Résultats de recherche pour « Magnetophononics »
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Abstract The emergence of magnetism in quantum materials creates a platform to realize spin-based applications in spintronics, magnetic memory, and quantum information science. A key to unlocking new functionalities in these materials is the discovery of tunable coupling between spins …
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Abstract The emergence of magnetism in quantum materials creates a platform to realize spin-based applications in spintronics, magnetic memory, and quantum information science. A key to unlocking new functionalities in these materials is the discovery of tunable coupling between spins and other microscopic degrees of freedom. We present evidence for interlayer magnetophononic coupling in the layered magnetic topological insulator MnBi 2 Te 4 . Employing magneto-Raman spectroscopy, we observe anomalies in phonon scattering intensities across magnetic field-driven phase transitions, despite the absence of discernible static structural changes. This behavior is a consequence of a magnetophononic wave-mixing process that allows for the excitation of zone-boundary phonons that are otherwise ‘forbidden’ by momentum conservation. Our microscopic model based on density functional theory calculations reveals that this phenomenon can be attributed to phonons modulating the interlayer exchange coupling. Moreover, signatures of magnetophononic coupling are also observed in the time domain through the ultrafast excitation and detection of coherent phonons across magnetic transitions. In light of the intimate connection between magnetism and topology in MnBi 2 Te 4 , the magnetophononic coupling represents an important step towards coherent on-demand manipulation of magnetic topological phases.
Abstract The direct, ultrafast excitation of polar phonons with electromagnetic radiation is a potent strategy for controlling the properties of a wide range of materials, particularly in the context of influencing their magnetic behavior. Here, we show that, contrary to …
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Abstract The direct, ultrafast excitation of polar phonons with electromagnetic radiation is a potent strategy for controlling the properties of a wide range of materials, particularly in the context of influencing their magnetic behavior. Here, we show that, contrary to common perception, the origin of phonon-induced magnetic activity does not stem from the Maxwellian fields resulting from the motion of the ions themselves or the effect their motion exerts on the electron subsystem. Through the mechanism of electron–phonon coupling, a coherent state of circularly polarized phonons generates substantial non-Maxwellian fields that disrupt time-reversal symmetry, effectively emulating the behavior of authentic magnetic fields. Notably, the effective fields can reach magnitudes as high as 100 T, surpassing by a factor of α−2≈2×104 the Maxwellian fields resulting from the inverse Faraday effect; α is the fine-structure constant. Because the light-induced nonreciprocal fields depend on the square of the phonon displacements, the chirality the photons transfer to the ions plays no role in magnetophononics.
Using a combination of first-principles and magnetization-dynamics calculations, we study the effect of the intense optical excitation of phonons on the magnetic behavior in insulating magnetic materials. Taking the prototypical magnetoelectric ${\mathrm{Cr}}_{2}{\mathrm{O}}_{3}$ as our model system, we show that excitation …
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Using a combination of first-principles and magnetization-dynamics calculations, we study the effect of the intense optical excitation of phonons on the magnetic behavior in insulating magnetic materials. Taking the prototypical magnetoelectric ${\mathrm{Cr}}_{2}{\mathrm{O}}_{3}$ as our model system, we show that excitation of a polar mode at 17 THz causes a pronounced modification of the magnetic exchange interactions through a change in the average Cr-Cr distance. In particular, the quasistatic deformation induced by nonlinear phononic coupling yields a structure with a modified magnetic state, which persists for the duration of the phonon excitation. In addition, our time-dependent magnetization dynamics computations show that systematic modulation of the magnetic exchange interaction by the phonon excitation modifies the magnetization dynamics. This temporal modulation of the magnetic exchange interaction strengths using phonons provides a route to creating nonequilibrium magnetic states and suggests avenues for fast manipulation of spin arrangements and dynamics.
Strategies for tuning the thermal conductivity of crystals by means of external fields are rare. Here, we predict the existence of large magnetophononic effects in materials that undergo antiferromagnetic (AFM) $\ensuremath{\leftrightarrow}$ ferromagnetic (FM) phase transitions, which allow for the modulation …
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Strategies for tuning the thermal conductivity of crystals by means of external fields are rare. Here, we predict the existence of large magnetophononic effects in materials that undergo antiferromagnetic (AFM) $\ensuremath{\leftrightarrow}$ ferromagnetic (FM) phase transitions, which allow for the modulation of the lattice heat conductivity, ${\ensuremath{\kappa}}_{L}$, via the application of magnetic fields. Specifically, by using first-principles methods we predict a large and anomalous ${\ensuremath{\kappa}}_{L}$ increase of $\ensuremath{\approx}40%$ for the metamagnetic phase transition occurring in bulk FeRh near room temperature. The disclosed magnetophononic effects are caused by large anharmonic spin-phonon couplings, namely, significant differences in the phase space of allowed phonon-phonon collision processes taking place in the respective AFM and FM phases.
