Laser-dressed photoelectron spectroscopy, employing extreme-ultraviolet attosecond pulses obtained by femtosecond-laser-driven high-order harmonic generation, grants access to atomic-scale electron dynamics. Limited by space charge effects determining the admissible number of photoelectrons ejected during each laser pulse, multidimensional (i.e. spatially or angle-resolved) attosecond photoelectron spectroscopy of solids and nanostructures requires high-photon-energy, broadband high harmonic sources operating at high repetition rates. Here, we present a high-conversion-efficiency, 18.4-MHz-repetition-rate cavity-enhanced high harmonic source emitting 5 × 105 photons per pulse in the 25-to-60-eV range, releasing 1 × 1010 photoelectrons per second from a 10-µm-diameter spot on tungsten, at space charge distortions of only a few tens of meV. Broadband, time-of-flight photoelectron detection with nearly 100% temporal duty cycle evidences a count rate improvement between two and three orders of magnitude over state-of-the-art attosecond photoelectron spectroscopy experiments under identical space charge conditions. The measurement time reduction and the photon energy scalability render this technology viable for next-generation, high-repetition-rate, multidimensional attosecond metrology.
At the beginning of this century, a series of seminal technological developments in the field of ultrafast lasers (reviewed, e.g., in ref. 1), led to the first photoelectron spectroscopy2 (PES) experiments performed with extreme-ultraviolet (XUV) radiation obtained by high-order-harmonic generation (HHG) driven by intense, visible/near-infrared (VIS/NIR) pulses in gases, in the presence of the (delayed) driving field3,4. In these experiments, the sub-optical-cycle temporal structure of HHG radiation, and its synchrony with the driving field providing a temporal reference, enabled laser-dressed XUV-PES with sub-femtosecond temporal resolution, marking the birth of attosecond metrology1. The two major PES-based tools employed in this emerging field, attosecond streaking1,5,6,7, using isolated attosecond pulses, and RABBITT (reconstruction of attosecond harmonic beating by interference of two-photon transitions)-based techniques8, using attosecond pulse trains4,9,10,11,12,13,14,15, rely on analysing the evolution of photoelectron spectra with varying delay between the two optical fields. Both approaches have been widely applied for measurements of attosecond photoemission delays from gases, providing insights into electron dynamics deep inside the atom (see e.g., refs. 1,7,13,14,16 and references therein). During the past decade, considerable efforts have addressed the extension of these techniques to solids6,9,10,11,12 and nanostructures17,18. For instance, very recently the combination of angle-resolved PES (ARPES) and RABBITT has enabled first band-specific measurements of correlated electron dynamics on metal surfaces9,10. Another example is the on-going effort to combine attosecond streaking with photoemission electron microscopy (PEEM) for the spatiotemporal study of complex plasmonic fields propagating on nanostructured metal surfaces17,18,19,20,21. Fundamental studies of correlated electron dynamics in these dense atomic systems are necessary for the development of novel materials and high technologies.
A severe shortcoming of laser systems employed in state-of-the-art attosecond-PES experiments, however, arises from their relatively low pulse repetition rate frep, usually well below 1 MHz, in the context of space charge22,23 (SC). Coulomb interaction of multiple photoelectrons released from the sample during a single pulse affects their velocities and trajectories towards the detector, leading to distortions of the observables, i.e., kinetic energy (and momentum or position)17,23. In fact, in the vast majority of setups for (multidimensional—i.e., energy, and angularly or spatially resolved) attosecond-PES on solids, space charge effects demand a significant attenuation of the HHG output9,17. At a space-charge-limited photoelectron flux and at typical frep values in the kHz range, the acquisition of (multidimensional) photoelectron spectra with sufficient signal-to-noise ratio necessitates impractically (or even prohibitively) long acquisition times of several hours10 to several tens of hours17. Over such periods, laser instabilities and sample contamination24 constitute severe technological challenges. This shortcoming can potentially be circumvented by HHG sources with repetition rates in the multi-MHz range. Fig. 1a shows an overview of state-of-the-art HHG sources illustrating that to date, however, the combination of high photon energies, high photon flux and high repetition rate has remained an unmet challenge. Although large-scale technologies such as FELs also offer high flux at high photon energies and repetition rates25 to date, they do not enable measurements with attosecond time resolution.
Here, we close this gap with a high-conversion-efficiency cavity-enhanced HHG source. Driving HHG at frep = 18.4 MHz with sub-40-fs, 1-µm pulses in argon results in XUV pulse trains with photon energies between 25 and 60 eV and, in particular, a record flux at >40 eV for high frep (Fig. 1a). In experiments demonstrating the potential of this source for time-resolved PES, a 10-µm-diameter spot on a tungsten surface was illuminated, generating between two and three orders of magnitude more photoelectrons than affordable in previous state-of-the-art, high-photon-energy attosecond-PES experiments under the same space-charge-imposed restrictions (Fig. 1b). Time-of-flight (ToF) detection allows for the simultaneous collection of photoelectrons from a large solid angle and in a broad range of kinetic energies, with a temporal detection duty cycle close to 100% (i.e., the time of flight dispersion corresponds to the pulse repetition period). Unlike other detection schemes (e.g., hemispherical or retarding-field analyzers), ToF spectrometers allow for the simultaneous detection of electron emission momentum (or spatial distribution) and kinetic energy without the need to scan over one of these parameters at the expense of a reduced flux. Furthermore, attosecond temporal resolution is inferred from the sideband modulation of laser-assisted photoemission4.
