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Melilite-type multiferroic oxides such as Ba&lt;sub&gt;2&lt;/sub&gt;MGe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;7&lt;/sub&gt; (M = Cu, Mn, Co) are the potential candidates for studying exotic quantum phenomena including low-energy magnetic, electronic and structural properties along with the magnetoelectric effect. Spontaneous electric polarization in Ba&lt;sub&gt;2&lt;/sub&gt;MnGe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;7&lt;/sub&gt;&lt;sub&gt; &lt;/sub&gt;arises due to the spin-dependent &lt;i&gt;d-p&lt;/i&gt; hybridization mechanism between the transition metal &lt;i&gt;3d&lt;/i&gt; and ligand &lt;i&gt;p&lt;/i&gt; orbitals like its sister compounds Ba&lt;sub&gt;2&lt;/sub&gt;CoGe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;7 &lt;/sub&gt;and Ba&lt;sub&gt;2&lt;/sub&gt;CuGe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;7&lt;/sub&gt; [1-3]&lt;sub&gt;. &lt;/sub&gt;While all the three compounds exhibit similar non-centrosymmetric tetragonal nuclear structure with space group P-42&lt;sub&gt;1&lt;/sub&gt;m (n.113) below the corresponding Néel temperatures (&lt;i&gt;T&lt;sub&gt;N&lt;/sub&gt;&lt;/i&gt;), they differ from each other mainly by their local spin microstructure [1, 4-6]. But there is no single report on any structural phase transition if exists in these materials from high-T to below &lt;i&gt;T&lt;sub&gt;N&lt;/sub&gt;&lt;/i&gt;. This is crucial to investigate in detail the structural evolution with temperature as the spin-dependent &lt;i&gt;d-p&lt;/i&gt; hybridization mechanism involving the coupling between transition metal ions and ligand oxygen atoms strongly depends on the corresponding bond-length inside the MO&lt;sub&gt;4&lt;/sub&gt; terahedron.&lt;br/&gt;&lt;br/&gt;Here we report a systematic structural study of the magnetoelectric Ba&lt;sub&gt;2&lt;/sub&gt;MnGe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;7&lt;/sub&gt; under varying temperature from RT to 673 K and cooling from 673 K to 110 K using single crystal synchrotron radiation diffraction at BM01, ESRF. Within this entire temperature range the structure was described in the same crystallographic space group P-42&lt;sub&gt;1&lt;/sub&gt;m with slight change in lattice parameters. From the reconstructed 2D reciprocal map obtained at the all temperatures we have observed no appearance of extra reflection or any extra symmetry extinction compared to RT phase (sg:P-42&lt;sub&gt;1&lt;/sub&gt;m), therefore no phase transition has been detected from 673 K down to 110 K. Interestingly, the forbidden reflections, which arise from multiple diffraction so called “Renninger effect” [7], observed at all temperatures. However, the structural parameters e.g. bond-lengths in the MnO4 tetrahedron, anisotropic displacement parameters (ADP) and lattice constant changes with temperature continuously.&lt;br/&gt;&lt;br/&gt;We have refined the structures in the space group P-42&lt;sub&gt;1&lt;/sub&gt;m using JANA2006 [8] and the results are presented in the Fig. 1. Lattice parameters were refined before the data reduction using CrysAlisPro [9] which give nice agreements with the reported values e.g. &lt;i&gt;a&lt;/i&gt; = &lt;i&gt;b&lt;/i&gt; = 8.4847(3) Å and &lt;i&gt;c&lt;/i&gt; = 5.5162(4) Å at RT. ADP ellipsoids of oxygen atoms at 673 K are enlarged due to high temperature effects while after cooling back to RT resemble well the starting value before heating. While cooling at 110 K, ADP ellipsoids of O3 atoms are flattened in one directions. Local arrangements of MnO&lt;sub&gt;4&lt;/sub&gt; tetrahedron and the electron density distributions are slightly different for those different temperatures. This feature could have a direct consequences to the observed dielectric relaxation (dipole relaxation) in Ba&lt;sub&gt;2&lt;/sub&gt;MnGe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;7&lt;/sub&gt; around 150 – 210 K [10], which was suggested to be results of changeable valence state of Mn transition metal ions though be observed in ceramic material. Changeable valence state of Mn atoms in Ba&lt;sub&gt;2&lt;/sub&gt;MnGe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;7&lt;/sub&gt; is more likely not the case, rather high-spin (S = 5/2) or low-spin (S =1/2) magnetic ground state is possible in the &lt;i&gt;d-p&lt;/i&gt; hybridization process [6]. Figure 2 shows the reconstructed (0KL) planes obtained at RT (starting phase), 673 K and 110 K. It is immediately noticeable that all the allowed structural Bragg reflections did not change with temperature except the intensity. In this space group forbidden reflections are found at (h00) and (0k0) = &lt;i&gt;2n+1&lt;/i&gt; which are marked as yellow circle. The evolution of the intensity of the main Bragg peak shown in fig. 2(d) is completely reversible while cooling from 673 K, whereas the change in intensity of the forbidden reflections are quite dramatic only during heating.&lt;br/&gt;&lt;br/&gt;In summary, our first systematic temperature dependent structural study on Ba&lt;sub&gt;2&lt;/sub&gt;MnGe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;7 &lt;/sub&gt;single crystal using synchrotron radiation diffraction indicates that no structural phase transition take place in the large temperature range from 673 to 110 K. The observed forbidden peaks of weak intensity are of purely parasitic nature (Renninger scattering). Their intensity ratio to the main Bragg peaks in the range of RT to 110 K are well consistent with our previous neutron diffraction study at 10 K and RT only. Detailed investigation of the structural parameters, especially the flattened electron density of O3 atoms in the MnO&lt;sub&gt;4&lt;/sub&gt; tetrahedral at 110 K, could relate the reported dielectric properties at low temperature region [10]. This study may sheds lights on the structural dependent &lt;i&gt;d-p&lt;/i&gt; hybridization mechanism when a finite electric polarization exist under the external magnetic field [1] far above the antiferromagnetic ordering temperature (&lt;i&gt;T&lt;sub&gt;N&lt;/sub&gt; &lt;/i&gt;~ 4 K). In our opinion this is the advanced and novel study in these Melilite multiferroic oxides where the knowledge of such structural information are crucial in the field of magnetoelectric coupling based device applications and important to have beforehand for studying magnetic structure, strongly correlated electronic properties and the temperature dependent crystal-electric-field (CEF) excitations.

**References:**

[1] H. Murakawa et al., Phys. Rev. B 85, 174106 (2012). [2] S. Miyahara et al., Journal of the Physical Society of Japan 80, 073708 (2011). [3] H. Murakawa et al., Phys. Rev. Lett. 105, 137202 (2010). [4] A. Zheludev et al., Phys. Rev. B 54, 15163 (1996). [5] A. Zheludev et al., Phys. Rev. B 68, 024428 (2003). [6] T. Masuda et al., Phys. Rev. B 81, 100402(R) (2010). [7] A. Sazonov et al., Inorg. Chem., 57, 5089−5095 (2018). [8] V. Petricek et al., Z. Kristallogr. 229 (5), 345-352 (2014). [9] CrysAlisPRO v.46, (2018), Oxford Diffraction /Agilent Technologies, England. [10] J. Su et al., (ISAF/ECAPD/PFM), 2012, vol. 1–3, pp. 9–13, doi: http://dx.doi.org/10.1109/ISAF.2012.6297818.

