Abstract
The unique functionalities of antiferromagnets offer promising routes to advance information technology. Their compensated magnetic order leads to spin resonances in the THzregime, which suggest the possibility to coherently control antiferromagnetic (AFM) devices orders of magnitude faster than traditional electronics. However, the required time resolution, complex sublattice interactions and the relative inaccessibility of the AFM order parameter pose serious challenges to studying AFM spin dynamics. Here, we reveal the temporal evolution of an AFM order parameter directly in the time domain. We modulate the AFM order in hexagonal YMnO_{3} by coherent magnon excitation and track the ensuing motion of the AFM order parameter using timeresolved optical secondharmonic generation. The dynamic symmetry reduction by the moving order parameter allows us to separate electron dynamics from spin dynamics. As transient symmetry reductions are common to coherent excitations, we have a general tool for tracking the ultrafast motion of an AFM order parameter.
Introduction
Recently, the appealing properties of antiferromagnets culminated in the demonstration of both optically^{1} and electrically^{2} induced switching of the AFM order. This illustrates the general usefulness of antiferromagnets for future applications^{3,4}, yet the dynamics occurring during the switching process remain uncertain as timeresolved (TR) access to the AFM order parameter is notoriously difficult. Consequently, detecting its motion in the time domain often relies on measuring one spin component, such as a transiently occuring uncompensated magnetic moment, and extrapolating the full orderparameter dynamics from models^{1}. A detailed study of all spin components during a ferromagnetic spin precession, however, revealed unexpected insights^{5,6}. Thus, a dependable analysis of the nontrivial spin dynamics during switching events in antiferromagnets necessitates direct and TR experimental access to all the orderparameter components.
While the uncompensated component is optically accessible by the Faraday effect, detection of the compensated part of the order parameter usually depends on more indirect processes, like magnetic linear birefringence, which is quadratic in the sublattice magnetisation. This leads to a loss of directionality and, thereby, of the ability to distinguish between spinreversed domain states^{2,7,8,9}. Here, optical secondharmonic generation (SHG), i.e., frequency doubling of a light wave in a material, is a powerful, symmetrysensitive technique that can couple linearly to the AFM order parameter, thus maintaining its directional information^{10,11}. The leading SHG contribution is given by \(P_i(2\omega ) = \epsilon _0{\cal{X}}_{ijk}E_j(\omega )E_k(\omega )\), where \(\epsilon _0\) is the vacuum permittivity, E is the electric field of the incoming light wave, \({\cal{X}}\) is the secondorder susceptibility tensor and P is the induced polarisation oscillating at twice the frequency ω of the incident light^{12}. Owing to the direct coupling of \({\cal{X}}\) to the AFM order parameter, SHG is ideal for the static characterisation of antiferromagnets^{11,13,14}. Despite this and despite the instantaneous nature of the SHG process, which allows probing ultrafast processes, TR SHG studies of optically induced dynamics are scarce. The methodical difficulty to discriminate between genuine magneticorderparameter dynamics, affecting \({\cal{X}}_{ijk}\), and electron dynamics, affecting the linear optical properties at ω and 2ω, hampers the interpretation of TR SHG measurements^{15}. In fact, distinguishing between orderparameter and electron dynamics is commonly believed to be a “practical impossibility”^{16}. This is particularly true for thermal excitations, where redistribution of resonantly excited charge carriers leads to substantial changes in the linear optical properties^{17,18,19,20}.
An optical excitation, however, can also act as a nonthermal stimulus to the magnetic order. A wellknown example is the inverse Faraday effect (IFE)^{16}, where a circularly polarised laser pulse generates a longitudinal effective magnetic field H_{IFE}. This field exists for the laser pulse duration only. The impulsive, nonresonant excitation results in a welldefined initial phase of the spin precession. This process is also effective in fully compensated antiferromagnets^{8,21,22,23,24,25,26}. Such a simple fundamental excitation is an ideal test case for us. Its wellunderstood dynamics allow us to demonstrate how to separate thermal electron dynamics from nonthermal spin dynamics and how to obtain the full orderparameter trajectory.
Here, we use a combination of Faraday rotation and SHG to track the orderparameter motion during a coherent spin precession in antiferromagnetic YMnO_{3}. We find that the coherent spin precession transiently reduces the pointgroup symmetry, which leads to the emergence of new SHG tensor components. We conclude this from a periodic modulation of the SHG anisotropy. In contrast to the Faraday rotation, which is sensitive to the outofplane spin component, we show that the SHG modulation reflects the inplane spin component. Moreover, we quantify both the inplane and outofplane spincanting angles, where we find a pronounced ellipticity of the spin precession. With this proofofconcept demonstration, we show that TR SHG is a valuable tool for the study of AFM spin dynamics providing complementary information that is inaccessible by other techniques.
Results
Experimental details
We choose hexagonal YMnO_{3} as a model system. The material is ferroelectric below T_{C} ≈ 1250 K^{27}. The three Mn^{3+} sublattices order antiferromagnetically below the Néel temperature T_{N} ≈ 70 K and form a quasitwo dimensional triangular lattice with a fully compensated spin structure. The spins in the sublattices point along the local x axes^{11}. The magnetic space group of the ground state is \(P6_3^\prime cm\prime\), which gives rise to a SHG contribution coupling bilinearly to the ferroelectric and the AFM order parameter^{10} (Supplementary Fig. 1). The magnetic structure yields three orthogonal magnon modes, named X, Y and Zmode, which differ in the direction of the transiently appearing oscillating uncompensated magnetisation component. The individual modes can be excited optically and probed selectively depending on the setting of pump and probelight polarisations^{23}. Here, we exemplarily focus on the Zmode, which has A_{2} symmetry^{28}.
The optical properties of YMnO_{3} are wellstudied^{29}. Owing to the hexagonal crystal structure, the material is optically uniaxial, which enables birefringencefree measurements along the z axis. The dielectric spectrum is characterised by a chargetransfer transition around 1.6 eV^{30} and lowoptical absorption in the nearinfrared regime^{31}. In order to minimise parasitic, thermally induced, incoherent dynamics^{24}, we optically pump the material at 0.97 eV, where the residual absorption is <10% for our 20 μm thin sample and nonthermal excitation via the IFE dominates. We probe the optically induced dynamics at ħω = 1.22 eV, where on the one hand, the high transmittivity enables measurements of the Faraday rotation and on the other hand, efficient SHG is ensured by resonant coupling to a d–d transition of the Mn^{3+} ions at 2ħω^{32}.
Our setup is sketched in Fig. 1. Via the IFE, a circularly polarised pump pulse cants the spins in the xy plane by an angle γμ_{0}H_{IFE}τ, where γ is the gyromagnetic ratio, μ_{0} is the vacuum permeability and τ is the duration of the effective magnetic field pulse^{33}. The transmitted linearly polarised probe pulse is split behind the sample by a dichroic mirror for separate, yet simultaneous, TR detection of the Faraday rotation and of the relative change of the SHG intensity (η = ΔI_{SHG}/I_{SHG}).
Zmode observation by Faraday rotation and SHG
A typical measurement at 10 K is shown in Fig. 2. The Faraday rotation in Fig. 2a exhibits sinelike behaviour with a frequency of Ω/2π = 95.2 ± 0.3 GHz. The initial phase changes by π upon changing the pump helicity, as is expected for a Zmode excitation via the IFE^{23}. In parallel to the Faraday rotation, we measured the SHG response η for a probe polarisation enclosing an angle of ϕ ≈15° with respect to a crystallographic x axis. We find a coherent modulation of η on an incoherent background. By taking (η_{−} − η_{+})/2 and (η_{−} + η_{+})/2, with the sign indicating the pump–pulse helicity, we can separate helicitydependent and helicityindependent contributions, respectively (Fig. 2b). We find that the oscillatory component of η is fully contained in the helicitydependent contribution, while the helicityindependent contribution follows a single exponential decay with a timeconstant that is typical for oxide systems^{17}. We thus attribute the helicityindependent dynamics to thermalisation processes, in particular also because the quasiinstantaneous effect of possible nonthermal, helicityindependent excitations^{34} cannot explain the exponentially progressing, delayed reduction of SHG intensity in Fig. 2b.
The helicitydependent SHG difference in Fig. 2b reveals a modulation at the same frequency Ω as the Faraday rotation. We can, therefore, safely conclude that, just like the Faraday rotation, the SHG modulation is based on the optically excited spin precession. Note, however, that the Faraday rotation, which is proportional to the net magnetisation along the z axis, and the SHG modulation are out of phase by π/2. Hence, the SHG modulation cannot be based on the outofplane spin component. Since the linear transmittance of the sample both at ω and 2ω does not show any periodic changes either (see Supplementary Fig. 2), we are left with the only option that the SHG modulation reflects the dynamics of the compensated inplane spin component. We conclude that we observe a modulation of \({\cal{X}}_{ijk}\) induced by dynamic changes of the AFM order parameter \(\ell\). There are two fundamentally different mechanisms that can affect \({\cal{X}}_{ijk}\) through \(\ell\): (i) symmetryconserving dynamics involving amplitude modulations of the existing components \({\cal{X}}_{ijk}\). Examples are longitudinal coherent dynamics^{35,36}, changes of the exchange interaction^{37,38} as well as thermally induced quenching dynamics^{17,20}. Or (ii) symmetrychanging dynamics leading to the appearance of new components \({\cal{X}}_{ijk}\). Besides, e.g., spinreorientation^{39} and AFM switching processes^{1}, this also includes transversal spin dynamics, where precessional spin motion causes a redistribution among the \({\cal{X}}\) components with periodically arising and vanishing contributions.
TR modulation of the SHG anisotropy
We distinguish the two cases by measuring the angledependent anisotropy of the SHG signal before and after the excitation. In contrast to Fig. 2, which shows the dynamics of one arbitrary angular component of the SHG anisotropy, measuring the full angledependent SHG anisotropy allows us to determine any symmetry changes that might occur. Figure 3a shows the SHG anisotropy prior to excitation. It is in agreement with the \(P6_3^\prime cm\prime\) symmetry of the magnetic ground state with the Mn^{3+} spins oriented along equivalent crystallographic x axis. The anisotropy exhibits six lobes of amplitude A spaced 60° each. We define their orientation as θ = 0°.
The timedependent SHG intensities at four representative angular components are visualised in Fig. 3b (see “Methods” for details). We find cosinelike modulations with opposite phases at the two sides of a lobe (violet and yellow), but no modulation of the SHG intensity at the minima (blue) or maxima (red). This behaviour cannot be explained by a symmetryconserving breathing of the SHG anisotropy. Such breathing would manifest itself as an inphase modulation at the two sides of a lobe and at the maximum. Instead, the observed dynamics are in accordance with a coherent, periodic, smallangle rotation of the SHG anisotropy. By fitting the full SHG anisotropy, we can extract the pump induced changes of the amplitude A and the orientation θ. The results are shown in Fig. 3c, d, respectively.
The amplitude A exhibits an exponential decrease of the order of 10%. The change of A cannot be caused by changes of the optical properties as the slight changes of the transmittivity at ω and 2ω (see Supplementary Fig. 2) are not sufficient to explain the 10% decrease of A. Instead, the isotropic, i.e., polarisationindependent, behaviour is indicative of an incoherent relaxation. We, therefore, attribute this decay to longitudinal orderparameter dynamics, i.e. to a reduction of the total sublattice magnetisation gμ_{B}S related to the relaxation of photoexcited charge carriers.
