Does the excitation of ultrafast magnetization require direct interaction between the photons of the optical pump pulse and the magnetic layer? Here, we demonstrate unambiguously that this is not the case. For this we have studied the magnetization dynamics of a ferromagnetic cobalt/palladium multilayer capped by an IR-opaque aluminum layer. Upon excitation with an intense femtosecond-short IR laser pulse, the film exhibits the classical ultrafast demagnetization phenomenon although only a negligible number of IR photons penetrate the aluminum layer. In comparison with an uncapped cobalt/palladium reference film, the initial demagnetization of the capped film occurs with a delayed onset and at a slower rate. Both observations are qualitatively in line with energy transport from the aluminum layer into the underlying magnetic film by the excited, hot electrons of the aluminum film. Our data thus confirm recent theoretical predictions.
Ultrafast demagnetization is a very intriguing phenomenon. The existence and origin of this rapid loss of a thin film’s magnetization on the femtosecond timescale has been controversially debated ever since its discovery in 19961. Recently, it has been proposed that the origin of this magnetization loss could be due to spin-dependent motion of the optically excited hot valence electrons causing a spatial redistribution of the magnetization, either to an adjacent metallic layer2,3 or within the magnetic layer itself4. Strong experimental evidence for this so-called superdiffusive spin transport has been found lately5,6,7,8.
However, the experiment of Eschenlohr and co-workers8, similar to our study reported here, has been challenged recently. Khorsand and co-workers9 showed that the Au cap layer employed in that experiment does not yield the postulated, and for the interpretation of the data crucial, attenuation of the incident IR pump pulse. Implementing a truly IR-opaque capping layer, we evade the limitation affecting the interpretation of the results of Eschenlohr and co-workers8. Proper characterization of the number of photons reaching the magnetic layer demonstrates that the transmitted intensity is by orders of magnitude too small to excite the ultrafast demagnetization process.
The experiment has been realized at the SXR instrument of the X-ray Free Electron laser LCLS10 equipped with the pnCCD camera11 using resonant magnetic small-angle scattering as probe technique for the temporal evolution of the local magnetization within the domains of a thin Co/Pd multilayer film. The data obtained undoubtedly prove that the ultrafast demagnetization process can be triggered without any direct interaction between the photons of the optical pump pulse and the magnetic layer. In addition, the data clearly resolve the presence of a delayed onset of this process as well as its slower evolution with respect to the dynamics directly induced by the IR pump pulse. We note that both these observations are consistent with an excitation process by hot electrons as proposed by Eschenlohr and co-workers8. However, and contrary to these authors, we think that those observations do not unambiguously prove that part of the magnetization is transferred to the metallic cap layer via superdiffusive spin transport3.
Samples fabrication and characterization
The thin-film samples studied in this experiment have been grown by DC magnetron sputtering on 50 nm thin X-ray transparent Si3N4 membranes (see Fig. 1(a)). Two ferromagnetic multilayer films were grown. One film was capped with a 3 nm thin Al layer to prevent oxidation of the magnetic multilayer. Since about 1.5 nm of this Al cap is instantaneously oxidized12, we refer to this film as uncapped Co/Pd film in the following. This is in contrast to the capped Co/Pd film on top of which a 40 nm thick Al film was grown.
To verify that this Al cap layer is indeed opaque for the IR pump pulse, a 40 nm thick Al layer has been grown on the same type of Si3N4 substrate. The transmission of this sample was measured to be 1.3 × 10−4 (sensitivity of the measurement has been 10−6). We will see below that this value corresponds to an Al opacity nearly two orders of magnitude larger than what is needed to exclude any direct IR photon excitation as origin of the observed demagnetization dynamics. Having also measured the IR reflectivity and transmission of the films, we can calculate the relative amount of pump pulse energy absorbed in the cap and magnetic layers of these films (Table 1). Finally, we can deduce from these data an absorption length of about 5.5 nm for the 800 nm IR light in Al, which is in line with values given in the literature13.