**Images:**

![](https://assets.underline.io/uploads/markdown_image/1/image/8c80799df7cf5583e2f5a3be8c8d1ca8.jpg)
Figure 1: (a) Chemical unit cell of Ba&lt;sub&gt;2&lt;/sub&gt;MnGe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;7&lt;/sub&gt; structure at RT. (b-d) Refined ADPs of all atoms in the unit cell at RT, 673 and 110 K where “R” denotes the refinement R-factor.

![](https://assets.underline.io/uploads/markdown_image/1/image/71503811fdc31e6e8aade34c26cdb309.png)
Figure 2: (a-c) reconstructed (0KL) reciprocal maps. (d) Intensity vs. temperature plot for main Bragg reflection (060) and forbidden reflection (050).

INTERMAG 2021

 In-situ single crystal synchrotron X-ray diffraction study on the structure of multiferroic antiferromagnet Ba2MnGe2O7 from low- to high-temperature

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This Conference provides an outstanding opportunity for worldwide participants to meet their colleagues and collaborators and discuss developments in all areas of magnetism research.

Melilite-type multiferroic oxides such as Ba2MGe2O7 (M = Cu, Mn, Co) are the potential candidates for studying exotic quantum phenomena including low-energy magnetic, electronic and structural properties along with the magnetoelectric effect. Spontaneous electric polarization in Ba2MnGe2O7 arises due to the spin-dependent d-p hybridization mechanism between the transition metal 3d and ligand p orbitals like its sister compounds Ba2CoGe2O7 and Ba2CuGe2O7 [1-3]. While all the three compounds exhibit similar non-centrosymmetric tetragonal nuclear structure with space group P-421m (n.113) below the corresponding Néel temperatures (TN), they differ from each other mainly by their local spin microstructure [1, 4-6]. But there is no single report on any structural phase transition if exists in these materials from high-T to below TN. This is crucial to investigate in detail the structural evolution with temperature as the spin-dependent d-p hybridization mechanism involving the coupling between transition metal ions and ligand oxygen atoms strongly depends on the corresponding bond-length inside the MO4 terahedron. Here we report a systematic structural study of the magnetoelectric Ba2MnGe2O7 under varying temperature from RT to 673 K and cooling from 673 K to 110 K using single crystal synchrotron radiation diffraction at BM01, ESRF. Within this entire temperature range the structure was described in the same crystallographic space group P-421m with slight change in lattice parameters. From the reconstructed 2D reciprocal map obtained at the all temperatures we have observed no appearance of extra reflection or any extra symmetry extinction compared to RT phase (sg:P-421m), therefore no phase transition has been detected from 673 K down to 110 K. Interestingly, the forbidden reflections, which arise from multiple diffraction so called “Renninger effect” [7], observed at all temperatures. However, the structural parameters e.g. bond-lengths in the MnO4 tetrahedron, anisotropic displacement parameters (ADP) and lattice constant changes with temperature continuously. We have refined the structures in the space group P-421m using JANA2006 [8] and the results are presented in the Fig. 1. Lattice parameters were refined before the data reduction using CrysAlisPro [9] which give nice agreements with the reported values e.g. a = b = 8.4847(3) Å and c = 5.5162(4) Å at RT. ADP ellipsoids of oxygen atoms at 673 K are enlarged due to high temperature effects while after cooling back to RT resemble well the starting value before heating. While cooling at 110 K, ADP ellipsoids of O3 atoms are flattened in one directions. Local arrangements of MnO4 tetrahedron and the electron density distributions are slightly different for those different temperatures. This feature could have a direct consequences to the observed dielectric relaxation (dipole relaxation) in Ba2MnGe2O7 around 150 – 210 K [10], which was suggested to be results of changeable valence state of Mn transition metal ions though be observed in ceramic material. Changeable valence state of Mn atoms in Ba2MnGe2O7 is more likely not the case, rather high-spin (S = 5/2) or low-spin (S =1/2) magnetic ground state is possible in the d-p hybridization process [6]. Figure 2 shows the reconstructed (0KL) planes obtained at RT (starting phase), 673 K and 110 K. It is immediately noticeable that all the allowed structural Bragg reflections did not change with temperature except the intensity. In this space group forbidden reflections are found at (h00) and (0k0) = 2n+1 which are marked as yellow circle. The evolution of the intensity of the main Bragg peak shown in fig. 2(d) is completely reversible while cooling from 673 K, whereas the change in intensity of the forbidden reflections are quite dramatic only during heating. In summary, our first systematic temperature dependent structural study on Ba2MnGe2O7 single crystal using synchrotron radiation diffraction indicates that no structural phase transition take place in the large temperature range from 673 to 110 K. The observed forbidden peaks of weak intensity are of purely parasitic nature (Renninger scattering). Their intensity ratio to the main Bragg peaks in the range of RT to 110 K are well consistent with our previous neutron diffraction study at 10 K and RT only. Detailed investigation of the structural parameters, especially the flattened electron density of O3 atoms in the MnO4 tetrahedral at 110 K, could relate the reported dielectric properties at low temperature region [10]. This study may sheds lights on the structural dependent d-p hybridization mechanism when a finite electric polarization exist under the external magnetic field [1] far above the antiferromagnetic ordering temperature (TN ~ 4 K). In our opinion this is the advanced and novel study in these Melilite multiferroic oxides where the knowledge of such structural information are crucial in the field of magnetoelectric coupling based device applications and important to have beforehand for studying magnetic structure, strongly correlated electronic properties and the temperature dependent crystal-electric-field (CEF) excitations.

**References:**

[1] H. Murakawa et al., Phys. Rev. B 85, 174106 (2012). [2] S. Miyahara et al., Journal of the Physical Society of Japan 80, 073708 (2011). [3] H. Murakawa et al., Phys. Rev. Lett. 105, 137202 (2010). [4] A. Zheludev et al., Phys. Rev. B 54, 15163 (1996). [5] A. Zheludev et al., Phys. Rev. B 68, 024428 (2003). [6] T. Masuda et al., Phys. Rev. B 81, 100402(R) (2010). [7] A. Sazonov et al., Inorg. Chem., 57, 5089−5095 (2018). [8] V. Petricek et al., Z. Kristallogr. 229 (5), 345-352 (2014). [9] CrysAlisPRO v.46, (2018), Oxford Diffraction /Agilent Technologies, England. [10] J. Su et al., (ISAF/ECAPD/PFM), 2012, vol. 1–3, pp. 9–13, doi: http://dx.doi.org/10.1109/ISAF.2012.6297818.

**Images:**

![](https://assets.underline.io/uploads/markdown_image/1/image/8c80799df7cf5583e2f5a3be8c8d1ca8.jpg)
Figure 1: (a) Chemical unit cell of Ba2MnGe2O7 structure at RT. (b-d) Refined ADPs of all atoms in the unit cell at RT, 673 and 110 K where “R” denotes the refinement R-factor.

![](https://assets.underline.io/uploads/markdown_image/1/image/71503811fdc31e6e8aade34c26cdb309.png)
Figure 2: (a-c) reconstructed (0KL) reciprocal maps. (d) Intensity vs. temperature plot for main Bragg reflection (060) and forbidden reflection (050).

