Ultrafast recovery dynamics of dimer stripes in IrTe2

Fuente: arXiv
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Autori principali: Rumo, M., Kremer, G., Heber, M., Wind, N., Nicholson, C. W., Ma, K. Y., Brenner, G., Pressacco, F., Scholz, M., Rossnagel, K., von Rohr, F. O., Kutnyakhov, D., Monney, C.
Natura: Preprint
Pubblicazione: 2025
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author Rumo, M.
Kremer, G.
Heber, M.
Wind, N.
Nicholson, C. W.
Ma, K. Y.
Brenner, G.
Pressacco, F.
Scholz, M.
Rossnagel, K.
von Rohr, F. O.
Kutnyakhov, D.
Monney, C.
author_facet Rumo, M.
Kremer, G.
Heber, M.
Wind, N.
Nicholson, C. W.
Ma, K. Y.
Brenner, G.
Pressacco, F.
Scholz, M.
Rossnagel, K.
von Rohr, F. O.
Kutnyakhov, D.
Monney, C.
contents The transition metal dichalcogenide IrTe2 displays a remarkable series of first-order phase transitions below room temperature, involving lattice displacements as large as 20 percents of the initial bond length. This is nowadays understood as the result of strong electron-phonon coupling leading to the formation of local multicentre dimers that arrange themselves into one-dimensional stripes. In this work, we study the out-of-equilibrium dynamics of these dimers and track the time evolution of their population following an infrared photoexcitation using free-electron lased-based time-resolved X-ray photoemission spectroscopy. First, we observe that the dissolution of dimers is driven by the transfer of energy from the electronic subsystem to the lattice subsystem, in agreement with previous studies. Second, we observe a surprisingly fast relaxation of the dimer population on the timescale of a few picoseconds. By comparing our results to published ultrafast electron diffraction and angle-resolved photoemission spectroscopy data, we reveal that the long-range order needs tens of picoseconds to recover, while the local dimer distortion recovers on a short timescale of a few picoseconds.
format Preprint
id arxiv_https___arxiv_org_abs_2510_24361
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Ultrafast recovery dynamics of dimer stripes in IrTe2
Rumo, M.
Kremer, G.
Heber, M.
Wind, N.
Nicholson, C. W.
Ma, K. Y.
Brenner, G.
Pressacco, F.
Scholz, M.
Rossnagel, K.
von Rohr, F. O.
Kutnyakhov, D.
Monney, C.
Strongly Correlated Electrons
The transition metal dichalcogenide IrTe2 displays a remarkable series of first-order phase transitions below room temperature, involving lattice displacements as large as 20 percents of the initial bond length. This is nowadays understood as the result of strong electron-phonon coupling leading to the formation of local multicentre dimers that arrange themselves into one-dimensional stripes. In this work, we study the out-of-equilibrium dynamics of these dimers and track the time evolution of their population following an infrared photoexcitation using free-electron lased-based time-resolved X-ray photoemission spectroscopy. First, we observe that the dissolution of dimers is driven by the transfer of energy from the electronic subsystem to the lattice subsystem, in agreement with previous studies. Second, we observe a surprisingly fast relaxation of the dimer population on the timescale of a few picoseconds. By comparing our results to published ultrafast electron diffraction and angle-resolved photoemission spectroscopy data, we reveal that the long-range order needs tens of picoseconds to recover, while the local dimer distortion recovers on a short timescale of a few picoseconds.
title Ultrafast recovery dynamics of dimer stripes in IrTe2
topic Strongly Correlated Electrons
url https://arxiv.org/abs/2510.24361