Modern MHz-repetition-rate ytterbium-based lasers (see refs. 26,27 and references therein) currently hold average power records for single-pass HHG with photon energies up to around 40 eV27,28,29, obtained from krypton and xenon (Fig. 1a), and have been successfully employed for narrowband PES measurements at these photon energies, both in single-pass26 and in cavity-enhanced HHG configuration30,31 (Fig. 1b).
However, with these technologies significantly higher photon energies (for which gases with a higher ionisation potential like argon or neon are typically employed) were so far only achieved at the cost of the repetition rate in single-pass HHG17,32,33 or of the photon flux in cavity-enhanced HHG34,35, see Fig. 1a. Here, we demonstrate that a combination of state-of-the-art fibre laser technology, nonlinear pulse compression and cavity-enhanced HHG can overcome these limitations.
The experimental setup is depicted in Fig. 2. The HHG source (see also Methods) consists of a master-oscillator-power-amplifier (MOPA) femtosecond frontend followed by a multi-pass bulk-compression stage and a femtosecond enhancement cavity (EC) housing the HHG gas target. The initial pulses were delivered by a titanium-sapphire oscillator with a repetition rate of 73.6 MHz. By means of a pulse picker after the oscillator, the repetition rate of the MOPA output36 was reduced to a quarter to permit sufficient energy dispersion in ToF-PES. The output of the MOPA was an 18.4-MHz train of 5.4-µJ, 250-fs pulses, spectrally centred at 1030 nm. Multi-pass nonlinear spectral broadening in bulk and subsequent chirp removal compensation with dispersive mirrors allowed for the temporal compression of these pulses down to sub-40-fs duration37 at an energy level up to one order of magnitude higher than in previous cavity-enhanced HHG setups with comparable pulse durations (see refs. 34,35 and references therein). After chirped-pulse amplification the pulses were coherently overlapped in a passive, 16.3-m roundtrip bowtie EC with a finesse of 140. At a power enhancement of 35, inside the EC, a 0.15-mJ, sub-40-fs circulating pulse was stably maintained over several minutes (Fig. 3a). The key technological aspect to achieving this high intensity and phase stability was using a feed-forward phase-stabilised Ti:Sa oscillator to seed the Yb-fibre amplifier37 (see Fig. 3b) and actively controlling the repetition frequency of the seed oscillator and the EC length with a fast and a slow loop, respectively. High harmonics of the circulating NIR radiation were generated in an argon gas target at the focus, and coupled out through a 340-µm-diameter on-axis opening in the resonator mirror following the focus34,35. Fig. 3c, d show the autocorrelation and the spectra of the pulses impinging and circulating in the EC, respectively.
Argon gas was delivered through an end-fire quartz nozzle with a 200-µm-diameter opening. The gas target position and the backing pressure were optimised for highest XUV yield around 40 eV after output coupling. An output coupled XUV flux of 1 × 1013 photons/second was measured, with energies ranging from 25 to 60 eV (Fig. 4). By combining state-of-the-art fibre laser technology with a novel nonlinear pulse compression scheme, a pulse energy of 4.5 µJ was available as a seed to the enhancement cavity, leading to 0.15-mJ intracavity pulses. Importantly, the moderate cavity finesse alleviates ionisation-related intensity limitations (clamping) that arise from the blueshift caused by self-phase-modulation in the gas target38,39,40. Together with relatively weak cumulative ionisation effects in the gas target (each atom traverses the beam diameter within 4 laser shots), this enabled an intracavity conversion efficiency around 10 times higher than in34,35 and, for the first time, approaching that obtained with single-pass HHG in argon (see Methods). This allowed for a highly efficient use of the EC concept, in particular leading to – to our knowledge – the highest usable XUV flux for photon energies beyond 40 eV at frep > 1 MHz reported so far (see Fig. 1).
Ultrafast photoelectron spectroscopy
For PES experiments, the XUV beam and, optionally, the NIR beam, were directed through a differentially pumped beamline and focused to a 10-µm-diameter spot onto the surface of a single-crystalline (110) tungsten target with a multilayer XUV mirror (Fig. 2). Photoelectrons were collected with a ToF spectrometer (equipped with a retarding grid) with two settings—drift mode (DM) and large-angular-dispersion mode (LAD)—differing in their capture angle and energy resolution (see Fig. 5a and Methods).
A first PES experiment was aimed at measuring the number of photoelectrons released from the sample and scrutinising the space-charge-induced spectral distortions. To this end, the XUV beam was separated from the 6-W average power NIR beam passing through the opening in the output-coupling mirror with a beam splitter. Thus, all of the detected photoelectrons stem from single-photon XUV photoemission. Although the use of XUV transmission optics was avoided, the reflective optics attenuated the XUV photon flux by 97%, resulting into 3 ×1011 photons/second at the sample, releasing an estimate of around 1 × 1010 photoelectrons/second. This value is in good agreement with that calculated from the ToF count rate, and results in an estimated space charge distortion of ΔESC≈50 meV (see Methods). In accordance with the instrument resolution of 0.13–0.36 eV (limited by the spectral width of the harmonics, see Methods), no distortions of the spectra were discernible for both acquisition modes (see Fig. 5b, c).