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The control of magnetization by electric current plays an important role in the applications of magnetic recording, nonvolatile memories, etc. As a key way to realize the manipulation of magnetization efficiently, the application of spin transfer torque (STT) and spin-orbit torques (SOT) requires materials with high spin polarization in electron transport.1-3 Besides, magnetic materials with low magnetization could reduce the critical switching current effectively due to the switching current is proportional to the saturation magnetization.4 Antiperovskite type Mn4N films have attracted a lot of attention due to the perpendicular magnetic anisotropy (PMA) and low saturation magnetization.5,6 However, the details about electronic transport properties in Mn4N films are not yet clear. Thus, the electronic transport properties of the Mn4N films with different thicknesses on MgO substrates have been investigated systematically. Fig. 1(a) presents the ρxx(T)/ρxx(300 K) of Mn4N films with different thicknesses on MgO(001) substrates. It is obvious that the resistivity continuously increases as the temperature increases in most films, showing a metallic conductance mechanism for the Mn4N films. However, there is an abnormal trend in the 4.7-nm-thick Mn4N films whose resistivity decreases as the temperature increases. In order to evaluate the purity and integrity of the Mn4N films, the residual resistivity ρxx0 at 0 K originated from impurity scattering is extracted from the ρxx-T curves.7 Fig. 1(b) shows the ρxx-T and fitting curve of the 78.8-nm-thick Mn4N film. The ρxx0 is obtained by fitting the ρxx-T at low temperatures using the expression as ρxx(T) = ρxx0+αTβ, where ρxx0 and T are the residual resistivity and temperature, and the coefficient α and β will change with the scattering model. The calculated ρxx0 of the 78.8-nm-thick Mn4N film is 30.56 μΩ cm, which is slightly less than ρxx(2 K) = 30.95 μΩ cm. The calculated β is 2.014 below 85 K, which is closely proportional to 2 for the ferromagnets. And the ρxx0 of other thicknesses were obtained by fitting the ρxx-T curves with the thickness from 7.8 to 47.3 nm in the same way. The thickness-dependent ρxx0(t) curve is shown in the inset of Fig. 1(b). It is obvious that the ρxx0 increases with the decrease of the film thickness, which imply the enhancement of the electron-electron interaction effects and interfacial scattering.8 Anomalous Hall effect of the Mn4N films were measured in the temperature range of 5-300K and in magnetic fields to 7 T. The Hall bars were used for measuring the Hall resistivity ρxy of Mn4N films with the thickness of 4.7-78.8 nm. The AHE is analyzed by the expression as ρxy=ρOH+ρAH=R0H+RsM, where R0 and Rs are ordinary and anomalous Hall coefficients, respectively. Fig. 2(a)-(h) shows the hysteretic property of the Hall resistivity ρxy for the different thickness as a function of applied magnetic field H at the temperatures of 5-300 K. The hysteretic property of ρxy due to the AHE caused by quantum mechanical spin-orbit interaction, and the linear property at the high-field regions due to the ordinary Hall effect (OHE) originated from the Lorentz force.9 The definition of MR is [ρxx(H)-ρxx(0)]/ρxx(0)×100%, where ρxx(0) is the resistivity of the film at 0 T. MR of the Mn4N film displays a negative signal and butterfly shape. The films with the thickness of 47.3 nm and 23.6 nm show a sudden lift as the magnetic field increases from 0 to 0.5 T, and the sign of MR is positive. Then, MR gradually decreases and sign turns negative with the increasing magnetic field above 0.5 T. The MR of 11.0 nm and 7.8 nm thick films shows the same trend except for the turning point at about 1 T. The upturn of MR in the low fields is mainly due to the Lorentz force effect, which causes a decline of mean free paths and a rise of the scattering rates.10 And the downturn of MR at high fields could be attributed to the enhancement of ferrimagnetic order and the reduction of electron scattering by spin-wave excitations and local magnetic anisotropy.11 At a certain temperature, MR of the Mn4N films increases with the increase of film thickness. These results provide experimental basis for application of SOT devices. This work is supported by National Natural Science Foundation of China (51871161 and 52071233).

**References:**

[1] S. Picozzi, A. Continenza, and A. J. Freeman, Phys. Rev. B 66, 094421 (2002). [2] Y. Takahashi, A. Srinivasan, B. Varaprasad, et al, Appl. Phys. Lett. 98, 152501 (2011). [3] A. Schmehl, V. Vaithyanathan, A. Herrnberger, S. Thiel, et al, Nature Mater. 6, 882-887 (2007). [4] K. Yamada, K. Oomaru, S. Nakamura, et al, Appl. Phys. Lett. 106, 042402 (2015). [5] Y. Yasutomi, K. Ito, T. Sanai, K. Toko, et al, J. Appl. Phys. 115, 17A935 (2014). [6] K. Ito, Y. Yasutomi, K. Kabara, et al, AIP Adv. 6, 056201 (2016). [7] G. Su, Y. Li, D. Hou, et al, Phys. Rev. B 90, 214410 (2014). [8] A. Cottey, Thin Solid Films 1, 297-307 (1968). [9] S. Onoda, N. Sugimoto, and N. Nagaosa, Phys. Rev. B 77, 165103 (2008). [10] X. Feng, W. Mi, and H. Bai, J. Appl. Phys. 110, 053911 (2011). [11] B. Raquet, M. Viret, E. Sondergard, O. Cespedes, and R. Mamy, Phys. Rev. B 66, 024433 (2002).

**Images:**

![](https://assets.underline.io/uploads/markdown_image/1/image/33b2abbb653ccc1887899b2f70a1a699.jpg)
Figure 1. (a) Temperature-dependent ρxx(T)/ρxx(300 K) of Mn4N films with different thicknesses on MgO substrates. (b) The longitudinal resistivity ρxx(T) of the 78.8-nm-thick Mn4N film and the fitting curve obtained below 85 K (blue line). The inset shows the thickness-dependent ρxx0

![](https://assets.underline.io/uploads/markdown_image/1/image/10105250aa2ccde783d9f5ac35cb2723.jpg)
Figure 2. Magnetic field-dependent Hall resistivity ρxy(H) of the (a) 78.8 nm, (b) 47.3 nm, (c) 31.5 nm, (d) 23.6 nm, (e) 15.8 nm, (f) 11.0 nm, (g) 7.8 nm and (h) 4.7 nm thick Mn4N films at different temperatures

