Light can be used to modify and control properties of media, as in the case of electromagnetically induced transparency or, more recently, for the generation of slow light or bright coherent extreme ultraviolet and X-ray radiation. Particularly unusual states of matter can be created by light fields with strengths comparable to the Coulomb field that binds valence electrons in atoms, leading to nearly free electrons oscillating in the laser field and yet still loosely bound to the core1,2. These are known as Kramers–Henneberger states3, a specific example of laser-dressed states2. Here, we demonstrate that these states arise not only in isolated atoms4,5, but also in rare gases, at and above atmospheric pressure, where they can act as a gain medium during laser filamentation. Using shaped laser pulses, gain in these states is achieved within just a few cycles of the guided field. The corresponding lasing emission is a signature of population inversion in these states and of their stability against ionization. Our work demonstrates that these unusual states of neutral atoms can be exploited to create a general ultrafast gain mechanism during laser filamentation.


It is often assumed that photo-ionization happens faster in more intense fields. Yet, since the late 1980s, theorists have speculated that atomic states become more stable when the strength of the laser field substantially exceeds the Coulomb attraction to the ionic core1,6,7,8,9,10,11,12,13,14. The electron becomes nearly but not completely free: rapidly oscillating in the laser field, it still feels residual attraction to the core, which keeps it bound. The effective binding potential, averaged over the electron oscillations, is sketched in Fig. 1a. It has a characteristic double-well structure, the wells occur when the oscillating electron turns around near the core. The laser-modified potential also modifies the spectrum, with laser-induced shifts adding to the familiar ponderomotive shift associated with nearly free electron oscillations. We refer to these states as ‘strongly driven laser-dressed states’. In spite of many theoretical predictions, it took three decades before their existence was inferred in experiments2,4,5, showing neutral atoms surviving laser intensities as high as I≈1015 –1016 W cm2.

Fig. 1: Kramers–Henneberger potential and simulated absorption spectra of an Ar atom dressed by a strong IR pulse.
Fig. 1

a, The KH potential for different pulse intensities, for 800 nm, developing the characteristic double-well shape. The insets show the potential in cylindrical coordinates. b,c, Time- and frequency-resolved absorption profiles, (where negative absorption signifies gain and positive absorption signifies loss), for a Gabor window of T = 500 a.u. and intensities of 1.4 × 1014 W cm2 (b) and 1.9 × 1014 W cm2 (c). d, Frequency-resolved absorption during the IR pulse. Different curves correspond to different peak intensities of the dressing IR field.

But are such unusual states really exotic? Can they also form in gases at ambient conditions, at intensities well below 1015–1016 W cm2? After all, for excited electronic states bound by a few electronvolts, the laser field overpowers the Coulomb attraction to the core at I≈1013−1014 W cm2. If so, would these states manifest inside laser filaments, the self-guiding light structures created by the nonlinear medium response at I≈1014 W cm2 (ref. 15)?

The formation of the Kramers–Henneberger (KH) states should modify both the real16 and imaginary17 parts of the medium's refractive index. While their response is almost free-electron-like, they do form discrete states and lead to new resonances. Crucially, at sufficiently high intensities, theory predicts the emergence of population inversion in these states, relative to the lowest excited states5,18. If the inversion is created inside a laser filament18, it would lead to amplification of the filament spectrum at the transition frequencies between the stabilized states.

We first confirm these expectations by directly solving the time-dependent Schrödinger equation (TDSE). We then observe these states experimentally via the emergence of absorption and stimulated emission peaks at transition wavelengths not present in the field-free atom or ion. Notably the gain takes place in neutral atoms, and we are able to achieve gain only by using shaped laser pulses, tailored to a few-cycle resolution. We also confirm theoretically that for our experimental conditions such resonances do not appear in standard filamentation models.

At present, lasing during laser filamentation in atmospheric gases is an active research field15,19,20,21,22,23,24,25,26,27,28. Recent work was also performed in low-pressure argon and krypton29,30, while stimulated X-ray emission has been observed from rare gas plasmas31. Our mechanism is novel and general for any gas: it relies on laser-dressed states in neutral atoms and uses pulse shaping to control their population and seed gain.