To evaluate the statistics of the PES measurements we calculated the relative standard deviation σ of several measurements, for varying integration time T of each measurement. The results are shown in Fig. 6a. A statistical behaviour (decrease of σ with \(\sqrt T\)) was observed for T< 160 s, resulting in σ < 1%. Long-term drifts led to an increase of σ to ~2.5% after T = 15 min.
To demonstrate the suitability of the HHG source for attosecond-resolution PES, we performed XUV-pump-NIR-probe measurements. The XUV-NIR beam splitter was replaced by a gold mirror, enabling NIR intensities in the 1011-W/cm² range at the target. For introducing a mutual delay, the XUV and the NIR beams leaving the EC were spatially separated by a coaxial optic featuring a small 300-nm-thick aluminium filter covering the centre of the beam, held in position by thin metal wires. The outer part is transparent for the NIR pulses, whereas the central part is only transparent for the XUV. A variable temporal delay was introduced by a two-segment spherical mirror (Fig. 2). The fixed outer gold-coated ring reflects the NIR radiation and a movable, 5-mm-diameter multilayer-coated inner segment reflects the time-delayed XUV pulse trains with a peak reflectivity of 14% at 44 eV and in a bandwidth of 10 eV. This common-path geometry renders the XUV-NIR interferometer inherently stable. Fig. 6b shows the intensity of the sideband peak at 37.9 eV as a function of the pump-probe delay. Its delay-dependent oscillation at twice the fundamental laser frequency is caused by the interference of two different two-photon-transitions4. This sinusoidal curve (Fig. 6b) contains information on the relative time delay between the NIR and XUV fields, on the spectral phase of the adjacent harmonics, as well as on the delay of the photoemission process itself and, thus, on the underlying electron dynamics in the sample. Using the RABBITT-technique4,8, this information can be extracted from the phases of these sideband modulations10,41. In order to determine an upper bound of the time resolution of our instrument, a sine curve with three free parameters (amplitude offset and phase) at a fixed wavelength of 1030 nm was fitted to the data. The resulting fit error of the phase indicates a timing precision of the interferometer of 36 as, which is comparable to state-of-the-art attosecond-PES experiments10,11. Notably, the common-path XUV-NIR interferometer does not necessitate active stabilisation10,11 of the delay line. In the photoelectron spectra at a kinetic energy of 12 eV, a distinct peak that we attribute to the tungsten 4f doublet state is visible (Fig. 7). Its energy separation from the highest valence band peak corresponds well to the literature value of the binding energy of the tungsten 4f 7/2 state of 31.4 eV42. Since it is difficult to discern peaks below 12 eV due to the background of secondary electrons, we generated significantly higher harmonics in neon and used a multilayer mirror centred at 65 eV to spectrally filter them without changing anything within the cavity but the gas, its pressure and the position of the gas nozzle. As it can be seen in Fig. 7, the higher photon energies of neon HHG allow to clearly observe several photoelectron peaks originating from the 4f-state. Due to spin-orbit coupling, the 4f-state is split into two peaks separated by 2.2 eV which differs by only 0.2 eV from the separation of 2.4 eV between two high harmonics. Consequently, a photoelectron peak from the deeper bound 4f 5/2 state excited by photons of a specific high harmonic would be separated by only 0.2 eV from the photoelectron peak resulting from the 4f 7/2 state and photons from the next lower harmonic. Although this can hardly be distinguished by eye in this particular measurement, techniques to separate such features reliably in time-resolved measurements (e.g., in the Fourier space) have recently been developed and applied successfully43,44. The different appearance of the valence band electrons of neon and argon high harmonics can be explained by the better separation from the secondary electron background in combination with the narrower bandwidth of the XUV mirror.
We have presented a HHG source affording a combination of high repetition rate (frep = 18.4 MHz), high photon energies (up to 60 eV) and high photon flux (5 × 105 photons per pulse). Proof-of-principle PES measurements on tungsten evidence the advantages of this parameter regime for PES-based attosecond metrology, over state-of-the-art HHG sources employed in this field. In particular, we demonstrated an improvement of the photoelectron flux by more than two orders of magnitude in space-charge-limited attosecond-PES. Considering the relatively strong attenuation of the XUV flux between the HHG source and the sample (almost two orders of magnitude), in principle an even higher photoelectron flux could be achieved with this HHG source. In addition, PES statistics attest the stability of this source for a comparatively very large number of laser shots. For measurement times of 160 s and 15 min, photoelectron spectra with standard deviations of less than 1% and ~2.5%, respectively, were taken. At our repetition rate, these two durations correspond to 2.9 × 109 and 1.7 × 1010 shots, respectively. For comparison, at a repetition rate of 10 kHz, typical for state-of-the-art attosecond-PES experiments9,10,11,13,14,17,45,46, this would correspond to 3.4 and 19 days of continuous measurement, respectively. A particularly important aspect of the decrease in measurement time is the fact that this large number of shots can be recorded over a duration shorter than the typical sample contamination time under ultra-high vacuum conditions. Typically, at a pressure of 10–10 mbar, a monolayer of residual gas particles builds up in around 2 h24. This requires periodic cleaning, which considerably increases the overall measurement time and experiment complexity.
