77 Se and 87 Rb nuclear magnetic resonance (NMR) experiments on Rb 0.74 Fe 1.6 Se 2 reveal clearly distinct spectra originating from a majority antiferromagnetic (AF) and a minority metallic-superconducting (SC) phase. The very narrow NMR line of the SC phase evidences the absence of Fe vacancies and any trace of AF order. The Rb content of the SC phase is deduced from intensity measurements identifying Rb 0.3(1) Fe 2 Se 2 as the actual composition of the SC fraction. The resulting estimate of 0.15 electrons/Fe brings this class of superconductors 245 family closer to the other Fe-based superconductor families.DOI:
We have studied the low-energy spin-excitation spectrum of the single-crystalline Rb 2 Fe 4 Se 5 superconductor (T c = 32 K) by means of inelastic neutron scattering. In the superconducting state, we observe a magnetic resonant mode centered at an energy of hω res = 14 meV and at the (0.5 0.25 0.5) wave vector (unfolded Fe-sublattice notation), which differs from the ones characterizing magnetic resonant modes in other iron-based superconductors. Our finding suggests that the 245-iron-selenides are unconventional superconductors with a sign-changing order parameter, in which bulk superconductivity coexists with the 5 × 5 magnetic superstructure. The estimated ratios of hω res /k B T c ≈ 5.1 ± 0.4 and hω res /2∆ ≈ 0.7 ± 0.1, where ∆ is the superconducting gap, indicate moderate pairing strength in this compound, similar to that in optimally doped 1111-and 122-pnictides. PACS numbers: 74.70.Xa, 74.25.Ha, 78.70.Nx, 74.20.Rp Soon after the discovery of arsenic-free iron-selenide superconductors A 2 Fe 4 Se 5 (A = K, Rb, Cs), also known as 245-compounds [1], their unprecedented physical properties came to light, such as the coexistence of high-T c superconductivity with strong antiferromagnetism [2,3]. The pairing mechanism and the symmetry of the superconducting (SC) order parameter in this family of compounds still remain among the major open questions. In the majority of other Fe-based superconductors, it is widely accepted that the strong nesting between the holelike Fermi surface (FS) at the Brilliouin zone (BZ) center and electronlike FS at the BZ boundary leads to the sign-changing s-wave (s ± -wave) pairing symmetry [4]. This scenario has been supported by different experimental methods, such as angle-resolved photoemission spectroscopy (ARPES) [5], quasi-particle interference [6], and inelastic neutron scattering (INS) [7,8].On the other hand, recent theoretical calculations [9] and ARPES experiments [10, 11] on the 245-system revealed the absence of holelike FS at the BZ center in the electronic structure, implying that the nesting between the hole-and electronlike FS sheets is no longer present. Hence, several theoretical studies proposed alternative pairing instabilities, such as d-wave or another type of s ± -wave symmetry with sign-changing order parameter between bonding and antibonding states [12][13][14]. As a hallmark of sign-changing SC order parameter, several authors theoretically predicted a resonant mode in the magnetic excitation spectrum below the SC transition, yet its precise position in momentum space still remains controversial [12,13].A major complication in treating the 245-compounds theoretically arises from the presence of a crystallographic superstructure of Fe vacancies that has been consistently reported both from x-ray and neutron diffraction experiments [15]. This 5 × 5 superstructure is closely related to the static antiferromagnetic (AFM) order persisting up to the Néel temperature, T N ≈ 540 K [16]. Although most of the existing band structure calculations have so far negle...
