Chinese Journal of Chemical Physics   2016, Vol. 29 Issue (4): 462-466

The article information

Lin Ju, Tong-shuai Xu, Yong-jia Zhang, Li Sun
鞠林, 徐同帅, 张雍家, 孙礼
First-Principles Study of Magnetism in Transition Metal Doped Na0.5Bi0.5TiO3 System
过渡金属掺杂在Na0.5Bi0.5TiO3体系中诱导产生磁性的第一性原理研究
Chinese Journal of Chemical Physics , 2016, 29(4): 462-466
化学物理学报, 2016, 29(4): 462-466
http://dx.doi.org/10.1063/1674-0068/29/cjcp1602023

Article history

Received on: February 2, 2016
Accepted on: May 4, 2016
First-Principles Study of Magnetism in Transition Metal Doped Na0.5Bi0.5TiO3 System
Lin Jua, Tong-shuai Xua, Yong-jia Zhangb, Li Sunb     
Dated: Received on February 2, 2016; Accepted on May 4, 2016
a. School of Physics and Electric Engineering, Anyang Normal University, Anyang 455000, China;
b. Department of Physics, Taiyuan University of Technology, Taiyuan 030024, China
Author: Li Sun, sunlitut@163.com
Abstract: The origins of magnetism in transition-metal doped Na0.5Bi0.5TiO3 system are investigated by ab initio calculations. The calculated results indicate that a transition-metal atom substitution for a Ti atom produces magnetic moments, which are due to the spin-polarization of transition-metal 3d electrons. The characteristics of exchange coupling are also calculated, which shows that in Cr-/Mn-/Fe-/Co-doped Na0.5Bi0.5TiO3 system, the antiferromagnetic coupling is favorable. The results can successfully explain the experimental phenomenon that, in Mn-/Fe-doped Na0.5Bi0.5TiO3 system, the ferromagnetism disappears at low temperature and the paramagnetic component becomes stronger with the increase of doping concentration of Mn/Fe/Co ions. Unexpectedly, we find the Na0.5Bi0.5Ti0.67V0.33iO3 system with ferromagnetic coupling is favorable and produces a magnetic moment of 2.00 μB, which indicates that low temperature ferromagnetism materials could be made by introducing V atoms in Na0.5Bi0.5TiO3. This may be a new way to produce low temperature multiferroic materials.
Key words: Transition-metal atom     Substitution     Magnetic moment     First-principles calculation    
Ⅰ INTRODUCTION

In recent years, multiferroic materials have drawn increasing interest due to their attractive physical properties and potential applications in spintronics, information storage and sensors [1-4]. The coupling between the magnetic and electric properties could lead to magnetoelectric effect [1] in which the magnetization can be controlled by application of electric fields, and vice versa. Multiferroic properties have been found in some oxides with perovskite structure [5-7]. The observed single-phase multiferrioc materials are few [8], due to the contradiction between the conventional mechanism for cation off-centering in ferroelectrics (which generally requires d$^0$ orbitals), and the formation of magnetic moments (which usually results from partially filled d or f orbitals). Related studies on magnetic ferroelectrics have signalled a revival of interest in this phenomenon [2]. Several reports show that doping of transition metal ions in a ferroelectric oxide could induce ferromagnetism, a similar case to that of diluted magnetic semiconductors [9, 10].

Na$_{0.5}$Bi$_{0.5}$TiO$_3$ attracts much attention as a promising environmental friendly lead-free ferroelectric material due to its possible applicability to electromechanical actuators, sensor, and transducers [11]. It is one among the non-lead free relaxor ferroelectrics having very high remanent polarization $P_\textrm{r}$=36 $\mu $C/cm$^2$ with a coercive field of about 70 kV/cm [12]. At temperatures below 255 $^{\circ}$C Na$_{0.5}$Bi$_{0.5}$TiO$_3$ has a rhombohedral structure with R3c space group which has anti-phase ($\bar a\; \bar a\; \bar a$) octahedral tilting and ion displacements along the [111] direction of the pseudo-cubic cell, making Na$_{0.5}$Bi$_{0.5}$TiO$_3$ exhibit unique ferroelectric and piezoelectric properties [13]. In such systems inducing a multifunctional behavior by site specific substitution will be inevitable. In Na$_{0.5}$Bi$_{0.5}$TiO$_3$, diluted magnetic behavior has been observed by transition-metal substitution at B-site, such as Fe-/Mn-/Co-doped Na$_{0.5}$Bi$_{0.5}$TiO$_3$ [14-16]. All the results above indicate that the substitutional doping with transition metals play a very important role in tuning the electronic and magnetic properties of Na$_{0.5}$Bi$_{0.5}$TiO$_3$ and related systems. However, the mechanisms of electronic and magnetic of TM-doped Na$_{0.5}$Bi$_{0.5}$TiO$_3$ remain unclear.

