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Achievement of Diverse Domain Structures in Soft Magnetic Thin Film through Adjusting Intrinsic Magnetocrystalline Anisotropy


Oriented soft magnetic hcp-Co1 − x Ir x films with a fixed thickness of 120 nm were fabricated. All prepared films exhibit soft magnetic properties but various magnetocrystalline anisotropies with the variation of Ir content. The measured data shows that diverse domain structures including the Néel wall, Bloch wall, and stripe domains present in a fixed film thickness. It is singular for the single-layer soft magnetic film to possess diverse domains in a fixed thickness. This phenomenon was explained by introducing intrinsic magnetocrystalline anisotropy energy into soft magnetic films rather than the structural parameters of the film, inner stress, and microstructure effect.


In past decades, soft magnetic films have been applied in information storage technology and sensors. Their potential applications in the high-frequency area, such as inductor, noise suppressor, and field generation layer inside a spin torque oscillator, further spur researchers to investigate the moment distribution and property manipulation of soft magnetic thin films. In soft magnetic thin films [14], their moment distribution and macroscopic properties are strongly affected by the domain structure and the domain structure even determines their practical applications [5, 6]. In perpendicular magnetic recording, the existence of the Bloch wall in a soft magnetic underlayer causes the appearance of an out-of-plane stray field [7]. This feature leads to an additional noise signal during information reading. In the film which needs a rotatable anisotropy, the formation of a stripe domain structure is necessary [8, 9]. For a uniform soft magnetic single layer with in-plane isotropy, the domain structure is determined by competition of the exchange energy, magnetostatic energy, and magnetic anisotropy energies which are composed of magnetocrystalline anisotropy energy and stress-induced anisotropy energy. Generally, the magnetocrystalline anisotropy energy in traditional soft magnetic films can be neglected due to the weak magnetocrystalline anisotropy of grains. For this kind of soft magnetic films, all magnetic moments strictly lie in the film plane and the domain structure is formed through the Néel wall when the film thickness is small. The Néel wall will transform into the Bloch wall as the film thickness exceeds a critical value. The critical value of the Fe- and Co-based soft magnetic film with negligible magnetocrystalline anisotropy is approximately 20–40 nm [1012]. When the film thickness is large enough, the stripe domain in which nearly all magnetic moments deviate from the film plane appears due to the weak perpendicular magnetic anisotropy originating from inner stress or a microstructure effect [13, 14].

Besides the film thickness, the domain structure can also be affected by the substrate and sputtering conditions which determine the inner stress and overall microstructure in magnetic layers and hence determine the perpendicular anisotropy which is the important origin for the stripe domain structure. According to reported literatures, the perpendicular anisotropy originating from the inner stress and microstructure effect in soft magnetic layers is usually very weak. When the film thickness is fixed, the accomplishment of dramatic variation of domain structures by changing the microstructure or stress without external manipulation is difficult. If the domain structure in soft magnetic layers can be changed easily through intrinsic magnetic parameters, the manipulation of domain structures will become easier and the expected domain structure can also exist in a fixed film thickness. This can promote the application of soft magnetic films in a wider area. In previous researches, the method for introducing magnetocrystalline anisotropy into a soft magnetic CoIr alloy film with orientation growth has been reported [15, 16]. The magnetocrystalline anisotropy constant of the CoIr alloy can even change from positive to negative with the variation of the Ir content [15]. In this study, the manipulation of the domain structure in soft magnetic CoIr films with a fixed film thickness was deeply investigated by adjusting the intrinsic magnetocrystalline anisotropy.


Oriented hcp-Co1 − x Ir x films were fabricated on Si wafers with surface oxidation by magnetron sputtering. The layer structure of the samples, which is shown in Fig. 1a, is substrate/Ti (9 nm)/Au (10 nm)/Co1 − x Ir x (120 nm). The Ti layer was used to enhance adhesiveness of the Au seed layer and to induce the (111) orientation of the Au layer [17], and the Au seed layer was used to obtain the oriented hcp-CoIr alloy with its c axis perpendicular to the film plane. The pure Co with small Ir pieces on its surface was used as the target. The concentration of Ir can be manipulated by the number of Ir pieces to change the magnetocrystalline anisotropy of the CoIr grain. The thickness of all magnetic Co1 − x Ir x layers was fixed as 120 nm. The sputter pressure was 0.25 and 0.30 Pa for the seed and CoIr layers, respectively. The crystal structure of the prepared films was analyzed by X-ray diffraction (XRD) with CuKα1 radiation (source wavelength is 1.5406 Å). A vibrating sample magnetometer (VSM) was used to measure their static magnetic properties and determine the magnetocrystalline anisotropy field of the CoIr alloy. A magnetic force microscope (MFM) was used to distinguish the domain structure of the prepared magnetic layers. Chemical composition of the magnetic layers was measured by an energy dispersive spectrometer (EDS).