Platelet-like single crystals of the Ca(Fe 1-x Co x ) 2 As 2 series having lateral dimensions up to 15 mm and thickness up to 0.5 mm were obtained from the high temperature solution growth technique using Sn flux. Upon Co doping, the c-axis of the tetragonal unit cell decreases, while the a-axis shows a less significant variation. Pristine CaFe 2 As 2 shows a combined spin-density-wave and structural transition near T = 166 K which gradually shifts to lower temperatures and splits with increasing Co-doping. Both transitions terminate abruptly at a critical Co-concentration of x c = 0.075. For x ≥ 0.05, superconductivity appears at low temperatures with a maximum transition temperature T C of around 20 K. The superconducting volume fraction increases with Co concentration up to x = 0.09 followed by a gradual decrease with further increase of the doping level. The electronic phase diagram of Ca(Fe 1-x Co x ) 2 As 2 (0 ≤ x ≤ 0.2) series is constructed from the magnetization and electric resistivity data. We show that the low-temperature superconducting properties of Co-doped CaFe 2 As 2 differ considerably from those of BaFe 2 As 2 reported previously. These differences seem to be related to the extreme pressure sensitivity of CaFe 2 As 2 relative to its Ba counterpart.
Resonant magnetic excitations are recognised as hallmarks of unconventional superconductivity in copper oxides, iron pnictides and heavy-fermion compounds. model calculations have related these modes to the microscopic properties of the pair wave function, but the mechanisms of their formation are still debated. Here we report the discovery of a similar resonant mode in the non-superconducting antiferromagnetic heavy-fermion metal CeB 6 . unlike conventional magnons, the mode is non-dispersive and is sharply peaked around a wave vector separate from those characterising the antiferromagnetic order. It is likely associated with a co-existing order parameter of the unusual antiferro-quadrupolar phase of CeB 6 , which has long remained hidden to neutron-scattering probes. The mode energy increases continuously below the onset temperature for antiferromagnetism, in parallel to the opening of a nearly isotropic spin gap throughout the Brillouin zone. These attributes are similar to those of the resonant modes in unconventional superconductors. This unexpected commonality between the two disparate ground states indicates the dominance of itinerant spin dynamics in the ordered lowtemperature phases of CeB 6 and throws new light on the interplay between antiferromagnetism, superconductivity and 'hidden' order parameters in correlated-electron materials.
Inelastic neutron scattering is employed to study the reciprocal-space structure and dispersion of magnetic excitations in the normal and superconducting states of single-crystalline Rb 0.8 Fe 1.6 Se 2 . We show that the recently discovered magnetic resonant mode in this compound has a quasi-two-dimensional character, similar to overdoped iron-pnictide superconductors. Moreover, it has a rich in-plane structure that is dominated by four elliptical peaks, symmetrically surrounding the Brillouin zone corner, without 5 × 5 reconstruction. We also present evidence for the dispersion of the resonance peak, as its position in momentum space depends on energy. Comparison of our findings with the results of band structure calculations provides strong support for the itinerant origin of the observed signal. It can be traced back to the nesting of electronlike Fermi pockets in the doped metallic phase of the sample in the absence of iron-vacancy ordering. [3,6], which is at the same time the optimal composition for the ordering of Fe vacancies into a 5 × 5 superstructure, grouping the occupied iron sites in plaquettes of four ferromagnetically aligned moments. On the one hand, experiments [3,7,8] and band structure calculations [9,10] suggest this superstructure to be insulating. On the other hand, angle-resolved photoelectron spectroscopy (ARPES) revealed a Fermi surface (FS) dominated by a large electron pocket at the M point [11,12]. Recent reports reconcile these seemingly contradictory findings by the observation of several coexisting phases, seen in transmission electron microscopy (TEM) [13][14][15][16] , TEM measurements suggested that the second phase is an iron-vacancy disordered state [13,14]. The phase separation scenario clearly needs more clarification in terms of the structure and stoichiometry of the SC phase for a consistent understanding of these observations.In iron pnictides, it is established that the SC order parameter changes its sign between the hole-and electronlike sheets of the FS [22][23][24]. Despite the absence or strong reduction of the hole Fermi pocket in iron selenides [25], different kinds of a sign-changing gap have also been suggested [26][27][28]. The recent finding of a magnetic resonant mode in the low-energy spin-excitation spectrum of [13,16,32]. However, to the best of our knowledge, first-principles calculations of the spin-excitation spectrum are not yet available for any of these alternative scenarios.To be able to differentiate between the mentioned possibilities and thus try to verify the origin of the spin-excitation spectrum, we have performed a detailed study of the reciprocal-space structure and the dispersion of the previously reported resonant mode. We show that the resonant magnetic excitations in the SC state of Rb x Fe 2− y Se 2 are quasi-two-dimensional (2D) and exhibit a complex in-plane pattern, dominated by four elliptical peaks that symmetrically surround the corner of the unfolded Brillouin zone (BZ) [33]. This result is consistent with the dynamic spin susc...
