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# Decoupling of static and dynamic criticality in a driven Mott insulator

## Abstract

Strongly driven antiferromagnetic Mott insulators have the potential to exhibit exotic transient phenomena that are forbidden in thermal equilibrium. However, such far-from-equilibrium regimes, where conventional time-dependent Ginzburg-Landau descriptions fail, are experimentally challenging to prepare and to probe especially in solid state systems. Here we use a combination of time-resolved second harmonic optical polarimetry and coherent magnon spectroscopy to interrogate n-type photo-doping induced ultrafast magnetic order parameter dynamics in the antiferromagnetic Mott insulator Sr2IrO4. We find signatures of an unusual far-from-equilibrium critical regime in which the divergences of the magnetic correlation length and relaxation time are decoupled. This violation of conventional thermal critical behavior arises from the interplay of photo-doping and non-thermal magnon population induced demagnetization effects. Our findings, embodied in a non-equilibrium phase diagram, provide a blueprint for engineering the out-of-equilibrium properties of quantum matter, with potential applications to terahertz spintronics technologies.

## Introduction

Dynamically driven interacting quantum many-body systems have the potential to exhibit properties that defy the laws of equilibrium statistical mechanics. A widely studied model is the impulsively driven antiferromagnetic (AFM) Mott insulator, which is predicted to realize exotic transient phenomena including dynamical phase transitions into thermally forbidden states1,2,3 and highly non-thermal magnon distributions4. The single-layer perovskite iridate Sr2IrO4 is a prototypical spin-orbit coupled AFM Mott insulator, serving as an ideal platform to explore such out-of-equilibrium behaviors. The low energy electronic structure of Sr2IrO4 consists of a completely filled band of spin-orbital entangled pseudospin Jeff = 3/2 states and a narrow half-filled band of Jeff = 1/2 states, which splits into lower and upper Hubbard bands due to on-site Coulomb repulsion5. Short-range AFM correlations between Jeff = 1/2 moments within a layer are established well above room temperature6,7. But owing to weak interlayer exchange coupling (Jc < 10−3Jab)7,8, three-dimensional (3D) long-range AFM ordering only occurs below a Néel temperature TN = 230 K. The ordered structure exhibits a weak in-plane ferromagnetic moment in each layer due to pseudospin canting, which is staggered along the c-axis (Fig. 1a). Resonant x-ray and neutron scattering measurements of La-doped Sr2IrO4 have shown that a small concentration of n-type carriers destroys c-axis ordering, leaving behind a paramagnetic state with short-range 2D AFM correlations9,10,11. As such, n-type photo-doping, which may be simulated by optically pumping electrons from the electronically inert Jeff = 3/2 band into the upper Hubbard band, provides a potential pathway to impulsively quench long-range AFM order.

Recently, both ultrafast optical and free-electron laser-based resonant x-ray scattering (RXS) methods have been used to probe photo-doping induced pseudospin dynamics in iridates12,13,14,15,16. In the case of Sr2IrO4, one study showed that it could be made magneto-optically active by aligning the canted moments in an external magnetic field14. Transient magnetization dynamics were then probed in the near-equilibrium weak photo-doping limit using time-resolved magneto-optical Kerr effect (MOKE) spectroscopy. The recovery time of the net magnetization was observed to diverge at TN, which was explained within a time-dependent Ginzburg–Landau framework. In another pair of studies, time-resolved RXS was used to probe long-range AFM order parameter dynamics without a field in a far-from-equilibrium strong photo-doping regime12,13. A non-thermal melting of the AFM order was achieved, but no critical dynamics were resolved across this phase transition.

The behavior of a system near a dynamical phase boundary should be sensitive to small changes in excitation density. In order to resolve out-of-equilibrium critical dynamics, it is therefore imperative that the excitation density be uniform throughout the probed volume and finely sampled near the phase boundary. Since the pump excitation density invariably decays with depth into the sample, one should in principle probe exclusively within a small interval of depth to minimize the effects of averaging over different excitation densities, which might otherwise obscure features of criticality (Supplementary Notes 1 and 2).

Here we meet this condition by using time-resolved second harmonic generation rotational anisotropy (SHG-RA). In combination with time-resolved MOKE, we probe the transient suppression and recovery of long-range magnetic order in Sr2IrO4 induced by n-type photo-doping. We report signatures of an unusual far-from-equilibrium critical regime in which the divergences of the magnetic correlation length and relaxation time are decoupled.