One route to the control of quantum magnetism at ultrafast timescales is magnetophononics, the modulation of magnetic interactions by coherently driven lattice excitations. Theoretical studies of a gapped quantum magnet subject to continuous, single-frequency driving of one strongly coupled phonon …
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One route to the control of quantum magnetism at ultrafast timescales is magnetophononics, the modulation of magnetic interactions by coherently driven lattice excitations. Theoretical studies of a gapped quantum magnet subject to continuous, single-frequency driving of one strongly coupled phonon mode find intriguing phenomena including mutually repelling phonon-bitriplon excitations and global renormalization of the spin excitation spectrum. Because experiments are performed with ultrashort pulses that contain a wide range of driving frequencies, we investigate phonon-bitriplon physics under pulsed laser driving. We use the equations of motion to compute the transient response of the driven and dissipative spin-phonon system, which we characterize using the phonon displacement, phonon number, and triplon occupations. In the Fourier transforms of each quantity we discover a low-frequency energetic oscillation between the lattice and spin sectors, which is an intrinsically nonequilibrium collective mode, and demonstrate its origin as a beating between mutually repelling composite excitations. We introduce a phonon-bitriplon approximation that captures all the physics of hybridization, collective mode formation, and difference-frequency excitation, and show that sum-frequency phenomena also leave clear signatures in the response. We model the appearance of such magnetophononic phenomena in the strongly coupled spin-chain compound CuGeO 3 , whose overlapping phonon and spin excitation spectra are well characterized, to deduce the criteria for their possible observation in quantum magnetic materials.
Harnessing the most advanced capabilities of quantum technologies will require the ability to control macroscopic quantum states of matter. Quantum magnetic materials provide a valuable platform for realizing highly entangled many-body quantum systems, and have been used to investigate phenomena …
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Harnessing the most advanced capabilities of quantum technologies will require the ability to control macroscopic quantum states of matter. Quantum magnetic materials provide a valuable platform for realizing highly entangled many-body quantum systems, and have been used to investigate phenomena ranging from quantum phase transitions (QPTs) to fractionalization, topological order and the entanglement structure of the quantum wavefunction. Although multiple studies have controlled their properties by static applied pressures or magnetic fields, dynamical control at the fundamental timescales of their magnetic interactions remains completely unexplored. However, major progress in the technology of ultrafast laser pulses has enabled the dynamical modification of electronic properties, and now we demonstrate the ultrafast control of quantum magnetism. This we achieve by a magnetophononic mechanism, the driving of coherent lattice displacements to produce a resonant excitation of the quantum spin dynamics. Specifically, we apply intense terahertz laser pulses to excite a collective spin state of the quantum antiferromagnet SrCu2(BO3)2 by resonance with the nonlinear mixing frequency of the driven phonons that modulate the magnetic interactions. Our observations indicate a universal mechanism for controlling nonequilibrium quantum many-body physics on timescales many orders of magnitude faster than those achieved to date.
Magnetophononics, the modulation of magnetic interactions by driven infrared-active lattice excitations, is emerging as a key mechanism for the ultrafast dynamical control of both semiclassical and quantum spin systems by coherent light. We demonstrate that, in a quantum magnetic material …
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Magnetophononics, the modulation of magnetic interactions by driven infrared-active lattice excitations, is emerging as a key mechanism for the ultrafast dynamical control of both semiclassical and quantum spin systems by coherent light. We demonstrate that, in a quantum magnetic material with strong spin-phonon coupling, resonances between the driven phonon and the spin excitation frequencies exhibit a giant self-blocking effect. Instead of absorbing more energy, the spin system acts as a strong brake on the driven phonon, causing it to absorb only a tiny fraction of the power available from the laser. Using the quantum master equations governing the nonequilibrium steady states of the coupled spin-lattice system, we show how self-blocking dominates the dynamics, demonstrate the creation of mutually repelling hybrid spin-phonon states, and control the nonequilibrium renormalization of the lattice-driven spin excitation band.
Data from Raman spectroscopy, pump-probe reflectivity, and density functional theory calculations.
Magnetophononics, the modulation of magnetic interactions by driving infrared-active lattice excitations, is emerging as a key mechanism for the ultrafast dynamical control of both semiclassical and quantum spin systems by coherent light. We demonstrate that, in a quantum magnet with …
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Magnetophononics, the modulation of magnetic interactions by driving infrared-active lattice excitations, is emerging as a key mechanism for the ultrafast dynamical control of both semiclassical and quantum spin systems by coherent light. We demonstrate that, in a quantum magnet with strong spin-phonon coupling, resonances between the driven phonon and the spin excitation frequencies exhibit an intrinsic self-blocking effect, whereby only a fraction of the available laser power is absorbed by the phonon. Using the quantum master equations governing the nonequilibrium steady states of the coupled spin-lattice system, we show how self-blocking arises from the self-consistent alteration of the resonance frequencies. We link this to the appearance of mutually repelling collective spin-phonon states, which in the regime of strong hybridization become composites of a phonon and two triplons. We then identify the mechanism and optimal phonon frequencies by which to control a global nonequilibrium renormalization of the lattice-driven spin excitation spectrum and demonstrate that this effect should be observable in ultrafast THz experiments on a number of known quantum magnetic materials.
This file provides a readable version of Figure S2 associated with our research article published in ACS Nano (DOI: 10.1021/acsnano.6c06828).Due to an unintended Word-to-PDF conversion issue, the figure (Figure S2) appears black in the published Supporting Information [https://pubs.acs.org/doi/10.1021/acsnano.6c06828?goto=supporting-info].The version provided …
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This file provides a readable version of Figure S2 associated with our research article published in ACS Nano (DOI: 10.1021/acsnano.6c06828).Due to an unintended Word-to-PDF conversion issue, the figure (Figure S2) appears black in the published Supporting Information [https://pubs.acs.org/doi/10.1021/acsnano.6c06828?goto=supporting-info].The version provided here reproduces the original figure without altering the underlying data or analysis. This file is provided by the authors independently for clarity and does not constitute a formal correction to the published article.published article.