First, we solve the TDSE for an argon atom interacting with an intense, 800 nm laser field (see Methods). We use a shaped infrared (IR) pulse with a sharp (~5 fs) front, which optimizes the population of the ‘nearly free’ laser-dressed states. Indeed, in IR fields their ionization rate maximizes at I≈1013 W cm2 (known as ‘death valley’), before decreasing again at higher intensities1,8,11,12,13. Thus, the ‘death valley’ should be crossed quickly. The sharp front is followed by a flat top, so that the laser-dressed states are better defined. Next, we compute the linear response of the dressed atom in the visible frequency range to identify gain lines. To this end, the dressed atom is probed by a weak broadband (~5 fs) probe, carried at wavelength λ = 600 nm and centred in the middle of the pump pulse (t = 0). The time-dependent response to the probe, ∆d(t), is extracted from the full polarization d(t) = <Ψ(t)|\(\hat{d}\)|Ψ(t)> as described in ref. 17: ∆d(t) = d(t)−dIR(t). Here dIR(t) = <ΨIR(t)|\(\hat{d}\)|ΨIR(t)>, where d is the dipole operator in the acceleration form, and Ψ(t) and ΨIR(t) are the time-dependent wavefunctions computed with both fields or the strong IR pump only, respectively.

The key quantity is Im[∆D(ω)], the imaginary part of the Fourier transform of ∆d(t): a negative imaginary part signifies gain, whereas a positive imaginary part signifies loss. Figure 1b,c shows a window Fourier transform of ∆d(t), using the sliding Gabor window, G2(t,t0) = exp[−(tt0)2/T2] (where T = 500 atomic units (a.u.)), which allows us to time-resolve the emission. Below I = 1014 W cm2, the time-dependent gain is offset by the loss, but the situation changes radically above this intensity: at I = 1.4 × 1014 W cm2 gain dominates and amplification lines arise around 550–570 nm and 630–650 nm (Fig. 1c,d). The lines are asymmetric, more Fano-like than Lorentzian (Fig. 1d), as expected in the presence of a strong driving field32. Importantly, the gain has a threshold nature and occurs intra-pulse.

Thus, theory predicts the emergence of gain at intensities I≈1014 W cm2, which will manifest in the forward spectrum from only shaped (that is, sharp rise time) laser pulses. Experimentally, we look for new, atypical absorption and emission structures with asymmetric Fano-like shapes, between 400 nm and 700 nm. Second, the population inversion should arise intra-pulse and depend on the pulse shape (rise time and duration). Third, the emission should have lasing characteristics and occur at transitions absent in the field-free atom or ion. To test these predictions we employ a pulse-shaping set-up33 with a resolution down to two cycles. We use a self-phase-modulated broadened and compressed chirped pulse amplified (CPA) Ti:Sapphire laser in combination with a 640-pixel spatial light modulator (SLM), providing 50 μJ pulses centred at 800 nm34 (Supplementary Fig. 1b, Methods). The pulses are focused into a chamber by a 300 mm off-axis spherical mirror, leading to a short filament (4 mm, see Supplementary Fig. 1a and Methods) in Ar or Kr (2–9 bar). The pulse is shaped such that it acquires the required sharp rise at the beginning of the filament, maximizing the population of the stabilized, strongly driven laser-dressed states. The pre-compensation of the desired pulse shape is achieved by acoustic shock wave optimization at the focus (see Methods). Pulse fronts of ~5 fs are generated, as measured using a spectral phase interferometry for direct electric field reconstruction (SPIDER).

Figures 2, 3 show the experimental results. The strongly driven laser-dressed states are best accessed using pulses with a sharp rise time. Thus we can compare the forward emission from pulses with the same spectra, but different temporal shapes. The red line in Fig. 2a shows the supercontinuum generated inside the filament, for a smooth, 40 fs, broad Gaussian laser pulse. This standard pulse yields a typical supercontinuum spectrum in the forward direction, with no resonant lines attributable to atoms or ions. In contrast, when the pulse rise is fast (that is, a 7 fs pulse), we observe dramatically different spectra with distinct asymmetric (Fano-like) amplification lines at 530 nm, 550 nm, 570 nm and 625 nm (Fig. 2a), as predicted by the theory. The Gaussian pulse has the seed radiation for gain or loss, but the slow rise time cannot populate the laser-driven states efficiently.