## Results

### Pump-induced instantaneous SHG response

The SHG-RA technique (Fig. 1b) was recently shown to be directly sensitive to the magnetization of the topmost layer of Sr2IrO4 in zero magnetic field17,18. We note that while an additional hidden order has been reported in Sr2IrO419,20, there is no indication that SHG couples to any hidden order18, contrary to a previous interpretation21. In an SHG-RA experiment, light is focused obliquely onto the (001) face of Sr2IrO4 and the intensity of light reflected at twice the incident frequency I(2ω) is measured as the scattering plane is rotated about the surface normal. In equilibrium, SHG-RA patterns acquired above TN exhibit four-fold (C4) rotational symmetry, arising from bulk electric-quadrupole (EQ) radiation from its centrosymmetric crystallographic point group18. Below TN, an additional surface magnetization-induced electric-dipole (SMIED) contribution turns on and interferes with the EQ contribution, lowering the symmetry of the SHG-RA pattern from C4 to C1 (Fig. 1c).

To study the effects of n-type photo-doping, we developed time-resolved pump-probe SHG-RA using the apparatus depicted in Fig. 1b. The pump beam, which was tuned on resonance with the Jeff = 3/2 band to upper Hubbard band transition, and probe beam were focused within a single magnetic domain for our experiments. Figure 1d shows transient SHG-RA data acquired at the instant of pump excitation (t = 0) as a function of pump fluence (F). In the un-pumped case (F = 0), the C1 symmetry of the SHG-RA pattern is manifested through the presence of a dominant intensity lobe, indicating a finite SMIED contribution and thus a finite magnetic order parameter. As F increases, the intensity of the dominant lobe decreases linearly until it plateaus above a critical fluence Fc ≈ 0.9 mJ/cm2. Beyond Fc, the non-magnetic C4 symmetry is fully restored to the SHG-RA pattern, signaling a collapsed SMIED contribution. The slightly higher C4-EQ yield from the pump-induced compared to heating-induced non-magnetic state likely arises from un-relaxed bulk magneto-elastic deformations that will be discussed in more detail below. The prompt change in the SHG-RA pattern within the time resolution of our instrument (<200 fs) for all fluences is consistent with a photo-doping scenario. Specifically, AFM order is suppressed by magnetic defects that are left in the wake of propagating doublons (Fig. 1b), which are generated on the timescale of the nearest-neighbor hopping (<20 fs)14,22,23. Moreover, the observed critical fluence corresponds to an excitation density (nex) of approximately 0.05 per iridium site, which is close to the reported critical La-doping level to suppress AFM order9,10, suggestive of an optical n-type doping induced quench mechanism.

More detailed comparisons between the properties of Sr2IrO4 in and out-of-equilibrium can be made by mapping the fluence versus temperature magnetic phase diagram. This is accomplished by collecting an array of SHG-RA patterns immediately after optical excitation across different starting temperatures and pump fluences and then tracking the onset of the SMIED contribution. For F = 0, the SMIED contribution emerges below TN as expected (Fig. 2a). With increasing F, this transition shifts monotonically to lower temperatures, indicating that Fc increases upon cooling. By plotting TN as a function of nex, or equivalently Fc as a function of T, a sharp out-of-equilibrium magnetic phase boundary is identified. Despite an instantaneous electronic temperature that already far exceeds TN at F ≈ 0.2 mJ/cm2 based on the electronic specific heat of Sr2IrO4 (see Supplementary Note 3), the photo-doping and La-doping phase boundaries nearly coincide over the small La-doping range where AFM order exists in equilibrium9,10 (Fig. 2b). This indicates that heat transfer from the charge to pseudospin subsystem is negligible near t = 0. Since chemical doping differs from photo-doping in non-trivial ways, including the introduction of a disorder that is known to nucleate non-magnetic metallic puddles in La-doped Sr2IrO49,24, we refrain from drawing more detailed comparisons.

