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Light-induced nonequilibrium response of the superconducting cuprate La$_{2-x}$Sr$_{x}$CuO$_4$

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 Added by Hiroaki Niwa
 Publication date 2019
  fields Physics
and research's language is English




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We report the dynamics of the cuprate superconductor La$_{2-x}$Sr$_{x}$CuO$_4$ ($x = 0.14$) after intense photoexcitation utilizing near-infrared (800 nm) optical pump-terahertz probe spectroscopy. In the superconducting state at 5 K, we observed a redshift of the Josephson plasma resonance that sustains for hundreds of picoseconds after the photoexcitation, indicating the destruction of the $c$-axis superconducting coherence. We show that the metastable spectral features can be described by the photoinduced surface heating of the sample. We also demonstrate that the conventional analysis used to extract the spectra of the photoexcited surface region can give rise to artifacts in the nonequilibrium response.

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153 - J. Chang , J. S. White , M. Laver 2012
We use small angle neutron scattering to study the superconducting vortex lattice in La$_{2-x}$Sr$_x$CuO$_4$ as a function of doping and magnetic field. We show that near optimally doping the vortex lattice coordination and the superconducting coherence length $xi$ are controlled by a van-Hove singularity crossing the Fermi level near the Brillouin zone boundary. The vortex lattice properties change dramatically as a spin-density-wave instability is approached upon underdoping. The Bragg glass paradigm provides a good description of this regime and suggests that SDW order acts as a novel source of disorder on the vortex lattice.
We have performed a temperature-dependent angle-integrated photoemission study of lightly-doped to heavily-overdoped La$_{2-x}$Sr$_{x}$CuO$_4$ and oxygen-doped La$_2$CuO$_{4.10}$. We found that both the magnitude $Delta$* of the (small) pseudogap and the temperature textit{T}* at which the pseudogap is opened increases with decreasing hole concentration, consistent with previous studies. On the other hand, the superconducting gap $Delta_{sc}$ was found to remain small for decreasing hole concentration. The results can be explained if the superconducting gap opens only on the Fermi arc around the nodal (0,0)-($pi,pi$) direction while the pseudogap opens around $sim$($pi$, 0).
We investigated transient optical responses in an optimally-doped high-Tc superconductor La2-xSrxCuO4 (x=0.15) by using 800-nm optical pump and terahertz probe spectroscopy. With increasing the photoexcitation intensities, the Josephson plasma resonance shows a gradual redshift, indicating the suppression of superconductivity by the photoexcitation. With further increasing the photoexcitation intensities, a new longitudinal mode in the loss function spectrum appears and grows from the high energy side, accompanied by a new transverse mode as manifested in the conductivity spectrum. The observed spectra are described by the multilayer model with alternating interlayer Josephson couplings. The new longitudinal and transverse modes sustain much longer than several hundred picoseconds after the photoexcitation, indicating that the new metastable phase with possessing alternating interlayer Josephson couplings is induced by the strong photoexcitation.
We present results of inelastic light scattering experiments on single-crystalline La$_{2-x}$Sr$_{x}$CuO$_4$ in the doping range $0.00 le x=p le 0.30$ and Tl$_2$Ba$_2$CuO$_{6+delta}$ at $p=0.20$ and $p=0.24$. The main emphasis is placed on the response of electronic excitations in the antiferromagnetic phase, in the pseudogap range, in the superconducting state, and in the essentially normal metallic state at $x ge 0.26$, where no superconductivity could be observed. In most of the cases we compare B$_{1g}$ and B$_{2g}$ spectra which project out electronic properties close to $(pi,0)$ and $(pi/2, pi/2)$, respectively. In the channel of electron-hole excitations we find universal behavior in B$_{2g}$ symmetry as long as the material exhibits superconductivity at low temperature. In contrast, there is a strong doping dependence in B$_{1g}$ symmetry: (i) In the doping range $0.20 le p le 0.25$ we observe rapid changes of shape and temperature dependence of the spectra. (ii) In La$_{2-x}$Sr$_{x}$CuO$_4$ new structures appear for $x < 0.13$ which are superposed on the electron-hole continuum. The temperature dependence as well as model calculations support an interpretation in terms of charge-ordering fluctuations. For $x le 0.05$ the response from fluctuations disappears at B$_{1g}$ and appears at B$_{2g}$ symmetry in full agreement with the orientation change of stripes found by neutron scattering. While, with a grain of salt, the particle-hole continuum is universal for all cuprates the response from fluctuating charge order in the range $0.05 le p < 0.16$ is so far found only in La$_{2-x}$Sr$_{x}$CuO$_4$. We conclude that La$_{2-x}$Sr$_{x}$CuO$_4$ is close to static charge order and, for this reason, may have a suppressed $T_c$.
We use angle-resolved photoemission spectroscopy to study the doping evolution of infinite-layer Sr$_{1-x}$La$_{x}$CuO$_{2}$ thin films grown by molecular-beam epitaxy. At low doping, the material exhibits a dispersive lower Hubbard band typical of the superconducting cuprate parent compounds. As carriers are added to the system, a continuous evolution from charge-transfer insulator to superconductor is observed, with the initial lower Hubbard band pinned well below the Fermi level and the development of a coherent low-energy band with electron doping. This two-component spectral function emphasizes the important role that strong local correlations play even at relatively high doping levels. Electron diffraction probes reveal a ${p(2times2)}$ surface reconstruction of the material at low doping levels. Using a number of simple assumptions, we develop a model of this reconstruction based on the polar nature of the infinite-layer structure. Finally, we provide evidence for a thickness-controlled transition in ultrathin films of SrCuO$_2$ grown on nonpolar SrTiO$_3$, highlighting the diverse structural changes that can occur in polar complex oxide thin films.
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