Fig. 2: Forward emission spectrum from different pulse shapes filamenting in argon at 9 bar.
Fig. 2

a, Gaussian pulse shape with a 40 fs duration, a 7 fs Fourier-limited pulse, a sawtooth shaped pulse, where the sharp front (5 fs), arrives first followed by a trailing 20 fs decay and the reversed sawtooth, with a 20 fs front rise time and a 5 fs decay time. The curves are offset for clarity. b, Incoherent sidewards emitted spectrum from a Fourier-limited, 7 fs pulse during filamentation in the same argon cell in green, and overlaid are the corresponding Ar I and Ar II plasma recombination lines taken from the NIST database, which are not visible in the forward, coherent spectrum. c, Forward emitted spectra, following filamentation in the same argon cell, of a 10 fs rise time, 5 fs plateau and 10 fs decay time, for increasing pulse energies. Two absorption features are visible at 625 nm and 560 nm, which become gain features at 33 µJ and 28 µJ, respectively, and a broad gain feature emerging at 600 nm. d, Forward emitted spectra, following filamentation in the same argon cell, of a 10 fs rise time, 10 fs plateau and 10 fs decay time, for increasing pulse energies. Gain features are visible at 605 nm, 625 nm and 670 nm. In both c and d, red arrows indicate the movement of emission peaks with increasing input energy, and the dashed lines are to guide the eye to specific lasing peaks. An input white light spectrum is shown in Supplementary Fig. 6.

Pulse-shaping control of gain is demonstrated when comparing an asymmetric triangular-like pulse (5 fs rise, 20 fs decay) against the reverse shape (20 fs rise, 5 fs decay). They have identical spectra but opposite spectral phase. The pulse with the fast rise generates strong gain lines, while the pulse with the slow rise leads to absorption at the same wavelengths. The gain lines are absent at wavelengths where no supercontinuum is present (that is, below 450 nm), as the supercontinuum acts as the lasing seed.

All the emission lines are observed only in the forward direction, indicative of emission coherent with the dressing pulse. Their divergence, measured from lateral photographs using spectral filtering, is 39 mrad in the 600 nm region, below that of the 800 nm driving pulse (50 mrad). Their polarization is coincident with that of the driving pulse, as expected of stimulated, rather than amplified spontaneous emission. The side spectra (Fig. 2b) do not exhibit lines at these wavelengths, but instead show well-known argon plasma incoherent recombination lines around 350 nm and 800 nm (taken from the National Institute of Standards and Technology (NIST) database), thus the emission is not amplification of fluorescence. Above a certain threshold, the output emission intensity grows roughly linearly with the intensity of the seeding spectrum contained in the supercontinuum tail of the pulse, as expected for stimulated emission (see Supplementary Fig. 2).

We now examine the dependence of gain on power and identify the lasing threshold. We use trapezoid-like pulse shapes (10 fs rise, 5 fs plateau, 10 fs decay; Fig. 2c), increasing the input laser energy. In Fig. 2c, the emission lines at 557 nm and 625 nm undergo absorption at lower pulse energies, but show gain when the pulse energy exceeds ~28 μJ. (For a 10 fs rise, 10 fs plateau, 10 fs decay, lasing commences at 33 µJ; Fig. 2d). The lasing output power versus the input power, in Supplementary Fig. 3, yields a lasing threshold of 1.5 GW (I≈1014 W cm2). We stress that gain lines in the 610–690 nm region (highlighted resonances near 625 nm and 675 nm; Fig. 2d) have no counterpart in the field-free spectrum of argon, and cannot be explained by emission after the pulse.

The key role of the laser-dressed (KH) states is confirmed by the theoretical results in Fig. 3. We cross-check the shape and spectrum of the trapezoidal input pulse (10 fs rise, 10 fs plateau, 10 fs decay) at the onset of filament, using numerical pulse propagation simulations (see Methods). We then use the experimental pulse in the TDSE simulations to calculate the intensity of the emitted radiation. The simulated output spectrum is normalized to the input spectrum at the 800 nm carrier wavelength, as in the experiment. Figure 3b shows the emergence of strong emission lines, as in the experiment (Fig. 3a). Note these peaks emerge where Fig. 1d shows gain. Figure 3b also shows that the observed lines cannot be attributed to standard nonlinear effects during propagation: a simulation of laser filamentation using standard propagation models (see Methods) does not lead to any peaks in the spectral region of interest.