Infrared pump soft X-ray probe experiment
As in previous experiments5,14, we have employed resonant magnetic small-angle X-ray scattering as probe technique, which characterizes in the presence of a magnetic domain structure a material’s local magnetization with nanometer spatial resolution. Prior to the experiment, a demagnetization procedure with an oscillating, successively decreasing magnetic field oriented parallel to the film surface has been employed to obtain a magnetic domain structure of well-aligned stripe domains15 (see Fig. 1(b)). Tuning the X-ray photon energy to the magnetically dichroic Co L3 edge, this grating-like magnetic domain structure gives rise to localized scattering intensities corresponding to the grating’s positive and negative diffraction orders. The clear visibility of up to the 5th scattering order in the pattern reproduced in Fig. 2 indicates the high degree of domain alignment present in these films.
The resonantly excited scattering pattern originating from a single X-ray pulse shown in the inset of Fig. 2 is representative for the ones recorded on both, the uncapped and the capped Co/Pd multilayer film. For this pattern recorded with negative pump probe delay (X-rays first), we see that the number of CCD counts within each of the two first order scattering peaks (roughly from 2 × 102 to 104 counts) is well above the noise level of the detector (a few counts). Such scattering patterns have been recorded for different IR pump fluence values while changing the IR-pump - X-ray probe delay continuously as discussed above. The magnetic scattering intensity is extracted from these pattern by integration of the plus and minus first order scattering peaks. Note that the scattering intensity is proportional to the square of the local magnetization within the domains5,14. Plotting these scattering intensities against the IR-pump – X-ray probe delay yields the curves shown in Fig. 3(a), which characterize the temporal evolution of the magnetization of the two Co/Pd films as a function of IR pump fluence. On a first glance one notes that the magnetization exhibits in all cases the typical behavior associated with the ultrafast demagnetization phenomenon1: a drastic drop of the magnetization occurring on a sub-picosecond time scale, which is followed by a partial magnetization recovery taking place with a slower time constant on the order of one to a few picoseconds. On the other hand, the comparison of the two films reveals that the onset of the magnetization dynamics of the capped film is clearly delayed with respect to the one of the uncapped film. We note that this delayed onset is the expected signature of the demagnetization dynamics induced by the hot electrons generated by the IR pump pulse in the metallic capping layer. This point is further discussed below.
The demagnetization curves of the uncapped Co/Pd film were excited with IR pump pulse energies of 20 μJ, 25 μJ and 50 μJ. Taking the reflectivity and absorption values from Table 1 we can derive values for the IR absorbed energy: 6 μJ, 7.5 μJ and 15 μJ respectively, giving rise to a maximum degree of demagnetization at about 0.5 ps delay of 24%, 38% and 57%. It has to be noted that this absorbed energy values might not correspond to the actual absorbed energy since the exact IR transmission through the transport line was not measured accurately. However, these values give us a very good relative scale to compare with the absorbed energy in the capped sample. Furthermore, the pump beam profile at the sample position was not measured with a sufficiently high accuracy to obtain an absolute fluence value. However, previous measurements on similar samples14,16 show that the fluences reached here should approximately be in the range of 5 to 15 mJ cm−2.
In case of the capped Co/Pd film, the IR pump pulse energy needed to be increased to 65 μJ to reach a demagnetization of 12%. Taking the film’s reflectivity and the layers’ absorption from Table 1, the IR photon pulse energy directly absorbed in the Co/Pd layer is estimated to be lower than 0.06 μJ. This corresponds to a fluence value within the focus area of 0.06 mJ cm−2 (see Methods). Clearly, this amount of energy is more than one order of magnitude too small to trigger any noticeable demagnetization16. Within the 40 nm thick Al layer, on the other hand, 10.4 mJ are absorbed.
To analyse the data in more detail, we have renormalized the demagnetization curves to exhibit the same degree of demagnetization. The resulting curves are plotted in Fig. 3(c). Comparing the time traces of the uncapped Co/Pd film with each other (red symbols) one observes for all three the very same initial rapid magnetization decrease. This observation implies that the temporal evolution of this initial demagnetization phase is independent of the specific IR pump fluence. On the other hand, once the magnetization minimum has been reached at about 0.5 ps, the curves exhibit distinctly different dynamics: The partial recovery of the magnetization taking place during this time range is increasingly slowed down with increasing IR pump fluence as it has been observed previously, e.g., in ref. 14,17.
