4ESRF, 6 rue Jules Horowitz, BP 220, F-38043 Grenoble Cedex, France
5Synchrotron SOLEIL, L′Orme des Merisiers, Saint-Aubin - BP 48, 91192 Gif-sur-Yvette, France
6Dipartimento di Scienze Fisiche, Informatiche e Matematiche, Università di Modena e Reggio Emilia, via Campi 213/A, I-41125 Modena, Italy
7Universite de Strasbourg, Institut de Physique et de Chimie des Materiaux de Strasbourg, CNRS UMP 7504, 23 Rue du Loess, 67034 Strasbourg Cedex 2, France
Guest Editors: H. D. Gleiter and T. Schimmel
Beilstein J. Nanotechnol. 2013, 4, 320–324. doi:10.3762/bjnano.4.36
Received 04 Mar 2013, Accepted 30 Apr 2013, Published 21 May 2013
The magnetic and electronic properties of single-molecule magnets are studied by X-ray absorption spectroscopy and X-ray magnetic circular dichroism. We study the magnetic coupling of ultrathin Co and Ni films that are epitaxially grown onto a Cu(100) substrate, to an in situ deposited submonolayer of TbPc2 molecules. Because of the element specificity of the X-ray absorption spectroscopy we are able to individually determine the field dependence of the magnetization of the Tb ions and the Ni or Co film. On both substrates the TbPc2 molecules couple antiferromagnetically to the ferromagnetic films, which is possibly due to a superexchange interaction via the phthalocyanine ligand that contacts the magnetic surface.
Keywords: magnetic anisotropy; magnetic coupling; single molecule magnets; X-ray absorption spectroscopy
Molecular spintronic devices as building blocks for future applications in information technology may be a big improvement and lead to higher efficiency [1-9]. Therefore several groups have studied the properties of potential organic molecules intensively over the past few years. Single-molecule magnets (SMMs) meet the requirements because of their magnetic remanence at low temperature without the need for long-range ordering. While most of the well-known SMMs consist of several interacting metal ions [10-13], bis(phthalocyaninato) terbium(III) (TbPc2) has only one rare-earth ion, coordinated by two organic phthalocyanine ligands consisting of nitrogen, carbon and hydrogen atoms (Figure 1a). The SMM properties arise simply from the single ion anisotropy of the Tb ion exhibiting a total angular momentum of J = 6 . The crucial point with regards to the applicability of magnetic molecules for industrial usage is the control of the magnetic properties. Mn- and Fe-porphyrin molecules were successfully coupled to ferromagnetic thin films, leading to the alignment of the magnetic moments of the metal ions parallel to the film [15-17] or antiparallel due to an interlayer of oxygen [18,19]. Recently, it was shown that TbPc2 molecules can be magnetically coupled to a ferromagnetic Ni substrate . The magnetic anisotropy and field dependence were also studied for TbPc2 in a submonolayer on Cu(100)  and on antiferromagnetic substrates . Spin quantum tunnelling at zero magnetic field leads to vanishing magnetization of the molecules, showing typical butterfly hysteresis [23-25]. Only at very low temperatures below 4 K is the relaxation slow enough for observation of magnetic remanence . Here we demonstrate that it is possible to block this relaxation and conserve the magnetization without any external field by coupling the molecules to a ferromagnetic substrate. By X-ray absorption spectroscopy and X-ray magnetic circular dichroism we study the electronic and magnetic properties of a submonolayer coverage of TbPc2 molecules on ultrathin Co and Ni films, focusing on the magnetic coupling between the substrate and the molecules.
Figure 2 shows spectra of circularly polarized (top) and linearly polarized X-rays (bottom) and the corresponding circular or linear dichroism at the Tb M4,5 absorption edges of TbPc2 on Cu(100). The XMCD signal has the shape typical for a Tb3+ ion, in agreement with what has been already reported for this molecule [20,21,24,25]. The high XMCD intensity at the M5 edge and the low intensity at the M4 edge indicate the large orbital moment of the Tb ion [27,28]. From the X-ray linear dichroism (XLD) at 45° X-ray incidence, one can deduce the orientation of the molecules. The typical shape at the M5 edge, with the sign changing from negative to positive, indicates that the molecules lie flat, with the phthalocyanine planes parallel to the surface, as expected for the submonolayer coverage .
The 15 ML thick Ni film has a well-defined easy magnetic axis perpendicular to the plane  and the TbPc2 molecule is known for its large magnetic anisotropy with the easy axis of magnetization perpendicular to the phthalocyanine plane . Thus, the easy axis of the molecules is parallel to the one of the underlying Ni film. From the field-dependent XMCD at both Tb M5 and Ni L3 absorption edges presented in Figure 3, the influence of the Ni film on the magnetization of the molecules is visible. While the magnetic moments of Tb align parallel to the external magnetic field when the field is strong enough, they align antiparallel in a small magnetic field. This antiparallel alignment is caused by the magnetic coupling to the Ni substrate. At the top of Figure 3 one is able to identify the coupling by the magnetization sign changes. The signal crosses zero three times, twice when the exchange field and the external field cancel out each other and once when the Ni magnetization crosses zero. In the image below the coupling is even more visible. In this very small region around zero, one can see the remanence of the Ni substrate. For the Tb signal there is remanence as well, but with the opposite sign. The magnetization direction for Ni and Tb switch exactly at the same external field of about ±0.01 T, demonstrating the interaction between the molecules and the Ni film. Please note that the connecting lines for the Ni data in the upper picture of Figure 3 do not represent the Ni hysteresis curve, because of the low density of magnetic field steps. A more precise representation of the Ni hysteresis and the corresponding coercive field can be seen in the lower figure. Since the identical system was investigated by Lodi Rizzini et al. , it is remarkable that we obtain a significant difference in the exchange field and the amplitude of the antiparallel signal at the Tb M5 edge, probably as a result of a weaker coupling. However, the main issue of the present manuscript is the demonstration of an antiferromagnetic coupling of rare-earth–Pc2 molecules to ferromagnetic substrates. The quantitative analysis of the antiferromagnetic coupling strength goes beyond the scope of this manuscript. This can be achieved by experimental investigation by means of a detailed temperature-dependent XMCD study together with comparison to ab initio calculations, e.g., by utilizing density functional theory (DFT).
