Elsa Abreu

THz spectroscopy of VO2 epitaxial films: controlling the anisotropic properties through strain engineering

We investigate far-infrared properties of strain engineered vanadium dioxide nanosheets through epitaxial growth on a (100)R TiO2 substrate. The nanosheets exhibit large uniaxial strain leading to highly uniform and oriented cracks along the rutile c-axis. Dramatic anisotropy arises for both the metal-insulator transition temperature, which is different from the structural transition temperature along the cR axis, and the metallic state conductivity. Detailed analysis reveals a Mott-Hubbard like behavior along the rutile cR axis. §contributed equally to this work

Symmetry breaking and geometric confinement in VO2: Results from a three-dimensional infrared nano-imaging

Epitaxial strain can play an important role in controlling the local phase dynamics of transition metal oxides. With scattering-type scanning near-field optical microscopy, we visualize the three dimensional landscape of phase inhomogeneity in strained VO2 films grown on [100]R TiO2 substrates. We demonstrate that three different symmetries are spontaneously broken in the vicinity of the VO2 phase transition: (1) Monoclinic-tetragonal (rutile) crystal symmetry breaking due to the structural phase transition, (2) in-plane (x-y plane) rotational symmetry breaking due to the formation of periodic strain domains, and (3) out-of-plane (z-axis) mirror symmetry breaking at the film cross-section due to substrate-induced epitaxial strain.

Dynamic conductivity scaling in photoexcited V 2 O 3 thin films

Optical-pump terahertz-probe spectroscopy is used to investigate ultrafast far-infrared conductivity dynamics during the insulator-to-metal transition (IMT) in vanadium sesquioxide (V2O3). The resultant conductivity increase occurs on a tens of ps timescale, exhibiting a strong dependence on the initial temperature and fluence. We have identified a scaling of the conductivity dynamics upon renormalizing the time axis with a simple power law (alpha = 1/2) that depends solely on the initial, final, and conductivity onset temperatures. Qualitative and quantitative considerations indicate that the dynamics arise from nucleation and growth of the metallic phase which can be described by the Avrami model. We show that the temporal scaling arises from spatial scaling of the growth of the metallic volume fraction, highlighting the self-similar nature of the dynamics. Our results illustrate the important role played by mesoscopic effects in phase transition dynamics.

k-resolved susceptibility function of 2H-TaSe2 from angle-resolved photoemission

The connection between the Fermi surface and charge-density-wave (CDW) order is revisited in 2H-TaSe2. Using angle-resolved photoemission spectroscopy, ab initio band-structure calculations, and an accurate tight-binding model, we develop the empirical k-resolved susceptibility function, which we use to highlight states that contribute to the susceptibility for a particular q vector. We show that although the Fermi surface is involved in the peaks in the susceptibility associated with CDW order, it is not through conventional Fermi surface nesting, but rather through finite energy transitions from states located far from the Fermi level. Comparison with monolayer TaSe2 illustrates the different mechanisms that are involved in the absence of bilayer splitting.

Modeling of soft x-ray induced ablation in solids

Powerful free electron lasers (FELs) operating in the soft X-ray regime are offering new possibilities for creating and probing materials under extreme conditions. We describe here simulations to model the interaction of a focused FEL pulse with metallic solids (niobium, vanadium, and their deuterides) at 13.5 nm wavelength (92 eV) with peak intensities between 1015 to 1018 W/cm2 and a fixed pulse length of 15 femtoseconds (full width at half maximum). The interaction of the pulse with the metallic solids was modeled with a non-local thermodynamic equilibrium code that included radiation transfer. The calculations also made use of a self-similar isothermal fluid model for plasma expansion into vacuum. We find that the time-evolution of the simulated critical charge density in the sample results in a critical depth that approaches the observed crater depths in an earlier experiment performed at the FLASH free electron laser in Hamburg. The results show saturation in the ablation process at intensities exceeding 1016 W/cm2. Furthermore, protons and deuterons with kinetic energies of several keV have been measured, and these concur with predictions from the plasma expansion model. The results indicate that the temperature of the plasma reached almost 5 million K after the pulse has passed.

Ultrafast Electron-Lattice Coupling Dynamics in VO2 and V2O3 Thin Films

Ultrafast optical pump--optical probe and optical pump--terahertz probe spectroscopy were performed on vanadium dioxide (

Large strain-induced conductivity anisotropy in VO 2 thin films probed by THz spectroscopy

{\mathrm{VO}}_{2}

Turning solid aluminium transparent by intense soft X-ray photoionization

) and vanadium sesquioxide (

Anisotropic electronic state via spontaneous phase separation in strained vanadium dioxide films.

{\mathrm{V}}_{2}{\mathrm{O}}_{3}

Phase transition in bulk single crystals and thin films of VO2 by nanoscale infrared spectroscopy and imaging

) thin films over a wide temperature range. A comparison of the experimental data from these two different techniques and two different vanadium oxides, in particular a comparison of the spectral weight oscillations generated by the photoinduced longitudinal acoustic modulation, reveals the strong electron-phonon coupling that exists in both materials. The low-energy Drude response of