We remark that the fluence independence of the initial demagnetization rate appeared already in our previous demagnetization study, which exploited at a high harmonic generation source the magnetic contrast of the Co M2,3 resonance as scattering contrast14. Since these M-edges of the transition metals are energetically low-lying (60 eV for Co), it could be argued that the strong, non-resonant contribution of valence electrons might affect these measurements. The replication of these observations obtained here at the Co L3 resonance therefore erases any such doubts. We also point out that the absence of any significant variation in the onset of the demagnetization dynamics demonstrates that any timing drift, which may have occurred during this experiment, is correctly accounted for by the optical IR – X-ray pulse cross-correlator.
The renormalized evolution of the capped Co/Pd film is represented by the dark blue circles in Fig. 3(c). The clear “horizontal” separation between the traces of the two films reveals unquestionably the presence of a significant delay between the onset of the respective demagnetization dynamics. As discussed below, we estimate this delay to be about 270 fs. In addition, the comparison reveals a clear difference in the demagnetization rate, which is about a factor of two slower in case of the capped Co/Pd film. These differences show up even more clearly by shifting the curve of the capped film by −380 fs (light blue squares in Fig. 3(c)) so that the minima of the curves for capped and uncapped (weakest pump) films overlap. Interestingly, one notes that the dynamics of the partial recovery of the magnetization of the capped film superposes with the one of the weakly pumped uncapped film (6 μJ). This similarity indicates that about 400 fs after excitation of the magnetization dynamics, the nature of the excitation process itself does not influence the dynamics anymore.
where is the variation in scattering intensity, S0 is the scattering intensity of the unpumped system, τM is the demagnetization time, τE the time constant characterizing the partial magnetization recovery, and Θ(t) the step function. The experimental time resolution enters as Γ(t), which we represent as a Gaussian function with a full width at half maximum (FWHM) of τG. This τG is the convolution of the pump and probe pulse width with the uncertainty of the optical IR – X-ray cross-correlator measurement. We remark that prior to the experiment, coarse pump-probe time overlap was determined with a coaxial antenna and this time reference was unchanged during the experiment. The timing of the individual pump-probe events of each time trace was after the experiment corrected with the simultaneously recorded data of the optical IR – X-ray pulse cross-correlator. Finally, to simplify data presentation, we shifted the time axis texp of all curves by the same amount such that t = 0 corresponds to pump-probe time overlap of the trace recorded for the uncapped Co/Pd film with low fluence pumping (t0,u). The time variable in eqn. 1 thus corresponds to with t0 a free fit parameter characterizing the onset of the demagnetization dynamics of the actual data trace. Definition of all other parameters can be found in the literature2.
In line with the visual similarity of the initial part of the three demagnetization curves of the uncapped Co/Pd film in Fig. 3(b), the fits of these curves yield within its accuracy identical values for onset (t0 = 0, see above), demagnetization time (τM = 160 fs) and τG = 150 fs. We thus fitted these three sets of data with the same time constants. The results are listed in Table 2.
When analyzing the temporal evolution of the capped Co/Pd film, one finds that the demagnetization dynamics can be well-reproduced by the same fit model. In particular this implies that the initial dynamics are correctly reproduced by a single exponential decay function. One notes, however, that this agreement can be reached in two ways: by either increasing the characteristic time scale of the demagnetization process (τM) or – and – the experimental time resolution (τG). We can actually understand this inter-dependence within the model put forward by Eschenlohr and co-workers8: the strong absorption of IR light by Al leads to the excitation of very hot valence electrons within the top 5–10 nm of the Al cap layer. These thermalize by electron-electron (and also electron-phonon) scattering thus giving rise to a very large number of hot electrons. Interchange between this hot-electron distribution with the colder one of the underlying Co/Pd multilayer acts as trigger for the observed ultrafast demagnetization process as discussed in more detail below.
The conversion of the incident IR laser pulse into a cascade of hot electrons can thus be seen as a temporal stretching of the excitation pulse. Within our fit model this leads to a higher value for the parameter τG, which combines pump and probe pulse duration with their relative arrival time jitter. It is however not possible to distinguish whether this increase in pump pulse duration is the unique source of the observed slowing down of the demagnetization rate or whether an increase in the time constant of the demagnetization process itself contributes, too. The reason for this is that the only other time scale of relevance here, namely the one of the partial magnetization recovery, is too long to be significantly influenced by a slightly longer pump pulse as attested by the overlap of the uncapped and weakly pumped capped film’s dynamic after the minimum magnetization has been reached (Fig. 3(c)).
