Searcharxiv⌕ Search

arXiv subjects

Robert J. Birgeneau

Publications and source records attributed to Robert J. Birgeneau.

78 records · Page 5Linked to original sources

Elucidating the magnetic and superconducting phases in the alkali metal intercalated iron chalcogenides

The complex interdigitated phases have greatly frustrated attempts to document the basic features of the superconductivity in the alkali metal intercalated iron chalcogenides. Here, using elastic neutron scattering, energy-dispersive x-ray spectroscopy, and resistivity measurements, we elucidate the relations of these phases in Rb$_{1-δ}$Fe$_y$Se$_{2-z}$S$_z$. We find: i) the iron content is crucial in stabilizing the stripe antiferromagnetic (AF) phase with rhombic iron vacancy order ($y\approx1.5$), the block AF phase with $\sqrt{5}\times \sqrt{5}$ iron vacancy order ($y\approx1.6$), and the iron vacancy-free phase ($y\approx2$); ii) the superconducting phase ($z=0$) evolves into a metallic phase ($z>1.5$) with sulfur substitution due to the progressive decrease of the electronic correlation strength. Both the stripe AF phase and the block AF phase are Mott insulators. Our data suggest that there are miscibility gaps between these three phases. The existence of the miscibility gaps in the iron content is the key to understanding the relationship between these complicated phases.

cond-mat.supr-con↗

The evolution of antiferromagnetic susceptibility to uniaxial pressure in Ba(Fe{1-x}Co{x})2As2

Neutron diffraction measurements are presented measuring the responses of both magnetic and structural order parameters of parent and lightly Co-doped Ba(Fe{1-x}Co{x})2As2 under the application of uniaxial pressure. We find that the uniaxial pressure induces a thermal shift in the onset of antiferromagnetic order that grows as a percentage of T_N as Co-doping is increased and the superconducting phase is approached. Additionally, as uniaxial pressure is increased within parent and lightly-doped Ba(Fe{1-x}Co{x})2As2 on the first order side of the tricritical point, we observe a decoupling between the onsets of the orthorhombic structural distortion and antiferromagnetism. Our findings place needed constraints on models exploring the nematic susceptibility of the bilayer pnictides in the tetragonal, paramagnetic regime.

cond-mat.supr-con↗

Photoelectron spin-flipping and texture manipulation in a topological insulator

Recently discovered materials called three-dimensional topological insulators constitute examples of symmetry protected topological states in the absence of applied magnetic fields and cryogenic temperatures. A hallmark characteristic of these non-magnetic bulk insulators is the protected metallic electronic states confined to the material's surfaces. Electrons in these surface states are spin polarized with their spins governed by their direction of travel (linear momentum), resulting in a helical spin texture in momentum space. Spin- and angle-resolved photoemission spectroscopy (spin-ARPES) has been the only tool capable of directly observing this central feature with simultaneous energy, momentum, and spin sensitivity. By using an innovative photoelectron spectrometer with a high-flux laser-based light source, we discovered another surprising property of these surface electrons which behave like Dirac fermions. We found that the spin polarization of the resulting photoelectrons can be fully manipulated in all three dimensions through selection of the light polarization. These surprising effects are due to the spin-dependent interaction of the helical Dirac fermions with light, which originates from the strong spin-orbit coupling in the material. Our results illustrate unusual scenarios in which the spin polarization of photoelectrons is completely different from the spin state of electrons in the originating initial states. The results also provide the basis for a novel source of highly spin-polarized electrons with tunable polarization in three dimensions.

cond-mat.mtrl-sci↗

Incommensurate lattice distortion in the high temperature tetragonal phase of La$_{2-x}$(Sr,Ba)$_{x}$CuO$_{4}$

We report incommensurate diffuse (ICD) scattering appearing in the high-temperature-tetragonal (HTT) phase of La$_{2-x}$(Sr,Ba)$_{x}$CuO$_{4}$ with $0.07 \leq x \leq 0.20$ observed by the neutron diffraction technique. For all compositions, a sharp superlattice peak of the low-temperature-orthorhombic (LTO) structure is replaced by a pair of ICD peaks with the modulation vector parallel to the CuO$_6$ octahedral tilting direction, that is, the diagonal Cu-Cu direction of the CuO$_2$ plane, above the LTO-HTT transition temperature $T_s$. The temperature dependences of the incommensurability $δ$ for all samples scale approximately as $T/T_s$, while those of the integrated intensity of the ICD peaks scale as $(T-T_s)^{-1}$. These observations together with absence of ICD peaks in the non-superconducting $x=0.05$ sample evince a universal incommensurate lattice instability of hole-doped 214 cuprates in the superconducting regime.

cond-mat.supr-con↗

Neutron scattering study of soft phonons and diffuse scattering in insulating La$_{1.95}$Sr$_{0.05}$CuO$_{4}$

Soft phonons and diffuse scattering in insulating La$_{2-x}$Sr$_{x}$CuO$_4$ ($x=0.05$) have been studied by the neutron scattering technique. The X-point phonon softens from high temperature towards the structural transition temperature $T_{s}=410$ K, and the Z-point phonon softens again below 200 K. The Z-point phonon softening persists to low temperature, in contrast to the behavior observed in the superconducting $x=0.15$ compound, in which the Z-point phonon hardens below $T_c$. The diffuse scattering associated with the structural phase transition at 410 K appears at commensurate positions. These results highlight interesting differences between superconducting and insulating samples.

cond-mat.supr-con↗

Smectic ordering in liquid crystal - aerosil dispersions II. Scaling analysis

Liquid crystals offer many unique opportunities to study various phase transitions with continuous symmetry in the presence of quenched random disorder (QRD). The QRD arises from the presence of porous solids in the form of a random gel network. Experimental and theoretical work support the view that for fixed (static) inclusions, quasi-long-range smectic order is destroyed for arbitrarily small volume fractions of the solid. However, the presence of porous solids indicates that finite-size effects could play some role in limiting long-range order. In an earlier work, the nematic - smectic-A transition region of octylcyanobiphenyl (8CB) and silica aerosils was investigated calorimetrically. A detailed x-ray study of this system is presented in the preceding Paper I, which indicates that pseudo-critical scaling behavior is observed. In the present paper, the role of finite-size scaling and two-scale universality aspects of the 8CB+aerosil system are presented and the dependence of the QRD strength on the aerosil density is discussed.

cond-mat.soft↗