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Atomic and Laser Physics
Credit: Jack Hobhouse

Andrea Cavalleri

Professor of Physics

Sub department

  • Atomic and Laser Physics
andrea.cavalleri@physics.ox.ac.uk
Telephone: 01865 (2)72365
Clarendon Laboratory, room 316.3
  • About
  • Publications

Ultrafast single-shot diffraction imaging of nanoscale dynamics

Nature Photonics 2:7 (2008) 415-419

Authors:

A Barty, S Boutet, MJ Bogan, S Hau-Riege, S Marchesini, K Sokolowski-Tinten, N Stojanovic, R Tobey, H Ehrke, A Cavalleri, S Düsterer, M Frank, S Bajt, BW Woods, MM Seibert, J Hajdu, R Treusch, HN Chapman

Abstract:

The transient nanoscale dynamics of materials on femtosecond to picosecond timescales is of great interest in the study of condensed phase dynamics such as crack formation, phase separation and nucleation, and rapid fluctuations in the liquid state or in biologically relevant environments. The ability to take images in a single shot is the key to studying non-repetitive behaviour mechanisms, a capability that is of great importance in many of these problems. Using coherent diffraction imaging with femtosecond X-ray free-electron-laser pulses we capture time-series snapshots of a solid as it evolves on the ultrafast timescale. Artificial structures imprinted on a Si 3 N 4 window are excited with an optical laser and undergo laser ablation, which is imaged with a spatial resolution of 50nm and a temporal resolution of 10ps. By using the shortest available free-electron-laser wavelengths and proven synchronization methods this technique could be extended to spatial resolutions of a few nanometres and temporal resolutions of a few tens of femtoseconds. This experiment opens the door to a new regime of time-resolved experiments in mesoscopic dynamics. © 2008 Macmillan Publishers Limited. All rights reserved.
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Optical switching in v O2 films by below-gap excitation

Applied Physics Letters 92:18 (2008)

Authors:

M Rini, Z Hao, RW Schoenlein, C Giannetti, F Parmigiani, S Fourmaux, JC Kieffer, A Fujimori, M Onoda, S Wall, A Cavalleri

Abstract:

We study the photoinduced insulator-metal transition in V O2, correlating its threshold and dynamics with excitation wavelength. In single crystals, switching can only be induced with photon energies above the 670 meV gap. This contrasts with the case of polycrystalline films, where formation of the metallic state can be initiated also with photon energies as low as 180 meV, which are well below the bandgap. Perfection of this process may become conducive to schemes for optical switches, limiters, and detectors operating at room temperature in the mid-infrared. © 2008 American Institute of Physics.
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Enhanced photosusceptibility near Tc for the light-induced insulator-to-metal phase transition in vanadium dioxide (vol 99, art no 226401, 2007)

PHYSICAL REVIEW LETTERS 100:1 (2008) ARTN 019906

Authors:

DJ Hilton, RP Prasankumar, S Fourmaux, A Cavalleri, D Brassard, MA El Khakani, JC Kieffer, AJ Taylor, RD Averitt
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Enhanced photosusceptibility near Tc for the light-induced insulator-to-metal phase transition in vanadium dioxide.

Phys Rev Lett 99:22 (2007) 226401

Authors:

DJ Hilton, RP Prasankumar, S Fourmaux, A Cavalleri, D Brassard, MA El Khakani, JC Kieffer, AJ Taylor, RD Averitt

Abstract:

We use optical-pump terahertz-probe spectroscopy to investigate the near-threshold behavior of the photoinduced insulator-to-metal (IM) transition in vanadium dioxide thin films. Upon approaching Tc a reduction in the fluence required to drive the IM transition is observed, consistent with a softening of the insulating state due to an increasing metallic volume fraction (below the percolation limit). This phase coexistence facilitates the growth of a homogeneous metallic conducting phase following superheating via photoexcitation. A simple dynamic model using Bruggeman effective medium theory describes the observed initial condition sensitivity.
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Chemistry. All at once.

Science 318:5851 (2007) 755-756
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