At later time delays, the charge, pseudospin, and lattice subsystems are typically expected to thermalize and thus the out-of-equilibrium phase diagrams mapped at t ≈ 0 and t 0 should be different. Figure 2c shows the intensity of the dominant SHG-RA lobe over a range of fluence values, converted into effective temperatures using the total specific heat of Sr2IrO4 (see Supplementary Note 3), acquired at t = 10 ps, which far exceeds the reported charge and lattice relaxation timescales but is much shorter than the timescale for heat to escape the probed region23,25. At low fluences, we find excellent agreement with the un-pumped temperature dependence data, confirming a pure optical heating effect. Surprisingly however, there is increasing bifurcation of the curves above F ≈ 0.8 mJ/cm2, leading to a growing mismatch between the out-of-equilibrium phase boundary mapped at t = 10 ps and that calculated assuming pure optical heating as a function of fluence (Fig. 2d). This indicates that thermalization of the pseudospin subsystem is impeded at high fluences.

A hallmark of the La-doping induced paramagnetic state is the persistence of short-range intralayer AFM correlations, manifested through remnant dispersive 2D magnons detected by resonant inelastic x-ray scattering10,11. To search for similar intralayer correlations in the photo-induced paramagnetic phase of Sr2IrO4, we leverage the fact that the zone center 2D magnon mode with B2g symmetry is weakly gapped (≈2 meV) and Raman active26,27. This allows the magnon to be coherently excited by our pump pulse via impulsive stimulated Raman scattering and optically tracked in the time domain using ultrafast MOKE spectroscopy28. Figure 2e, f show typical SHG and MOKE transients acquired in the high pump fluence (FFc) regime. Despite a complete collapse of the magnetic order parameter over the displayed 10 ps time window (Fig. 2e) as evidenced by an absence of any SMIED contribution, coherent oscillations of the infinite wavelength B2g magnon continue to be supported (Fig. 2f). This provides clear evidence of a significant 2D magnetic correlation length in the transient paramagnetic state, suggesting a non-thermal analog of La-doped Sr2IrO4 is realized. These results are consistent with and complementary to a time-resolved RXS study of Sr2IrO412, which showed that photo-doping strongly suppresses an AFM Bragg peak but does not alter the main high energy and short-wavelength features of the intralayer magnon spectrum (see Supplementary Note 4).

### Temporal evolution of the SHG response

Having comprehensively mapped the transient magnetic phase diagram of Sr2IrO4, we now finely examine the out-of-equilibrium critical dynamics. Figure 3a, b show the time-dependent change in intensity ΔI(2ω) of the dominant SHG-RA lobe acquired at T = 80 K over a range of pump fluences. For FFc (Fig. 3a), we observe a rapid drop in ΔI(2ω) at t = 0 signifying a reduction of the SMIED contribution. This is followed by an exponential recovery with rise time τ ≈ 1–2 ps towards a value negatively offset from the t < 0 intensity, which we showed (Fig. 2c, d) represents a thermalized state with a slightly elevated temperature. As F increases, τ rises slightly but exhibits no discontinuity at Fc despite the SMIED contribution vanishing. However, as F exceeds Fc, the point where C4 symmetry is restored, τ continues to grow and eventually diverges around F* ≈ 1.6 mJ/cm2 (Fig. 3b, c). Similar dynamics are observed if instead F is kept fixed and T is varied (inset Fig. 3a). These data reveal that the divergence of the magnetic correlation length and relaxation time occur along separated critical lines in the out-of-equilibrium phase diagram marked by Fc and F* respectively (inset Fig. 3c). Such a decoupling is forbidden in equilibrium and is also not observed across dynamical phase transitions in weakly correlated ferromagnets29 and charge density wave systems30.

We note the presence of a subtle exponential drop just after t = 0 that becomes more pronounced at large F. This causes ΔI(2ω) to drop below the instantaneous EQ value (gray bar in Figs. 1 and 3a, b) and ultimately plateau at the high-temperature EQ value upon reaching F*. Given that magneto-elastic deformations are known to occur below TN in Sr2IrO48 and can cause small changes in the EQ response, a possible origin of this exponential component is lattice relaxation following impulsive suppression of the magnetic order parameter. Therefore, only at large F when τ sufficiently exceeds the relevant phonon timescales do the magneto-elastic deformations have time to fully relax (see Supplementary Note 5).

