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Analogy Between the “Hidden Order” and the Orbital Antiferromagnetism in URu2xFexSi2

H.-H. Kung, S. Ran, N. Kanchanavatee, V. Krapivin, A. Lee, J. A. Mydosh, K. Haule, M. B. Maple, and G. Blumberg
Phys. Rev. Lett. 117, 227601 – Published 22 November 2016
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Abstract

We study URu2xFexSi2, in which two types of staggered phases compete at low temperature as the iron concentration x is varied: the nonmagnetic “hidden order” (HO) phase below the critical concentration xc, and unconventional antiferromagnetic (AFM) phase above xc. By using polarization resolved Raman spectroscopy, we detect a collective mode of pseudovectorlike A2g symmetry whose energy continuously evolves with increasing x; it monotonically decreases in the HO phase until it vanishes at x=xc, and then reappears with increasing energy in the AFM phase. The mode’s evolution provides direct evidence for a unified order parameter for both nonmagnetic and magnetic phases arising from the orbital degrees-of-freedom of the uranium-5f electrons.

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  • Received 29 August 2016

DOI:https://doi.org/10.1103/PhysRevLett.117.227601

© 2016 American Physical Society

Physics Subject Headings (PhySH)

Condensed Matter, Materials & Applied Physics

Authors & Affiliations

H.-H. Kung1,*, S. Ran2,3, N. Kanchanavatee2,3, V. Krapivin1, A. Lee1, J. A. Mydosh4, K. Haule1, M. B. Maple2,3, and G. Blumberg1,5,†

  • 1Department of Physics & Astronomy, Rutgers University, Piscataway, New Jersey 08854, USA
  • 2Department of Physics, University of California San Diego, La Jolla, California 92093, USA
  • 3Center for Advanced Nanoscience, University of California San Diego, La Jolla, California 92093, USA
  • 4Kamerlingh Onnes Laboratory, Leiden University, 2300 RA Leiden, The Netherlands
  • 5National Institute of Chemical Physics and Biophysics, 12618 Tallinn, Estonia

  • *hk458@physics.rutgers.edu
  • girsh@physics.rutgers.edu

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Vol. 117, Iss. 22 — 25 November 2016

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Images

  • Figure 1
    Figure 1

    (a) The upper panel shows the phase diagram of URu2Si2 system, where the black lines show the phase boundaries. The measurements on the iron substituted URu2xFexSi2 crystals from neutron diffraction [22] (blue triangle), electrical resistivity [2] (green square), magnetic susceptibility [2] (purple triangle), and heat capacity [3] (yellow diamond), are overlaid with the neutron diffraction results for URu2Si2 under hydrostatic pressure [4] (open square) to show the similarity between the two tuning parameters. The lower panel shows the dependence of the A2g collective mode energy on the Fe concentration, x [Fig. 2]. At the critical concentration, x=0.1, the mode maximum is below the accessible energy cutoff. Therefore, the data point is placed at zero energy, with the error bar reflecting the instrumental cutoff. (b)–(g) Schematics of the Ginzburg-Landau free energy in Eq. (1) at various special points in the phase diagram [solid gray circles in (a)]. ψHO and ψAFM are the real and imaginary part of the hexadecapole order parameter, respectively [26, 27].

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  • Figure 2
    Figure 2

    Low temperature Raman response in the A2g symmetry channel, χA2g′′(ω,T) [28]. The upper panels show intensity plots, where the intensities are color coded in logarithmic scale. The lower panels show the spectra at about half the transition temperature to emphasize the collective mode, where the error bars represent one standard deviation, and the red solid lines are guides to the eye. The energies of this mode as function of the Fe concentration x are shown in Fig. 1.

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  • Figure 3
    Figure 3

    The static Raman susceptibility in the A2g symmetry channel (open squares) χA2g(0,T), compared with the magnetic susceptibility with field applied along the c axis [3] (solid line).

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  • Figure 4
    Figure 4

    The crystal structure of URu2xFexSi2 in (a) the HO and (b) the LMAF phases. Illustrations capturing the symmetries of the charge distributions of the ground state wave functions are placed at the uranium atomic sites. On the right are illustrations showing the in-plane structures of the wave functions. In the HO phase, the crystal field state with the lowest energy has A2g symmetry with 8 nodal lines, |A2g, which mixes with the first excited state with A1g symmetry, |A1g, to form the local wave functions in the HO phase, |HO±cosθ|A2g±sinθ|A1g. In the LMAF phase, the ordering of the crystal field states switches, and the new wave functions in the LMAF phase are, |AFM±cosθ|A1g±isinθ|A2g. Here, θarcsin(V/ω0) and θarcsin(V/ω0), respectively. ω0 is the splitting between the lowest lying crystal field states in the minimal model. V and V are the order parameter strength in the HO and LMAF phases, respectively.

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