Furthermore, the measurement time reduction is expected to lead to a corresponding improvement of the temporal resolution in attosecond-PES experiments. In particular, the measurement of the sinusoidal oscillation of the laser-assisted XUV-photoemission sideband shown in Fig. 6b was done within 105 s which lies well within the time that the system behaves statistically (Fig. 5a), implying that multidimensional PES measurements can be repeated multiple times in the absence of drifts. The high flux and repetition rate of our system could even enable delay scans within less than a millisecond, which would decrease the impairment of the time resolution by acoustic vibrations. As was recently demonstrated7, averaging the results of a large number of measurements can enable the determination of photoionisation delays with absolute errors in the sub-attosecond range.
The current configuration of our apparatus is particularly suited for RABBITT-based attosecond metrology. For measurements of photoionisation delays, these techniques exhibit a few distinct advantages. For instance, they combine high temporal resolution, given by the individual attosecond bursts in the XUV pulse train, with high spectral resolution afforded by the discrete nature of the harmonics, and they offer high signal-to-noise ratios due to the evaluation of sideband modulations rather than shifts of broad photoelectron spectra9,10,11,13,14. In particular in combination with ARPES, very recently broadband RABBITT measurements have led to a number of insights into band-specific multi-electron attosecond correlation dynamics in solids9,10,11. The instrument presented here offers the prospect of a reduction of the measurement time in such investigations, promising the application of these attosecond tools to a wide range of material systems in the near future.
In contrast to previous multi-MHz HHG sources, our apparatus generates photons with energies of several tens of eV at a significantly higher flux. In addition, due to geometrical XUV output coupling, the architecture is photon-energy scalable to 100 eV or more34,35. Besides the general advantages of rendering PES less sensitive to external fields and of affording a better temporal resolution and a better energy separation of primary from secondary electrons, high photon energies are crucial for accessing deeply bound states of the system under study. This enables the comparison of photoemission delays from different initial states for self-referencing6,7 and is desirable for experiments on X-ray magnetic circular dichroism, e.g., at the M-edge of nickel or cobalt47. We demonstrated that the high photon energies of our setup enable addressing such a deeply bound state in tungsten, as it can be seen in Fig. 7. This may allow one to compare photoemission delays between the valence band and a deeper bound state in a solid material utilizing the RABBITT-technique.
The femtosecond-laser technologies presented here can be extended both to longer and to shorter48,49 pulses. Driving HHG with longer intracavity pulses is a way towards higher spectral resolution for RABBITT-based measurements. Shorter pulses, together with cavity-enhanced gating methods offer the prospect of the generation of temporally isolated attosecond pulses at multi-MHz repetition rates50. Such pulses could be used, for example, in multidimensional attosecond-streaking-based measurements, such as attosecond photoelectron emission microscopy of nanoplasmonic fields17,18,19,21. Beyond attosecond metrology the high-power multi-MHz-repetition-rate HHG source presented here could benefit applications such as XUV frequency comb spectroscopy51 for precision-measurements of electronic energy levels of atoms52, or for referencing to nuclear transitions53 for future nuclear clocks.
Estimation of space charge effects
The effect of space charge on the photoelectron spectra is estimated by using the Long-Itchkawitz-Kabler (LIK) model54. The model is based on the assumption of a radially expanding spherical, initially monoenergetic charge distribution and yields an energy broadening ΔESC of the spectrum given by ΔESC[eV] = 3 × 10−3 Ne/(0.5dfocus[µm])22,54, where Ne denotes the number of emitted electrons per pulse and dfocus is the diameter of the emission spot. The validity of the model has been confirmed by classical many-body calculations. It has been shown to also be applicable to photoelectrons uniformly distributed in energy by changing the factor on the right-hand side of the above equation to 0.5 × 10−3(±0.12 × 10−3) for electrons on the high-energy side of the spectrum22. Furthermore, the simulations showed that the broadening is usually accompanied by an energy shift of roughly the same magnitude. We used this modified relation to estimate the space-charge-caused broadening. To relate the number of XUV photons to the number of emitted electrons, and to calculate the expected space charge effect for the various experiments shown in Fig. 1b (for a fixed spot size), the total photoemission probability including scattered and secondary electrons is needed. In the case of our experiment, we determined a photoemission probability of 3.3% from the measurement of the number of emitted electrons per pulse and taking into account the attenuation of ~97% of the output coupled XUV radiation along the beam path to the tungsten surface (the attenuations due to one Nb2O5 beam splitter, one gold mirror and a scandium-silicon XUV multilayer mirror amount to 50%, 40 and 90%, respectively). This value is in satisfactory agreement with the quantum efficiency of tungsten photocathodes experimentally determined previously to decrease from roughly 10% at 25 eV to about 6% at 50 eV55. The discrepancy can be attributed to the uncertainty of the attenuation estimation (including geometrical losses at the 5-mm-diameter XUV mirror, angle uncertainties, surface roughness etc.). For typical PES experiments, an energy resolution on the order of 100 meV is sufficient to distinguish different initial states in the electronic bandstructure of a solid10, which justifies the choice of the admissible space-charge-induced energy broadening in the discussion. Furthermore, we assumed a typical focal spot diameter of 50 µm for the comparison, while in our experiment, to scrutinise the presence of space charge effects, we utilized a smaller spot size of 10 µm in order to increase the sensitivity to these effects. In attosecond-PES, in order to have homogeneous conditions for all emitted electrons, the focal spot of the XUV focus is restricted to be smaller than the spot size of the pump beam. The latter, in turn, is limited by the requirement to provide high enough intensities to generate detectable signals. In case of RABBITT -experiments, NIR- intensities of 1011 W/cm² are well suited to generate a high flux of two-photon transitions while still preventing a significant portion of higher-order transitions. More generally in the case of non-homogenous samples (e.g. nanostructures for PEEM-experiments) such spot sizes are crucial.
