ترغب بنشر مسار تعليمي؟ اضغط هنا

Inelastic Electron Tunneling Spectroscopy at High-Temperatures

86   0   0.0 ( 0 )
 نشر من قبل Prosper Ngabonziza
 تاريخ النشر 2020
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

Ion conducting materials are critical components of batteries, fuel cells, and devices such as memristive switches. Analytical tools are therefore sought that allow the behavior of ions in solids to be monitored and analyzed with high spatial resolution and in real time. In principle, inelastic tunneling spectroscopy offers these capabilities. However, as its spectral resolution is limited by thermal softening of the Fermi-Dirac distribution, tunneling spectroscopy is usually constrained to cryogenic temperatures. This constraint would seem to render tunneling spectroscopy useless for studying ions in motion. We report here the first inelastic tunneling spectroscopy studies above room temperature. For these measurements, we have developed high-temperature-stable tunnel junctions that incorporate within the tunnel barrier ultrathin layers for efficient proton conduction. By analyzing the vibrational modes of O-H bonds in BaZrO3-based heterostructures, we demonstrate the detection of protons with a spectral resolution of 20 meV at 400 K (FWHM). Overturning the hitherto existing prediction for the spectral resolution limit of 186 meV (5.4 kBT at 400 K), this resolution enables high-temperature tunneling spectroscopy of ion conductors. With these advances, inelastic tunneling spectroscopy constitutes a novel, valuable analytical tool for solid-state ionics.

قيم البحث

اقرأ أيضاً

We investigated the localized electronic properties of nanoporous gold films by using an ultra-high vacuum scanning tunneling microscope at low temperature (4.2 K). Second derivative scanning tunneling spectroscopy shows the plasmon peaks of the nano porous gold films, which are excited by inelastic tunneling electrons. We propose that the nanorod model is appropriate for nanoporous gold studies at the nanometer-scale. These results are supported by a 3D electron tomography analysis and theoretical calculations of nanoporous gold with ellipsoid shape.
We address local inelastic scattering from vibrational impurity adsorbed onto graphene and the evolution of the local density of electron states near the impurity from weak to strong coupling regime. For weak coupling the local electronic structure i s distorted by inelastic scattering developing peaks/dips and steps. These features should be detectable in the inelastic electron tunneling spectroscopy, $d^2I/dV^2$, using local probing techniques. Inelastic Friedel oscillations distort the spectral density at energies close to the inelastic mode. In the strong coupling limit, a local negative $U$-center forms in the atoms surrounding the impurity site. For those atoms, the Dirac cone structure is fully destroyed, that is, the linear energy dispersion as well as the V-shaped local density of electron states is completely destroyed. We further consider the effects of the negative $U$ formation and its evolution from weak to strong coupling. The negative $U$-site effectively acts as local impurity such that sharp resonances appear in the local electronic structure. The main resonances are caused by elastic scattering off the impurity site, and the features are dressed by the presence of vibrationally activated side resonances. Going from weak to strong coupling, changes the local electronic structure from being Dirac cone like including midgap states, to a fully destroyed Dirac cone with only the impurity resonances remaining.
We report a detailed study of tunneling spectra measured on 2H-Ta$_x$Nb$_{1-x}$Se$_2$ ($x=0sim 0.1$) single crystals using a low-temperature scanning tunneling microscope. The prominent gap-like feature unintelligible for a long time was found to be accompanied by some in-gap fine structures. By investigating the second-derivative spectra and their temperature and magnetic field dependencies, we were able to prove that inelastic electron tunneling is the origin of these features and obtain the Eliashberg function of 2H-Ta$_x$Nb$_{1-x}$Se$_2$ at atomic scale, providing a potential way to study the local Eliashberg function and phonon spectra of the related transition-metal dichalcogenides.
78 - N. Medvedev , I. Milov 2020
Electron-phonon coupling, being one of the most important parameters governing the material evolution after ultrafast energy deposition, yet remains the most unexplored one. In this work, we applied the dynamical coupling approach to calculate the no nadiabatic electron-ion energy exchange in nonequilibrium solids with the electronic temperature high above the atomic one. It was implemented into the tight-binding molecular dynamics code, and used to study electron-phonon coupling in various elemental metals. The developed approach is a universal scheme applicable to electronic temperatures up to a few electron-Volts, and to arbitrary atomic configuration and dynamics. We demonstrate that the calculated electron-ion (electron-phonon) coupling parameter agrees well with the available experimental data in high-electronic-temperature regime, validating the model. The following materials are studied here - fcc metals: Al, Ca, Ni, Cu, Sr, Y, Zr, Rh, Pd, Ag, Ir, Pt, Au, Pb; hcp metals: Mg, Sc, Ti, Co, Zn, Tc, Ru, Cd, Hf, Re, Os; bcc metals: V, Cr, Fe, Nb, Mo, Ba, Ta, W; diamond cubic lattice metals: Sn; specific cases of Ga, In, Mn, Te and Se; and additionally semimetal graphite and semiconductors Si and Ge. For many materials, we provide the first and so far the only estimation of the electron-phonon coupling at elevated electron temperatures, which can be used in various models simulating ultrafast energy deposition in matter. We also discuss the dependence of the coupling parameter on the atomic mass, temperature and density.
We present a theoretical study of the spin transport properties of mono-atomic magnetic chains with a focus on the spectroscopical features of the I-V curve associated to spin-flip processes. Our calculations are based on the s-d model for magnetism with the electron transport treated at the level of the non-equilibrium Greens function formalism. Inelastic spin-flip scattering processes are introduced perturbatively via the first Born approximation and an expression for the associated self-energy is derived. The computational method is then applied to describe the I-V characteristics and its derivatives of one dimensional chains of Mn atoms and the results are then compared to available experimental data. We find a qualitative and quantitative agreement between the calculated and the experimental conductance spectra. Significantly we are able to describe the relative intensities of the spin excitation features in the I-V curve, by means of a careful analysis of the spin transition selection rules associated to the atomic chains.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا