Abstract
Exotic electronic states resulting from entangled spin and orbital degrees of freedom are hallmarks of strongly correlated f-electron systems. A spectacular example is the so-called hidden-order (HO) phase transition1 in the heavy-electron metal URu2Si2, which is characterized by the huge amount of entropy lost at THO=17.5āK (refs 2, 3). However, no evidence of magnetic/structural phase transition has been found below THO so far. The origin of the HO phase transition has been a long-standing mystery in condensed-matter physics. Here, on the basis of a first-principles theoretical approach, we examine the complete set of multipole correlations allowed in this material. The results uncover that the HO parameter is a rank-5 multipole (dotriacontapole) order with nematic Eā symmetry, which exhibits staggered pseudospin moments along the [110] direction. This naturally provides comprehensive explanations of all key features in the HO phase including anisotropic magnetic excitations, the nearly degenerate antiferromagnetic-ordered state and spontaneous rotational-symmetry breaking.
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In the rare-earth and actinide compounds, f electrons behave like well-localized moments at high temperatures. As the temperature is lowered, f electrons begin to delocalize owing to the hybridization with conduction electron wavefunctions. At yet lower temperatures the f electrons become itinerant, forming a narrow conduction band with heavy effective electron mass, which is largely enhanced from the free-electron mass. Notable many-body effects within the narrow band lead to a plethora of fascinating physical phenomena including multipole order, quantum phase transition and unconventional superconductivity. Among them, perhaps the appearance of a HO state in URu2Si2 is one of the most mysterious phenomena. Identification of the microscopic order parameter and mechanism that drives the HO transition continues to be a central question in strongly correlated f-electron systems1.
There are several unique features that seem to be clues for understanding the HO in URu2Si2. In the paramagnetic state above THO, the magnetic susceptibility exhibits the Ising-like anisotropy2,4. In the HO state below THO, an electronic excitation gap is formed on a large portion of the Fermi surface5,6 (FS) and most of the carriers disappear7,8. Closely related to this, the gap formation also occurs in the magnetic excitation spectra at commensurate and incommensurate wave numbers, QC=(0ā0ā1) and QIC=(0.6ā0ā0), respectively, as revealed by the neutron inelastic scattering9,10,11. The HO ground state changes to the large-moment antiferromagnetic (AFM) state with the ordering vector QC on applying hydrostatic pressure12,13, but the FS has a striking similarity between these different phases14,15, implying that the HO is nearly degenerate with the AFM order. The magnetic torque measurements reveal the nematicity, which breaks the in-plane rotational (tetragonal) symmetry in the HO16. The challenge for the theory has been to identify the order parameter that explains all of the above key features.
The theories that have been proposed to describe the HO state can be divided into two prevailing approaches; one is based on the localized 5f-electron model17,18,19,20,21,22,23 and the other the itinerant one24,25,26,27,28,29. Recent angle-resolved photoemission spectroscopy results clearly demonstrate that all 5f electrons are itinerant30 and the crystalline electric field, which is a signature of the localized nature, has never been observed. Moreover, the nuclear magnetic resonance measurements31 show a formation of the coherent heavy-electron state well above THO. Therefore, it is natural to discuss the electronic structure on the basis of the itinerant picture. However, reliable calculation of the physical quantities by taking into account the complicated band structure is a difficult task. For this purpose, we use a state-of-the-art ab initio downfolding (Supplementary Section SI) and dissect the electronic structure obtained from the density-functional theory (DFT) calculations. The obtained tight-binding Hamiltonian is constructed from 56 orbitals of U 5f, U 6d, Ru 4d and Si 3p. Introducing the on-site Coulomb interactions between 5f electrons, we obtain a realistic itinerant model, that is, a 56-band Anderson-lattice model including the spināorbit interaction. On the basis of this realistic model Hamiltonian, magnetic and multipole correlations are analysed by the random-phase approximation (RPA) and beyond. To account for the mass renormalization effect in the Fermi-liquid theory, the energy and temperature scale is reduced by a factor of 10 throughout this study2,14,15, which makes comparisons to the experiments straightforward.
Figure 1 shows the paramagnetic FS and the band structure near the Fermi level, respectively. The energy bands crossing the Fermi level have mainly the total angular momentum j=5/2 multiplet of U 5f. Each jz component of j=5/2 multiplet is coloured by weight. It turns out that each separated FS is mainly composed of a rather specific jz component without large mixing, except for the outer FS around the Z point (Fig. 1). Such a jz component map is quite useful in that we are able to capture valuable information such as which parts of the FS play an essential role for the HO formation. Indeed, the disentanglement of FS orbital characters has also been an important theoretical advance to understand the electronic properties in iron-pnictide superconductors32.
First we discuss the RPA analysis of rank-1 (dipole) correlation, which is the conventional static magnetic correlation. The regime with jz=Ā±5/2, shown in red, in the outer FS around the Z point is well nested with the outer FS around the Ī point by the vector QC, as indicated by the arrow in Fig. 1 (ref. 33). This nesting gives rise to a sharp peak of the correlation parallel to the c axis (dipole Jz) at Z (0 0 1) shown in Fig. 2a. Another salient feature is the hump structure at around (0.6 0 0) and the equivalent points, whose Q-vectors coincide with QIC. We point out that these peak and hump structures in the paramagnetic phase are directly related to the magnetic excitation gap at QC and QIC in the HO phase11 because the gap opening occurs at the nested parts of the FS. We also note that the in-plane magnetic correlations, Jx and Jy, are not enhanced in contrast to Jz (Fig. 2b), which is also consistent with the Ising-like magnetic susceptibility2,4 and polarized-neutron measurements10.
Next we examine the higher-rank multipole correlations. According to the group theory, there are 36 multipole moments up to the fifth rank in j=5/2 subspace (Supplementary Table S1). Figure 2cāf shows the correlations between the basis functions belonging to rank 2 (quadrupole), 3 (octupole), 4 (hexadecapole) and 5 (dotriacontapole), respectively. What is remarkable is that as in the case for the dipole Jz, the QC correlation at the Z point is strongly enhanced in some cases such as O20 (rank 2), Hx(y)b (rank 4), D4 (rank 5) and so on. Generally, these bases are mixed in the tetragonal symmetry, as shown by finite off-diagonal terms (red lines). The multipole correlations obtained by the diagonalization are depicted in Fig. 2g, in which each correlation at QC is classified by the irreducible representations and the dominant component is denoted in parentheses (Supplementary Section SIII). At low temperatures, A2ā(Jz), Eā(Dx(y)) and A1ā(D4) symmetries exhibit the first, second and third strongest enhancement. The first and the last two correspond to the AFM and dotriacontapole states, respectively. Within the RPA, the AFM state always overcomes the dotriacontapole states. To go beyond the RPA, we consider a staggered particleāhole pairing (generalized multipole orders at the Z point) mediated by the RPA fluctuation from an analogy with unconventional superconductivity (Supplementary Section SIV). This corresponds to the inclusion of the modeāmode coupling. From an analogue of the superconducting gap equation for the staggered ordering, we calculate the maximum eigenvalue Ī». The corresponding multipole correlation increases proportionally to ā¼1/(1āĪ»), and then Ī»=1 provides the transition temperature. The temperature dependence of Ī» of each symmetry is shown in Fig. 3a. As the temperature is lowered, Ī» of Eā(Dx(y)) is most strongly enhanced and the condition Ī»=1 is fulfilled at finite temperature, indicating a phase transition to the Eā(Dx(y))state. We emphasize that Eā(Dx(y)) symmetry breaks the in-plane four-fold symmetry, which naturally accounts for the nematicity observed in the magnetic torque results16,34. In addition, the Eā(Dx(y)) state breaks the time-reversal symmetry, which is consistent with the nuclear magnetic resonance measurements31. These lead us to conclude that the HO is Eā(Dx(y)) dotriacontapole order.
The present calculations also reproduce well other key features of the HO, that is, near degeneracy of the HO and AFM states and the anisotropic temperature dependence of the uniform susceptibility. Figure 3a demonstrates that Ī» of Eā(Dx(y)) is very close to that of A2ā(Jz). This indicates that both states are nearly degenerate and a small perturbation can change the HO to the AFM state. Indeed, we can construct a phase diagram by tuning the interactions (Supplementary Fig. S4), which is consistent with the pressureātemperature phase diagram (Fig. 3b). The temperature dependence of the uniform susceptibility Ļc(0) parallel to the c axis exhibits a broad maximum at around 40āK, whereas Ļab(0) perpendicular to the c axis is smaller and nearly temperature independent (Fig. 3c), in good agreement with experiments2,4. The low-temperature decrease of Ļc(0) arises from the deep dip structure in the density of states near the Fermi level (Supplementary Fig. S1b). The Ising-like susceptibility including its temperature dependence has been discussed in terms of the crystalline electric field excitations of the localized 5f electrons so far. However, the present results demonstrate that the susceptibility can be well accounted for by the itinerant scenario.
