1. Introduction
One of the main drives for ultrafast magnetization dynamics studies is applications in magnetic storage technology and logic operations with spintronic devices [
1]. For example, breaking the current nanosecond time scale limit for magnetization manipulation would allow to create ultrafast magnetic devices as needed for future Big Data or Artificial Intelligence applications. To achieve this goal, it is not sufficient to only demagnetize a system as demonstrated on the femtosecond time scale in 1996 [
2]; instead, it is necessary to completely control its magnetization. In that regard, the experiment realized by Vicario et al. [
3] is remarkable. Using a terahertz (THz) pump, these authors were able to initiate a non resonant precession of the magnetization in a thin cobalt film on the time scale of a picosecond. This observation opens up the way to the deterministic control of magnetization with ultrashort pulses.
THz pulses have a longer wavelength than infrared (IR) pulses, hence a lower frequency. Consequently, the THz photon energy is lower (by almost three orders of magnitude) than that of a near IR photon which is generally used as pump in ultrafast magnetization experiments (0.004 eV versus 1.6 eV). Therefore, absorption of a THz photon can only occur by electrons very close to the Fermi level and only into lower energy levels than it is the case of an IR pump pulse (
Figure 1). The THz pulse induced dynamics is then dominated by the interaction between the sample and the strong magnetic field of the THz pulse rather than by absorption and heating. An interesting question arises therefore, at which wavelength, or over which wavelengths range, we can observe the transition between the two behaviors. This knowledge will be fundamental to tailor ultrafast magnetic devices. Our goal is thus to study the transition from such a coherent coupling to the non-coherently excited ultrafast demagnetization phenomenon.
Recently, the generation of THz pulses with much higher field amplitudes has become possible, which permitted a conceptually new approach for investigating low energy degrees of freedom in matter [
4]. Additionally, advancements of accelerator technology achieved, for example at BL3 beamline of FLASH (DESY, Hamburg, Germany), made it possible to produce carrier-envelope phase stable THz pulses with high fields and adjustable high repetition rates [
5]. Appropriate parameters settings of the THz undulator allows for the generation of narrow-band THz frequency and intense pulses, which can be used to trigger magnetization dynamics coherently.
In the present work, we use synchronized THz-pump to an X-ray Free Electrons Laser (XFEL) source to investigate the THz induced magnetization dynamics in a Permalloy (Py) film. The tunable THz undulator allows us to select the pulse duration and the wavelength. A filter is used to remove higher orders generated by the undulator and to obtain a single frequency THz pulse. The extreme ultraviolet (XUV) radiation delivered by the XFEL, a powerful tool for probing magnetic phenomena at the nanometer and femtosecond scales [
6,
7,
8,
9], is used to study the resonant magneto-optic response at the Ni
absorption edges (around
) [
10]. Unfortunately, we did not succeed to achieve any ultrafast coherent magnetization control by the THz pump with a fundamental frequency of 100 μm because the THz intensity was too low.
However, after the removal of the filter from the THz undulator beam path, an ultrafast demagnetization of the Py film can be evidenced. The pump radiation is now composed of the fundamental frequency but also higher harmonics, that span from THz to IR wavelength range, which are responsible for this non coherent dynamics. The dynamics is more complex than the usual demagnetization response and allowed us to reconstruct the shape of the fundamental THz electric field. This method will provide an in-situ and fast way to obtain a characterization of the THz pulse, which is fundamental for the interpretation of future coherent magnetization control experiments, in addition to more conventional characterization methods which can be difficult to implement during an experiment [
5,
11].
2. Materials and Methods
THz radiation is produced by the THz undulator of the BL3 beamline at FLASH, a purpose built planar electromagnetic undulator with 9 full periods of 40
[
12]. It can generate radiation in a very broad spectral range from the mid infrared to the far infrared spectral regions corresponding to wavelengths between 1 μm and 300 μm (respectively 300 THz and 1 THz). The pulse duration and intensity depends on the wavelength chosen: the THz pulse has about ten optical cycles (corresponding to a pulse duration of about
and 10 ps respectively) and the maximum pulse energy is 150
[
5].
The THz undulator is implemented in series, and can be operated simultaneously to the XUV undulator of FLASH for the realization of THz pump–XUV probe experiments (see
Figure 2). To do so, an electron bunch is accelerated in the tunnel, passes into the XUV undulator and generates an XUV pulse. The electrons bunch then passes through the THz undulator and generates a THz pulse. Those two pulses are separated by a holey mirror and then recombine onto the sample thanks to a series of mirrors. Since both THz and XUV pulses are emitted from the same electron bunch, they are inherently synchronized [
5,
12].
In more detail, the experimental setup consists of two vacuum chambers. The incoming XUV beam (red in
Figure 2) passes through the first chamber and is reflected back and focused by a spherical mirror in the second chamber (not shown in the
Figure 2). The tilts of this back mirror are motorized in order to be able to change the position of the beam on the sample. This allow us to find the spatial overlap of the probe beam with the THz beam. The reflected and focused XUV beam comes back to the main chamber, passes through a center aperture in the THz off-axis parabola (orange in the zoom of
Figure 2) and eventually arrives on the sample. In the meantime, the THz beam enters the main chamber perpendicularly to the XUV beam and is focused onto the sample by the off-axis parabola. The exact spots sizes on the sample could not be measure in-situ but the characteristics of the beams and the focusing mirrors should yield a focal spot diameter of lower than 100
for XUV and larger than 400
for THz ensuring a uniform excitation of the probed area.