Heavy-fermion metals exhibit a plethora of low-temperature ordering phenomena . Among these are the so-called hidden-order phases that, in contrast to conventional magnetic order, are invisible to standard neutron diffraction experiments. One of the structurally most simple hidden-order compounds, CeB6, has been intensively studied for an elusive phase that was attributed to the antiferroquadrupolar ordering of cerium-4f moments . As the ground state of CeB6 is characterized by a more conventional antiferromagnetic (AFM) order , the low-temperature physics of this system has generally been assumed to be governed solely by AFM interactions between the dipolar and multipolar Ce moments . Here we overturn this established picture by observing an intense ferromagnetic (FM) low-energy collective mode that dominates the magnetic excitation spectrum of CeB6. Inelastic neutron-scattering data reveal that the intensity of this FM excitation significantly exceeds that of conventional spin-wave magnons emanating from the AFM wavevectors, thus placing CeB6 much closer to a FM instability than previously anticipated. This propensity for ferromagnetism may account for much of the unexplained behaviour of CeB6, and should lead to a re-examination of existing theories that have so far largely neglected the role of FM interactions.
We investigate magnetic ordering in metallic Ba(Fe 1−x Mn x ) 2 As 2 and discuss the unusual magnetic phase, which was recently discovered for Mn concentrations x > 10%. We argue that it can be understood as a Griffiths-type phase that forms above the quantum critical point associated with the suppression of the stripe-antiferromagnetic spin-density-wave (SDW) order in BaFe 2 As 2 by the randomly introduced localized Mn moments acting as strong magnetic impurities. While the SDW transition at x = 0, 2.5% and 5% remains equally sharp, in the x = 12% sample we observe an abrupt smearing of the antiferromagnetic transition in temperature and a considerable suppression of the spin gap in the magnetic excitation spectrum. According to our muon-spin-relaxation, nuclear magnetic resonance and neutron-scattering data, antiferromagnetically ordered rare regions start forming in the x = 12% sample significantly above the Néel temperature of the parent compound. Upon cooling, their volume grows continuously, leading to an increase in the magnetic Bragg intensity and to the gradual opening of a partial spin gap in the magnetic excitation spectrum. Using neutron Larmor diffraction, we also demonstrate that the magnetically ordered volume is characterized by a finite orthorhombic distortion, which could not be resolved in previous diffraction studies most probably due to its coexistence with the tetragonal phase and a microstrain-induced broadening of the Bragg reflections. We argue that Ba(Fe 1−x Mn x ) 2 As 2 could represent an interesting model spin-glass system, in which localized magnetic moments are randomly embedded into a SDW metal with Fermi surface nesting.
Cerium hexaboride is a cubic f-electron heavy-fermion compound that displays a rich array of low-temperature magnetic ordering phenomena which have been the subject of investigation for more than 50 years. Its complex behaviour is the result of competing interactions, with both itinerant and local electrons playing important roles. Investigating this material has proven to be a substantial challenge, in particular because of the appearance of a 'magnetically hidden order' phase, which remained elusive to neutron-scattering investigations for many years. It was not until the development of modern x-ray scattering techniques that the long suspected multipolar origin of this phase was confirmed. Doping with non-magnetic lanthanum dilutes the magnetic cerium sublattice and reduces the f-electron count, bringing about substantial changes to the ground state with the emergence of new phases and quantum critical phenomena. To this day, Ce1-x La x B6 and its related compounds remain a subject of intense interest. Despite the substantial progress in understanding their behaviour, they continue to reveal new and unexplained physical phenomena. Here we present a review of the accumulated body of knowledge on this family of materials in order to provide a firm standpoint for future investigations.
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