In the following, we fix the demagnetization time fit parameter to the value obtained for the uncapped film (τM = 160 fs), which is motivated by the absence of any IR fluence dependence of the initial magnetization dynamics of the uncapped film. The obtained fit, shown as solid blue line in Fig. 3(a,b), reproduces the data with excellent precision. For the delay of the onset of the magnetization dynamics it yields a value of t0 = 270 fs and a time constant τE = 1.01 ps for the dynamics of the partial magnetization recovery. As expected from the visual agreement with the uncapped film in case of the lowest pump, this latter value is close to the value of the uncapped film. Finally, τG is found to be 430 fs. From this we can derive for the excitation pulse width a value of about 400 fs making the reasonable assumption that neither the X-ray pulse length nor the arrival time correction have changed with respect to the experiment on the capped film realized just minutes before. The main parameters obtained from fitting the experimental data to equation 1 are summarized in Table 2.
The observation of the ultrafast demagnetization dynamics in case of the capped Co/Pd film, for which the IR pump is completely absorbed in the capping layer, demonstrates without doubt that ultrafast demagnetization does not require direct interaction between the electromagnetic pump pulse and the magnetic film. This result therefore resolves the controversy between Eschenlohr et al.8 and Khorsand et al.9. Moreover, our observations are in qualitative agreement with the model proposed by Eschenlohr and co-workers8, which attributes the photonless excitation of the demagnetization process to the hot electrons generated in the metallic capping layer by absorption of the IR pump pulse. Indeed, the delay between the demagnetization of the capped Co/Pd film compared to the one of the uncapped sample can be seen as the traveling time of the hot electrons through the Al cap layer. And the slowing down of the observed demagnetization dynamics can be understood as a broadening of the excitation pulse due to the stochastic electron-electron scattering cascade. It has to be noted that heat diffusion at the speed of sound (of the order of 5000 ms−1 in Al) is at least one order of magnitude too slow to explain our observations.
A detailed calculation of these processes is beyond the scope of this article. We note, however, that the observed delay of the onset of the demagnetization process (t0 = 270 fs) and the reduced rate of the demagnetization process are qualitatively compatible with the timescales found in previous calculations3,8. We further remark that in comparison to the values calculated by Eschenlohr et al. for their Au (30 nm)/Ni (15 nm)/Al (buffer) trilayer (t0 = 70 ± 40 fs and tM = 400 ± 160 fs)8, our larger delay value is in line with our 10 nm thicker cap layer as well as the shorter hot-electron lifetime in our Al layer with respect to the Au layer18.
The demagnetization process itself is described within the model of Eschenlohr and co-workers8 as consequence of superdiffusive exchange between the initially cold, spin polarized electrons of the ferromagnetic layer and the hot, spin-neutral electrons of the cap layer. Due to the different mobility of spin majority and minority electrons within the ferromagnetic layer, a net transport of magnetic moment out of the ferromagnetic layer occurs into the neighboring non-magnetic, metallic cap and buffer layer. We note that our observations are in agreement with this prediction, however, we do not consider them as providing strong experimental evidence for this model. To obtain such evidence, or even proof, the amount of spin polarization injected from the ferromagnetic layer into the neighboring, non-magnetic layers should be characterized experimentally. Then, a comparison between the amount of lost and gained spin polarization could quantitatively determine the relevance/contribution of superdiffusive spin transport to the overall demagnetization dynamics.
In conclusion, we have demonstrated that ultrafast demagnetization does not require direct excitation of the ferromagnetic material by a photon pulse. In order to prove that affirmation we have measured the magnetization dynamics of a magnetic film capped by a thick Al layer. Contrary to pioneering previous work8 the optical properties of this capping layer have been thoroughly characterized and found to strongly absorb the IR pump pulse. The remaining photon pulse reaching the underlying magnetic film is three orders of magnitude too weak to trigger the demagnetization observed. Comparison between the dynamics of this capped film with the ones of an uncapped reference film showed that the onset of the demagnetization dynamics is delayed and the initial loss in magnetization is slowed down. These observations are compatible with a demagnetization process triggered by a flux of hot valence band electrons from the Al cap layer to the underlying magnetic film. The mechanism by which these hot electrons trigger the demagnetization remains to be elucidated.