 Electronic transport properties of antiperovskite Mn4N epitaxial films

I. INTRODUCTION Thermoelectric generators (TEG) that convert waste heat to electricity is regarded as alternative and environment-friendly technology for harvesting and recovering heat [1]. Although the conventional thermoelectric devices based on the Seebeck effect (SE) are promising, SE-based TEGs suffer from the high fabrication cost due to their complex structure and the usage of toxic, rare, and expensive elements. Furthermore, the one-dimensional relationship between the heat and carrier transports defined in SE makes it very challenging to achieve a high energy conversion efficiency and be only limited to a flat heat source surface [1, 2]. Recently its counterpart, the anomalous Nernst effect (ANE) in ferromagnetic materials, has gained increasing interests with its potential merits to further improve the figure-of-merit, ZT, simplify a thermopile structure with low-cost materials, and be applicable for a non-flat surface [2, 3]. However, to date, the reported thermoelectric conversion efficiency of the ANE is too small compared with the SE, which hampers its application as TEG. Thus, it is quite meaningful to explore valid approaches to achieve larger ANE output. In this study, we focus on the multilayer structure with full Heusler alloy Co2MnGa which is a famous ferromagnet exhibiting the large ANE thanks to its characteristic electronic band structure [3, 4]. In addition to the ANE originating from the bulk property of Co2MnGa, we expect the enhancement of ANE in the multilayer structures as reported previously [5, 6]. Here, polycrystalline Co2MnGa/AlN multilayer films were prepared on the amorphous substrates, the layer thickness dependence of ANE was investigated. We found that the large anomalous Nernst thermopower (SANE) of 4.9 ± 0.4 µV K-1 can be obtained even for the polycrystalline Co2MnGa. II. EXPERIMENTAL METHOD The film stacking structure is Si/SiO2/AlN(20)/[Co2MnGa(t)/AlN(5)]25/t (t = 2.5, 5.0, 12.5, and 25.0, thickness in nm), which was fabricated by DC magnetron sputtering at room temperature. Then all the films were post-annealed at 500 oC for 3 hours. For the ANE measurement, the thin films were first patterned into Hall-cross shapes through the use of photolithography and Ar ion milling. After milling, the on-chip thermometers made of the 100-nm-thick sputtered Pt were prepared by the lift-off process. The in-plane temperature gradient was generated by an on-chip heater, and the temperature on the cold and hot sides of the sample was monitored by two Pt on-chip thermometers. An external magnetic field (± 2 T) was applied perpendicular to the sample plane. III. RESULT AND DISCUSSION The structural characterization was carried out using the x-ray diffraction. For all samples, the Co2MnGa layers showed the (110)-oriented textures on the SiO2 substrate. The 25-nm-thick Co2MnGa film (single layer) exhibited the weak Co2MnGa 220 peak. On the other hand, [Co2MnGa (12.5)/AlN (5)]2 multilayer film (multilayer) with the Co2MnGa layers sandwiched by dielectric AlN layers shows a much stronger (110) texture. Moreover, the satellite peaks were observed around 2θ = 44.6° of the multilayer sample, indicating shape and abrupt Co2MnGa/AlN interfaces. Furthermore, the largest SANE of 4.9 ± 0.1 µV K-1 was achieved for the multilayer film while the value of SANE was 3.8 ± 0.4 µV K-1 for the single layer film. Although the present SANE of 4.9 ± 0.1 µV K-1 is smaller than the record-high value of SANE which is ~ 8.0 μV K−1 for single crystal Co2MnGa bulk [7], it is still promising one order of magnitude larger than those for other ferromagnets with similar magnetizations [8]. The results indicate that the large ANE output can be obtained even for the polycrystalline Co2MnGa which quite meaningful for practical application. This fact also implies that multilayers and/or superlattices with low dimension and sharp interfaces are promising platform/candidates to achieve large ANE. The present results provide new insight into the correlation between microstructure and ANE. We consider that the size and interface effect are the primary origins for the enhancement of ANE in the proposed Co2MnGa/AlN multilayer films. There are three possible scenarios for explaining the enhancement of ANE in the multilayer samples. First, the distinct thermal expansion coefficient, elastic modulus, and lattice mismatch between metals (Here Co2MnGa) and ceramics (here AlN) would introduce tremendous interface stress during the annealing, i.e. heating and cooling processes. The interface stress in the Co2MnGa layer may be a driving force to promote the chemical ordering of Co2MnGa. Second, the lattice distortion in Co2MnGa due to the interface stress will modify its electronic band structures. Third, the composition variation in the Co2MnGa layers may occur via the interdiffusion through the interface. The detailed structural analyses will be addressed in the presentation. This work successfully demonstrated a way to achieve giant ANE thermopower for the polycrystalline Co2MnGa layer on the amorphous substrate by exploiting the dielectric AlN layers. This is an important finding for practical applications. This work was supported by KAKENHI (18H05246) and CSRN.

**References:**

[1] S. Twaha, et al., Renew Sustain Energy Rev, 65, 698 (2016) [2] Y. Sakuraba, Scr. Mater. 111, 29 (2016) [3] A. Sakai, et al., Nat Phys. 14, 1119 (2018) [4] K. Sumida et al., Commun Mater 1, 89 (2020) [5] K. Uchida et al., Phys. Rev. B 92, 094414 (2015) [6] C. Fang et al., Phys. Rev. B 93, 054420 (2016) [7] Xu, L. et al., Phys. Rev. B 101, 180404 (R) (2020) [8] S. N. Guin et al., NPG Asia Mater. 11, 16 (2019)

**Images:**

 Enhancement of the Anomalous Nernst Effect in Polycrystalline Co2MnGa/AlN Multilayers

Half-metallic ferromagnets (HMFs) have attracted much interest as promising materials in spintronics devices since they generate highly spin-polarized current due to the absence of one spin-channel at the Fermi level (EF). Among the known HMFs, the use of Co2-based Heusler alloys enables enhancing the giant-magnetoresistance, tunnel-magnetoresistance, and spin-accumulation effects, thereby improving the performance of spintronic devices [1-3]. Despite the large magnetoresistance (MR) ratio observed in Heusler based devices, the structural disorder is still one of the remaining issues which lower the P. Therefore, it is essential to have a highly ordered Heusler structure to realize the half-metallicity. The structural order (B2→L21) of the Heusler alloys e.g., Co2MnSi [4] and Co2FeGe0.5Ga0.5 [1] have been promoted by annealing at high temperatures (&gt;500°C) resulting in an enhanced MR ratio. However, for various applications, the permissible maximum annealing temperature is restricted, e.g., for a magnetic read head in a hard disk drive (HDD) the annealing temperature is limited to 300°C because of the temperature tolerance of the NiFe shield. Therefore, it is desirable to search for other Heusler alloys that crystallize in L21-order below 300°C. The present work is motivated by Okubo et al. [5]’s report, where the L21 to B2-order transition temperature of Co2MnZ (Z = Ge, Sn) Heusler alloys is very high (&gt;1500K) suggesting high energetical stability of L21-structure; and hence L21-order is expected to appear even in the as-deposited state or by low-temperature annealing. Co2MnZ (Z = Ge, Sn) and reference Co2FeGe0.5Ga0.5 films were deposited on MgO (001) single crystal substrate using an ultra-high vacuum magnetron sputter system at room temperature and then post-annealed in-situ at Tann = 200-700°C to induce the atomic-ordering. Here, Co50Fe50 (3nm) was used as a buffer layer to deposit Co2MnZ films to suppress a phase separation. Co2MnSn films with two different compositions Co:Mn:Sn = 53.4:29.3:17.3 and 47.4:25.5:27.1 were deposited, which we refer to as Sn-poor and Sn-rich films, respectively. The crystal structure of the films was analyzed using a high-resolution X-ray diffractometer with Cu-Kα radiation. Finally, to quantify the P of the conduction electron in the bulk region, Co2MnZ and Co2FeGe0.5Ga0.5 films were microfabricated into a non-local spin valve (NLSV) device using electron-beam lithography, Ar-ion milling, and the lift-off techniques. X-ray diffraction revealed that Co2MnZ and Co2FeGe0.5Ga0.5 films are epitaxially grown along (001) direction. The degree of L21-ordering (SL21) as a function of Tann of Co2MnZ, Co2FeGe0.5Ga0.5, and Co2MnSi [4] films are shown in Fig.1(a). In the case of Co2FeGe0.5Ga0.5 and Co2MnSi, L21-ordering was observed above 500°C. Interestingly, in Co2MnZ films, L21-ordering appeared even in the as-deposited state and it enhances systematically with increasing Tann. Figure 2(a) shows a scanning electron microscopy (SEM) image of a typical NLSV device using Co2MnGe and Cu and the schematic of non-local measurement. We observed a clear spin-accumulation signal (△RS) in all our NLSV devices, which decays with increasing the gap-length (d); as Fig.2(b) shows a representative △RS-d curve of Co2MnGe film (Tann = 300°C). To evaluate P, the measured △RS in the Cu channel was analyzed by one-dimensional spin diffusion model [6]. The evaluated P of the films are displayed in Fig.1(b), which varies systematically with increasing Tann. The spin-polarization P of Co2MnGe at Tann = 300°C is higher (~0.65) than that of Co2MnSn and Co2FeGe0.5Ga0.5 due to a higher SL21, suggesting that Co2MnGe is a promising material for various practical applications. For Co2MnSn, however, low P was found in both compositions, despite high SL21. Because first-principle calculations predict highly spin-polarized electronic structure in the Sn-rich composition, it is desirable to check the microstructure by transmission-electron microscopy to understand the origin of low P. In conclusion, we elucidated that Co2MnGe is a promising material to obtain high atomic order and large P in the sputtered film without high-temperature annealing. Since the present Co2MnGe film has a slightly Co-rich composition which is not suitable to obtain high P due to the formation of the Co antisite disorder, optimization of the composition ratio is expected to lead to higher P.