Fig. 1
figure 1

a Layer structure of the sputtered films with Ti (9 nm)/Au (10 nm)/Co1 − x Ir x (120 nm). b Crystal structure of CoIr alloy. c XRD patterns of the oriented Co1 − x Ir x films

Results and Discussion

Figure 1b is a hexagonal crystalline system. The magnetocrystalline anisotropy energy of this system can be expressed by

$$ {E}_{\mathrm{grain}}={K}_1 \sin {}^2\theta +{K}_2 \sin {}^4\theta +{K}_3 \sin {}^6\theta +{K}_4 \sin {}^6\theta \cos 6\varphi $$

Here, the coefficients with a twofold symmetry term are summarized as \( {K}_u^{\mathrm{grain}} \), and K 4 is negligible due to that it is usually very small in this system. When \( {K}_u^{\mathrm{grain}} \) is positive, the easy magnetization direction is along the c axis. This easy axis turns into a hard axis, and the magnetic moments prefer to lie in the c plane when \( {K}_u^{\mathrm{grain}} \) is negative.

Figure 1c is the XRD patterns of the Co1 − x Ir x films grown on the Au seed layer, which is measured by the θ–2θ scan method. Only two diffraction peaks are observed in a film. The peak at the lower angle is the (111) plane for Au. The strong peak at the higher angle corresponds to the (002) plane of the hcp-CoIr alloy due to that the hcp-Co alloy prefers to grow with its (002) plane on the (111) plane of Au [17]. This unique strong peak of the (002) plane reveals that the c crystal plane of Co1 − x Ir x is parallel to the film plane. As the atomic diameter of Ir is bigger than that of Co, the lattice constant of the CoIr becomes smaller with the decrease of Ir content. This is verified by the left drift of the diffraction angle.

To get the magnetocrystalline anisotropy constant \( {K}_u^{\mathrm{grain}} \) of the Co1 − x Ir x films with various Ir content, the initial magnetization curves parallel and perpendicular to the film plane were measured. Figure 2a shows typical results of the Co91.1Ir8.9 film. The total out-of-plane anisotropy field H out can be obtained by calculating the area between two magnetization curves. The H out should be composed of demagnetization field 4πM s and magnetocrystalline anisotropy field \( {K}_u^{\mathrm{grain}} \). The demagnetization field can be obtained from the measured saturation magnetization shown in Fig. 2b. The \( {K}_u^{\mathrm{grain}} \) can be gotten by − [(H out − 4πM s )M s ]/2. When H out is larger than 4πM s , \( {K}_u^{\mathrm{grain}} \) is negative; on the contrary, \( {K}_u^{\mathrm{grain}} \) is positive. Figure 2b shows the calculated \( {K}_u^{\mathrm{grain}} \) values from the measured data. When x = 18.9, the film has the strongest magnetocrystalline anisotropy with a negative \( {K}_u^{\mathrm{grain}} \). As x decreases, the magnetocrystalline anisotropy becomes weak while \( {K}_u^{\mathrm{grain}} \) keeps the negative value. When x = 8.9, \( {K}_u^{\mathrm{grain}} \) turns to be a small positive value. The positive \( {K}_u^{\mathrm{grain}} \) indicates the c axis in the CoIr alloy is the easy axis. As the c axis of the CoIr alloy grows perpendicular to the film plane, the positive \( {K}_u^{\mathrm{grain}} \) results in a perpendicular magnetic anisotropy of Co91.1Ir8.9 in the film.