## Discussion

To check whether the divergence of τ simply results from a prolonged photo-dopant lifetime, we performed simultaneous transient linear reflectivity (ΔR/R) and SHG-RA measurements below TN to directly compare the charge and pseudospin dynamics. As shown in Fig. 4a–c, the generation of photo-dopants and their subsequent suppression of the SMIED contribution both occur within the time resolution of our experiment. However, unlike the SHG response, we observe no saturation in the amplitude of ΔR/R and no significant change in its characteristic recovery time (τ0 ≈ 1 ps) as a function of fluence (inset Fig. 4a), demonstrating that the slow dynamics observed at F* occur exclusively in the pseudospin sector. This suggests that τ must be governed by the relaxation of excess magnons that are emitted upon doublon decay. One possibility is that the magnons rapidly thermalize to a higher temperature and that τ represents the timescale for the hot pseudospin subsystem to cool via heat exchange with the lattice and charge subsystems. However, a three-temperature model describing this process predicts that magnons should cool faster at higher excitation densities. Moreover, it fails to produce any diverging timescale (Supplementary Notes 3 and 6). This points to the alternative possibility that τ represents the timescale for the pseudospin subsystem to internally thermalize.

The rate-limiting step for recovering long-range magnetic order is the establishment of c-axis correlations (Fig. 2e, f). Therefore τ must be set by the thermalization time of interlayer c-axis magnons. However, the large mismatch between Jc (≈10 μeV)7,8 and both the charge gap (≈250 meV)31 and lowest optical phonon energy (≈10 meV)27 of Sr2IrO4 should impede c-axis magnon thermalization via charge or phonon excitation processes, leaving magnon–magnon scattering as the dominant thermalization channel. Building on the seminal work of Hohenberg and Halperin32, we study the critical dynamics after doublon decay of this effectively closed c-axis magnon subsystem via a general stochastic Langevin equation for a real order parameter in one spatial dimension (Supplementary Note 7):

$${\partial }_{t}{\varphi }_{k}\left(t\right)=-\left({{k}^{2}+\tau }_{0}^{-1}\right){\varphi }_{k}\left(t\right)-\lambda \int \frac{d{k}_{1}}{2\pi }\int \frac{d{k}_{2}}{2\pi }{\varphi }_{{k}_{1}}\left(t\right){\varphi }_{{k}_{2}}\left(t\right){\varphi }_{{k-k}_{1}-{k}_{2}}\left(t\right)+{\xi }_{k}\left(t\right)$$
(1)

where $${\varphi }_{k}\left(t\right)$$ is the k-th Fourier component of the magnetic order parameter field $$\varphi \left(z,t\right)$$ that parameterizes the ordering of the intralayer Néel vector along the c-axis (Fig. 4d, e), $${\tau }_{0}^{-1}$$ is a temperature-dependent mass term that is equivalent to the thermalization rate in a linearized Boltzmann equation33, and λ parameterizes the interaction between magnons. Going beyond conventional time-dependent Ginzburg–Landau descriptions, we introduce a Gaussian noise term $${\xi }_{k}\left(t\right)$$ with $$\langle {\xi }_{k}(t){\xi }_{k^{\prime} }(t^{\prime} )\rangle =\delta (t-t^{\prime} )\delta (k+k^{\prime} )({k}^{2}+{\tau }_{0}^{-1})[2{n}_{k}(t)+1]$$ that imprints a non-equilibrium fluctuation-dissipation relation for some general magnon distribution function $${n}_{k}\left(t\right)$$, in which the modes transverse to the c-axis are assumed to relax much faster and are thus integrated out34. To leading order, the equation of motion for the magnetic order parameter $${{\Phi }}\left(t\right)=\langle {\varphi }_{k = 0}(t)\rangle$$ is given by $${\partial }_{t}{{\Phi }}\left(t\right)=-{\tau }^{-1}{{\Phi }}\left(t\right)-\lambda {{{\Phi }}\left(t\right)}^{3}$$, and the Boltzmann equation for the magnon distribution is given by $${\partial }_{t}{n}_{k}\left(t\right)=-\left|{\tau }^{-1}\right|\left[{n}_{k}\left(t\right)-{n}_{k}^{T}\right]$$, where $${\tau }^{-1}={\tau }_{0}^{-1}-\lambda {N}_{{{{{{{{\rm{mag}}}}}}}}}$$ and $${n}_{k}^{T}$$ is the Bose distribution function corresponding to the final equilibrated magnon temperature T. These equations show that, in a closed system, the rate at which the magnetic order parameter recovers to its equilibrium value at T via magnon thermalization is a decreasing function of the total number of excited magnons (Nmag). This provides an explanation for all key features of the data in Fig. 3c. In the low pump fluence limit where Nmag 1/τ0λ, τ approaches a lower bound that is naturally set by the photo-dopant decay time τ0. As Nmag grows with fluence, τ exhibits a power-law increase following the reduced curvature of the Mexican hat potential. Finally once Nmag reaches 1/τ0λ at the critical fluence F*, τ diverges even though the total energy of the magnetic subsystem remains sub-critical (see Supplementary Note 7). For F ≥ F*, thermalization can still eventually occur through the weak coupling between c-axis magnons and phonons, which is likely responsible for the slow (>100 ps) recovery of the magnetic order parameter observed by time-resolved RXS measurements at high fluences12,13. Ultimately, on even longer timescales, the system cools back to the initial temperature via heat diffusion out of the pumped region (Fig. 4d, e).

