Ultrafast disordering of vanadium dimers in photoexcited VO2

Cita com:
hdl:2117/123715
Document typeArticle
Defense date2018-11-02
PublisherAmerican Association for the Advancement of Science.
Rights accessOpen Access
This work is protected by the corresponding intellectual and industrial property rights.
Except where otherwise noted, its contents are licensed under a Creative Commons license
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Attribution-NonCommercial-NoDerivs 3.0 Spain
ProjectAGR-INSTITUTO DE CIENCIAS FOTONICAS (MINECO-SEV-2015-0522)
CONTROL EN FEMTOSEGUNDOS DE REDES CRISTALINAS (MINECO-FIS2015-67898-P)
SeeSuper - Probing nanoscale and femtosecond fluctuations in high temperature superconductors (EC-H2020-758461)
CONTROL EN FEMTOSEGUNDOS DE REDES CRISTALINAS (MINECO-FIS2015-67898-P)
SeeSuper - Probing nanoscale and femtosecond fluctuations in high temperature superconductors (EC-H2020-758461)
Abstract
Time-resolved x-ray scattering can be used to investigate the dynamics of materials during the switch from one structural phase to another. So far, methods provide an ensemble average and may miss crucial aspects of the detailed mechanisms at play. Wall et al. used a total-scattering technique to probe the dynamics of the ultrafast insulator-to-metal transition of vanadium dioxide (VO2) (see the Perspective by Cavalleri). Femtosecond x-ray pulses provide access to the time- and momentum-resolved dynamics of the structural transition. Their results show that the photoinduced transition is of the order-disorder type, driven by an ultrafast change in the lattice potential that suddenly unlocks the vanadium atoms and yields large-amplitude uncorrelated motions, rather than occurring through a coherent displacive mechanism.
CitationWall, S. [et al.]. Ultrafast disordering of vanadium dimers in photoexcited VO2. "Science", 2 Novembre 2018, vol. 362, núm. 6414, p. 572-576.
ISSN0036-8075
Publisher versionhttp://science.sciencemag.org/content/362/6414/572
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