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Persistent order due to transiently enhanced nesting in an electronically excited charge density wave

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Cortés Rodriguez,  Rocio
Fachbereich Physik, Freie Universität Berlin;
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Wolf,  Martin
Fachbereich Physik, Freie Universität Berlin;
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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ncomms10459.pdf
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Citation

Rettig, L., Cortés Rodriguez, R., Chu, J.-H., Fisher, I. R., Schmitt, F., Moore, R. G., et al. (2016). Persistent order due to transiently enhanced nesting in an electronically excited charge density wave. Nature Communications, 7: 10459. doi:10.1038/ncomms10459.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0029-B52A-3
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.