Ultrafast light pulses can modify the electronic properties of quantum materials by perturbing the underlying, intertwined degrees of freedom. In particular, iron-based superconductors exhibit a strong coupling among electronic nematic fluctuations,
spins, and the lattice, serving as a playground for ultrafast manipulation. Here we use time-resolved x-ray scattering to measure the lattice dynamics of photo-excited BaFe2As2. Upon optical excitation, no signature of an ultrafast change of the crystal symmetry is observed, but the lattice oscillates rapidly in time due to the coherent excitation of an A1g mode that modulates the Fe-As-Fe bond angle. We directly quantify the coherent lattice dynamics and show that even a small photo-induced lattice distortion can induce notable changes in the electronic and magnetic properties. Our analysis implies that transient structural modification can generally be an effective tool for manipulating the electronic properties of multi-orbital systems, where electronic instabilities are sensitive to the orbital character of bands near the Fermi level.
The goal of this paper is to provide an intuitive and useful tool for analyzing the impurity bound state problem. We develop a semiclassical approach and apply it to an impurity in two dimensional systems with parabolic or Dirac like bands. Our metho
d consists of reducing a higher dimensional problem into a sum of one dimensional ones using the two dimensional Green functions as a guide. We then analyze the one dimensional effective systems in the spirit of the wave function matching method as in the standard 1d quantum model. We demonstrate our method on two dimensional models with parabolic and Dirac-like dispersion, with the later specifically relevant to topological insulators.
Chiral edge modes of topological insulators and Hall states exhibit non-trivial behavior of conductance in the presence of impurities or additional channels. We will present a simple formula for the conductance through a chiral edge mode coupled to a
disordered bulk. For a given coupling matrix between the chiral mode and bulk modes, and a Green function matrix of bulk modes in real space, the renormalized Green function of the chiral mode is expressed in closed form as a ratio of determinants. We demonstrate the usage of the formula in two systems: i) a 1d wire with random onsite impurity potentials for which we found the disorder averaging is made simpler with the formula, and ii) a quantum Hall fluid with impurities in the bulk for which the phase picked up by the chiral mode due to the scattering with the impurities can be conveniently estimated.
The interplay among charge, spin and lattice degrees of freedom in solids gives rise to intriguing macroscopic quantum phenomena such as colossal magnetoresistance, multiferroicity and high-temperature superconductivity. Strong coupling or competitio
n between various orders in these systems presents the key to manipulate their functional properties by means of external perturbations such as electric and magnetic fields or pressure. Ultrashort and intense optical pulses have emerged as an interesting tool to investigate elementary dynamics and control material properties by melting an existing order. Here, we employ few-cycle multi-terahertz pulses to resonantly probe the evolution of the spin-density-wave (SDW) gap of the pnictide compound BaFe2As2 following excitation with a femtosecond optical pulse. When starting in the low-temperature ground state, optical excitation results in a melting of the SDW order, followed by ultrafast recovery. In contrast, the SDW gap is induced when we excite the normal state above the transition temperature. Very surprisingly, the transient ordering quasi-adiabatically follows a coherent lattice oscillation at a frequency as high as 5.5 THz. Our results attest to a pronounced spin-phonon coupling in pnictides that supports rapid development of a macroscopic order on small vibrational displacement even without breaking the symmetry of the crystal.
We employ three dimensional x-ray coherent diffraction imaging to map the lattice strain distribution, and to probe the elastic properties of a single crystalline Ni (001) nanowire grown vertically on an amorphous Si02 || Si substrate. The reconstruc
ted density maps show that with increasing wire width, the equilibrium compressive stress in the core region decreases sharply while the surface tensile strain increases, and gradually trends to a nonzero constant. We use the retrieved projection of lattice distortion to predict the Youngs Modulus of the wire based on the elasticity theory.
Intrinsic magnetoelectric coupling describes the interaction between magnetic and electric polarization through an inherent microscopic mechanism in a single phase material. This phenomenon has the potential to control the magnetic state of a materia
l with an electric field, an enticing prospect for device engineering. We demonstrate giant magnetoelectric cross-field control in a single phase rare earth titanate film. In bulk form, EuTiO3 is antiferromagnetic. However, both anti and ferromagnetic interactions coexist between different nearest neighbor europium ions. In thin epitaxial films, strain can be used to alter the relative strength of the magnetic exchange constants. Here, we not only show that moderate biaxial compression precipitates local magnetic competition, but also demonstrate that the application of an electric field at this strain state, switches the magnetic ground state. Using first principles density functional theory, we resolve the underlying microscopic mechanism resulting in the EuTiO3 G-type magnetic structure and illustrate how it is responsible for the giant cross-field magnetoelectric effect.
Using resonant x-ray diffraction, we observe an easy c-axis collinear antiferromagnetic structure for the bilayer Sr$_3$Ir$_2$O$_7$, a significant contrast to the single layer Sr$_2$IrO$_4$ with in-plane canted moments. Based on a microscopic model H
amiltonian, we show that the observed spin-flop transition as a function of number of IrO$_2$ layers is due to strong competition among intra- and inter-layer bond-directional pseudo-dipolar interactions of the spin-orbit entangled $J_{eff}$=1/2 moments. With this we unravel the origin of anisotropic exchange interactions in a Mott insulator in the strong spin-orbit coupling regime, which holds the key to the various types of unconventional magnetism proposed in 5$d$ transition metal oxides.
We report on a lattice simulation result for four-dimensional {cal N}=1 SU(2) super Yang-Mills theory with the dynamical overlap gluino. We study the spectrum of the overlap Dirac operator at three different gluino masses m=0.2, 0.1 and 0.05 with the
Iwasaki action on a 8^3 times 16 lattice. We find that the lowest eigenvalue distributions are in good agreement with the prediction from the random matrix theory. Moreover the mass dependence of the condensate is almost constant, which gives a clean chiral limit. Our results for the gluino condensate in the chiral limit is < bar{psi} psi > r_0^3 = 0.63(12), where r_0 is the Sommer scale.
Rare earth (R) half-Heusler compounds, RBiPt, exhibit a wide spectrum of novel ground states. Recently, GdBiPt has been proposed as a potential antiferromagnetic topological insulator (AFTI). We have employed x-ray resonant magnetic scattering to elu
cidate the microscopic details of the magnetic structure in GdBiPt below T_N = 8.5 K. Experiments at the Gd L_2 absorption edge show that the Gd moments order in an antiferromagnetic stacking along the cubic diagonal [1 1 1] direction satisfying the requirement for an AFTI, where both time-reversal symmetry and lattice translational symmetry are broken, but their product is conserved.
Oxygen octahedral rotations have been measured in short-period (LaNiO$_3$)$_n$/(SrMnO$_3$)$_m$ superlattices using synchrotron diffraction. The in-plane and out-of-plane bond angles and lengths are found to systematically vary with superlattice compo
sition. Rotations are suppressed in structures with $m>n$, producing a nearly cubic form of LaNiO$_3$. Large rotations are present in structures with $m<n$, leading to reduced bond angles in SrMnO$_3$. The metal-oxygen-metal bond lengths decrease as rotations are reduced, in contrast to behavior previously observed in strained, single layer films. This result demonstrates that superlattice structures can be used to stabilize non-equilibrium octahedral behavior in a manner distinct from epitaxial strain, providing a novel means to engineer the electronic and ferroic properties of oxide heterostructures.