Fig. 2
figure 2

a Initial magnetization curves of the Co91.1Ir8.9 film parallel and perpendicular to the film plane. b Extracted magnetocrystalline anisotropy constant of the Co1 − x Ir x alloy

Figure 3 gives the in-plane hysteresis loops of the films measured at room temperature. The inset shows the coercivities of the samples. For the films with negative \( {K}_u^{\mathrm{grain}} \), the coercivity and applied magnetic field required for saturation are all small. When \( {K}_u^{\mathrm{grain}} \) is negative, the c crystal plane of CoIr alloy is the easy magnetization plane and K 4 is very small in this system. As the fabricated films are composed of oriented CoIr grains with its c crystal plane parallel to the film plane, this leads to good soft magnetic properties along the film plane although the magnetocrystalline anisotropy of the film is strong. Moreover, in this situation, both the demagnetization field and magnetocrystalline anisotropy field spur magnetic moments to lie in the film plane. When x = 8.9, the sample exhibits quite different properties. The magnetization process appears to be a transcritical hysteresis loop, which is a strong signature of the formation of stripe domain structures [8, 9, 14]. It is speculated that the perpendicular magnetic anisotropy originating from positive \( {K}_u^{\mathrm{grain}} \) of the CoIr alloy supports the formation of stripe domain structures. It should be noticed that the coercivity in the film with stripe domain is larger compared with that of the films without stripe domain structures. This result is quite consistent with other reports on films with stripe domains and can be interpreted in terms of rotatable anisotropy often found in thin films with stripe domains [8, 9, 14, 18].

Fig. 3
figure 3

Room temperature of the in-plane hysteresis loops of the samples

Figure 4 displays the MFM images of the films in demagnetization state with an area of 5 μm × 5 μm. For the Co1 − x Ir x film with x = 18.9, any out-of-plane stray field is not detected. All magnetic moments should strictly lie in the film plane, and the domain structure should be formed through the Néel wall. The schematic of the domain structure was shown in Fig. 5a. Generally, the transition thickness of the magnetic layer from the Néel wall to the Bloch wall for Fe- and Co-based soft magnetic film with negligible magnetocrystalline anisotropy is about 20–40 nm. However, the oriented soft magnetic Co91.1Ir8.9 film with a thickness of 120 nm still possesses a Néel wall. This is due to the enhanced transition thickness from the Néel wall to the Bloch wall, which can be explained by the following equations for the Néel wall energy E Néel and the Bloch wall energy E Bloch [15]:

Fig. 4
figure 4

MFM pattern of Co1-xIrx films with a scanning area of 5μm×5μm. a out-of-plane stray field is not detected for Co81.1Ir18.9; (b)-(c) out-of-plane stray field in transition area of magnetic moment reversal is detected for Co85.7Ir14.3 and Co90.2Ir9.8, respectively (d) a stripe domain structure is clearly shown with bright and black stripes for Co91.1Ir8.9

Fig. 5
figure 5

The schematics of the domain structure. a Néel wall. b Bloch wall. c Stripe domain structure

$$ {E}_{\mathrm{N}\acute{\mathrm{e}} \mathrm{el}}={A}_1\frac{\pi^2}{\sigma }+\frac{\pi {M_s}^2{\sigma}^2}{t+\sigma } $$
$$ {E}_{\mathrm{Bloch}}={A}_1\frac{\pi^2}{\sigma }+\frac{-{K}_u^{\mathrm{grain}}}{2}\sigma +\frac{\pi {M_s}^2t{\sigma}^2}{t+\sigma } $$

where t, σ, and A 1 denote magnetic layer thickness, domain wall thickness, and exchange stiffness constant, respectively. The type of domain wall depends on which is smaller for E Néel and E Bloch. The critical transition thickness of the magnetic layer from the Néel wall to the Bloch wall can be achieved when E Néel = E Bloch. The dependence of the critical transition thickness from the Néel wall to the Bloch wall on \( {K}_u^{\mathrm{grain}} \) by using M s of Co81.1Ir18.9 (1000 G) and the exchange stiffness constant of pure cobalt are shown in Fig. 6. The critical thickness increases with the increase of \( \left|{K}_u^{\mathrm{grain}}\right| \). For the oriented Co81.1Ir18.9 film, its \( {K}_u^{\mathrm{grain}}=-6.3\times {10}^6\mathrm{erg}/\mathrm{cc} \). The calculated transition thickness is 130 nm. Hence, the Co81.1Ir18.9 film with a thickness of 120 nm still possesses the Néel wall. When x = 14.3 and 9.8, the magnetocrystalline anisotropy of the films becomes weaker compared with the Co81.1Ir18.9 film and the domain wall characterized by black and white lines in the MFM images is obviously detected. This domain wall should be a Bloch wall due to that the out-of-plane stray field in the transition area of the magnetic moment reversal is detected by MFM and the magnetic moments except the domain wall area still lie in the film plane. The schematic of the domain structure was shown in Fig. 5b. Figure 6 also shows the critical thickness dependence of \( {K}_u^{\mathrm{grain}} \) by using M s of Co85.7Ir14.3 (1100 G) and Co90.2Ir9.8 (1190 G). The calculated transition thicknesses are only 38 and 28 nm for the Co85.7Ir14.3 and Co90.2Ir9.8 films, respectively. As the actual film thickness is much larger than the transition thicknesses, the Bloch wall should exist.

