Ultrafast control of magnetic interactions via light-driven phonons

Resonant ultrafast excitation of infrared-active phonons is a powerful technique with which to control the electronic properties of materials that leads to remarkable phenomena such as the light-induced enhancement of superconductivity1,2, switching of ferroelectric polarization3,4 and ultrafast insulator-to-metal transitions5. Here, we show that light-driven phonons can be utilized to coherently manipulate macroscopic magnetic states. Intense mid-infrared electric field pulses tuned to resonance with a phonon mode of the archetypical antiferromagnet DyFeO3 induce ultrafast and long-living changes of the fundamental exchange interaction between rare-earth orbitals and transition metal spins. Non-thermal lattice control of the magnetic exchange, which defines the stability of the macroscopic magnetic state, allows us to perform picosecond coherent switching between competing antiferromagnetic and weakly ferromagnetic spin orders. Our discovery emphasizes the potential of resonant phonon excitation for the manipulation of ferroic order on ultrafast timescales6

Superstripes and complexity in high-temperature superconductors

While for many years the lattice, electronic and magnetic complexity of high-temperature superconductors (HTS) has been considered responsible for hindering the search of the mechanism of HTS now the complexity of HTS is proposed to be essential for the quantum mechanism raising the superconducting critical temperature. The complexity is shown by the lattice heterogeneous architecture: a) heterostructures at atomic limit; b) electronic heterogeneity: multiple components in the normal phase; c) superconducting heterogeneity: multiple superconducting gaps in different points of the real space and of the momentum space. The complex phase separation forms an unconventional granular superconductor in a landscape of nanoscale superconducting striped droplets which is called the "superstripes" scenario. The interplay and competition between magnetic orbital charge and lattice fluctuations seems to be essential for the quantum mechanism that suppresses thermal decoherence effects at an optimum inhomogeneity.Comment: 20 pages, 3 figures; J. Supercon. Nov. Mag. 201

Figure source data for 'Coherent spin-wave transport in an antiferromagnet'

This repository contains figure source data for 'Coherent spin-wave transport in an antiferromagnet' Contents Figure 1: (a) optical absorption DyFeO3 for different photon energies: 1a_absorption.txt (b)Penetration depth for different photon energies: 1a_penetetrationdepth.txt (c) Time-resolved polarization rotation for transmission and reflection geometries: 1c_time-resolved.txt Fourier amplitude spectra for different geometrie: 1c_FourierInsets Figure 2: (b) Extracted oscillation frequencies as function of temperature: 2b_frequencies.txt Figure 3 (a) Time-resolved polarization rotation for different photon energies (folder figure3a) (b) Amplitude spectra of the time-resolved polarization rotation for different photon energies (folder figure3b) (c) Amplitude vs penetration depth: 3c.txt Figure 4 (a) Time- and space dependent amplitude: 4a.txt (b) Fourier spectra for different incidence angles + data-inset: 4b.txt (c) Fourier spectra for different probe wavelengths: 4c.txt (d) Extracted central frequencies and calculated group velocity for different wavenumbers: 4de.txt . Copyright: Creative Commons Attribution 4.0 International Open Acces

Coherent spin-wave transport in an antiferromagnet

Magnonics is a research field complementary to spintronics, in which the quanta of spin waves (magnons) replace electrons as information carriers, promising lower dissipation1–3. The development of ultrafast, nanoscale magnonic logic circuits calls for new tools and materials to generate coherent spin waves with frequencies as high and wavelengths as short as possible4,5. Antiferromagnets can host spin waves at terahertz frequencies and are therefore seen as a future platform for the fastest and least dissipative transfer of information6–11. However, the generation of short-wavelength coherent propagating magnons in antiferromagnets has so far remained elusive. Here we report the efficient emission and detection of a nanometre-scale wavepacket of coherent propagating magnons in the antiferromagnetic oxide dysprosium orthoferrite using ultrashort pulses of light. The subwavelength confinement of the laser field due to large absorption creates a strongly non-uniform spin excitation profile, enabling the propagation of a broadband continuum of coherent terahertz spin waves. The wavepacket contains magnons with a shortest detected wavelength of 125 nm that propagate into the material with supersonic velocities of more than 13 km s–1. This source of coherent short-wavelength spin carriers opens up new prospects for terahertz antiferromagnetic magnonics and coherence-mediated logic devices at terahertz frequencies

Ultrathin complex oxide nanomechanical resonators

Complex oxide thin films and heterostructures exhibit a variety of electronic phases, often controlled by the mechanical coupling between film and substrate. Recently it has become possible to isolate epitaxially grown single-crystalline layers of these materials, enabling the study of their properties in the absence of interface effects. In this work, we use this technique to create nanomechanical resonators made out of SrTiO 3 and SrRuO 3 . Using laser interferometry, we successfully actuate and measure the motion of the nanodrum resonators. By measuring the temperature-dependent mechanical response of the SrTiO 3 resonators, we observe signatures of a structural phase transition, which affects both the strain and mechanical dissipation in the resonators. Here, we demonstrate the feasibility of integrating ultrathin complex oxide membranes for realizing nanoelectromechanical systems on arbitrary substrates and present a novel method of detecting structural phase transitions in these exotic materials. </p

Berry phase engineering at oxide interfaces

Three-dimensional strontium ruthenate (SrRuO3) is an itinerant ferromagnet that features Weyl points acting as sources of emergent magnetic fields, anomalous Hall conductivity, and unconventional spin dynamics. Integrating SrRuO3 in oxide heterostructures is potentially a novel route to engineer emergent electrodynamics, but its electronic band topology in the two-dimensional limit remains unknown. Here we show that ultrathin SrRuO3 exhibits spin-polarized topologically nontrivial bands at the Fermi energy. Their band anticrossings show an enhanced Berry curvature and act as competing sources of emergent magnetic fields. We control their balance by designing heterostructures with symmetric (SrTiO3/SrRuO3/SrTiO3 and SrIrO3/SrRuO3/SrIrO3) and asymmetric interfaces (SrTiO3/SrRuO3/SrIrO3). Symmetric structures exhibit an interface-tunable singlechannel anomalous Hall effect, while ultrathin SrRuO3 embedded in asymmetric structures shows humplike features consistent with multiple Hall contributions. The band topology of two-dimensional SrRuO3 proposed here naturally accounts for these observations and harmonizes a large body of experimental results