## Conclusions

Altogether, our results provide experimental signatures that static and dynamic critical behavior can be decoupled in a Mott antiferromagnet upon driving due to a subtle interplay of photo-doping and magnon thermalization processes (Fig. 4d, e). The hierarchy of magnetic, phononic and charge gap energy scales that enables this behavior in Sr2IrO4 is typical for layered transition metal oxide based AFM Mott insulators including the high-Tc superconducting cuprates, suggesting that our reported phenomena may be operational in numerous layered quantum materials. This raises the intriguing prospect of fine-tuning parameters such as τ0, Fc, and F* to optimize desired out-of-equilibrium properties. For example, extending τ0 may be a pathway for realizing metastable electronic instabilities in a photo-doped Mott insulator, while the combination of a small τ0 and Fc with a large F* would be favorable for low-power high-speed AFM switching applications.

## Methods

### Sample growth

Single crystals of Sr2IrO4 were grown using a self-flux technique from off-stoichiometric quantities of IrO2, SrCO3, and SrCl2. The ground mixtures of powders were melted at 1470C in partially capped platinum crucibles. The soaking phase of the synthesis lasted for >20 h and was followed by a slow cooling at 2 °C/h to reach 1400 C. From this point, the crucible is brought to room temperature through rapid cooling at a rate of 100 °C/h. Crystals were cleaved along the (001) face just prior to measurements and immediately pumped down to a pressure < 5 × 10−6 torr in an optical cryostat.

### Time-resolved spectroscopic probes

#### Time-resolved SHG-RA

Experiments were performed by splitting light from a regeneratively amplified Ti:sapphire laser, which produces 100 fs pulses with central wavelength λ = 800 nm at a repetition rate of 100 kHz, into pump and probe arms. The pump beam feeds an optical parametric amplifier, whose 1400 nm output beam is linearly polarized and sent through a delay line before being focused at normal incidence onto a 90 μm spot (FWHM) located within a single magnetic domain of a Sr2IrO4 crystal. As shown in Fig. 1b, the circularly polarized probe laser pulse (λ = 800 nm) traverses a linear input polarizer, phase mask, and collimating lens and is focused at oblique incidence (≈10) onto a 30 μm spot within the pumped sample area using an objective lens. The reflected SHG pulse (λ = 400 nm) is re-collimated by the objective lens, linearly polarized by an output polarizer and then deflected onto a CCD camera by a triad of dichroic mirrors, which measures the SHG intensity at a fixed time delay with respect to the pump. The probe fluence was fixed to 1.5 mJ/cm2. A complete instantaneous SHG-RA pattern is acquired by mechanically co-rotating the input polarizer, phase mask, and output polarizer, which implements a rotation of the probe scattering plane about the sample surface normal, and then projecting the SHG light reflected at each scattering plane angle onto different positions along a circular locus of points on the CCD camera (see ref. 35 for further details). The procedure for converting raw CCD data to the polar SHG-RA plots shown in the main text is described in Supplementary Note 8. The SHG dynamics shown in Fig. 3 were reproduced under different polarization geometries and different scattering plane angles as shown in Supplementary Note 9.

#### Time-resolved linear reflectivity

Transient reflectivity measurements were performed using exactly the same setup as that used for time-resolved SHG-RA as described above. Identical experimental conditions were preserved for the reflectivity and SHG-RA measurements, with the only change between experimental runs being the spectral filtering optics before the CCD camera to either isolate the 800 nm or 400 nm output.

