It is unexpected that a spin-glass transition, which generally occurs only in the system with some form of disorder, was observed in the ThCr2Si2-type compound PrAu2Si2 at a temperature of ~3 K. This puzzling phenomenon was later explained based on a
novel dynamic frustration model that does not involve static disorder. We present the results of re-verification of the reported spin-glass behaviors by measuring the physical properties of three polycrystalline PrAu2Si2 samples annealed under different conditions. Indeed, in the sample annealed at 827 C for one week, a spin-glass transition does occur at a temperature of Tf=2.8 K as that reported previously in the literature. However, it is newly found that the spin-glass effect is actually more pronounced in the as-cast sample, and almost completely disappears in the well-annealed (at 850 C for 4 weeks) sample. The apparent sample dependence of the magnetic characteristics of PrAu2Si2 is discussed by comparing it with similar phenomena observed in the isomorphic compounds URh2Ge2 and CeAu2Si2. Our experimental results strongly suggest that the spin-glass behavior observed in the as cast and insufficient annealed samples is most likely due to the presence of small amount of crystalline impurities and/or partial site disorder on the Au and Si sublattices, and thus is not the inherent characteristic of ideal ThCr2Si2-type PrAu2Si2. The perfectly ordered PrAu2Si2 should be regarded as a paramagnetic system with obvious crystal-field effects.
Magnetic skyrmions are the self-organized topological spin textures behaving like particles. Because of their fast creation and typically long lifetime, experimental verification of skyrmions creation/annihilation processes has been challenging. Here
we successfully track skyrmions dynamics in defect-introduced Co9Zn9Mn2, by using pump-probe Lorentz transmission electron microscope. Following the nanosecond-photothermal excitation, we resolve 160-nm-skyrmions proliferation at <1 ns, contraction at 5 ns, drift from 10 ns to 4 microsecond and coalescence at 5 microsecond. These motions relay the multiscale arrangement and relaxation of skyrmion clusters in a repeatable cycle of 20 kHz. Such repeatable dynamics of skyrmions, arising from the weakened but still persistent topological protection around defects, enables us to visualize the whole life of the skyrmions, as well as demonstrating the possible high-frequency manipulations of topological charges brought by skyrmions.
Controlling acoustic phonons, the carriers of sound and heat, has been attracting great attention toward the manipulation of sonic and thermal properties in nanometric devices. In particular, the photo-acoustic effect using ultrafast optical pulses h
as a promising potential to optically manipulate phonons in picoseconds time regime. However, its mechanism has been so far mostly based on the commonplace thermoelastic expansion in isotropic media, limiting the spectrum of potential applications. We investigate a conceptually new mechanism of photo-acoustic effect involving the structural instability, by utilizing a transition-metal dichalcogenide VTe$_2$ with the ribbon-type charge-density-wave (CDW). Ultrafast electron microscope imaging and diffraction measurements reveal the generation and propagation of unusual acoustic waves in the nanometric thin plate associated with the optically induced instantaneous charge-density-wave dissolution. Our results highlight the capability of photo-induced structural instability as a source of coherent acoustic waves.
In differential phase contrast scanning transmission electron microscopy (DPC-STEM), variability in dynamical diffraction resulting from changes in sample thickness and local crystal orientation (due to sample bending) can produce contrast comparable
to that arising from the long-range electromagnetic fields probed by this technique. Through simulation we explore the scale of these dynamical diffraction artefacts and introduce a metric for the magnitude of their confounding contribution to the contrast. We show that precession over an angular range of a few milliradian can suppress this confounding contrast by one-to-two orders of magnitude. Our exploration centres around a case study of GaAs near the [011] zone-axis orientation using a probe-forming aperture semiangle on the order of 0.1 mrad at 300 keV, but the trends found and methodology used are expected to apply more generally.
The electronic nematic phase is an unconventional state of matter that spontaneously breaks the rotational symmetry of electrons. In iron-pnictides/chalcogenides and cuprates, the nematic ordering and fluctuations have been suggested to have as-yet-u
nconfirmed roles in superconductivity. However, most studies have been conducted in thermal equilibrium, where the dynamical property and excitation can be masked by the coupling with the lattice. Here we use femtosecond optical pulse to perturb the electronic nematic order in FeSe. Through time-, energy-, momentum- and orbital-resolved photo-emission spectroscopy, we detect the ultrafast dynamics of electronic nematicity. In the strong-excitation regime, through the observation of Fermi surface anisotropy, we find a quick disappearance of the nematicity followed by a heavily-damped oscillation. This short-life nematicity oscillation is seemingly related to the imbalance of Fe 3dxz and dyz orbitals. These phenomena show critical behavior as a function of pump fluence. Our real-time observations reveal the nature of the electronic nematic excitation instantly decoupled from the underlying lattice.
The low energy electronic structure of LaFeAsO1-xHx (0.0 < x < 0.60), the system which exhibits two superconducting domes in its phase diagram, is investigated by utilizing the laser photoemission spectroscopy. From the precise temperature-dependent
measurement of the spectra near the Fermi level, we find the suppression of the density of states with cooling, namely the pseudogap formation, for all doping range. The pseudogap in the low x range (i.e. the first superconducting dome regime) gets suppressed with increasing x, more or less similarly to the previous results in F-doped LaFeAsO system. On the other hand, the pseudogap behavior in the second superconducting dome regime at high-x becomes stronger with increasing the H-doping level. The systematic doping dependence shows that the pseudogap is enhanced toward the both ends of the phase diagram where the different types of antiferromagnetic order exist.
We report the lattice dynamics of transition metal thin films by using the ultrafast electron diffraction. We observe a suppression of the diffraction intensity in a few picosecond after the photoexcitation, which is directly interpreted as the latti
ce heating via the electron-phonon interaction. The electron-phonon coupling constants for Au, Cu and Mo are quantitatively evaluated by employing the two-temperature model, which are consistent with those obtained by optical pump-probe methods. The variation in the lattice dynamics of the transition metals are systematically explained by the strength of the electron-phonon coupling, arising from the elemental dependence of the electronic structure and atomic mass.
We investigate the in-plane anisotropy of Fe 3d orbitals occurring in a wide temperature and composition range of BaFe2(As1-xPx)2 system. By employing the angle-resolved photoemission spectroscopy, the lifting of degeneracy in dxz and dyz orbitals at
the Brillouin zone corners can be obtained as a measure of the orbital anisotropy. In the underdoped regime, it starts to evolve on cooling from high temperatures above both antiferromagnetic and orthorhombic transitions. With increasing x, it well survives into the superconducting regime, but gradually gets suppressed and finally disappears around the non-superconducting transition (x = 0.7). The observed spontaneous in-plane orbital anisotropy, possibly coupled with anisotropic lattice and magnetic fluctuations, implies the rotational-symmetry broken electronic state working as the stage for the superconductivity in BaFe2(As1-xPx)2.
We study the color-dependent confining forces between two quarks by the quenched lattice simulations of Coulomb gauge QCD. The color-singlet and color-antitriplet instantaneous potentials yield attractive forces. The ratio of the string tensions obta
ined from them is approximately 2 and have little volume dependence. Meanwhile, the color-octet and color-sextet channels give a minor contribution for two-quark system. We finally find that the infrared self-energy of the color-nonsinglet channels diverges in the infinite volume limit; however, the degree of the divergence on the finite lattice can be understood in terms of color factors.