The samples have been grown in an argon atmosphere of 1 × 10−3 mbar. The base pressure of the instrument has been 1 × 10−8 mbar. The multilayers samples have been deposited on a 2 nm thick Pd seed layer. The deposition rate used were respectively 0.03 nm s−1, 0.05 nm s−1 and 0.12 nm s−1 for Al, Co and Pd. Taking into account the measured transmission of the single Al layer and the theoretical transmission values of the Al/Si3N4 and Si3N4/air interfaces (0.24 and 0.89) the absortion in the 40 nm Al layer is estimated to be (note that multiple reflections and interference effects have been neglected within this approximation).
The 800 nm pump pulses triggering the magnetization dynamics were delivered by the femtosecond IR laser of the SXR end station10,19. To uniformly excite the magnetic film on the 50 μm square membranes, a focusing lens (f = 75 cm) was positioned just in front of the beamline’s standard in-coupling mirror, which yields close to collinear beam propagation. The spatial beam profile and position of the IR pump beam was monitored during the experiment using an out-of-vacuum replica of the IR focus. Since the IR pulse length in the SXR hutch is about 50 fs, we chose a comparable X-ray probe pulse length. Both pulse durations are thus below the temporal resolution of the X-ray arrival time jitter correction, which sets the overall time resolution of the experiment to about 130 ± 20 fs20.
The bending of the Kirkpatrick-Baez mirrors was set to obtain an X-ray spot size of about 50 μm in diameter comparable to the size of the membranes 50 × 50 μm2. The incident X-ray photon flux density (FX) was limited to a value at least 20 times lower than the modification treshold of the magnetic domains structure21, i.e. FX < 2 mJ cm−2. One can calculate that of these about 3% are absorbed within the Al cap layer, 50% in the Co/Pd multilayer, 2% in the Pd buffer and 4% in the Si3N4 membrane. The dynamics is thus safely dominated by the IR excitation.
A particularity of this experiment has been the use of the pnCCD camera11 to record single X-ray pulse scattering patterns at the full 120 Hz repetition rate of LCLS. The detector’s central opening adds the possibility to accurately determine the transmitted X-ray intensity with a photodiode and thus to normalize the recorded scattering pattern to the intensity of the photon pulse incident on the spatially constrained Si3N4 membrane. Within minutes tens of thousands of correctly intensity normalized scattering pattern can thus be recorded. This high data rate can be exploited in an IR pump - X-ray scattering probe experiment by continuously varying the pump-probe delay during data accumulation. We employed for this a random walk scheme centered around pump-probe time overlap and extending towards the desired delay range with decreasing sampling rate. Adding as further ingredient an accurate measure of the individual X-ray arrival time jitter using the optical cross-correlator installed permanently at SXR (timing tool)19,20, the recorded data are then grouped in time bins matching the desired time resolution of the respective temporal region. The efficiency of this experimental approach is demonstrated by the excellent signal-to-noise ratio of the delay scans shown in Fig. 3(a), which have been recorded within a few minutes each.
How to cite this article: Vodungbo, B. et al. Indirect excitation of ultrafast demagnetization. Sci. Rep. 6, 18970; doi: 10.1038/srep18970 (2016).
The authors gratefully acknowledge financial support received from the PEPS SASLELX of the French CNRS, from the German Federal Ministry of Education and Research within FSP-301 and FSP-302 under contracts 05K10KTB and 05K13KT4, and from the DFG within SFB 925. Portions of this research were carried out on the SXR Instrument at the Linac Coherent Light Source (LCLS), a division of SLAC National Accelerator Laboratory and an Office of Science user facility operated by Stanford University for the U.S. Department of Energy. The SXR Instrument is funded by a consortium whose membership includes the LCLS, Stanford University through the Stanford Institute for Materials Energy Sciences (SIMES), Lawrence Berkeley National Laboratory (LBNL), University of Hamburg through the BMBF priority program FSP 301, and the Center for Free Electron Laser Science (CFEL). Part of this work was supported by the Department of Energy, Office of Science, Basic Energy Sciences, Materials Sciences and Engineering Division, under Contract DE-AC02-76SF00515. M. H. B. would like to acknowledge the Knut and Alice Wallenberg Foundation for their financial support.
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