Fig. 6
figure 6

The dependence of the critical transition thickness from the Néel wall to the Bloch wall on \( {K}_u^{\mathrm{grain}} \) at M s  = 1000, 1100, and 1190 G

When \( {K}_u^{\mathrm{grain}} \) turns to be positive, the film with x = 8.9 clearly exhibits a stripe domain structure (Fig. 5c displays its schematic), due to that the MFM image is composed of bright and black stripes. This MFM image is consistent with the transcritical hysteresis loop in Fig. 3 which is a signature of the formation of the stripe domain structure. According to the reported literatures, the film thickness possessing the stripe domain is about several hundred nanometers and the stripe domain comes from the weak perpendicular magnetic anisotropy that resulted from a stain and microstructure effect [8, 13, 1922]. Its critical thickness can be described by

$$ {t}_{\mathrm{stripe}}^{\mathrm{crit}}=2\pi \sqrt{A/{K}^{\mathrm{perp}}} $$

K perp originating from stress or a microstructure effect is generally very weak. This leads to a larger \( {t}_{\mathrm{stripe}}^{\mathrm{crit}} \) from the above equation. In this study, the oriented Co91.1Ir8.9 thin film exhibits the stripe domain structure in a relatively small thickness. In the oriented Co91.1Ir8.9 thin film, there is the uniaxial magnetocrystalline anisotropy \( {K}_u^{\mathrm{grain}} \) perpendicular to the film plane. This \( {K}_u^{\mathrm{grain}} \) has the same effect as K perp on the formation of the stripe domain structure. Moreover, the positive \( {K}_u^{\mathrm{grain}} \) can be manipulated easily by varying the Ir content, so the \( {t}_{\mathrm{stripe}}^{\mathrm{crit}} \) can also be adjusted easily in this film system.


In summary, the diverse domain structures in oriented soft magnetic Co1 − x Ir x thin films with a fixed thickness were reported. The magnetocrystalline anisotropy energy was introduced into total energy in soft magnetic films to adjust the domain structure. When \( {K}_u^{\mathrm{grain}} \) varies from negative to positive, the domain structure exhibits a diverse change from the Néel wall domain to the Bloch wall domain and then to the stripe domain with all magnetic moments deviating from the film plane. All these changes are accomplished only by adjusting the intrinsic magnetic parameters. This work offers a new avenue to manipulate the domain structure in single-layer soft magnetic films except film thickness, inner stress, and microstructure determined by sputtering conditions.



Energy dispersive spectrometer


Magnetic force microscope


Vibrating sample magnetometer


X-ray diffraction


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We thank the National Natural Science Foundations of China (Nos. 11204115 and 11574122) and the Fundamental Research Funds for the Central Universities (lzujbky-2015-115) for the support provided.

Authors’ Contributions

TW, TYM, YW, and FSL conceived and coordinated the project. JYJ and TW carried out the experimental work and wrote the manuscript. All authors read and approved the manuscript.

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The authors declare that they have no competing interests.

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Correspondence to Tao Wang.

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Jiao, J., Wang, T., Ma, T. et al. Achievement of Diverse Domain Structures in Soft Magnetic Thin Film through Adjusting Intrinsic Magnetocrystalline Anisotropy. Nanoscale Res Lett 12, 21 (2017).

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  • Soft magnetic film
  • Domain structure
  • Magnetocrystalline anisotropy