In addition, the admissible electron flux might be limited by space-charge-induced distortions within the detector, e.g., if additional electron optics with intermediate foci are used. For instance, for attosecond photoemission electron microscopy it has been estimated, that the spatial resolution can be severely affected already at an electron flux of about 0.01 e/µm217. This corresponds to only 20 electrons per pulse within a 50-µm-diameter emission spot, which is a factor of 20 below our electron flux, thus imposing even stronger limitations than in the example considered in Fig. 1b.
High-flux, high-photon-energy 18.4-MHz HHG source
The seed for the MOPA system is a 300-µW, 73.6-MHz train of pulses spectrally centred at 1030 nm, split off from the output of a titanium-sapphire oscillator. Utilising a synchronous acousto-optic-frequency-shifter-based pulse picker56, a feed-forward carrier-envelope-offset (CEO) frequency stabilisation57 and three successive chirped-pulse Yb-doped fibre amplification stages (with temporal stretching to 200 ps), after the reflection-grating compressor an 18.4-MHz train of 5.4-µJ, 250-fs pulses is obtained. Previous studies have shown that the amplification and the pulse picking processes preserve the phase and intensity stability of the oscillator nearly perfectly36,56. The MOPA output is spectrally broadened by self-phase modulation in a multi-pass-cell with 49 passes through a 12-mm thick fused-silica medium and temporally compressed by dispersive mirrors to sub-40 fs duration. The efficiency of the nonlinear compression unit is 88%37. To minimise fluctuations of the spatial overlap between the compressed pulses and the EC at the input coupler, an active beam pointing stabilisation was installed, and the majority of the setup was placed in a housing to reduce air fluctuations. The bowtie enhancement cavity consisted of 8 mirrors, 7 of which are highly reflective quarter-wave stacks and one is a 97%-reflectivity input coupler. Taking into account the input power (80 W), the circulating average power (2.8 kW) and the overlap of 60%, we determine the finesse of the EC to be 140 and the losses at the pierced mirror to be 1.5%. This value is slightly higher than the expected losses of 1% our 4.2 × 3.1-mm-radius mode experiences at the 340-µm aperture in the XUV output coupler. This might be due to slight deformations of the pierced mirror around the whole. The output coupler was pierced by inverse laser drilling58. During the drilling, the substrate surface was protected by an optically bonded cover, leading to an excellent edge quality59. The focusing mirrors with a radius of curvature of 600 mm were chosen according to two design criteria: (i) the large cavity eigenmode (beam diameter 8.4 mm × 6.2 mm) on the 1”-diameter mirrors (close to the inner stability edge) prevents damages and achieves a trade-off between losses at the aperture in the output coupler and output coupling efficiency (Fig., 4 shows an estimation of the output coupling efficiency calculated by 3+1 D simulations); (ii) the focus size is maximised under the constraint of an on-axis peak intensity in the range 1–2 × 1014 W/cm2 (focus radius wx × wy = 25 µm × 32 µm). The gas target was provided by a fused-silica 200-µm end-fire nozzle. Highest XUV flux around 40 eV was achieved with a backing pressure of 4.5 bar of argon gas at the nozzle, which increased the background pressure in the cavity vacuum chamber to 1 × 10−2 mbar (a 1600 l/s turbo-molecular pump with a 110-m3/h pre-pump were used for evacuation). Reabsorption in the residual gas along the XUV beam path (1.5 m) amounted to 26% (calculated using transmission data from60 and our measured XUV spectrum). In order to operate the cavity at its preferred offset frequency of 5.5 MHz61, we locked the CEO frequency of the MOPA system to 5.5 MHz using a feed forward scheme57. In the presence of the gas target, an intra-cavity power of 2.8 kW at 38-fs pulse duration was achieved over several minutes without any measures of realignment, and over several hours with only minor occasional realignment of the cavity. To prevent mirror contamination, the two cavity mirrors following the HHG target, the NIR/XUV beam splitter and the following gold mirror are constantly flushed with ozone. The cavity lock was implemented according to the Pound-Drever-Hall scheme with two feed-back loops: one slow loop which acts on the cavity length and a fast one adjusting the repetition frequency of the titanium-sapphire oscillator by varying the length of its cavity. To estimate the XUV conversion efficiency in the gas target, we corrected for the output coupling efficiency and for reabsorption in the background gas, resulting in a conversion efficiency of 5 × 10−8 at 40 eV. State-of-the art single-pass systems using argon as the generation medium and 1-µm driving pulses62,63 reach conversion efficiencies between 5x10−8 and 2x10−7 at comparable photon energies. The output coupling efficiency (Fig. 4) was estimated with the 3+1 D HHG model described in ref. 64 by varying the target gas density and selecting the value with optimum flux around 40 eV, and assuming a gas target position of one Rayleigh range before the focus. This target position was experimentally determined by scanning the nozzle position and observing the clamping of the intracavity power due to plasma-induced blueshift.
