Neutron Diffraction Investigation of the DyFe11Ti Magnetic Structure and Its Spin Reorientations

Olivier Isnard*, Eder J. Kinast

a University Grenoble Alpes, Institut Néel du CNRS, 25 rue des Martyrs, Grenoble 38042, France

b Universidade Estadual do Rio Grande do Sul, Porto Alegre, RS 90010-191, Brazil

Keywords:

A B S T R A C T In this article, we report on the magnetic structure of DyFe11Ti and its thermal evolution as probed by neutron powder diffraction. A thermodiffraction technique was used to follow the temperature dependence of the magnetic moments, as well as their orientation. The Dy and Fe moments were coupled to each other in an antiparallel manner to form a ferrimagnet, where the easy magnetization direction at 2 K was the [110] axis in the basal (a, b) plane. This magnetic structure underwent two successive spin reorientation phenomena with increasing temperature.A large Dy magnetic moment of 9.7 Bohr magneton (μB) was obtained at low temperatures, and the magnitude decreased rapidly to 7.5μB at 200 K. The largest Fe magnetic moment was observed on the Fe 8i position.A ThMn12-type crystal structure was preserved in the studied temperature range,despite the large changes of the magnetic structure.A sharp tilt was observed at the first-order spin reorientation, TSR1; the angle between the easy magnetization axis and the crystal c axis was reduced from 90° at 2 K to about 20° at 200 K (where c is the easy axis above 200 K); and the Dy and Fe magnetic moments maintained an antiparallel coupling.

1. Introduction

The investigation of iron (Fe)-rich intermetallic compounds containing rare-earth metals (R) has attracted considerable interest during the last three decades,due to the potential of these compounds to act as hard magnetic materials. These remarkable materials can potentially combine a high ordering temperature and high magnetization with significant magnetocrystalline anisotropy and coercivity. In addition to their potential for application,R-Fe intermetallic compounds offer researchers the opportunity to perform extensive fundamental studies of the magnetic behavior of itinerant 3d electrons and localized 4f electronic states. Several studies have investigated the unusual behavior of RFe12-xMxintermetallic compounds [1-3]. Firstly, no RFe12compound has been reported as a bulk sample; secondly, the use of a stabilizing element, M, is necessary in order to obtain the RFe12-xMxphase and observe a ThMn12structure type. When M = Ti, a relatively high Curie temperature can be obtained for these phases, and can be further improved by the insertion of a light element within the crystal lattice,such as hydrogen(H),carbon(C),or nitrogen(N)[4,5]. These materials are also of interest due to their relatively complex magnetic phase diagram when the R and Fe sub-lattices have different preferential anisotropy directions [1,2,4].

The ThMn12structure, which was originally determined by Florio et al. [6], is closely related to the CaCu5structure type by an ordered substitution of a rare-earth element by a pair of 3d transition metals following the relation 2RM5- R + 2M →RM12.Half of the R atoms are consequently replaced by M atoms at the 8i position. This substitution results in a change of crystal symmetry, and the tetragonal I4/mmm space group is retained. In addition to the 2a position occupied by the rare-earth element,transition metal atoms are observed on three inequivalent atomic positions:8i,8j,and 8f[1,7,8].The ThMn12structure is also related to the parent Th2Ni17structure. For a detailed description of the relationships between these structures, the reader is referred to the work of Hu et al. [8].

This article focuses on the magnetic structure of DyFe11Ti compounds and on its temperature dependence. This compound has attracted a great deal of research interest due to its original magnetic behavior and the presence of two spin reorientation transitions. At room temperature, DyFe11Ti exhibits a uniaxial alignment of the magnetic moments along the c axis, as has been derived from single-crystal studies and from M?ssbauer spectroscopy [9-12]. The low-temperature behavior is more complex,and has been the subject of several magnetic studies.Contradicting conclusions were drawn from the studies of different sets of single crystals[9-14],particularly in regards to the first-or second-order nature of the lowest temperature spin reorientation,TSR1.However,those researchers agreed that TSR2, the spin reorientation above 200 K, is of the second order.Nevertheless, no direct investigation of the magnetic structure by neutron diffraction has been reported to date.This is the purpose of the present study,which focuses on the low-temperature magnetic behavior around TSR1with the aim of shedding new light on the complex magnetic phase diagram of DyFe11Ti.