Fig. 3: A comparison between simulated and experimental emission spectra from a 10 fs rise, 10 fs plateau, 10 fs decay laser pulse shape.
Fig. 3

a, Experimentally measured forward emission for filamentation in argon, at 50 µJ, showing the input (blue) and output (orange) spectra. b, Theoretically calculated emission spectrum of the strongly dressed atom for the experimental pulse at the input of the filament: input (blue), output (orange). The green line shows the results of filamentation propagation simulations (see Methods) without including the laser-dressed states. c, Position of the KH states as a function of laser intensity. To demonstrate the origin of the emission in the spectral region 650 nm ± 50 nm, the lowest excited KH state (blue) is shifted up (dashed and shaded blue): it enters the dense manifold of weakly bound states (grey region) at I≈0.9 × 1014 W cm2. d, Relative population difference between key field-free states, which can contribute to emission, between 500 nm and 700 nm, for two different intensities: 0.92 × 1014 W cm2 (diamonds) and 1.37 × 1014 W cm2 (circles). Dashed blue lines indicate that the population of the energetically lower state is higher than that of the energetically higher state. Orange lines indicate population inversion between the states. The population is calculated at the end of the pulse.

Finally, we focus on the spectral region between 610 nm and 690 nm. There are no field-free lines in the argon spectrum that coincide with the observed strong amplification lines at 625 nm and near 675 nm. However, Fig. 3c shows that transitions between the laser-dressed states (calculated in the KH frame, see Methods) do move into this region at I≈0.9 × 1014 W cm2. Note that Fig. 3c does not show the overall pondermotive shift of the excited states and demonstrates only the additional shift. This shift is small compared to the pondermotive shift, which reaches 6 eV at 1014 W cm2 (for λ = 800 nm). Figure 3d shows the population difference between the field-free states that move into this region at intensities around 1014 W cm2. These are the states with field-free transition frequencies between 500 nm and 600 nm, which acquire population inversion at intensities around 1014 W cm2.

The lasing mechanism is not specific to argon. Similar results were found in krypton (see Fig. 4 and Supplementary Fig. 7). The lasing transitions are at different energies than in argon, reflecting the different atom, but also exhibit both broad and narrow gain features and asymmetric Fano-like lineshapes.

There is no direct connection between the observed resonant widths of laser-dressed states, their lifetime and pulse duration. Indeed, the laser-dressed states undergo ultrafast dynamics intra-pulse and their positions are intensity-dependent, leading to ‘inhomogeneous’ broadening due to the spatial and temporal intensity distributions. In a 7 fs pulse, the dressed states shift rapidly with changing pulse intensity, so that resonances should broaden with increasing peak intensity (Fig. 4a, from 3 nm to 7 nm at 617 nm). For a long ‘trapezoidal’ pulse (10 fs rise, 40 fs plateau,10 fs decay), transition lines shift with intensity but keep their widths (~7 nm at 624 nm and ~12 nm at 613 nm; Fig. 4b).

Fig. 4: The forward emission spectra of trapezoid pulse shapes in krypton at 9 bar, with increasing pulse energy.
Fig. 4

a, A Fourier-limited pulse, 7 fs duration. A shift in the transition lines is observed with increasing pulse energy of 3–5 nm over 50 µJ, and at 20 µJ the weak emission/absorption lines are strongly enhanced and the linewidths broadened (from 3 nm to 7 nm). b, Trapezoid pulses with 10 fs rise time, 40 fs plateau and 10 fs decay time. Narrow and broad gain features are visible, experiencing a spectral shift of about 3–5 nm over an energy increase of 50 µJ, but with less broadening. A distinct Fano lineshape emerges at 627 nm. Dashed lines and white arrows are to guide the eye, between the figures, to show the shift in emission wavelengths between different pulse durations and also to highlight the field dependence of the states involved. The temporal pulse shape is shown in red for each graph.

The observation of gain lines specific to the atom dressed by an intense, I > 1014 W cm2, laser field, and absent in the spectrum of field-free transitions, shows that the seemingly exotic KH states are ubiquitous even in dense (1–9 bar) gases interacting with strong laser fields. At high intensities, the laser-driven atom can become an inverted medium, inside the laser pulse, where electrons respond almost as free, yet remain bound and can be used as a multi-photon pumped gain medium during laser filamentation. Amplification at the inverted transitions between the dressed states, resulting in the emergence of gain lines during the pump pulse, can trigger additional wave-mixing processes with the strong pump, possibly leading to additional parametric gain lines in the spectrum. After the end of the pulse, coherent free induction decay can also seed lasing between the field-free states carrying population inversion. Our findings illustrate new opportunities for enhancing and controlling lasing inside laser filaments by optimizing the shape of the input laser pulse.


