provide the ultimate topographical imaging capability to SECM, but previous attempts are limited. Here, the conversion of a general scanning electrochemical probe microscopy (SEPM) platform to facilitate contact electrical conductance (C)‐ and electron tunnelling (T)‐SECM measurements is considered. Measurements in air under ambient conditions with a Pt/Ir wire tip are used to assess the performance of the piezoelectric positioning system. A hopping‐mode imaging protocol is implemented, whereby the tip approaches the surface at each pixel until a desired current magnitude is exceeded, and the corresponding z position (surface height) is recorded at a set of predefined xy coordinates in the plane of the surface. At slow tip approach rates, the current shows an exponential dependence on tip‐substrate distance, as expected for electron tunnelling. For measurements in electrochemical environments, in order to overcome well‐known problems with leakage currents at coated‐wire tips used for electrochemical STM, Pt‐sensitised carbon nanoelectrodes are used as tips. The hydrogen evolution reaction on 2D Au nanocrystals serves as an exemplar system for the successful simultaneous mapping of topography and electrochemical activity

    Can single cell respiration be measured by scanning electrochemical microscopy (SECM)?

    Get PDF
    Ultramicroelectrode (UME), or, equivalently, microelectrode, probes are increasingly used for single-cell measurements of cellular properties and processes, including physiological activity, such as metabolic fluxes and respiration rates. Major challenges for the sensitivity of such measurements include: (i) the relative magnitude of cellular and UME fluxes (manifested in the current); and (ii) issues around the stability of the UME response over time. To explore the extent to which these factors impact the precision of electrochemical cellular measurements, we undertake a systematic analysis of measurement conditions and experimental parameters for determining single cell respiration rates via the oxygen consumption rate (OCR) in single HeLa cells. Using scanning electrochemical microscopy (SECM), with a platinum UME as the probe, we employ a self-referencing measurement protocol, rarely employed in SECM, whereby the UME is repeatedly approached from bulk solution to a cell, and a short pulse to oxygen reduction reaction (ORR) potential is performed near the cell and in bulk solution. This approach enables the periodic tracking of the bulk UME response to which the near-cell response is repeatedly compared (referenced) and also ensures that the ORR near the cell is performed only briefly, minimizing the effect of the electrochemical process on the cell. SECM experiments are combined with a finite element method (FEM) modeling framework to simulate oxygen diffusion and the UME response. Taking a realistic range of single cell OCR to be 1 × 10–18 to 1 × 10–16 mol s–1, results from the combination of FEM simulations and self-referencing SECM measurements show that these OCR values are at, or below, the present detection sensitivity of the technique. We provide a set of model-based suggestions for improving these measurements in the future but highlight that extraordinary improvements in the stability and precision of SECM measurements will be required if single cell OCR measurements are to be realized

    Scanning ion conductance microscopy reveals differences in the ionic environments of gram-positive and negative bacteria

    Get PDF
    This paper reports on the use of scanning ion conductance microscopy (SICM) to locally map the ionic properties and charge environment of two live bacterial strains: the Gram-negative and the Gram-positive . SICM results find heterogeneities across the bacterial surface and significant differences among the Gram-positive and Gram-negative bacteria. The bioelectrical environment of the was found to be considerably more negatively charged compared to . SICM measurements, fitted to a simplified finite element method (FEM) model, revealed surface charge values of -80 to -140 mC m for the Gram-negative . The Gram-positive show a much higher conductivity around the cell wall, and surface charge values between -350 and -450 mC m were found using the same simplified model. SICM was also able to detect regions of high negative charge near , not detected in the topographical SICM response and attributed to the extracellular polymeric substance. To further explore how the cell wall structure can influence the SICM current response, a more comprehensive FEM model, accounting for the physical properties of the Gram-positive cell wall, was developed. The new model provides a more realistic description of the cell wall and allows investigation of the relation between its key properties and SICM currents, building foundations to further investigate and improve understanding of the Gram-positive cellular microenvironment

    Jet energy measurement and its systematic uncertainty in proton–proton collisions at √s=7 TeV with the ATLAS detector

    Get PDF
    The jet energy scale (JES) and its systematic uncertainty are determined for jets measured with the ATLAS detector using proton–proton collision data with a centre-of-mass energy of √s=7 TeV corresponding to an integrated luminosity of 4.7 fb −1. Jets are reconstructed from energy deposits forming topological clusters of calorimeter cells using the anti-kt algorithm with distance parameters R=0.4 or R=0.6, and are calibrated using MC simulations. A residual JES correction is applied to account for differences between data and MC simulations. This correction and its systematic uncertainty are estimated using a combination of in situ techniques exploiting the transverse momentum balance between a jet and a reference object such as a photon or a Z boson, for 20≤pTjet1 TeV. The calibration of forward jets is derived from dijet pT balance measurements. The resulting uncertainty reaches its largest value of 6 % for low-pT jets at |η|=4.5. Additional JES uncertainties due to specific event topologies, such as close-by jets or selections of event samples with an enhanced content of jets originating from light quarks or gluons, are also discussed. The magnitude of these uncertainties depends on the event sample used in a given physics analysis, but typically amounts to 0.5–3 %

    Angular analysis of D0π+πμ+μD^0 \to \pi^+\pi^-\mu^+\mu^- and D0K+Kμ+μD^0 \to K^+K^-\mu^+\mu^- decays and search for CPCP violation

    Get PDF
    The first full angular analysis and an updated measurement of the decay-rate CPCP asymmetry of the D0π+πμ+μD^0 \to \pi^+\pi^-\mu^+\mu^- and D0K+Kμ+μD^0 \to K^+K^-\mu^+\mu^- decays are reported. The analysis uses proton-proton collision data collected with the LHCb detector at centre-of-mass energies of 7, 8 and 13 TeV. The data set corresponds to an integrated luminosity of 9 fb1^{-1}. The full set of CPCP-averaged angular observables and their CPCP asymmetries are measured as a function of the dimuon invariant mass. The results are consistent with expectations from the standard model and with CPCP symmetry.Comment: All figures and tables, along with any supplementary material and additional information, are available at https://cern.ch/lhcbproject/Publications/p/LHCb-PAPER-2021-035.html (LHCb public pages

    Observation of the Decay Λ0b→Λ+cτ−¯ν

    Get PDF
    The first observation of the semileptonic b-baryon decay Λb0→Λc+τ-ν¯τ, with a significance of 6.1σ, is reported using a data sample corresponding to 3 fb-1 of integrated luminosity, collected by the LHCb experiment at center-of-mass energies of 7 and 8 TeV at the LHC. The τ- lepton is reconstructed in the hadronic decay to three charged pions. The ratio K=B(Λb0→Λc+τ-ν¯τ)/B(Λb0→Λc+π-π+π-) is measured to be 2.46±0.27±0.40, where the first uncertainty is statistical and the second systematic. The branching fraction B(Λb0→Λc+τ-ν¯τ)=(1.50±0.16±0.25±0.23)% is obtained, where the third uncertainty is from the external branching fraction of the normalization channel Λb0→Λc+π-π+π-. The ratio of semileptonic branching fractions R(Λc+)B(Λb0→Λc+τ-ν¯τ)/B(Λb0→Λc+μ-ν¯μ) is derived to be 0.242±0.026±0.040±0.059, where the external branching fraction uncertainty from the channel Λb0→Λc+μ-ν¯μ contributes to the last term. This result is in agreement with the standard model prediction
    corecore