#### Time-resolved MOKE

Experiments were performed by splitting light from a regeneratively amplified Ti:sapphire laser (repetition rate 1 kHz; pulse energy 6 mJ; pulse duration 100 fs; central wavelength λ = 800 nm) into pump and probe arms. The pump arm feeds a collinear dual-stage optical parametric amplifier, whose 1300 nm output beam is circularly polarized and then focused onto the sample at normal incidence (F = 4.6 mJ/cm2). The probe arm (λ = 800 nm) is linearly S-polarized and focused near normal incidence onto the sample. To measure the polarization rotation (Kerr) angle of the reflected probe light, the reflected probe beam is sent through a half-wave plate followed by a Wollaston prism. These optics are oriented such that in the absence of a pump beam (θk = 0), two equally intense beams of orthogonal linear polarization are produced, which are fed into the two input channels of a balanced photo-detector.

### Conversion from F to nex

The number of photo-excitations nex created by the pump beam was calculated using the following equation:

$${n}_{{{{{{{{\rm{ex}}}}}}}}}=\frac{F\left(1-R\right){V}_{{{{{{{{\rm{u.c.}}}}}}}}}}{{N}_{{{{{{{{\rm{Ir}}}}}}}}}{E}_{{{{{{{{\rm{ph}}}}}}}}}\delta }$$
(2)

where F is the pump fluence, R = 0.2 and δ = 100 nm are the sample reflectivity and penetration depth respectively at the pump wavelength λ = 1400 nm36,37, Vu.c. is the unit cell volume of Sr2IrO4, NIr is the number of Ir atoms per unit cell, and Eph the pump photon energy (0.89 eV).

### Exponential fitting procedure for linear reflectivity

Transient linear reflectivity curves were fit to a double exponential function of the form $${{\Delta }}R/R=A{e}^{-t/{\tau }_{0}}+B{e}^{-t/{\tau }_{1}}+C$$. A high quality of fit is achieved as shown in Fig. 4a. The timescales extracted for τ0 (≈1 ps) and τ1 (≈200 fs) agree with the two exponential timescales associated with the decay of photo-induced midgap states observed by ultrafast angle-resolved photoemission spectroscopy measurements23, attributed to acoustic phonon and optical phonon mediated photo-carrier relaxation processes respectively. Since the rate-limiting step for photo-carrier relaxation is τ0, that is what we plot in the inset of Fig. 4a. We note that ref. 23, also reported an absence of any fluence dependence for τ0, which is consistent with our observations (inset Fig. 4a).

## Data availability

All relevant data presented in this paper are available from the corresponding author upon reasonable request.

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## Acknowledgements

We thank L. Balents, A. Cavalleri, S. K. Cushing, E. Demler, S. Di. Matteo, M. Endres, B. Fine, N. Gedik, D. Kennes, O. Mehio, H. Ning, M. Norman, and M. Sentef for useful discussions. This work is supported by ARO MURI Grant No. W911NF-16-1-0361. D.H. also acknowledges support for instrumentation from the David and Lucile Packard Foundation and from the Institute for Quantum Information and Matter (IQIM), an NSF Physics Frontiers Center (PHY-1733907). A.d.l.T. acknowledges support from the Swiss National Science Foundation through an Early Postdoc Mobility Fellowship (P2GEP2165044). M.B. acknowledges support from the Alexander von Humboldt foundation. N.J.L. acknowledges support from an IQIM Fellowship. G.C. acknowledges NSF support via a grant DMR-1712101.

## Author information

Authors

### Contributions

X.C., S.D.W., and G.C. synthesized and characterized the Sr2IrO4 crystals. A.d.l.T., K.L.S., and I.P. performed the SHG-RA measurements. J.W.H., L.Z., and A.d.l.T. built the SHG-RA apparatus. G.Z. and R.D.A. performed the MOKE measurements. M.B., Y.B., and G.R. performed the Langevin theory calculations. A.d.l.T., N.J.L., and D.H. analyzed the data. A.d.l.T. and D.H. wrote the paper with input from all authors.

### Corresponding author

Correspondence to David Hsieh.

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### Competing interests

The authors declare no competing interests.

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de la Torre, A., Seyler, K.L., Buchhold, M. et al. Decoupling of static and dynamic criticality in a driven Mott insulator. Commun Phys 5, 35 (2022). https://doi.org/10.1038/s42005-022-00813-6

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• DOI: https://doi.org/10.1038/s42005-022-00813-6