The important difference between the Co and the Ni substrate is the orientation of the magnetic easy axis that is parallel to the surface for the 10 ML thick Co film . The magnetic coupling between the Co substrate and the molecule is therefore only between the out-of-plane component of the Co magnetization. The parallel component cannot polarize the molecules because of their large magnetic anisotropy . The top graph of Figure 4 shows the magnetic signal of Tb in an external field between −6 T and 6 T. The shape is dominated by a paramagnetic signal that one would expect for a free molecule at a temperature of T ≈ 10 K. But close to zero field the superposition of a second contribution becomes visible. In order to highlight the contribution, we subtracted the magnetization signal expected for the free molecule, which is simply a linear background at this temperature. The outcome is the lower graph of Figure 4. Compared to the Co magnetization curve (red line), one can see the antiparallel signal of the Tb magnetization. This antiferromagnetic contribution is very small compared to the dominating paramagnetic signal, because the Co magnetization direction is not in the direction of the molecular easy axis. If a very large coupling strength between the molecules and the Co substrate exceeds the magnetic anisotropy barrier, the magnetic moment of Tb could be forced in the plane. However, because of the large magnetic anisotropy barrier of the TbPc2 molecules of 73 meV [20,31], we expect the magnetic moment of the Tb ions not to be forced to the in-plane direction by the Co magnetization since the coupling energies presented in  are in the regime of 1 meV. Nevertheless, this needs to be demonstrated, e.g., by angle-dependent measurements. In addition, the calculated coupling strength compared to the anisotropy energy would answer this question. But as mentioned above, this goes beyond the scope of this manuscript. Another reason for a smaller antiferromagnetic coupling strength may be the higher temperature for the measurements on Co (T ≥ 10 K) than on Ni (8 K). This temperature difference may cause changes in the field dependence of the XMCD, because a significant temperature dependence of the magnetic coupling is expected .
We have shown that the magnetic moments of TbPc2 molecules can be ordered by coupling to a ferromagnetic substrate. At a temperature of 8 K it is possible to get a remanent magnetization, originating from an antiferromagnetic coupling to the Ni substrate. We observe an antiferromagnetic coupling also on the Co substrate, whose magnetic easy axis is in the plane and thus perpendicular to the one of the terbium(III) total angular momentum of J = 6. This antiferromagnetic contribution is much smaller than on the Ni film, partially due to the higher measuring temperature, but primarily because of the large magnetic anisotropy of the molecule. Therefore the magnetization curve is dominated by the paramagnetic signal.
The samples were prepared in situ at a base pressure of 10−10 mbar directly before the measurements. By cycles of Ar+ bombardment and annealing the Cu(100) surface was cleaned. Afterwards the ferromagnetic films were grown epitaxially via electron beam evaporation. The 10 ML thick Co film was produced with a rate of 0.5 ML/min and the 15 ML thick Ni film with a rate of 0.3 ML/min. The TbPc2 molecules were thermally evaporated at a temperature of about 400 °C from a Knudsen cell onto the substrate held at room temperature.
The XAS measurements of the system TbPc2/Co/Cu(100) were performed in magnetic fields up to 6 T at the DEIMOS beamline at the synchrotron SOLEIL, the XAS measurements of the system TbPc2/Ni/Cu(100) in a magnetic field up to 4 T at the ID08 beamline at the ESRF. The lowest possible temperature was reached by cooling with liquid helium (T = 4 K), while the real temperature at the sample was limited by the quality of the thermal contact, leading to temperatures above 4 K. In detail we were able to measure at T ≈ 8 K at the ESRF and T ≥ 10 K at SOLEIL, although the temperature at the sample holder was 4 K.
To determine the thermal stability of TbPc2, the sample was exposed to high-temperature sublimation under high vacuum in the sublimation apparatus consisting of a tube flask dipped into a heating mantle and a condenser. This method is carried out by heating 80 mg of the crude solid, while simultaneously evacuating the system. Upon reaching 400–420 °C at the bottom of the round flask and at a standard pressure in the system of about 2.8·10−2 mbar, the sublimate appears on the cooled condenser. After 40 min about half of the crude solid was collected on the condenser. Both the sublimate and the residual molecules in the tube flask were exposed to mass-spectrometric and spectroscopic analysis as was the rest of the sample from a Knudsen cell. MALDI-TOF and UV–vis spectra did not reveal any difference compared to the initial sample. The presence of a binuclear complex (Tb2Pc3) in the MALDI-TOF spectrum as an evidence of thermal degradation was detected only in the rest of the sample in the tube flask after exposure to more than 450 °C for not less than 30 min. This allows us to assert that sublimation at 400 °C leaves the molecules unaffected.
One part of the experiments was performed on the DEIMOS beamline at SOLEIL Synchrotron, France (proposal number 20120073). We are grateful to the SOLEIL staff for smoothly running the facility. We also acknowledge the European Synchrotron Radiation Facility for financial support (Project HE 3739) and we would like to thank the beamline staff for assistance in using beamline ID08. This work was partially supported also by the MIUR Project PRIN Contract No. 20105ZZTSE