To probe the magnetization dynamics, we used the time-resolved Transverse Magneto-Optical Kerr Effect (T-MOKE). The basic principles of this technique have been presented in many reports [
13,
14,
15]. The geometry is represented in
Figure 3. The incident angle on the sample is chosen to be close to 45° to maximize the T-MOKE signal. Two avalanche photodiodes (APD) measure the XUV beam incoming intensity,
, and the reflected signal,
, from the sample. An electromagnet is used to magnetize the sample in plane in two opposite directions,
and
, giving rise to two different signal intensities,
and
, measured as
for positive and negative magnetizations respectively.
The sample studied consisted of a 10 thin Py film sputtered on a silicon substrate with a 3 thin Ta buffer and capped with a 3 thin Al layer to prevent oxidation. To measure the magnetization dynamics of this sample, we tuned the XFEL to a photon energy of , in resonance with the absorption edges of Ni, and recorded and for delays between the THz pump and the XUV probe ranging from −5 ps to 15 ps.
3. Results
First, we tuned the THz undulator to obtain a fundamental wavelength of 100 μm. To suppress higher harmonics, we used a 50 μm long-pass filter. This should results in a pump pulse consisting of about 10 oscillations of a 3 THz electromagnetic field and a pulse duration of about 3.3 ps. The coupling between the magnetic field of this radiation and the magnetization of the sample should results in oscillations in the magnetic signal with a period of about 333
(the period of the THz radiation and hence of the associated magnetic field). From previous experiments [
3], a THz fluence of about 10 mJ cm
−1 should be sufficient to trigger this effect (1 mJ cm
−1 were enough for a single cycle 2.1 THz pulse).
Figure 4a shows the sample reflectivity as function of time delay for the two opposite magnetization direction of the sample. Because of T-MOKE, the reflectivity for
is almost 3 times higher than the reflectivity for
. However, there is no effect of the THz field on the magnetization of the sample. After investigating at different THz wavelengths we came to the conclusion that the magnetic field associated to the THz pump was too weak to induce a magnetic response. This was most probably due to a combination of two factors: the intensity in the fundamental was a little lower than expected and the focal spot was too large to compensate and obtain the right fluence.
To increase the pump pulse intensity, we removed the long-pass filter. This should increase the pulse intensity by a factor of at least 4 [
5]. By doing so, we were able to trigger a modification of the sample magnetization state with the THz pump (
Figure 4b). To analyze this magnetization dynamics in more detail, we have plotted the so-called asymmetry, defined as
, in
Figure 5 for two different THz fundamental wavelength, 45 and 100 μm. The curves appear very similar to the typical curves obtained by performing a demagnetization experiment with femtosecond IR pulses.
The magnetization dynamics is nonetheless very different to the typical ultrafast demagnetization in transition metals thin films [
16,
17]. First, as seen on
Figure 5, the demagnetization occurs on a much longer timescale of a few picoseconds. Moreover, the timescale of the dynamics depends on the fundamental wavelength of the THz pump. Finally, the demagnetization curves appear to be the results of several different demagnetization processes triggered successively. All together, these point out to the fact that our measurements are dominated by the shape of the THz pulse.
To characterize this pulse shape, we fitted our data with the following equation which is often used to describe ultrafast demagnetization [
7,
18]:
where
is the unpumped asymmetry,
and
are constants,
and
are the electrons-phonons and spins relaxation times,
the Heaviside function and
the temporal intensity profile of the pump beam. To simplify the analysis, we considered that the pump beam consisted of 10 cycles (given the number of period of the THz undulator) of a single THz frequency of either 3 or 6.7 THz (corresponding to pulse durations of about 3.3 ps and 1.5 ps respectively). This ignores the fact that the higher harmonics will distort the shape of the THz pulse [
11] but a more accurate description would not match the time resolution of our data.
The results of the fits are shown in
Figure 6. The most evident observation is that the intensity is not uniformly spread among cycles for both THz pump wavelengths. This was to be expected by observing the demagnetization curves on
Figure 5 which presented broken lines demagnetization slopes. Moreover, the most intense cycles are not situated at the same position within the pulse for 45 and 100 μm fundamental wavelengths: respectively in the middle and at the end of the THz pulse. This observations are in rough agreement with proper measurements of the THz pulse shape which showed that the exact shape of the THz pulse is highly dependent on the XFEL parameters and can drastically change upon variation of these parameters during an experiment [
5].
4. Discussion
Given the pump fluence of our experiment we were not able to trigger a detectable coherent magnetization dynamics with a single frequency THz radiation pump pulse. Adding higher harmonics to the pump pulse resulted in a clearly visible reduction of the sample’s magnetization occurring on the picosecond timescale. However, there is no signature of the magnetization to be directly affected by the magnetic field of the THz pump pulse, the observed dynamics appears to be driven by a pure demagnetization process. This observation indicates that the magnetic field strength has been too low at any given time to trigger a coherent response of the sample’s magnetization, while incoherent energy transfer through energy absorption accumulating over the successive cycles of the THz pump pulse induced the observed demagnetization dynamics. To be able to observe the THz induced coherent magnetization dynamics in a follow-up experiment, it is therefore necessary to increase the THz fluence, which can be achieved by improving the focusing of the THz beam.
Our results also showed that the THz pulse envelope emitted by the FLASH undulator source is highly non-uniformly structured. This indicates that an analysis of an experiment of coherent THz control of magnetization dynamics at this source will require a detailed characterization of the THz pulse shape. Such a diagnostic is not yet permanently accessible at the THz beamline of FLASH, but the results reported here provide due to the rather simple setup an attractive way to do so.