Author
Listed:
- L. Rettig
(Fakultät für Physik, Universität Duisburg-Essen
Fachbereich Physik, Freie Universität Berlin
Present address: Swiss Light Source, Paul Scherrer Institut, CH-5232 Villigen PSI, Switzerland)
- R. Cortés
(Fachbereich Physik, Freie Universität Berlin
Fritz-Haber-Institut der MPG
Present address: Physical Review Letters, American Physical Society, 1 Research Road, Ridge, 11961 New York, USA)
- J.-H. Chu
(Geballe Laboratory for Advanced Materials
SLAC National Accelerator Laboratory, Stanford Institute for Material and Energy Sciences)
- I. R. Fisher
(Geballe Laboratory for Advanced Materials
SLAC National Accelerator Laboratory, Stanford Institute for Material and Energy Sciences)
- F. Schmitt
(Geballe Laboratory for Advanced Materials)
- R. G. Moore
(SLAC National Accelerator Laboratory, Stanford Institute for Material and Energy Sciences)
- Z.-X. Shen
(Geballe Laboratory for Advanced Materials
SLAC National Accelerator Laboratory, Stanford Institute for Material and Energy Sciences)
- P. S. Kirchmann
(SLAC National Accelerator Laboratory, Stanford Institute for Material and Energy Sciences)
- M. Wolf
(Fachbereich Physik, Freie Universität Berlin
Fritz-Haber-Institut der MPG)
- U. Bovensiepen
(Fakultät für Physik, Universität Duisburg-Essen
Fachbereich Physik, Freie Universität Berlin)
Abstract
Non-equilibrium conditions may lead to novel properties of materials with broken symmetry ground states not accessible in equilibrium as vividly demonstrated by non-linearly driven mid-infrared active phonon excitation. Potential energy surfaces of electronically excited states also allow to direct nuclear motion, but relaxation of the excess energy typically excites fluctuations leading to a reduced or even vanishing order parameter as characterized by an electronic energy gap. Here, using femtosecond time- and angle-resolved photoemission spectroscopy, we demonstrate a tendency towards transient stabilization of a charge density wave after near-infrared excitation, counteracting the suppression of order in the non-equilibrium state. Analysis of the dynamic electronic structure reveals a remaining energy gap in a highly excited transient state. Our observation can be explained by a competition between fluctuations in the electronically excited state, which tend to reduce order, and transiently enhanced Fermi surface nesting stabilizing the order.
Suggested Citation
L. Rettig & R. Cortés & J.-H. Chu & I. R. Fisher & F. Schmitt & R. G. Moore & Z.-X. Shen & P. S. Kirchmann & M. Wolf & U. Bovensiepen, 2016.
"Persistent order due to transiently enhanced nesting in an electronically excited charge density wave,"
Nature Communications, Nature, vol. 7(1), pages 1-6, April.
Handle:
RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms10459
DOI: 10.1038/ncomms10459
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