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arxiv: 2501.15771 · v1 · pith:YGWAWAO5 · submitted 2025-01-27 · cond-mat.str-el · cond-mat.supr-con

Absence of two-phonon quasi-elastic scattering in the normal state of doped--SrTiO₃ by THz pump-probe spectroscopy

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classification cond-mat.str-el cond-mat.supr-con
keywords energyscatteringindicatesnonlinearrelaxationelectronicmetallicpump-probe
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Multi-pulse nonlinear THz spectroscopies enable a new understanding of interacting metallic systems via their sensitivity to novel correlation functions. Here, we investigated the THz nonlinear properties of the dilute metallic phase of doped-SrTiO$_3$ thin films using nonlinear terahertz 2D coherent spectroscopy. We observed a large $\chi^{(3)}$ response in the low temperature region where the dc electrical resistivity follows a T$^2$-dependence. This is largely a pump-probe response, which we find is governed by a single energy relaxation rate that is much smaller at all temperatures than the momentum relaxation rates obtained from the optical conductivity. This indicates that the processes that dominate the resistive scattering are not the same as those that remove energy from the electronic system. Moreover the fact that the energy relaxation rate is an increasing function of temperature indicates that the excitations that do carry away energy from the electronic system cannot be considered as quasi-elastic and as such soft two-phonon electron scattering does not play a major role in the physics as proposed. This indicates that these materials' resistive T$^2$ scattering likely originates in electron-electron interactions despite the very small Fermi wave vectors at the lowest dopings.

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Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score.

  1. Energy relaxation due to two-phonon scattering of electrons: Breakdown of the energy diffusion model

    cond-mat.str-el 2026-04 unverdicted novelty 7.0

    Two-phonon scattering overtakes single-phonon scattering for electron energy relaxation above the Bloch-Grüneisen temperature, invalidating the energy-diffusion picture.