Why is such a high-rank multipole state (rank 5) with Eā(Dx(y)) symmetry realized in URu2Si2? Similar high-rank multipole states have been proposed already; a rank-4 A2+ state by the DFT+DMFT (dynamical mean field theory) method20, and a rank-5 A2ā state by the DFT+U method27. However, these states obtained in the strong correlation limit are inconsistent with the nematic behaviour34. Detailed comparisons with other proposed HO parameters are listed in Supplementary Table S2. In our approach from the itinerant limit, the FS nesting with the QC vector plays an essential role in the multipole fluctuations. What is crucially important is that the FS regions connected by this QC are dominated by the Ā±5/2 components, as shown in Fig. 1. In this situation, we can consider a subspace consisting of only two components jz=5/2 and ā5/2, which allows us to map jz=Ā±5/2 to pseudospin ā and ā. Then the dipole Jz is described by the Pauli matrix Ļz spanned in the pseudospin space, as it has only diagonal elements corresponding to . In the same way, Dx(y) is given by Ļx(y), representing off-diagonal components describing the transition (Supplementary Section SV), which accompanies the angular momentum change of 5ā allowed only in rank 5. In this pseudospin space, the staggered Jz state corresponds to the NĆ©el order along the caxis. On the other hand, the Dx(y) state corresponds to the in-plane order breaking the rotational symmetry, where in-plane pseudospin moments are antiferromagnetically coupled along the c axis (Fig. 3d). Thus, the pressure-induced first-order transition from the HO to AFM state can be explained by the pseudospin staggered moment flip from the in-plane to the out-of-plane direction. The experimentally observed nematicity along the [110] direction corresponds to the linear combination of the two-fold degenerate Dx and Dy. The HO parameter is then represented by
where fk Ī± is an annihilation operator for an f electron with momentum k and pseudospin Ī±. It should be noted that under in-plane 180Ā° rotation, the pseudospins change their direction, which discriminates this state from a nematic phase in the strict sense. However, its staggered nature leads to the two-fold nematic symmetry of the bulk susceptibility as observed experimentally.
Figure 4a shows the FS in the HO and AFM states, which is calculated by applying the effective multipole field so as to open the gap of 4āmeV observed by scanning tunnelling microscopy5,6. The lattice doubling in the AFM phase with QC also occurs in the HO phase. Most of the FS having jz=Ā±5/2 components disappears as a result of the gap opening at the nested parts of the paramagnetic FS. Around the Ī-point, small electron and large hole (Ī±) pockets, the FS with a cage-like structure and four electron pockets (Ī²) exist. The FS in the HO phase bears a striking resemblance to that in the AFM state (Supplementary Section SVII), consistent with the quantum oscillation measurements. However, the broken four-fold symmetry in the HO state can be seen clearly in the FS with a cage-like structure (Fig. 4b), in sharp contrast to the AFM state.
The present approach based on the first-principles calculation is able to give a comprehensive explanation to the problem of HO, which has been a quarter-century mystery. Why has the HO been hidden for a long time? The reason is that in conventional experimental techniques, such as resonant X-ray and neutron measurements, extremely high-resolution measurements should be required for the direct detection of the high-rank multipole order parameter. We also point out that the present rank-5 order induces a very tiny but finite in-plane dipole moment belonging to the same symmetry Eā, which is roughly estimated as 10ā2ā10ā3Ī¼B(Supplementary Section SVI). The detection of such a tiny moment remains a future issue. The itinerant multipole ordering with nematicity revealed in the present study is a new type of electron ordering, which is expected to be ubiquitously present in strongly correlated electron systems when spin and orbital degrees of freedom are entangled.
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Acknowledgements
We thank K. Ueda, K. Haule, G. Kotliar, M. Sigrist and T. M. Rice for helpful discussions and suggestions. This work was supported by a Grant-in-Aid for the Global COE programme āThe Next Generation of Physics, Spun from Universality and Emergenceā, a Grant-in-Aid for Scientific Research on Innovative Areas āHeavy Electronsā (20102002, 20102006) from MEXT, and KAKENHI from JSPS.
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H.I. and R.A. developed a methodology for the DFT+RPA and beyond. M-T.S. analysed the fermiology in some ordered states. T.T. provided group-theoretical arguments of multipoles. H.I., T.S. and Y.M. wrote the text. All authors contributed to critical discussion of the physical interpretation of the results.
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Ikeda, H., Suzuki, MT., Arita, R. et al. Emergent rank-5 nematic order in URu2Si2. Nature Phys 8, 528ā533 (2012). https://doi.org/10.1038/nphys2330
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DOI: https://doi.org/10.1038/nphys2330
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