**References:**

[1] S. Li et al., Appl. Phys. Lett. 103, 042405 (2013). [2] H. Liu et al., Appl. Phys. Lett. 101, 132418 (2012). [3] Ikhtiar et al., J. Appl. Phys. 115, 173912 (2014). [4] Y. Sakuraba et al., Phys. Rev. B 82, 094444 (2010). [5] A. Okubo et al., Appl. Phys. Lett. 96, 222507 (2010). [6] S. Takahashi and S. Maekawa, Phys. Rev. B 67, 052409 (2003).

**Images:**

![](https://assets.underline.io/uploads/markdown_image/1/image/8902ea3d787672d1d6b6265fa50d0219.jpg)
Fig.1. Tann dependence of (a). SL21, and (b). bulk spin-polarization P measured in NLSV devices. SL21 exceeding 1 is expected to be caused by off-stoichiometry in the films.

![](https://assets.underline.io/uploads/markdown_image/1/image/1c520a3f468d3d48a7c2ba59af666eb7.jpg)
Fig.2. (a). An SEM image of a typical NLSV device using Co2MnGe and Cu, and the schematic of non-local measurement. (b). The gap-length (d) dependence of △RS of NLSV based on Co2MnGe film (Tann = 300°C). The solid line indicates the fitting curve using one-dimensional spin diffusion model [6].

 Enhancement of L21-atomic order and spin-polarization in Co2MnZ (Z = Ge, Sn) Heusler thin films by low-temperature annealing process

Room temperature magnetoelectric (ME) compounds are rare and high-quality artificially multilayered ones are in general difficult and costly to produce. In this respect, magnetic Naturally Layered Perovskite structures (NLP) with improper ferroelectricity [1, 2], such as the Ruddlesden-Popper (RP) calcium manganite compound Ca3Mn2O7 [2], offer an alternative route to achieve non-expensive and high-performance room temperature MEs for information storage, sensors, and actuators or low power energy-efficient electronics. They allow exploring oxygen octahedra nonpolar rotations and cation site displacement to attain non-centrosymmetry. Additionally, due to their high sensitivity to lattice-distortions, their preparation in thin film form over crystalline substrates allows the manipulation of acentricity and enables the tuning of lattice, electric and magnetic interactions. However, crystallizing the desired layer with RP structure is challenging. Thus, the preparation conditions to obtain the envisaged Can+1MnnO3n+1 phases, with different n, need to be optimized. The objective of this study is to identify the deposition conditions that lead to different phases of (CaO)(CaMnO3)n with n = 2 (improper ferroelectric Ca3Mn2O7) and/or with n = ∞ (CaMnO3). Here we adopted the Laser ablation deposition method for developing (CaO)(CaMnO3)n thin films. As such, thin films of calcium manganate have been prepared over SrTiO3 substrates using Ca3Mn2O7 target by laser ablation. Polycrystalline Ca3Mn2O7 was synthesized using a conventional high-temperature ceramic route. The phase purity of the target was checked using XRD. The deposition parameters were studied, specifically oxygen partial pressures (from 10-3 to 10-1 mbar), laser fluences (10-5 J/cm2), substrate temperatures (from room temperature to 730 oC) and post-annealing influence. Further, a detailed structural study using X-ray diffraction (XRD), microstructural analysis by scanning electron microscopy (SEM), quantification of composition with energy-dispersive X-ray spectroscopy (EDS), magnetic property using SQUID magnetometer, and dielectric analysis by impedance analyzer were carried out. The XRD results show that for oxygen pressures in the range 10-2 - 10-1 mbar, deposition temperatures of 600 oC to 730 oC and laser fluences from 1.7 J/cm2 to 2.9 J/cm2, the films are polycrystalline, stabilizing in the CaMnO3 orthorhombic Pnma phase. The SEM measurements show dense films with smooth surfaces (Fig.1). The corresponding EDS measurements indicate a 1:1 atomic proportion in these samples. On the other hand, by decreasing the oxygen pressure, increasing the temperature and increasing the laser fluence, the Ca/Mn proportion increases, so that for films prepared on SrTiO3, at 730 oC, with 4 J/cm2 laser fluence, ~10-3 mbar oxygen pressure and with a post-annealing process, the Ca2Mn3O7 (n = 2) phase is stabilized, as confirmed by XRD (Fig.2). The corresponding EDS analysis further gives a Ca/Mn atomic ratio of ~1.5:1, consistent with the presence of this phase. The corresponding magnetic properties of the films, that are correlated with the stabilized phases and preparation conditions, will be present as well as the dielectric properties that were characterized by impedance spectroscopy.

**References:**

[1] Ghosez, P., Triscone, J.-M., Coupling of three lattice instabilities: Multiferroics, Nature Materials, vol. 10, n. 4, 2011, 269–270. [2] Rocha-Rodrigues, P., Santos, S. S. M., Miranda, I. P., Oliveira, G. N. P, Correia, J. G., Assali, L. V. C., Petrilli, H. M., Araújo, J. P., Lopes, A. M. L., Ca3Mn2O7 structural path unraveled by atomic-scale properties: A combined experimental and ab initio study, Physical Review B, 101, 064103, 2020.

**Images:**

![](https://assets.underline.io/uploads/markdown_image/1/image/0bee090bfd5ee13876d09318b47cab4d.jpg)
The cross-section image from SEM shows a dense film with a thickness of about 300 nm.

![](https://assets.underline.io/uploads/markdown_image/1/image/ff9a5f8b7a402acdcaca185e32eb98fb.jpg)
The XRD diffractogram confirms the stabilization of the Ca2Mn3O7 phase (n = 2).