Time-of-flight photoelectron detection
Three different principles are common in electron spectroscopy: retardation of the electrons by a potential barrier (retarding field analyser), dispersion of electrons in a magnetic (or in some cases an electric) field (e.g., hemispherical analysers) and time-of-flight (ToF) analysis. The first two options necessitate a scan over the energy range that is to be analysed, whereas ToF detection allows for the simultaneous detection of electrons of all accepted kinetic energies. More importantly, when combined with a spatially resolving detector, only ToF spectrometers enable the detection of 3D data at once: electron kinetic energy and two dimensions either in space (PEEM) or angle (ARPES). ToF spectrometers are ideal in combination with HHG sources due to the pulsed nature of the latter. The maximum admissible temporal dispersion of electrons is limited by the time between two subsequent laser pulses, which is 54 ns at our repetition rate. Secondary electrons with times of flight far above this value (for any reasonable drift distance) are filtered out by an additional retarding grid as a high-pass filter for electrons. For our drift distance of 880.5 mm (Themis 1000, SPECS GmbH) this typically results in a detectable window of 33–50 eV electron kinetic energy with a resolution of around 30 meV (determined from the measured temporal resolution of our 2D-delayline-detector). This energy range can be increased by accelerating electrons before or within the spectrometer at the expense of energy resolution. Without applying any additional field, our spectrometer collects a solid angle of 0.0016 sr in its so-called drift mode (DM). In its low angular dispersion mode (LAD), a complex multi-element electronic lens system within the spectrometer is used to image a larger solid angle of 0.047 sr on the detector. Since the electron lens system inevitably suffers from chromatic aberration, only a limited energy window can be correctly imaged, and a loss of energy resolution cannot be prevented. Although the earth magnetic field is compensated for down to a residual field of around 2 µT using Helmholtz-coils, this also can have a negative impact on the resolution. We experimentally determined the energy resolution in LAD mode for our settings to be ~1 eV (cf. Fig. 4b). Our instrument resolution can be calculated as the convolution of the detector resolution (30 meV in DM) and the width of the harmonics (between 0.13 eV and 0.35 eV) and amounts to values between 0.13 and 0.36 eV for the individual harmonics. Consequently, space-charge-induced distortions of the photoelectron spectra on the order of a few tens of meV cannot be resolved. In the LAD mode the number of photoelectron counts per second in the observed energy window reached the maximum admissible count rate of 1 MHz on our DLD-detector in its 3D resolved mode. In general, for PES applications a pulse repetition rate high enough so that space charge does not impair the application is desirable. However, an upper bound is set by cumulative effects in the HHG process that limit the XUV yield65,66. Furthermore, for ToF-PES there is a trade-off between repetition rate, energy resolution and observable energy window, caused by the ToF dispersion of the electrons. Here, we demonstrate that a repetition rate in the low tens of MHz dramatically increases the PE statistics while also granting a temporal detection duty cycle of nearly 100% and an energy bandwidth and resolution appropriate for solid-state PES while catching all electrons that are relevant for the measurement.
XUV-IR-interferometer delay stability
To obtain an estimation of the maximum achievable timing precision with our setup, we evaluated the delay stability of the piezo stage (P-621.1CD, Physik Instrumente GmbH) in our interferometer. The position is measured with sub-nanometer resolution using a built-in contact-free capacitive sensor. At a fixed position, in closed loop operation, we found that in 1491 measurements it deviates from the nominal value with a standard deviation of 1.5 nm which is close to the repeatability specified by the manufacturer (±1 nm) and corresponds to a timing jitter of 9.8 as. With state-of-the-art interferometric delay tracking techniques, the delay can in principle be determined with sub-as precision67.
The data that support the findings of this study are available from the corresponding author upon reasonable request.
Krausz, F. & Stockman, M. I. Attosecond metrology: from electron capture to future signal processing. Nat. Phot. 8, 205 (2014).
Hüfner, S. Photoelectron Spectroscopy. (Springer Verlag, Berlin, Heidelberg, 2003).
Drescher, M. et al. X-ray pulses approaching the attosecond frontier. Science 291, 1923 (2001).
Paul, P. M. et al. Observation of a train of attosecond pulses from high harmonic generation. Science 292, 1689–1692 (2001).
Itatani, J. et al. Attosecond streak camera. Phys. Rev. Lett. 88, 173903 (2002).
Cavalieri, A. L. et al. Attosecond spectroscopy in condensed matter. Nat 449, 1029 (2007).
Ossiander, M. et al. Attosecond correlation dynamics. Nat. Phys. 13, 280 (2016).
Muller, H. G. Reconstruction of attosecond harmonic beating by interference of two-photon transitions. Appl. Phys. B 74(S1), S17–S21 (2002).
Chen, C. et al. Distinguishing attosecond electron–electron scattering and screening in transition metals. Proc. Natl Acad. Sci. USA. 114, E5300–E5307 (2017).
Tao, Z. et al. Direct time-domain observation of attosecond final-state lifetimes in photoemission from solids. Science 353, 6294 (2016).
Locher, R. et al. Energy-dependent photoemission delays from noble metal surfaces by attosecond interferometry. Optica 2, 405 (2015).
Lucchini, M. et al. Light-matter interaction at surfaces in the spatiotemporal limit of macroscopic models. Phys. Rev. Lett. 115, 137401 (2015).
Cattaneo, L. et al. Comparison of attosecond streaking and RABBITT. Opt. Express 24, 29060 (2016).
Isinger, M. et al. Photoinoization in the time and frequency domain. Science 358, 893 (2017).
