We present a complementary experimental and theoretical investigation of relaxation dynamics in the charge-density-wave (CDW) system TbTe$_3$ after ultrafast optical excitation. Using time- and angle-resolved photoemission spectroscopy, we observe an unusual transient modulation of the relaxation rates of excited photocarriers. A detailed analysis of the electron self-energy based on a nonequilibrium Greens function formalism reveals that the phase space of electron-electron scattering is critically modulated by the photoinduced collective CDW excitation, providing an intuitive microscopic understanding of the observed dynamics.
We present angular dependent magneto-transport and magnetization measurements on alpha-(ET)2MHg(SCN)4 compounds at high magnetic fields and low temperatures. We find that the low temperature ground state undergoes two subsequent field-induced density-wave type phase transitions above a critical angle of the magnetic field with respect to the crystallographic axes. This new phase diagram may be qualitatively described assuming a charge density wave ground state which undergoes field-induced transitions due to the interplay of Pauli and orbital effects.
We present time- and angle-resolved photoemission spectroscopy measurements on the charge density wave system CeTe$_{3}$. Optical excitation transiently populates the unoccupied band structure and reveals a gap size of 2$Delta$ = 0.59 eV. The occupied Te-5p band dispersion is coherently modified by three modes at $Omega_{1}$ = 2.2 THz, $Omega_{2}$ = 2.7 THz and $Omega_{3}$ = 3 THz. All three modes lead to small rigid energy shifts whereas $Delta$ is only affected by $Omega_{1}$ and $Omega_{2}$. Their spatial polarization is analyzed by fits of a transient model dispersion and DFT frozen phonon calculations. We conclude that the modes $Omega_{1}$ and $Omega_{2}$ result from in-plane ionic lattice motions, which modulate the charge order, and that $Omega_{3}$ originates from a generic out-of-plane $A_{1g}$ phonon. We thereby demonstrate how the rich information from trARPES allows identification of collective modes and their spatial polarization, which explains the mode-dependent coupling to charge order.
Topological physics and strong electron-electron correlations in quantum materials are typically studied independently. However, there have been rapid recent developments in quantum materials in which topological phase transitions emerge when the single-particle band structure is modified by strong interactions. We here demonstrate that the room-temperature phase of (TaSe$_4$)$_2$I is a Weyl semimetal with 24 pairs of Weyl nodes. Owing to its quasi-1D structure, (TaSe$_4$)$_2$I hosts an established CDW instability just below room temperature. Using X-ray diffraction, angle-resolved photoemission spectroscopy, and first-principles calculations, we find that the CDW in (TaSe$_4$)$_2$I couples the bulk Weyl points and opens a band gap. The correlation-driven topological phase transition in (TaSe$_4$)$_2$I provides a route towards observing condensed-matter realizations of axion electrodynamics in the gapped regime, topological chiral response effects in the semimetallic phase, and represents an avenue for exploring the interplay of correlations and topology in a solid-state material.
Hysteresis underlies a large number of phase transitions in solids, giving rise to exotic metastable states that are otherwise inaccessible. Here, we report an unconventional hysteretic transition in a quasi-2D material, EuTe4. By combining transport, photoemission, diffraction, and x-ray absorption measurements, we observed that the hysteresis loop has a temperature width of more than 400 K, setting a record among crystalline solids. The transition has an origin distinct from known mechanisms, lying entirely within the incommensurate charge-density-wave (CDW) phase of EuTe4 with no change in the CDW modulation periodicity. We interpret the hysteresis as an unusual switching of the relative CDW phases in different layers, a phenomenon unique to quasi-2D compounds that is not present in either purely 2D or strongly-coupled 3D systems. Our findings challenge the established theories on metastable states in density wave systems, pushing the boundary of understanding hysteretic transitions in a broken-symmetry state.
Unconventional quasiparticle excitations in condensed matter systems have become one of the most important research frontiers. Beyond two- and fourfold degenerate Weyl and Dirac fermions, three-, six- and eightfold symmetry protected degeneracies have been predicted however remain challenging to realize in solid state materials. Here, charge density wave compound TaTe4 is proposed to hold eightfold fermionic excitation and Dirac point in energy bands. High quality TaTe4 single crystals are prepared, where the charge density wave is revealed by directly imaging the atomic structure and a pseudogap of about 45 meV on the surface. Shubnikov de-Haas oscillations of TaTe4 are consistent with band structure calculation. Scanning tunneling microscopy reveals atomic step edge states on the surface of TaTe4. This work uncovers that charge density wave is able to induce new topological phases and sheds new light on the novel excitations in condensed matter materials.
J. Maklar
,M. Schuler
,Y. W. Windsor
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(2021)
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"Coherent Modulation of Quasiparticle Scattering Rates in a Photoexcited Charge-Density-Wave System"
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Julian Maklar
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