In order to address exactly these above questions, we explore the electronic and magnetic properties of bulk of Na$_{0.5}$Bi$_{0.5}$TiO$_3$ with transition metals doping via the first-principles density functional theory (DFT). Results demonstrate that, for Na$_{0.5}$Bi$_{0.5}$TiO$_3$ system, magnetic moments can be induced when one Ti atom is substituted by a TM (TM=V, Cr, Mn, Fe, and Co) atom. We also compared the energies of ferromagnetic and antiferromagnetic couplings between two TM atoms substitutions in Na$_{0.5}$Bi$_{0.5}$TiO$_3$ super-cell. The type of preferential magnetic coupling of system depends upon both the doped transition-metal atoms and the distributions of the Ti atoms substituted. The TM doping concentration was defined as the molar ratio of TM/(TM+Ti).

Ⅱ COMPUTATIONAL DETAILS

DFT calculations were performed using the plane-wave pseudopotential method in the Vienna $ab$ $initio$ simulation package (VASP) [17, 18]. The projector augmented wave (PAW) [19, 20] potentials were employed. Considering the fact that LDA may underestimate the Coulomb repulsion and tend to localize the charge density, strong correlation effects were introduced by means of the LDA+$U$ scheme [19]. In our LDA+$U$ calculation, the on-site effective $U$ parameter ($U_{\textrm{eff}}$=$U$-$J$=5.8 eV) was proposed by Dudarev et al. [21]. The calculated lattice constants of ($a$=$b$=5.49 Å, $c$=13.51 Å, and $\alpha$=$\beta$=90$^{\circ}$, $\gamma$=120$^{\circ}$) are in good agreement with reported results by Jones and Thomas [13]. Special $k$ points were generated with a 3$\times$3$\times$3 grid based on Monkhorst-Pack scheme. We constructed a rhombohedral Na$_{0.5}$Bi$_{0.5}$TiO$_3$ periodic supercell containing 30 atoms, where a Ti atom is substituted by a TM atom (TM=V, Cr, Mn, Fe, and Co). Such substitution corresponds to Na$_{0.5}$Bi$_{0.5}$Ti$_{0.84}$V$_{0.16}$O$_3$ and the doping level is 16%. An energy cutoff of 400 eV was used for the plane wave expansion of the electronic wave function. The cases of pure Na$_{0.5}$Bi$_{0.5}$TiO$_3$ and TM atoms (TM=V, Cr, Mn, Fe, and Co) doped Na$_{0.5}$Bi$_{0.5}$TiO$_3$ are considered. The total energy is converged to be 1.0$\times$10$^{-4}$ eV/atom, while the Hellman-Feynman force is smaller than 0.01 eV/Å in the optimized structure.

Ⅲ RESULTS AND DISCUSSION

The rhombohedral Na$_{0.5}$Bi$_{0.5}$TiO$_3$, a complex perovskite-structure compound with Na and Bi ions at the A site of ABO$_3$ with a Na:Bi ratio of 1:1 are shown in Fig. 1. The density of state (DOS) for the pure system Na$_{0.5}$Bi$_{0.5}$TiO$_3$ is given in Fig. 2(a). In addition, the total DOS for pure Na$_{0.5}$Bi$_{0.5}$TiO$_3$ system also shows that no spin-polarization emerges around the Femi energy level, indicating that the pure Na$_{0.5}$Bi$_{0.5}$TiO$_3$ is nonmagnetic, as there are no unpaired electrons, the results are in good agreement with Zhang's report [22].

Figure 1 The schematic crystal structure of rhombohedral Na$_{0.5}$Bi$_{0.5}$TiO$_3$.
Figure 2 Total density of state of (a) pure Na$_{0.5}$Bi$_{0.5}$TiO$_3$, (b) Na$_{0.5}$Bi$_{0.5}$Ti$_{0.84}$V$_{0.16}$O$_3$, (c) Na$_{0.5}$Bi$_{0.5}$Ti$_{0.84}$Cr$_{0.16}$O$_3$, (d) Na$_{0.5}$Bi$_{0.5}$Ti$_{0.84}$Mn$_{0.16}$O$_3$, (e) Na$_{0.5}$Bi$_{0.5}$Ti$_{0.84}$Fe$_{0.16}$O$_3$ and (f) Na$_{0.5}$Bi$_{0.5}$Ti$_{0.84}$Co$_{0.16}$O$_3$, respectively. The vertical dotted line indicates the Fermi level.