2. Material and methods

The sample preparation was performed by means of highfrequency induction melting in a purified argon (Ar) atmosphere,starting from the pure elements. To homogenize the obtained ingot, annealing was performed in an evacuated quartz ampoule for ten days at 950 °C. Sample purity was investigated using X-ray diffraction and thermomagnetic measurements. Neutron diffraction measurements were performed on D1B, a powder diffractometer operated by the French National Center for Scientific Research(CNRS) as a Collaborative Research Group at Institut Laue-Langevin (ILL), in Grenoble, France. A wavelength of 2.52 ? was selected by a pyrolytic graphite monochromator. We used a multicounter containing 400 cells, with a step of 0.2° between neighboring cells; the detector covered a 2θ angular range of 80°.The detector was set at an initial position of 2θ = 20°, since no Bragg reflection was observed at a lower angle.The diffractograms were taken at different temperatures ranging from 1.5 to 202 K.The crystal structure and magnetic parameters were refined using the Rietveld method implemented in the FullProf program [15].The definition of the agreement factors is given in the corresponding FullProf program manual.In order to minimize neutron absorption by the dysprosium (Dy) nucleus, we used a special annular sample holder.

3. Results and discussion

Rietveld refinement of the neutron data revealed the presence of elemental iron as a minority phase in the studied compound(its content was below 1%). Neutron diffraction also indicated the presence of traces of TiFe2as impurity. A plot of the refinement of the diffraction pattern recorded at 2 K for DyFe11Ti is given in Fig. 1. Thanks to the large contrast between the atomic neutron coherent scattering length of the titanium (Ti) and Fe nuclei, the Ti atom location and content could be precisely determined. As shown in Table 1, the Ti atoms were located exclusively on the 8i position of the ThMn12structure type, whereas the Fe atoms were found on the remaining transition metal positions 8i, 8j, and 8f.This preferential location on the 8i site is in line with earlier reported results on isotype RFe11Ti intermetallics [7], and is attributed to the larger volume of the 8i position. The refined Ti content was in excellent agreement with the initial DyFe11Ti stoichiometry, confirming the very low content of ‘‘Ti-containing impurity.”An analysis of the magnetic contribution to the neutron diffraction pattern indicated that the Dy and Fe magnetic moments were coupled anti-ferromagnetically and were lying within the basal (a, b) plane, forming a 90° angle with the c axis. Due to the contradicting results on the orientation of the magnetic moments[9,13],two directions were tested:[100]and[110].Rietveld refinement at 2 K gave a significantly better fit when the magnetic moments were along the[110]direction—a result that agrees with Refs. [13,14]; consequently, the easy magnetization axis is [110].At 2 K, the magnetic moment carried by the Dy atoms, 9.7 Bohr magneton(μB),was very close to the 10μBthat was expected from the trivalent state. The Fe magnetic moment was found to be aligned ferromagnetically and to have different values for the three inequivalent Fe atomic positions; the largest moment was observed on the Fe 8i site, whereas the smallest was found on the 8f site.The large magnetic moment observed on the 8i position is a general feature of the RFe12-xMxcompounds,and has been suggested to result from both the large atomic volume and the possible presence of a significant orbital contribution to the Fe magnetic moment [16]. Such a sequence of Fe magnetic moments—that is,8i > 8j > 8f—is in good agreement with the hyperfine field derived for the three Fe positions in RFe11Ti isotype compounds[17,18].No magnetic moment was refined on the Ti atoms. This does not exclude the possibility of a weak moment due to polarization by the surrounding Fe and Dy atoms on titanium. However, such a weak moment is likely to be below the sensitivity of the powder neutron diffraction used in this work.