As already indicated by Fig. 3b, d reveals a striking periodic rotation of the SHG anisotropy. The modulation frequency of Δθ matches that of the Faraday rotation, which confirms the magnetic origin. As illustrated in Fig. 3e, a rotated anisotropy can be decomposed into a linear superposition of two sixfold anisotropies at θ = 0° (spins along x axis, space group \(P6_3^\prime cm\prime\), red curve) and θ = 90° (spins along y axis, space group \(P6_3^\prime c\prime m\), blue curve). The superposition corresponds to a coherent deviation of the spins from the x axis towards the y axis and, therefore, to a symmetry reduction to \(P6_3^\prime\) or lower (see Supplementary Fig. 3). With tan α = S_{y}/S_{x}, we can write the dynamic SHG tensor as \({\cal{X}}(t) = \cos \alpha (t)\widetilde {\cal{X}}^g + \sin \alpha (t)\widetilde {\cal{X}}^e\) with timeindependent tensors \(\widetilde {\cal{X}}^g\) and \(\widetilde {\cal{X}}^e\). Thus, complementary to the Faraday rotation, which is sensitive to the uncompensated z component of the spin precession, the rotation of the SHG anisotropy reflects the transversal dynamics of the compensated spin component in the xy plane. Furthermore, according to the Curie principle^{40}, the isotropic effect of a thermal excitation cannot reduce the symmetry of \({\cal{X}}\). Thus, the SHG anisotropy rotation is a pristine measure of the nonthermal spin dynamics. Separating thermal and nonthermal dynamics is therefore possible.
Discussion
We can use the SHG measurements to quantify the spin deflection angle α according to 3Δθ ≈ ρα (see Supplementary Note 1), where \(\rho = \widetilde {\cal{X}}^e/\widetilde {\cal{X}}^g = 0.6\) is the amplitude ratio of the realvalued susceptibilities \(\widetilde {\cal{X}}_{ijk}\)^{13,41,42}. Note that ρ changes by ±0.3 within the probe laser linewidth, which introduces a systematic error of that order. From Fig. 3d, we extrapolate Δθ(0) = 0.198° ± 0.007° and, hence, α(0) = 1.0° with a statistical and systematic uncertainty of 0.035° and 0.5°, respectively. This, in turn, allows us to quantify the effective magnetic field of the IFE as α(0) = γμ_{0}H_{IFE}τ, where 1° corresponds to μ_{0}H_{IFE} ≈760 mT for τ = 130 fs (assuming the free electron value γ = 176 s^{1}T^{1}). Note that the optically induced spin canting by nonresonant excitation via the IFE is comparable to resonant excitation via the magnetic field component of a strong THz pulse^{43}.
In addition to the quantification of the basalplane spincanting angle, we can use the TR Faraday rotation to estimate the maximum outofplane spincanting angle as 2.4 mdeg (see Supplementary Note 2). Such a highly anisotropic spin precession is a general phenomenon in antiferromagnets and highlights the dominance of the exchange interaction over the weak magnetic inplane anisotropy^{8,28}.
After relating the basalplane spincanting angle α and the total sublattice magnetisation gμ_{B}S to the SHG anisotropy orientation and amplitude, respectively, we understand the measurement shown in Fig. 2 as follows: The observed TR SHG response is a superposition of longitudinal and transversal spin dynamics and therefore a combination of scenarios (i) and (ii). The time dependence of α, and hence S_{y}, is reflected by the periodic SHG modulation. We combine this with the S_{z}sensitive Faraday rotation to obtain the full orderparameter motion. By plotting the transversal spin components in Fig. 4, one can clearly recognise the magnonic damped elliptical motion (solid line).
We thus present a proofofconcept experiment, where we track the full threedimensional motion of an AFM order parameter. In our model compound, YMnO_{3}, SHG and Faraday rotation are combined to obtain the trajectory of an optically induced coherent spin precession. While the outofplane spin canting induces an uncompensated magnetic moment that causes a Faraday rotation, the basalplane canting and the total sublattice magnetisation are reflected in the SHG measurements. We quantify the optically induced canting as approximately 1°, corresponding to an effective magnetic field of the IFE of 760 mT. Key to this analysis is not the symmetry of the magnetic ground state, but the transient symmetry reduction during the coherent excitation of an A_{2} magnon mode. This symmetry reduction directly affects the highly symmetrysensitive SHG anisotropy and allows us to separate nonthermal spin dynamics from thermal electron dynamics. We emphasise though that our approach is not at all limited to harmonic smallamplitude dynamics. Instead, we exploit a fundamental excitation to showcase the insights provided by a TR symmetry analysis, while at the same time establishing a general approach for accessing orderparameter dynamics at subpicosecond timescales. Tracking the full orderparameter motion instead of just one component is indispensable for understanding the highly complex dynamics occurring during ultrafast switching, spinreorientation and other nonequilibrium phenomena.