 Growth of Ruddlesden–Popper (CaO)(CaMnO3)n Thin Films by Laser Ablation Deposition

Complex oxide thin films have highly tunable magnetic properties, not only due to the correlated degrees of freedom within these materials, but also due to the constraints imposed by choice of substrate material. For example, the magnetic properties of manganite materials depend heavily on the bond lengths and angles, resulting in a dead layer at the substrate/film interface [1,2,3]. Recently, techniques have been developed to separate oxide thin films from the substrate after growth, decoupling structural and chemical degrees of freedom at the interface [4]. This technique therefore may allow us to reduce dead layers at the interface of manganite thin films. Thin films of (001)-oriented LaMnO3+δ (LMO) were grown using pulsed laser deposition on a water-soluble Sr3Al2O6 (SAO) film on top of a (001) SrTiO3 substrate. After coating the film with a 1μm thick support layer of PMMA polymer, the SAO was dissolved in water, allowing the film to be separated from the substrate; this freestanding film could then be transferred to a different substrate, in this case, oxidized Si or LSAT. X-ray diffraction measurements show that freestanding films remain highly crystalline and oriented, but are no longer strained to the substrate. Magnetometry measurements indicate very similar TC, magnetic anisotropy, and saturation magnetization for both freestanding and epitaxial films, and cannot discern any difference in dead layer. Therefore, polarized neutron reflectometry (PNR) was performed at multiple temperatures to understand the depth profile of both the nuclear and magnetic structure of these freestanding films. As shown in Fig. 1, the film transferred onto the LSAT substrate is very smooth and has an expected structure. Between the substrate and freestanding film is a region with slightly lower nuclear scattering length density (SLD); from STEM and EELS, we find that this region is caused by intermixing with or residue from the water-soluble layer. In contrast, the film transferred onto silicon has a much more complicated structure, as shown in Fig. 2. The PNR data can only be explained with a long-range corrugation or rumpling of the film when placed on the Si substrate, with water incorporated into the interfacial region. After chemical removal of the PMMA support, this corrugation remains. Regardless of the substrate material, the magnetic profile within the freestanding manganite film is uniform, and there is no evidence of the magnetically dead layers at the substrate/film interface seen in epitaxial films. Thus, although choice of substrate can still affect freestanding films through chemical effects – which may have implications for the integration of these freestanding films with silicon-based devices – removing the structural constraints imposed by epitaxial growth is a promising avenue to reduce the dead layer in manganites.

**References:**

[1] Zhai, X., Cheng, L., Liu, Y., et al. Nat. Commun. 5, 4283 (2014). [2] Moon, E. J., Balachandran, P. V., et al. Nano Lett. 14, 2509-2514 (2014). [3] Liao, Z., Zhang, J. Appl. Sci. 9, 144 (2019). [4] Lu, D., Baek, D. J., Hong, S. S., et al. Nat. Mater. 15, 1255–1260 (2016).

**Images:**

![](https://assets.underline.io/uploads/markdown_image/1/image/bd954455d1393d7baa1acecb08ea8393.jpg)
(a) PNR data and (b) spin asymmetry of a 20 nm LMO freestanding film transferred onto an LSAT substrate, taken at 50K in an in-plane magnetic field of 3T. (c) The nuclear and magnetic depth-profile used to generate the best-fit model.

![](https://assets.underline.io/uploads/markdown_image/1/image/f23f5b70115419a383466b864d2fe667.jpg)
(a) PNR data and (b) spin asymmetry of a 40 nm LMO freestanding film transferred onto a Si/SiOx substrate, taken at 7K in an in-plane magnetic field of 1.5T. (c) The nuclear and magnetic depth-profile used to generate the best-fit model.

 Interfacial Corrugation and Magnetism of Freestanding LaMnO3+δ Thin Films

Energy gap parameters can vary significantly in X2YZ Heusler alloys [1], where Y-elements are 3d-transition metals and Z-components are s- and p-elements. Therefore, changes in different physical properties, especially, in electronic and optical characteristics are observed. Some features may indicate conditions close to half-metallic ferromagnets (HMFs) [2] and spin gapless semiconductors (SGSs) [3]. Such compounds are promising materials for spintronics because they can possess almost 100% spin polarization of charge carriers. HMFs hold an energy gap near the Fermi level for the current carriers with spin down, while its absence for current carriers with spin up. In turn, SGSs are like HMFs for the spin projection down, however, for the opposite spin direction, the gap is being zero [2, 3]. Thus, the aim of the work is to follow the changes in the electronic transport, optical properties of the Co2YSi (Y = Ti, V, Cr, Mn, Fe, Co, Ni) Heusler alloys system experimentally, and to compare the results obtained with the electronic band structure calculation, to establish their interconnection and suggest possible proximity to HMF- and/or SGS-states in the Co2YSi system. According to the data of X-ray structural analysis, all compounds are found to be ordered in the L21 structure. The electrical resistivity was measured in a wide temperature range using a PPMS setup. The field and the temperature dependences of the magnetic properties being studied too on the SQUID magnetometer. The coefficients of the normal and anomalous Hall Effect were found. The values of current carrier concentration and their mobility were estimated. Results of optical measurements showed good agreement with electronic band structure calculation. Besides, the correlation between the changes in these electronic, optical characteristics, and the coefficient of the current carrier spin polarization depending on the number of valence electrons are observed, which may point to the possible states of the HMF or SGS in this system of Heusler alloys. The work was performed within the framework of the state assignment of the Ministry of Science and High Education of Russia (the themes “Spin”, No. AAAA-A18-118020290104-2-2 and “Electron” No. AAAA-A18-118020190098-5) with partial support from the RFBR (project No. 20-32-90065), and the Government of the Russian Federation (Decree No. 211, Contract No. 02.A03.21.0006).

**References:**

[1] T. Graf, C. Felser, and S.S.P. Parkin, Prog. Solid State Chem., Vol. 39, p. 1 (2011) [2] M.I. Katsnelson, V.Yu. Irkhin, L. Chioncel et al., Rev. Mod. Phys., Vol. 80, p. 315 (2008). [3] X.L. Wang, Phys. Rev. Lett. Vol. 100, p. 156404 (2008).

**Images:**

 Electronic properties and electronic structure of Co2YSi (Y = Ti, V, Cr, Mn, Fe, Co, Ni) Heusler alloys