Fig.1. Plot of the Rietveld refinement of the neutron diffraction pattern recorded at 2 K for DyFe11Ti. The red points are experimental data and the black curve corresponds to Rietveld fit. The first and second rows of green Bragg peaks refer to the nuclear and magnetic contribution,respectively.The third and fourth rows refer to the Bragg peak position of the traces(<1%)of alpha Fe and TiFe2,respectively,as impurities. A.u.: arbitrary units; Iobs: ovserved intensity; Icalc: calculated intensity.

In order to investigate the evolution of the magnetic structure of DyFe11Ti, diffraction patterns were recorded every 2.5 K during heating from 1.5 to 202 K. A zoom of the low-angle part(between 21° and 41° in 2θ) is plotted in Fig. 2, highlighting the main changes in diffraction intensities. This plot corresponds to the(110), (200), and (101) Bragg peaks, which were observed at 24°,34°, and 35°, respectively. Whereas the first two peaks showed an increase in intensity,the(101)presented the opposite behavior,with a rapidly decreasing intensity when approaching 100 K.Such behavior at low temperature is indicative of a spin reorientation of the magnetic moments, and motivated our further investigation.The presence of a magnetic contribution appearing at high temperature for the (110) and (200) peaks indicates the appearance of a magnetic moment component perpendicular to the scattering vector.Each of the 86 neutron diffraction patterns were refined in order to obtain the temperature dependence of the magnetic structure.The easy magnetization axis was[110]below TSR1.Up to about 89 K, the best fit was obtained by keeping a 90° angle between the Dy and Fe magnetic moments on the one hand, and the c axis on the other hand.Such easy plane orientation is in good agreement with the earlier reported57Fe M?ssbauer spectroscopy results[12,17].Above 91 K and up to 202 K,the diffraction patternswere fitted by refining the angle between the c axis and the magnetization direction. This gave significantly better refinement results.An example of the refinement is plotted for the 200 K pattern in Fig. 3. It is worth noting that the Dy magnetic moment experienced a large reduction of more than 2μBfrom 2 to 200 K.This finding confirms the strong temperature dependence of the 4f electron magnetic moments. The Fe magnetic moments are much less sensitive to temperature changes, and were reduced by only 0.2μBper Fe atom in this temperature range. This result can be attributed to the rather high ordering temperature of DyFe11Ti—that is, 552 K [12]—which led to a saturated state of Fe moments below 200 K.

Table 1 Crystal structure parameters as deduced from Rietveld refinement of the neutron powder diffraction data recorded for DyFe11Ti at 2 K.

Fig. 2. Temperature dependence of a low-angle portion of the neutron powder diffraction pattern recorded between 1.5 and 200 K for DyFe11Ti. The observed evolution reflects the occurrence of a spin reorientation transition upon temperature change.

Fig.3. Plot of the Rietveld refinement of the neutron diffraction pattern recorded at 200 K for DyFe11Ti. The red points are experimental data and the black curve corresponds to Rietveld fit. The first and second rows of Bragg peaks refer to the nuclear and magnetic contribution,respectively.The third and fourth rows refer to the Bragg peak position of the traces (< 1%) of alpha Fe and TiFe2, respectively, as impurities. The last row is the contribution of the vanadium tail of the cryostat.

The results of the Rietveld analysis of the thermodiffraction data are given in Figs. 4-6. Table 2 presents the structural and magnetic data obtained from Rietveld refinement of the pattern recorded for DyFe11Ti at 200 K.As derived from neutron diffraction,the thermal evolution of the angle between the easy magnetization direction and the c axis indicated that DyFe11Ti exhibits an easy plane anisotropy below 90 K, whereas an easy axis has been reported at 240 and 300 K from57Fe M?ssbauer spectroscopy[12]. As shown in Fig. 4, the first spin reorientation occurring at TSR1= 90 K is sharp and manifests itself by a sudden drop of the angle from 90°to 72°for 89 and 93 K,respectively.This angle then decreases much more slowly above 105 K. A smooth decrease is observed from 50° to 30°, followed by a slightly more pronounced decrease when approaching the second spin reorientation, TSR2,whose value is above 200 K.

