Local breaking of four-fold rotational symmetry by short-range magnetic order in heavily overdoped Ba(Fe1−x_{1-x}Cux_{x})2_{2}As2_{2}

We investigate Cu-doped Ba(Fe$_{1-x}$Cu$_x$)$_2$As$_2$ with transport, magnetic susceptibility, and elastic neutron scattering measurements. In the heavily Cu-doped regime where long-range stripe-type antiferromagnetic order in BaFe$_2$As$_2$ is suppressed, Ba(Fe$_{1-x}$Cu$_x$)$_2$As$_2$ (0.145 $\leq x \leq$ 0.553) samples exhibit spin-glass-like behavior in magnetic susceptibility and insulating-like temperature dependence in electrical transport. Using elastic neutron scattering, we find stripe-type short-range magnetic order in the spin-glass region identified by susceptibility measurements. The persistence of short-range magnetic order over a large doping range in Ba(Fe$_{1-x}$Cu$_x$)$_2$As$_2$ likely arises from local arrangements of Fe and Cu that favor magnetic order, with Cu acting as vacancies relieving magnetic frustration and degeneracy. These results indicate locally broken four-fold rotational symmetry, suggesting that stripe-type magnetism is ubiquitous in iron pnictides.Comment: accepted by Physical Review B Rapid Communication

Strict limit on in-plane ordered magnetic dipole moment in URu2Si2

Neutron diffraction is used to examine the polarization of weak static antiferromagnetism in high quality single crystalline URu2Si2. As previously documented, elastic Bragg-like diffraction develops for temperature T<T_{HO}= 17.5 K at q=(100) but not at wave vector transfer q=(001). The peak width indicates correlation lengths \xi_c=230(12) \AA \ and \xi_a=240(15) \AA. The integrated intensity of the T-dependent peaks corresponds to a sample averaged c-oriented staggered moment of \mu_{c}=0.022(1) \mu_B at T=1.7 K. The absence of T-dependent diffraction at q=(001) places a limit \mu_{\perp}<0.0011 \mu_B on an f- or d-orbital based in-plane staggered magnetic dipole moment, which is associated with multipolar orders proposed for URu_2Si_2.Comment: 9 pages, 7 figure

Temperature dependence of the resonance and low energy spin excitations in superconducting FeTe0.6_{0.6}Se0.4_{0.4}

We use inelastic neutron scattering to study the temperature dependence of the low-energy spin excitations in single crystals of superconducting FeTe$_{0.6}$Se$_{0.4}$ ($T_c=14$ K). In the low-temperature superconducting state, the imaginary part of the dynamic susceptibility at the electron and hole Fermi surfaces nesting wave vector $Q=(0.5,0.5)$, $\chi^{\prime\prime}(Q,\omega)$, has a small spin gap, a two-dimensional neutron spin resonance above the spin gap, and increases linearly with increasing $\hbar\omega$ for energies above the resonance. While the intensity of the resonance decreases like an order parameter with increasing temperature and disappears at temperature slightly above $T_c$, the energy of the mode is weakly temperature dependent and vanishes concurrently above $T_c$. This suggests that in spite of its similarities with the resonance in electron-doped superconducting BaFe$_{2-x}$(Co,Ni)$_x$As$_2$, the mode in FeTe$_{0.6}$Se$_{0.4}$ is not directly associated with the superconducting electronic gap.Comment: 7 pages, 6 figure

Short-range cluster spin glass near optimal superconductivity in BaFe2−x_{2-x}Nix_{x}As2_{2}

High-temperature superconductivity in iron pnictides occurs when electrons are doped into their antiferromagnetic (AF) parent compounds. In addition to inducing superconductivity, electron-doping also changes the static commensurate AF order in the undoped parent compounds into short-range incommensurate AF order near optimal superconductivity. Here we use neutron scattering to demonstrate that the incommensurate AF order in BaFe$_{2-x}$Ni$_{x}$As$_{2}$ is not a spin-density-wave arising from the itinerant electrons in nested Fermi surfaces, but consistent with a cluster spin glass in the matrix of the superconducting phase. Therefore, optimal superconductivity in iron pnictides coexists and competes with a mesoscopically separated cluster spin glass phase, much different from the homogeneous coexisting AF and superconducting phases in the underdoped regime.Comment: 4 figure

Electron doping evolution of the neutron spin resonance in NaFe1−x_{1-x}Cox_{x}As

Neutron spin resonance, a collective magnetic excitation coupled to superconductivity, is one of the most prominent features shared by a broad family of unconventional superconductors including copper oxides, iron pnictides, and heavy fermions. In this work, we study the doping evolution of the resonances in NaFe$_{1-x}$Co$_x$As covering the entire superconducting dome. For the underdoped compositions, two resonance modes coexist. As doping increases, the low-energy resonance gradually loses its spectral weight to the high-energy one but remains at the same energy. By contrast, in the overdoped regime we only find one single resonance, which acquires a broader width in both energy and momentum, but retains approximately the same peak position even when $T_c$ drops by nearly a half compared to optimal doping. These results suggest that the energy of the resonance in electron overdoped NaFe$_{1-x}$Co$_x$As is neither simply proportional to $T_c$ nor the superconducting gap, but is controlled by the multi-orbital character of the system and doped impurity scattering effect.Comment: accepted by PR