Klünder, K. et al. Probing single-photon ionization on the attosecond time scale. Phys. Rev. Lett. 106, 143002 (2011).
Schultze, M. et al. Delay in photoemission. Science 328, 1658 (2010).
Chew, S. H. et al. Time-of-flight-photoelectron emission microscopy on plasmonic structures using attosecond extreme ultraviolet pulses. Appl. Phys. Lett. 100, 051904 (2012).
Förg, B. et al. Attosecond nanoscale near-field sampling. Nat. Comm. 7, 11717 (2016).
Stockmann, M. I., Kling, M. F., Kleineberg, U. & Krausz, F. Attosecond nanoplasmonic-field microscope. Nat. Photonics 1, 539 (2007).
Hommelhoff, P. & Kling, M. F. Attosecond Nanophysics. (Wiley-VCH, Weinheim, 2015).
Schötz, J. et al. Reconstruction of nanoscale near fields by attosecond streaking. IEEE J. Sel. Top. Quantum Electron. 23, 8700111 (2017).
Hellmann, Rossnagel, S. K., Marczynski-Bühlow, M. & Kipp, L. Vacuum space-charge effects in solid-state photoemission. Phys. Rev. B 79, 035402 (2009).
Buckanie, N. M. et al. Space charge effects in photoemission electron microscopy using amplified femtosecond laser pulses. J. Phys. Condens. Matter 21, 314003 (2009).
Masel, R. Principles of Adsorption and Reaction on Solid Surfaces. (Wiley Interscience, New York, 1996).
Emma, P. et al. First lasing and operation of an ångstrom-wavelength free-electron laser. Nat. Photonics 4, 641–647 (2010).
Chiang, C.-T. et al. Boosting laboratory photoelectron spectroscopy by megahertz high-order harmonics. New J. Phys. 17, 013035 (2015).
Hädrich, S. et al. Exploring new avenues in high repetition rate table-top coherent extreme ultraviolet sources. Light Sci. Appl. 4, e320 (2015).
Wang, H. et al. Bright high-repetition-rate source of narrowband extreme-ultraviolet harmonics beyond 22 eV. Nat. Comm. 6, 7459 (2015).
Hädrich, S. et al. High photon flux table-top coherent extreme-ultraviolet source. Nat. Phot. 8, 779 (2014).
Mills, A. K. et al. An XUV source using a femtosecond enhancement cavity for photoemission spectroscopy. Proc. SPIE 9512, 95121 (2015).
Corder, C. et al. Ultrafast extreme ultraviolet photoemission without space charge. Struct. Dyn. 5, 054301 (2018).
Popmintchev, D. et al. Ultraviolet surprise. Efficient soft x-ray high-harmonic generation in multiply ionized plasmas. Science 350, 1225 (2015).
Rothhardt, J. et al. 53 W average power few-cycle fiber laser system generating soft x rays up to the water window. Opt. Lett. 39, 5224–5227 (2014).
Pupeza, I. et al. Compact high-repetition-rate source of coherent 100 eV radiation. Nat. Phot. 7, 608–612 (2013).
Carstens, H. et al. High-harmonic generation at 250 MHz with photon energies exceeding 100 eV. Optica 3, 366–369 (2016).
Saule, T. et al. Phase-stable, multi-µJ femtosecond pulses from a repetition-rate tunable Ti:Sa-oscillator-seeded Yb-fiber amplifier. Appl. Phys. B 123, 17 (2017).
Weitenberg, J., Saule, T., Schulte, J. & Rußbüldt, P. Nonlinear pulse compression to sub-40 fs at 4.5 μJ pulse energy by multi-pass-cell spectral broadening. IEEE J. Quantum Electron. 53, 6 (2017).
Holzberger, S. et al. Femtosecond enhancement cavities in the nonlinear regime. Phys. Rev. Lett. 115, 023902 (2015).
Carlson, D. R., Lee, J., Mongelli, J., Wright, E. M. & Jones, R. J. Intracavity ionization and pulse formation in femtosecond enhancement cavities. Opt. Lett. 36, 2991 (2011).
Allison, T. K., Cingöz, A., Yost, D. C. & Ye, J. Extreme nonlinear optics in a femtosecond enhancement cavity. Phys. Rev. Lett. 107, 183903 (2011).
Mairesse, Y. et al. Attosecond synchronization of high-harmonic soft x-rays. Science 302, 5650 (2003).
Fuggle, J. C. & Mårtensson, N. Core-level binding energies in metals. J. Electron Spectrosc. Relat. Phenom. 21, 275 (1980).
Jordan, I. & Wörner, H. J. Extracting attosecond delays from spectrally overlapping interferograms. J. Opt. 20, 024013 (2018).
Gruson, V. et al. Attosecond dynamics through a Fano resonance: monitoring the birth of a photoelectron. Science 354, 6313 (2016).
Mikkelsen, A. et al. Photoemission electron microscopy using extreme ultraviolet attosecond pulse train. Rev. Sci. Instr. 80, 123703 (2009).
Dakovski, G. L., Li, Y., Durakiewicz, T. & Rodriguez, G. Tunable ultrafast extreme ultraviolet source for time- and angle-resolved photoemission spectroscopy. Rev. Sci. Instr. 81, 073108 (2010).
Willems, F. et al. Probing ultrafast spin dynamics with high-harmonic magnetic circular dichroism spectroscopy. Phys. Rev. B 92, 220405 (2015).