Methods
Sample
Our YMnO_{3} sample is a single crystal grown by the floatingzone method. We oriented, cut and polished the sample to obtain a 20 μm thin slab with (0001)oriented surfaces for experiments in transmission geometry. The sample was mounted in a cryostat (Janis SVT400).
Pump–probe experimental setup
The fundamental light source of our setup is a regeneratively amplified Ti:Sapphire laser (Coherent, Legend, 2.5 W) producing 130 fs laser pulses at 1 kHz with a central photon energy of 1.55 eV. For our measurements, we used the output of two optical parametric amplifiers providing pump and probe pulses, respectively. To ensure excitation by the IFE, the circularly polarised pump pulses were tuned to 0.97 eV, where the absorption of YMnO_{3} is low. A residual absorption coefficient of ≈30 cm^{−1} at the pump photon energy and ≈40 cm^{−1} at the probe photon energy^{31} results in an absorption of ≈6% and ≈8%, respectively. The pump fluence was approximately 60 mJ cm^{−2}. Linearly polarised probe pulses at 1.22 eV allow for the detection of Faraday rotation and SHG. The pump and probe spots exhibit Gaussian profiles with diameters of approximately 180 and 150 μm, respectively. In order to observe the SHG modulation in Fig. 2, the linear polarisation was set to 15° relative to the crystallographic y axis, i.e., to an inclination point of the sixfold antiferromagnetic SHG anisotropy. The transmitted probe pulse passed a dichroic mirror that spatially separated the linear and nonlinear optical response. The Faraday rotation was detected using a balanced photodiode, while simultaneously a photomultiplier tube measured the SHG yield in the pumped and unpumped state.
SHG anisotropy measurements
All measurements were performed in nearnormal incidence. The polarisation dependence of the SHG anisotropy was obtained by keeping the sample fixed and rotating the light polarisation of the incoming probe laser pulse with a halfwave plate. The transmission direction of a GlanLaser prism inserted between the dichroic mirror and the photomultiplier tube (not shown in Fig. 1) was always set perpendicular to the polarisation of the incoming probe light. Each SHG anisotropy consists of 73 individual data points spaced by 5°. The changes of amplitude ΔA/A and orientation Δθ were extracted from a fit according to
The uncertainties shown in Fig. 3c, d denote standard errors of the amplitudes and orientations.
Figure 3b is obtained by normalising the SHG anisotropy for each delay time to its maximum, averaging each data point with its symmetry equivalent points, i.e.,
and plotting I_{ave}(0°), I_{ave}(±15°) and I_{ave}(−30°).
Data availability
The data that support the findings of this study are available from the corresponding author upon reasonable request.
References
Kimel, A. V. et al. Inertiadriven spin switching in antiferromagnets. Nat. Phys. 5, 727–731 (2009).
Wadley, P. et al. Electrical switching of an antiferromagnet. Science 351, 587–590 (2016).
Jungwirth, T., Marti, X., Wadley, P. & Wunderlich, J. Antiferromagnetic spintronics. Nat. Nanotechnol. 11, 231–241 (2016).
Gomonay, O., Baltz, V., Brataas, A. & Tserkovnyak, Y. Antiferromagnetic spin textures and dynamics. Nat. Phys. 14, 213–216 (2018).
Acremann, Y. et al. Imaging precessional motion of the magnetization vector. Science 290, 492–495 (2000).
Tesařová, N. et al. Direct measurement of the threedimensional magnetization vector trajectory in GaMnAs by a magnetooptical pumpandprobe method. Appl. Phys. Lett. 100, 102403 (2012).
Saidl, V. et al. Optical determination of the Néel vector in a CuMnAs thinfilm antiferromagnet. Nat. Photon. 11, 91–96 (2017).
Tzschaschel, Ch. et al. Ultrafast optical excitation of coherent magnons in antiferromagnetic NiO. Phys. Rev. B 95, 174407 (2017).
Zheng, Z. et al. Magnetooptical probe of ultrafast spin dynamics in antiferromagnetic CoO thin films. Phys. Rev. B 98, 134409 (2018).