In his theoretical study,Kuz’min[13]demonstrated that spatial inhomogeneities of the sample composition (e.g., Ti content) play an important role in the magnetic behavior and gradual character of the first-order spin reorientation in DyFe11Ti. The present neutron diffraction investigation performed on a sample with defined stoichiometry provides a clear picture of the magnetic phase diagram and the spin reorientation phenomenon observed on DyFe11Ti. The temperature dependence of the angle of rotation of the magnetization, as derived from neutron diffraction, is similar to that reported in Ref.[19].Indeed,a rapid tilt of the easy magnetization direction to the plane can be observed for T

Fig.4. Thermal evolution of the tilt angle between the easy magnetization direction and the c crystal axis as derived from the Rietveld refinement of the neutron powder diffraction patterns recorded for DyFe11Ti. The circles refer to the M?ssbauer data on the same sample [12], and the dotted line is a visual guide.

Fig. 5. Temperature dependence of the lattice parameters of DyFe11Ti in the temperature range of the two spin reorientation transitions.

Fig. 6. Thermal evolution of the atomic magnetic moments, as derived from the Rietveld refinement of the neutron powder diffraction patterns recorded for DyFe11Ti. MDy: magnetic moment of Dy; MFe: magnetic moment of Fe.

Table 2 Crystal structure parameters deduced from Rietveld refinement of the neutron powder diffraction data recorded for DyFe11Ti at 200 K.

It is interesting to note that no anomaly occurred in the temperature dependence of the lattice parameters at either TSR1or TSR2.On the contrary, the two lattice parameters exhibited a normal behavior, being almost constant up to 50 K and then increasing as a result of thermal expansion, with a rate of 2.3 × 10-5and 3.1 × 10-5?·K-1for c and a, respectively (Fig. 5). The absence of any features on the lattice parameters may be surprising, but is in agreement with the normal thermal expansion reported earlier for DyFe11Ti[20].In contrast,the magnetostriction has been found to be very sensitive to temperature changes in the vicinity of the spin reorientation phase transitions in single-crystal DyFe11Ti[21]. The magnitude of the atomic magnetic moments (Fig. 6)decreased upon increasing temperature, but did not seem to be influenced by the occurrence of spin reorientation at TSR1. A very small evolution of the Fe magnetic moment was observed in the studied temperature range, which is in good agreement with the relatively large ordering temperature of DyFe11Ti. The dysprosium magnetic moment was much more sensitive to temperature change and presented a quasi-linear dependence above 50 K,with a reduction rate of 0.0145μB·K-1.

4. Conclusions

Thanks to neutron diffraction analysis,the Ti content of DyFe11-Ti was determined and the crystal structure was investigated. Ti atoms were found to be exclusively located on the 8i position.The magnetic structure of DyFe11Ti exhibits a basal plane anisotropy at 2 K with an alignment of the Dy and Fe magnetic moments within the basal plane; the easy magnetization axis is along the[110] direction. The lowest temperature spin reorientation manifests itself at 90 K by an abrupt decrease of the angle between the easy magnetization direction and the [001] direction. At this TSR1, our experimental results favor the first-order spin reorientation transition scenario.A conical magnetic structure was observed in a wide temperature range above the basal plane anisotropy domain. Upon increasing the temperature further, the magnetic moments tilted toward the c axis,thus leading to the uniaxial character reported in the literature at 300 K.This transition from a conical magnetic structure to the easy plane occurred close to 200 K.A large temperature dependence of the Dy magnetic moment was observed, in contrast to the Fe moments, which remained almost identical in the studied temperature domain. A study of the thermal evolution of the lattice parameters did not present any anomalous behavior at the spin reorientation—a result that agrees with the earlier reported thermal expansion.Further studies are in progress to investigate the magnetic behavior of isotype RFe11Ti hydrides, and of DyFe11TiH in particular.

Acknowledgements

The use of the Collaborative Research Group instrument D1B operated by the CNRS at the ILL is warmly acknowledged, as well as the ILL for providing the neutron beam.

Compliance with ethics guidelines

Olivier Isnard and Eder J. Kinast declare that they have no conflict of interest or financial conflicts to disclose.