Antiferromagnets (AFMs) have regained strong attention from the magnetism community especially with the advent of antiferromagnetic spintronics [1]. The key operational element of spintronic devices is represented by information carriers, such as domain walls (DWs) and skyrmions. The simplest AFM DW separates two regions with the opposite orientation of the Neel order parameter. Although highly relevant, the experimental studies of AFM DWs (visualization, dynamics, mechanics) are challenging because of strict requirements on measurement techniques to access their properties. Here, we overcome these limitations and conduct detailed, quantitative studies of the mechanics and the nanoscale properties of individual, antiferromagnetic DWs in a single crystal Cr2O3 – a room-temperature, magnetoelectric, insulating AFM [2]. Our results reveal a remarkably pristine DW behaviour, which is governed by DW energy minimization and boundary conditions, but largely unaffected by pinning or disorder – a “textbook example” of antiferromagnetic DW physics. In our experiment, the crystal’s (0001) surface is patterned by a grid of mesas with mean thickness and width t=166 nm and w=2400 nm, respectively. The DW is nucleated by means of magnetoelectric field cooling by inverting the electric bias field over opposite halves of the sample. The DW may also be dragged through the mesa pattern by a focused laser spot. The magnetic texture is imaged using Nitrogen Vacancy (NV) magnetometry [3]. We find that the DW mimics an elastic surface with specific mechanical properties, determined by the interaction with the topographic features of the sample where the DW is (i) deflected from the straight plane crossing the mesa; (ii) bent around mesa corners. To address the DW behaviour theoretically, we perform large-scale spin-lattice simulations with GPU speed-up [4]. The analytical Ansatz is developed based on the numerically-obtained, three-dimensional DW profile. All main features of the DW behaviour can be determined taking into account the nearest-neighbour exchange and uniaxial anisotropy for a general model of a bipartite AFM. Crossing the mesa, the DW experiences an S-shaped distortion observed at the mesa surface, which is the result of exchange-driven boundary conditions at the side faces of the mesa, see Fig. 1. Below the top surface, the DW possesses a twist to match this distortion with the straight plane far below the sample’s surface. We find that the DW surface is deflected from the plane over a characteristic depth of 0.34w. Comparison of the equilibrium DW direction in bulk and at the mesa’s top surface allows us to derive an effective Snell’s law for the DW behaviour at the sample’s surface with the given incidence and refraction angles θ1 and θ2. The effective refraction coefficient is determined by the analytical energy minimization and reads neff = 1 + 3.1t/w + O(θ1). Controlled manipulation via laser not only enables DW dragging through the mesa, but also pinning at mesa corners. The shape of the DW surface is governed by its intrinsic elasticity. In terms of mechanics of an elastic ribbon, the corresponding tension coefficient is determined by the temperature-dependent exchange stiffness and anisotropy coefficient. This allows for curved DW states in which it is pinned at the opposite mesa sides. Using mesas as bistable pinning sites, we propose a potential DW-based AFM memory concept. Here, the memory state “0” or “1” is associated with the direction of the Neel order parameter at the mesa surface. We have realized such pinning sites experimentally and have shown manipulation of the state via laser dragging. In summary, we realize engineered DW potentials and control over DW trajectories by topographic structuring and manipulation of the DW position by means. The physics of AFM DWs in a single crystal with non-trivial surface topography is described theoretically by means of spin-lattice simulations and analytical model. A novel nanoscale AFM memory architecture is suggested.

**References:**

[1] T. Jungwirth, J. Sinova, A. Manchon et al, Nat. Phys. Vol. 14, p. 200 (2018); T. Jungwirth, X. Marti, P. Wadley et al, Nat. Nano. Vol. 11, p. 231 (2016); V. Baltz, A. Manchon, M. Tsoi et al, Rev. Mod. Phys. Vol. 90, p. 015005 (2018); O. V. Pylypovskyi, D. Y. Kononenko, K. V. Yershov et al, Nano Lett. Vol. 20, p. 8157 (2020) [2] N. Hedrich, K. Wagner, O. V. Pylypovskyi et al, arXiv:2009.08086 [3] L. Rondin, J.-P. Tetienne, T. Hingant et al, Rep. Prog. Phys. Vol. 77, p. 056503 (2014); N. Hedrich, D. Rohner, M. Batzer et al, Phys. Rev. Applied, Vol. 14, p. 064007 (2020) [4] SLaSi simulation package, http://slasi.knu.ua; O. V. Pylypovskyi, D. D. Sheka, Book of Abstracts, EUROPT Workshop, p. 11 (2013)

**Images:**

![](https://assets.underline.io/uploads/markdown_image/1/image/53f177df2920dadc9b01b189e65f13fb.jpg)
Fig. 1. The deflection of the DW from the straight path and distortion at the mesa surface shown by the stray magnetic field image taken using Nitrogen Vacancy microscopy. Inset shows the DW trajectory in spin-lattice simulations.

![](https://assets.underline.io/uploads/markdown_image/1/image/468d98b21c2bc9cd432573e88f7fb894.jpg)
Fig. 2. Concept of DW-based AFM memory with bits defined by the direction of the Neel order parameter at the mesa top surface (red or blue color, respectively).

 Domain walls in antiferromagnetic samples with non-trivial surface topography

Voltage-controlled magnetism, where magnetic properties are controlled via an applied electric field instead of current, could represent a significant increase in energy savings in future magnetically actuated devices. Practically, however, this approach faces several important obstacles, such as thickness limitations in electrically charged metallic films, mechanical failure in strain-mediated piezoelectric/magnetostrictive devices, and a lack of room-temperature multiferroics. Voltage-driven ionic motion (magneto-ionics) may provide a path forward by avoiding many of these drawbacks. Nevertheless, translating magneto-ionics into real world devices requires significant improvements in magneto-ionic rates, cyclability, and magnetization. Here, we report on the development of magneto-ionics in single-layer, semiconducting transition metal oxides and nitrides, and the subsequent enhancements in their performance. We first present electrolyte-gated and defect-mediated O transport in single-layer, paramagnetic Co3O4 at room temperature (i.e. without thermal assistance), which allows voltage-controlled magnetic switching (referred to here as ON-OFF ferromagnetism: Fig. 1) via internal reduction/oxidation processes[1]. Negative bias partially reduces Co3O4 to Co, resulting in films with Co- and O-rich areas (ferromagnetism: ON). Positive bias re-oxidizes Co back to Co3O4 (paramagnetism: OFF). We show that the bias-induced motion of O is caused by mixed vacancy clusters, with O motion promoted at grain boundaries and assisted by the development of O-rich diffusion channels. The generated ferromagnetism is shown to be stable, and easily erased by sufficient positive bias. This voltage-induced process is demonstrated to be compositionally, structurally, and magnetically reversible and self-contained. We then show that room-temperature magneto-ionic effects in electrolyte-gated paramagnetic Co3O4 films can be significantly increased, both in terms of generated magnetization (6 times larger) and speed (35 times faster), if the electric field is applied using an electrochemical capacitor configuration (utilizing an underlying conducting buffer layer: Fig. 2) instead of electric-double-layer transistor-like configuration (placing the electric contacts at the side of the semiconductor)[2]. In addition to gains in speed, magnetization measurements show a marked increase in the squareness ratio and a decrease in the switching field distribution of the hysteresis loops in Co3O4 biased in the capacitor configuration, the result of the formation of more uniform ferromagnetic regions. These results are attributed to the uniform electric field applied throughout the film, as confirmed by COMSOL simulations. As the measured films are quite thick, further miniaturization promises even greater magneto-ionic rates. We then demonstrate room-temperature voltage-driven nitrogen magneto-ionics (i.e., N transport) by electrolyte-gating of a CoN film[3]. Nitrogen magneto-ionics in CoN is compared to oxygen magneto-ionics in Co3O4, in films using an electrochemical capacitor configuration. Both materials are shown to be nanocrystalline (face-centered cubic structure), and show reversible voltage-driven ON-OFF ferromagnetism (Fig. 1). Nitrogen transport is found to occur uniformly throughout the film, creating a plane-wave-like migration front, without assistance of diffusion channels. Nitrogen magneto-ionics also requires lower threshold voltages and exhibits enhanced rates and cyclability, due to the combination of a lower critical electric field required to overcome the energy barrier for ion diffusion and the lower electronegativity of nitrogen with respect to oxygen, consistent with ab initio calculations contrasting N vs. O motion in cobalt stacks. These results place nitrogen magneto-ionics as a robust alternative for efficient voltage-driven effects and, along with oxygen magneto-ionics, may enable the use of magneto-ionics in devices that require endurance and moderate speeds of operation, such as brain-inspired/stochastic computing or magnetic micro-electro-mechanical systems.