Pulse-shape generation

To synthesize laser waveforms with pulse-shape control down to the few-cycle level, a CPA Ti:Sapphire laser, (780 nm, 1.5mJ, 40 fs, 1 kHz; details and a diagram can be found in Supplementary Fig. 1b) undergoes two-stage filamentation in air, through loose focusing with 2 m and 1.25 m focal length mirrors. The pulse, broadened (700–900 nm) by the first filamentation stage, is re-collimated and recompressed with a pair of chirped mirrors before refocusing for the second filamentation stage, with a pair of spherical mirrors. At the exit of this second stage, the pulse spectrum spans more than one octave (450 nm–1 µm) and is recompressed by a chirp mirror arrangement34. The final compression of higher spectral phase orders and the pulse shape control are achieved using a 4 f all-reflective pulse shaper with a dual mask, 640-pixel, liquid crystal modulator. In this configuration, few-cycle 5 fs pulses of up to 50 µJ can be produced, in addition to flat top, or sawtooth with sharp rise times. These are optimized using a pulse-shape optimization algorithm explained below.

Pulse-shape optimization and diagnostics

In order to compensate for dispersion arising from the chamber window and the propagation in the pressured gas before the focal point, we apply a phase detection algorithm35, onto the SLM, to get the shortest pulse (Fourier transform-limited) at the focus. The signal used for the optimization loop was the acoustic shock wave released by the plasma, representative of the free-carrier density produced by the laser. Using subsequent measurements we verify this procedure leads to the desired pulse shape, at the onset of the filament (Fourier transform-limited, sawtooth, flat top trapezoids). The pulse shapes are measured using a transient-grating frequency-resolved optical grating (FROG)34, as well as a SPIDER (Venteon), at pulse positions before and after filamentation. To measure the pulse shape within the filament, a 100 µm Al foil is placed in the filament path. The filament drills a self-adapted iris, arresting further filamentation and nonlinear propagation36, but preserving the temporal pulse shape at this distance. The remaining beam was analysed by a SPIDER. The SPIDER traces are shown in Supplementary Figs. 4 and 5.

Pulse propagation simulations

Numerical simulations, based on a unidirectional pulse propagation equation (UPPE)37, are used to simulate the laser filamentation process and cross-check the pulse-shape optimization routine detailed above. The propagation simulations are first carried out up to the onset of filamentation for sample pulses, and confirmed the desired experimental pulse shape. Next the same simulations were carried out throughout the full filamentation region to obtain the spectra both at the input and at the output of the filament. The numerical method and the code verification are described in detail elsewhere38. Briefly, the simulations are performed in a cylindrically symmetric geometry, reducing the dimensionality of the problem to two spatial dimensions plus one temporal dimension. The ionization model uses the standard Perelomov–Popov–Terent’ev ionization rates. All standard nonlinear effects, such as self-focusing, self-phase modulation and self-steepening, are included (see Supplementary Fig. 8).

Filamentation in pressured argon and krypton cells

A schematic of the experimental set-up can be found in Supplementary Fig. 1. The shaped pulses enter a pressurized chamber (2–9 bar) containing Ar or Kr via 5 mm ultraviolet fused silica windows, where a 300 mm off-axis gold spherical mirror generates a filament ~4–5 mm in length, before exiting the chamber through a 5 mm ultraviolet fused silica window. Spectra from the filament and its plasma are focused in the forward and transverse directions onto Ocean Optics fibre spectrometers (ultraviolet–visible and near-infrared). An image of the filament in the transverse direction is taken by a digital camera, and the acoustic shock wave is recorded with a microphone.

Theoretical methods

The theoretical results in Figs.1, 3 have been obtained by propagating the TDSE numerically, using the code described in ref. 39. We have used a radial box of 200.0 a.u., with a total number of radial points nr = 4000, and a radial grid spacing of 0.05 a.u. The maximum angular momentum included in the spherical harmonics expansion was Lmax = 50. The time grid had a spacing of Δt = 0.0025 a.u. In order to remove unwanted reflections from the border of the radial box, we have placed a complex absorbing potential40 at 32.7 a.u. before the end of the radial box. The argon potential used was fitted to reproduce energies and dipoles of the first few one-particle states of argon, as described in equation (22) of ref. 41:


To obtain the absorption spectra shown in Fig. 1, we have used the technique described in ref. 17. The probe absorption–emission signal is proportional to:

$$S({\Omega })\propto \frac{{\rm{Im}}[{E}_{{\rm{probe}}}^{* }\left({\Omega }\right){D}_{{\rm{probe}}}\left({\Omega }\right)]}{\int {\rm{d}}{\Omega }| {E}_{{\rm{probe}}}\left({\Omega }\right){| }^{2}}$$

where Eprobe(Ω) is the spectral amplitude of the XUV probe pulse and Dprobe is the frequency-resolved linear response of the IR-dressed system to the probe pulse:

$${D}_{{\rm{probe}}}\left({ \Omega }\right)=\frac{1}{{ \Omega }^{2}}\int {\rm{d}}t{{\rm{e}}}^{i{ \Omega }t}[d\left(t\right)-{d}_{{\rm{IR}}}\left(t\right)]$$

therefore removing the contribution of the standard nonlinear response induced by the IR. Here, d(t) and dIR(t) are the dipole responses calculated with both fields and with only the IR field present, respectively (see main text).

The infrared field used in the calculations consisted of a 4-cycle cos2 turn on, followed by a 32-cycle flat top part and a 4-cycle cos2 turn off. The carrier frequency of the dressing IR pulse is ω = 0.0569 a.u. (λ = 800 nm).

The probe pulse used for extraction of the absorption spectrum of the dressed system consisted of a Gaussian pulse with central frequency Ω = 0.075942 a.u. (λ = 600 nm) and a full-width at half-maximum (FWHM) of 164 a.u.. The pulse is timed at the middle of the infrared pulse. Prior to the Fourier transform, the calculated time-dependent dipole was multiplied by a temporal mask with a flat top ending at 500 a.u. and followed by an exponential turn off with a time-constant of 200 a.u., so that the response is effectively turned off when the dressing IR pulse is over. This was done to ensure that only the dressed atom response is tracked, and that the coherent beating between the field-free states after the end of the dressing laser pulse is removed in this calculation. For the window Fourier transform with the Gabor window in Fig. 1b,c, only the Gabor window was applied, without additional exponential damping. To obtain the laser-dressed (KH) states shown in Fig. 3c, the model argon potential was adapted to a different solver for the stationary Schrödinger equation written in cylindrical (rather than spherical) coordinates specifically for the diagonalization of the KH Hamiltonian. The approach is described elsewhere13. For better numerical convergence, the model potential was modified slightly while keeping the energies and the transition dipoles for all relevant states unchanged.

Data availability

The data that supports the plots within this paper and other findings of this study are available from the corresponding author upon reasonable request.

Additional information

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Change history

  • 18 June 2018

    In the version of this Letter originally published, the units of the bottom three values in the Fig. 1d legend were incorrect; they should have been W cm–2. This has now been corrected.


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The authors acknowledge the valuable contributions of M. Moret, for advanced technical assistance with the experimental set-up, S. Courvoisier, for technical assistance with graphical formatting, and L. Woeste, for constructive advice. J.P, J.G. and S.H. acknowledge funding from SNF NCCR MUST grant. J.P and J.K acknowledge funding from ERC grant Filatmo. M.M. acknowledges funding from MHV fellowship grant number: PMPDP2-145444 and NCCR MUST Women's Postdoc Awards. M.I. acknowledges the support of the DFG QUTIF grant number IV 152/7-1.

Author information


  1. GAP, University of Geneva, Geneva, Switzerland

    • Mary Matthews
    • , Julien Gateau
    • , Nicolas Berti
    • , Sylvain Hermelin
    • , Jérôme Kasparian
    •  & Jean-Pierre Wolf
  2. Max-Born-Institut für Nichtlineare Optik und Kurzzeitspektroskopie, Berlin, Germany

    • Felipe Morales
    • , Maria Richter
    • , Timm Bredtmann
    • , Olga Smirnova
    •  & Misha Ivanov
  3. Inst. für Exp. Physik, Freie Universitat Berlin, Berlin, Germany

    • Alexander Patas
    •  & Albrecht Lindinger
  4. Departamento de Química, Módulo 13, Universidad Autónoma de Madrid, Madrid, Spain

    • Maria Richter


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J-P.W. and M.I. conceived the experiment. M.I., F.M., M.R., T.B. and O.S. performed the calculations and developed the theoretical interpretation. N.B. performed filamentation propagation simulations. M.M., S.H., J.K. and J.G. designed the experimental apparatus. A.P. and A.L. designed and implemented the pulse-shaping process. M.M., A.P., A.L, J.G. and S.H. performed the experiment and pulse measurements. M.M., A.P. and J.K. analysed and processed the experimental data. All authors contributed to the writing of the manuscript.

Competing interests

The authors declare no competing interests.

Corresponding author

Correspondence to Mary Matthews.

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