Sa, D., Valentí, R. & Gros, C. A generalized GinzburgLandau approach to second harmonic generation. Eur. Phys. J. B 14, 301–305 (2000).
Fiebig, M., Pavlov, V. V. & Pisarev, R. V. Secondharmonic generation as a tool for studying electronic and magnetic structures of crystals: review. J. Opt. Soc. Am. B 22, 96–118 (2005).
Shen, Y. R. The Principles of Nonlinear Optics. (WileyInterscience, Hoboken, 2003).
Fiebig, M., Fröhlich, D., Lottermoser, Th. & Kohn, K. Spinangle topography of hexagonal manganites by magnetic secondharmonic generation. Appl. Phys. Lett. 77, 4401 (2000).
Chauleau, J.Y., Haltz, E., Carrétéro, C., Fusil, S. & Viret, M. Multistimuli manipulation of antiferromagnetic domains assessed by secondharmonic imaging. Nat. Mater. 16, 803–807 (2017).
Huber, L. et al. Coherent acoustic perturbation of secondharmonic generation in NiO. Phys. Rev. B 92, 094304 (2015).
Kirilyuk, A., Kimel, A. V. & Rasing, Th. Ultrafast optical manipulation of magnetic order. Rev. Mod. Phys. 82, 2731–2784 (2010).
Satoh, T., Van Aken, B. B., Duong, N. P., Lottermoser, Th. & Fiebig, M. Ultrafast spin and lattice dynamics in antiferromagnetic Cr_{2}O_{3}. Phys. Rev. B 75, 155406 (2007).
Matsubara, M., Kaneko, Y., He, J.P., Okamoto, H. & Tokura, Y. Ultrafast polarization and magnetization response of multiferroic GaFeO_{3} using timeresolved nonlinear optical techniques. Phys. Rev. B 79, 140411(R) (2009).
Sala, V. G. et al. Resonant optical control of the structural distortions that drive ultrafast demagnetization in Cr_{2}O_{3}. Phys. Rev. B 94, 014430 (2016).
Sheu, Y. M., Ogawa, N., Kaneko, Y. & Tokura, Y. Photocreating supercooled spiralspin states in a multiferroic manganite. Phys. Rev. B 94, 081107(R) (2016).
Satoh, T. et al. Spin oscillations in antiferromagnetic NiO triggered by circularly polarized light. Phys. Rev. Lett. 105, 077402 (2010).
Ivanov, B. A. Spin dynamics of antiferromagnets under action of femtosecond laser pulses (Review Article). Low Temp. Phys. 40, 91–105 (2014).
Satoh, T., Iida, R., Higuchi, T., Fiebig, M. & Shimura, T. Writing and reading of an arbitrary optical polarization state in an antiferromagnet. Nat. Photon. 9, 25–29 (2015).
Bossini, D. & Rasing, Th. Femtosecond optomagnetism in dielectric antiferromagnets. Phys. Scr. 92, 024002 (2017).
Satoh, T. et al. Excitation of coupled spinorbit dynamics in cobalt oxide by femtosecond laser pulses. Nat. Commun. 8, 638 (2017).
Němec., P., Fiebig, M., Kampfrath, T. & Kimel, A. V. Antiferromagnetic optospintronics. Nat. Phys. 14, 229–241 (2018).
Lilienblum, M. et al. Ferroelectricity in the multiferroic hexagonal manganites. Nat. Phys. 11, 1070–1073 (2015).
Toulouse, C. et al. Lattice and spin excitations in multiferroic hYMnO_{3}. Phys. Rev. B 89, 094415 (2014).
Wang, Y. T., Luo, C. W. & Kobayashi, T. Understanding multiferroic hexagonal manganites by static and ultrafast optical spectroscopy. Adv. Condens. Matter Phys. 2013, 104806 (2013).
Kalashnikova, A. M. & Pisarev, R. V. Electronic structure of hexagonal rareearth manganites RMnO_{3}. J. Exp. Theor. Phys. 78, 143–147 (2003).