**References:**

[1] A. Quintana, E. Menéndez, M. O. Liedke et al., ACS Nano, Vol. 12, p. 10291 (2018) [2] J. de Rojas, A. Quintana, A. Lopeandía et al., Advanced Functional Materials, Vol. 30, p. 2003704 (2020) [3] J. de Rojas, A. Quintana, A. Lopeandía et al., Nature Communications, Vol. 11, p. 5871 (2020)

**Images:**

![](https://assets.underline.io/uploads/markdown_image/1/image/2bda3c2e7c2cf2043f08b607447b7fbe.jpg)
Fig. 1. Hysteresis loops (M vs. H) of as-prepared, negatively-biased, and positively-biased CoN films at magneto-ionic activation voltages.

![](https://assets.underline.io/uploads/markdown_image/1/image/12893d420d32ae333459d12c5c0e4b71.jpg)
Fig. 2. A schematic of the electrochemical capacitor configuration used to bias cobalt-oxide (Co3O4) and cobalt-nitride (CoN) films.

 Oxygen vs. Nitogen Magneto-ionics

Interfacial electrochemical effects on magnetism, often also named magneto-ionic effects, are an emerging room-temperature and low-voltage approach in the research area of voltage control of magnetism [1]. In magneto-ionic systems, the magnetic layer is gated via a solid or liquid electrolyte and the applied voltage triggers ion migration and interfacial redox reactions, which impact the magnetic properties. In contrast to multiferroic systems and capacitive electronic charging, magneto-ionic concepts make significant magnetic property changes possible at room temperature and without the need for strain mediation [2], [3]. Since the mechanism is based on electrochemical charge transfer at the electrode/electrolyte interface, the morphology and the composition may be key to the magneto-ionic efficiency. We report magneto-ionic manipulation of ultrathin films in extended and stripe geometry and 3D nanoplatelet structures. In situ magnetic transport measurements are used in this study to determine and analyze the magneto-ionic effect. For FeOOH nanoplatelets, the application of a low voltage via liquid electrolyte gating yields an ON switching of magnetization (deduced from changes of the anomalous Hall resistance, see Figure 1a) [4]. The transformation proceeds via voltage-induced dissolution/redeposition, with the initially paramagnetic FeOOH structure as iron ion reservoir. The time-dependency of the reduction reaction enables the non-volatile setting of magnetic layers with different total magnetic moments. A large reversible magneto-ionic change of magnetization of up to 15% is achieved in the resulting iron films, which is explained by the enhanced roughness of the iron films obtained from the nanoplatelet structure. For thin Fe3O4/Fe films in stripe geometry, we achieved a tunable magnetoresistance by electrolytic gating (Figure 1b) [5]. Here, the tuning mechanism relies on voltage-triggered redox reactions, which locally affect the Fe3O4 regions. In the low-magnetic-field region (&lt;1 T), a crossover from positive to negative magnetoresistance is achieved by a voltage change of only 1.72 V. We will further present first results on the impact of the composition in iron triad magneto-ionic systems on magnetic properties by going beyond iron structures. The proposed approach is promising for the development of energy-efficient magnetic switches, sensors, and magnetic actuation, and may offer new avenues in magnetoelectronic devices.

**References:**

[1] K. Leistner, Current Opinion in Electrochemistry Vol. 25, p. 100636 (2021) [2] C. Navarro-Senent et al., APL Materials, Vol. 7, p. 030701 (2019) [3] K. Duschek et al., J. Mater. Chem. C, Vol. 6, p. 8411 (2018) [4] M. Nichterwitz et al., J. Phys. D: Appl. Phys., Vol. 53, p. 084001 (2020) [5] M. Nichterwitz et al., ACS Appl. Electron. Mater., Vol. 2, p. 2543 (2020)

**Images:**

![](https://assets.underline.io/uploads/markdown_image/1/image/e678a85b2d151bfa98d2f7b3f748549d.jpg)
Fig. 1 (a) electric “ON” switching of magnetism via electrolytic gating of FeOOH nanoplatelets. Magnetization curves as measured by anomalous Hall effect (AHE) after reduction at −1.27 V for different reduction times. The inset shows the cross-sectional REM image of a FeOOH pristine sample. (Adapted from [4]). (b) Voltage-control of the magnitude and the sign of magnetoresistance (MR) of FeOx/Fe nanocomposite thin films by electrolytic gating in LiOH. The inset shows a cross-sectional HR-TEM image of the pristine iron oxide-iron nanocomposite film. (Adapted from [5]).

 Magneto-ionic effect in iron triad nanostructures with different shapes and composition

Heterostructured artificial multiferroics have opened up the possibility for novel applications like multi-state memory or magnetic field sensors, as well as enhance performance of energy harvesters or tunable antennae or phase shifters. Magnetic thin films have been grown under strain with the goal of utilizing the large strain generated with a stress-induced interferroelectric phase transition in single crystal Pb(In1/2Nb1/2)O3-Pb(Mg1/3Nb2/3)O3-PbTiO3 (PIN-PMN-PT) [1] to optimized the magnetoelectric (ME) coupling. It was previously observed that for magnetostrictive phases laminated under zero stress, this phase transitional stress did not result in any ME coupling [2]. In this work, FeCo/Ag multilayered films were grown on (011) PIN-PMN-PT single crystals using sputter deposition. The FeCo/Ag multilayers were deposited onto two substrates: One with zero stress, while another was grown simultaneously with the substrate under an in-situ strain of ~1400 με along the [001] direction using a home-built stress fixture. The magnetic easy axes varied significant between the two films after the strain had been released due to the difference in the stresses in the film. The sample grown under zero strain showed a 90o rotation of the magnetic easy axis under the collective effect of tensile and compressive stresses in-plane imposed by the piezocrystal. The change in magnetization with applied voltage was large at zero stress but decreases with increased external stress applied to the sample, which is expected resulting from a stress-induced change in magnetic anisotropy that limits the effects of magnetoelastic-imposed stresses. In contrast, the magnetization loops for the sample grown in the stress fixture was unchanged with application of stress during the measurements, and zero magnetoelectric effect was observed. The possibility of high stresses beyond the plastic limit of FeCo due to both applied pre-stress and the intrinsic stress from sputter deposition are investigated, and the results will be compared.

**References:**

[1] P. Finkel, M. Staruch A. Amin, M. Ahart, and S.E. Lofland, Scientific Reports 5, 13770 (2015). [2] M. Staruch, J.F. Li, Y. Wang, D. Viehland, and P. Finkel, Appl. Phys. Lett. 105, 152902 (2014).

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In-situ single crystal synchrotron X-ray diffraction study on the structure of multiferroic antiferromagnet Ba2MnGe2O7 from low- to high-temperature

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In-situ single crystal synchrotron X-ray diffraction study on the structure of multiferroic antiferromagnet Ba2MnGe2O7 from low- to high-temperature

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