We use inelastic neutron scattering to show that superconductivity in electron-underdoped NaFe0.985Co0.015As induces a dispersive sharp resonance near Er1 = 3:25 meV and a broad dis- persionless mode at Er2 = 6 meV. However, similar measurements on o
verdoped superconducting NaFe0:955Co0:045As find only a single sharp resonance at Er = 7 meV. We connect these results with the observations of angle-resolved photoemission spectroscopy that the superconducting gaps in the electron Fermi pockets are anisotropic in the underdoped material but become isotropic in the overdoped case. Our analysis indicates that both the double neutron spin resonances and gap anisotropy originate from the orbital dependence of the superconducting pairing in the iron pnic- tides. Our discovery also shows the importance of the inelastic neutron scattering in detecting the multiorbital superconducting gap structures of iron pnictides.
In this work, we study the A$_{x}$Fe$_{2-y}$Se$_2$ (A=K, Rb) superconductors using angle-resolved photoemission spectroscopy. In the low temperature state, we observe an orbital-dependent renormalization for the bands near the Fermi level in which th
e dxy bands are heavily renormliazed compared to the dxz/dyz bands. Upon increasing temperature to above 150K, the system evolves into a state in which the dxy bands have diminished spectral weight while the dxz/dyz bands remain metallic. Combined with theoretical calculations, our observations can be consistently understood as a temperature induced crossover from a metallic state at low temperature to an orbital-selective Mott phase (OSMP) at high temperatures. Furthermore, the fact that the superconducting state of A$_{x}$Fe$_{2-y}$Se$_2$ is near the boundary of such an OSMP constraints the system to have sufficiently strong on-site Coulomb interactions and Hunds coupling, and hence highlight the non-trivial role of electron correlation in this family of iron superconductors.
In this paper we investigate the quantum phase transition from magnetic Bose glass to magnetic Bose-Einstein condensation induced by a magnetic field in NiCl2.4SC(NH2)2 (dichloro-tetrakis-thiourea-Nickel, or DTN), doped with Br (Br-DTN) or site dilut
ed. Quantum Monte Carlo simulations for the quantum phase transition of the model Hamiltonian for Br-DTN, as well as for site-diluted DTN, are consistent with conventional scaling at the quantum critical point and with a critical exponent z verifying the prediction z=d; moreover the correlation length exponent is found to be nu = 0.75(10) and the order parameter exponent to be beta = 0.95(10). We investigate the low-temperature thermodynamics at the quantum critical field of Br-DTN both numerically and experimentally, and extract the power-law behavior of the magnetization and of the specific heat. Our results for the exponents of the power laws, as well as previous results for the scaling of the critical temperature to magnetic ordering with the applied field, are incompatible with the conventional crossover-scaling Ansatz proposed by Fisher et al., [Phys. Rev. B 40, 546 (1989)], but they can all be reconciled within a phenomenological Ansatz in the presence of a dangerously irrelevant operator.
A microscopic model Hamiltonian for the ferroelectric field effect is introduced for the study of oxide heterostructures with ferroelectric components. The long-range Coulomb interaction is incorporated as an electrostatic potential, solved self-cons
istently together with the charge distribution. A generic double-exchange system is used as the conducting channel, epitaxially attached to the ferroelectric gate. The observed ferroelectric screening effect, namely the charge accumulation/depletion near the interface, is shown to drive interfacial phase transitions that give rise to robust magnetoelectric responses and bipolar resistive switching, in qualitative agreement with previous density functional theory calculations. The model can be easily adapted to other materials by modifying the Hamiltonian of the conducting channel, and it is useful in simulating ferroelectric field effect devices particularly those involving strongly correlated electronic components where ab-initio techniques are difficult to apply.
The low-temperature states of bosonic fluids exhibit fundamental quantum effects at the macroscopic scale: the best-known examples are Bose-Einstein condensation (BEC) and superfluidity, which have been tested experimentally in a variety of different
systems. When bosons are interacting, disorder can destroy condensation leading to a so-called Bose glass. This phase has been very elusive to experiments due to the absence of any broken symmetry and of a finite energy gap in the spectrum. Here we report the observation of a Bose glass of field-induced magnetic quasiparticles in a doped quantum magnet (Br-doped dichloro-tetrakis-thiourea-Nickel, DTN). The physics of DTN in a magnetic field is equivalent to that of a lattice gas of bosons in the grand-canonical ensemble; Br-doping introduces disorder in the hoppings and interaction strengths, leading to localization of the bosons into a Bose glass down to zero field, where it acquires the nature of an incompressible Mott glass. The transition from the Bose glass (corresponding to a gapless spin liquid) to the BEC (corresponding to a magnetically ordered phase) is marked by a novel, universal exponent governing the scaling on the critical temperature with the applied field, in excellent agreement with theoretical predictions. Our study represents the first, quantitative account of the universal features of disordered bosons in the grand-canonical ensemble.
The modulation of charge density and spin order in (LaMnO$_3$)$_{2n}$/(SrMnO$_3$)$_n$ ($n$=1-4) superlattices is studied via Monte Carlo simulations of the double-exchange model. G-type antiferromagnetic barriers in the SrMnO$_{3}$ regions with low c
harge density are found to separate ferromagnetic LaMnO$_{3}$ layers with high charge density. The recently experimentally observed metal-insulator transition with increasing $n$ is reproduced in our studies, and $n=3$ is found to be the critical value.
The origin of the spiral spin-order in perovskite multiferroic manganites $R$MnO$_{3}$ ($RE=$ Tb or Dy) is here investigated using a two $e_{rm g}$-orbitals double-exchange model. Our main result is that the experimentally observed spiral phase can b
e stabilized by introducing a relatively weak next-nearest-neighbor superexchange coupling ($sim10%$ of the nearest-neighbor superexchange). Moreover, the Jahn-Teller lattice distortion is also shown to be essential to obtain a realistic spiral period. Supporting our conclusions, the generic phase diagram of undoped perovskite manganites is obtained using Monte Carlo simulations, showing phase transitions from the A-type antiferromagnet, to the spiral phase, and finally to the E-type antiferromagnet, with decreasing size of the $R$ ions. These results are qualitatively explained by the enhanced relative intensity of the superexchanges.
Most previous investigations have shown that the surface of a ferromagnetic material may have antiferromagnetic tendencies. However, experimentally the opposite effect has been recently observed: ferromagnetism appears in some nano-sized manganites w
ith a composition such that the antiferromagnetic charge-ordered CE state is observed in the bulk. A possible origin is the development of ferromagnetic correlations at the surface of these small systems. To clarify these puzzling experimental observations, we have studied the two-orbital double-exchange model near half-doping n=0.5, using open boundary conditions to simulate the surface of either bulk or nano-sized manganites. Considering the enhancement of surface charge density due to a possible AO termination (A = trivalent/divalent ion composite, O = oxygen), an unexpected surface phase-separated state emerges when the model is studied using Monte Carlo techniques on small clusters. This tendency suppresses the CE charge ordering and produces a weak ferromagnetic signal that could explain the experimental observations.