Babonas, G.J., Grivel, J.C., Reza, A. & Girkantaite, R. Ellipsometric studies of ErMnO_{3} single crystals. Lith. J. Phys. 47, 309–314 (2007).
Degenhardt, C., Fiebig, M., Fröhlich, D., Lottermoser, Th. & Pisarev, R. V. Nonlinear optical spectroscopy of electronic transitions in hexagonal manganites. Appl. Phys. B 73, 139–144 (2001).
Landau, L. D., Pitaevskii, L. P. & Lifshitz, E. M. Electrodynamics of Continuous Media. (Pergamon, Oxford, 1984).
Mikhaylovskiy, R. V. et al. Ultrafast optical modification of exchange interactions in iron oxides. Nat. Commun. 6, 8190 (2015).
Sheu, Y. M., Ogawa, N., Tokunaga, Y., Chan, H. C. & Tokura, Y. Selective probe of coherent polar phonon and quasiferromagnetic resonance modes in multiferroic GdFeO_{3}. Phys. Rev. B 98, 100301(R) (2018).
Mankowsky, R., von Hoegen, A., Först, M. & Cavalleri, A. Ultrafast reversal of the ferroelectric polarization. Phys. Rev. Lett. 118, 197601 (2017).
Melnikov, A. et al. Coherent optical phonons and parametrically coupled magnons induced by femtosecond laser excitation of the Gd(0001) surface. Phys. Rev. Lett. 91, 227403 (2003).
Matsubara, M. et al. Ultrafast optical tuning of ferromagnetism via the carrier density. Nat. Commun. 6, 6724 (2015).
Kimel, A. V., Kirilyuk, A., Tsvetkov, A., Pisarev, R. V. & Rasing, Th. Laserinduced ultrafast spin reorientation in the antiferromagnet TmFeO_{3}. Nature 429, 850–853 (2004).
Hargittai, I. & Vainshtein, B. K. Crystal Symmetries. (Pergamon, Amsterdam, 1989).
IizukaSakano, T., Hanamura, E. & Tanabe, Y. Secondharmonicgeneration spectra of the hexagonal manganites RMnO_{3}. J. Phys. 13, 3031–3055 (2001).
Lottermoser, Th. Elektrische und Magnetische Ordnung Hexagonaler Manganite. (PhD Thesis, Dortmund, 2002).
Baierl, S. et al. Terahertzdriven nonlinear spin response of antiferromagnetic nickel oxide. Phys. Rev. Lett. 117, 197201 (2016).
Acknowledgements
The authors thank Morgan Trassin and Mads Weber for valuable discussions. T.S. was supported by Japan Society for the Promotion of Science (JSPS) KAKENHI (Nos. JP15H05454, JP19H01828 and JP26103004) and JSPS CoretoCore Programme (A. Advanced Research Networks). C.T. and M.F. acknowledge support from the SNSF project 200021/147080 and by FAST, a division of the SNSF NCCR MUST. M.F. thanks ETH Zurich and CEMS at RIKEN for support of his research sabbatical.
Author information
Authors and Affiliations
Contributions
T.S. conceived the project. C.T. designed, conducted and evaluated the experiments. T.S. and M.F. supervised the project. All authors discussed the results and contributed to the writing of the paper.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Peer review information: Nature Communications thanks Alireza Qaiumzadeh, and other anonymous reviewer(s) for their contribution to the peer review of this work. Peer reviewer reports are available.
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Tzschaschel, C., Satoh, T. & Fiebig, M. Tracking the ultrafast motion of an antiferromagnetic order parameter. Nat Commun 10, 3995 (2019). https://doi.org/10.1038/s41467019119619
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41467019119619
Further reading

Coherent helicitydependent spinphonon oscillations in the ferromagnetic van der Waals crystal CrI3
Nature Communications (2022)

Large ultrafastmodulated Voigt effect in noncollinear antiferromagnet Mn3Sn
Nature Communications (2021)

Ultrafast reorientation of the Néel vector in antiferromagnetic Dirac semimetals
npj Computational Materials (2021)

Efficient spin excitation via ultrafast dampinglike torques in antiferromagnets
Nature Communications (2020)
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.