Fritsch, K., Poetzlberger, M., Pervak, V., Brons, J. & Pronin, O. All-solid-state multipass spectral broadening to sub-20 fs. Opt. Lett. 43, 4643–4636 (2018).
Lilienfein, N. et al. Enhancement cavities for few-cycle pulses. Opt. Lett. 42, 271–274 (2017).
Högner, M., Saule, T., Lilienfein, N., Pervak, V. & Pupeza, I. Tailoring the transverse mode of a high-finesse optical resonator with stepped mirrors. J. Opt. 20, 024003 (2018).
Cingöz, A. et al. Direct frequency comb spectroscopy in the extreme ultraviolet. Nat 482, 68–71 (2012).
Herrmann, M. et al. Feasibility of coherent xuv spectroscopy on the 1S−2S transition in singly ionized helium. Phys. Rev. A. 79, 052505 (2009).
Panov, A. D. Quantitative conversion spectroscopy of the ultrasoft isomeric transition of uranium-235 and the electronic structure of uranium oxides. J. Exp. Theor. Phys. 85, 313 (1997).
Long, J. P., Itchkawitz, B. S. & Kabler, M. N. Photoelectron spectroscopy of laser-excited surfaces by synchrotron radiation. J. Opt. Soc. Am. B 13, 201 (1996).
Saloman, E. B. Typical photoefficiency between 20-250 eV of windowless XUV photodiodes with tungsten and anodized aluminum oxide photocathodes. Appl. Opt. 17, 1489–1490 (1978).
de Vries, O. et al. Acousto-optic pulse picking scheme with carrier-frequency-to-pulse-repetition-rate synchronization. Opt. Express 23, 19586 (2015).
Lücking, F., Assion, A., Apolonski, A., Krausz, F. & Steinmeyer, G. Long-term carrier-envelope-phase-stable few-cycle pulses by use of the feed-forward method. Opt. Lett. 37, 2076 (2012).
Esser, D. Laser-manufactured mirrors for geometrical output coupling of intracavity-generated high harmonics. Opt. Express 21, 26797 (2013).
Esser, D. Fused-silica mirror substrates with laser-microstructured openings with reduced chipping. CLEO Europe, CE_10_3 (2015)
Henke, B. L., Gullikson, E. M. & Davis, J. C. X-ray interactions: photoabsorption, scattering, transmission, and reflection at E=50-30000 eV, Z=1-92. At. Data Nucl. Data Tables 54, 181–342 (1993).
Holzberger, S. et al. Enhancement cavities for zero-offset-frequency pulse trains. Opt. Lett. 40, 2165–2168 (2015).
Rothhardt, J. et al. High-repetition-rate and high-photon-flux 70 eV high-harmonic source for coincidence ion imaging of gas-phase molecules. Opt. Exp. 24, 18133 (2016).
Lorek, E. et al. High-order harmonic generation using a high-repetition-rate turnkey laser. Rev. Sci. Instr. 85, 123106 (2014).
Högner, M., Tosa, V. & Pupeza, I. Generation of isolated attosecond pulses with enhancement cavities—a theoretical study. New J. Phys. 19, 033040 (2017).
Porat, G. et al. Phase-matched extreme-ultraviolet frequency-comb generation. Nat. Phot. 12, 387–391 (2018).
Saule, T. et al. Cumulative plasma effects in cavity-enhanced high-order harmonic generation in gases. APL Phot. 3, 101301 (2018).
Schweinberger, W. et al. Interferometric delay tracking for high-precision Mach-Zehnder-type scanning measurements. Opt. Exp. 27, manuscript in press (2019).
Takahashi, E., Nabekawa, Y. & Midorikawa, K. Generation of 10-µJ coherent extreme-ultraviolet light by use of high-order harmonics. Opt. Lett. 27, 1920 (2002).
Takahashi, E., Nabekawa, Y. & Midorikawa, K. Low-divergence coherent soft x-ray source at 13 nm by high-order harmonics. Appl. Phys. Lett. 84, 4 (2004).
Frietsch, B. et al. A high-order harmonic generation apparatus for time- and angle-resolved photoelectron spectroscopy. Rev. Sci. Instr. 84, 075106 (2013).
Ozawa, A., Zhao, Z., Kuwata-Gonokami, M. & Kobayashi, Y. High average power coherent vuv generation at 10 MHz repetition frequency by intracavity high harmonic generation. Opt. Exp. 23, 15107 (2015).
This work was supported by the project MEGAS in the frame of the Fraunhofer-Max-Planck Cooperation and by the German Research Foundation (DFG) via the Munich Centre for Advanced Photonics (MAP). J.S. and M.F.K. acknowledge support via the Max Planck Society via IMPRS-APS, I.P. acknowledges support from the European Research Council (ERC) under grant no. 617173.
The authors declare no competing interests.
Journal peer review information: Nature Communications thanks the anonymous reviewers for their contribution to the peer review of this work.
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Saule, T., Heinrich, S., Schötz, J. et al. High-flux ultrafast extreme-ultraviolet photoemission spectroscopy at 18.4 MHz pulse repetition rate. Nat Commun 10, 458 (2019). https://doi.org/10.1038/s41467-019-08367-y
Nature Photonics (2021)
Nature Communications (2021)
Nature Communications (2020)
Nature Photonics (2019)