Experimental evidence has shown that the transition-metal atoms replace the Ti atoms at B-site [14, 15]. Calculations have been performed on Na$_{0.5}$Bi$_{0.5}$Ti$_{0.84}$V$_{0.16}$O$_3$ (TM=V, Cr, Mn, Fe and Co). The total DOSs of Na$_{0.5}$Bi$_{0.5}$Ti$_{0.84}$V$_{0.16}$O$_3$ (TM=V, Cr, Mn, Fe, and Co) are shown in Fig. 2 (b)-(f). An obvious spin-split in the spin-up and spin-down total DOS at/near the Fermi level can be found. Clearly, V-, Cr-, Fe-, and Co-doped Na$_{0.5}$Bi$_{0.5}$TiO$_3$ are all half-metals and magnetic with 100% spin polarization. The Mn-doped Na$_{0.5}$Bi$_{0.5}$TiO$_3$ is magnetic semiconductors, because both the majority and minority spin DOSs are zero at the Fermi level and there is a clear spin polarization between the DOSs of the two spin channels around the Fermi level. According to our calculations, the values of magnetic moments are 1.00, 2.00, 3.00, 2.00, and 1.01 $\mu _\textrm{B}$ for 16% V-, Cr-, Mn-, Fe-, and Co-doped Na$_{0.5}$Bi$_{0.5}$TiO$_3$, respectively.

The total energies of the supercell with Na$_{0.5}$Bi$_{0.5}$Ti$_{0.84}$TM$_{0.16}$O$_3$ (TM=V, Cr, Mn, Fe and Co) for spin-polarized and nonspin-polarized modes are also calculated. The corresponding energy difference $\Delta E_{\textrm{N-M}}$=$E_\textrm{N}$-$E_\textrm{M}$ between the total energies of nonmagnetic state $E_\textrm{N}$ and the magnetic state $E_\textrm{M}$ are 0.12, 0.64, 1.32, 0.47 and 0.07 eV for 16% V-, Cr-, Mn-, Fe-, and Co-doped Na$_{0.5}$Bi$_{0.5}$TiO$_3$, respectively. All the results show that the magnetic state is more stable than the nonmagnetic one. Figure 3(a)-(e) show the spin-density distribution (spin-up minus spin-down) for Na$_{0.5}$Bi$_{0.5}$Ti$_{0.84}$TM$_{0.16}$O$_3$ (TM=V, Cr, Mn, Fe, and Co). The spin density is mainly distributed on the TM atoms.

Figure 3 Three-dimensional iso-surfaces of magnetization density for (a) Na$_{0.5}$Bi$_{0.5}$Ti$_{0.84}$V$_{0.16}$O$_3$, (b) Na$_{0.5}$Bi$_{0.5}$Ti$_{0.84}$Cr$_{0.16}$O$_3$, (c) Na$_{0.5}$Bi$_{0.5}$Ti$_{0.84}$Mn$_{0.16}$O$_3$, (d) Na$_{0.5}$Bi$_{0.5}$Ti$_{0.84}$Fe$_{0.16}$O$_3$, and (e) Na$_{0.5}$Bi$_{0.5}$Ti$_{0.84}$Co$_{0.16}$O$_3$. The yellow iso-surfaces represent the spin density of spin up. The iso-value is 0.01 Å$^3$.

In order to further understand the electronic structure, the atom-, orbital-, and spin-projected density of the TM atom (TM=V, Cr, Fe and Co) d states, Na atoms s, p states, Bi atoms s, p, d states, Ti s, p, d states, and O p states are calculated and presented in Fig. 4 for V-, Cr-, Fe-, and Co-doped Na$_{0.5}$Bi$_{0.5}$TiO$_3$. Obviously, the TM 3d DOS shows an exchange splitting between the spin-up and spin-down DOS peaks at/near the Fermi level, which results in a magnetic moment. As shown in Fig. 3(c)-(e), small induced magnetic moments are also observed for the O atoms. The differencebetween the spin-up and spin-down DOS of O p states can be found, which can been in Fig. 4(a)-(d). The O atoms around the 3d TM atoms are polarized while other O atoms are not. That is to say, the polarized electrons are decided by the distance between the O atom and the TM atom. The spin-projected DOS of spin-up orbitals (or spin-down orbitals) pass through the Fermi level and spin-down orbitals (or spin-up orbitals) can exhibit the characteristics of semiconductor. Therefore, V-, Cr-, Fe-, and Co-doped Na$_{0.5}$Bi$_{0.5}$TiO$_3$ are the half-metal materials.

Figure 4 Partial DOS of TM d states, Na s, p states, Bi s, p, d states, Ti s, p, d states, V d states, and O p states for Na$_{0.5}$Bi$_{0.5}$Ti$_{0.84}$TM$_{0.16}$O$_3$ and TM=(a) V, (b) Cr, (c) Fe and (d) Co, respectively. The vertical dotted line indicates the Fermi level.

Subsequently, we perform spin polarized calculations on the Na$_{0.5}$Bi$_{0.5}$TiO$_3$ supercell with two TM (TM=V, Cr, Mn, Fe and Co) atoms substituting for Ti atoms in the lattice. Such substitution corresponds to Na$_{0.5}$Bi$_{0.5}$Ti$_{0.67}$TM$_{0.33}$O$_3$ and the doping level is 33%. In the supercell, we investigate three distributions of the two Ti atoms, which are replaced by TM atoms. The three cases are: (ⅰ) the two TM atoms are located at the sites of Ti1 and Ti2, respectively, (ⅱ) the two TM atoms are located at the sites of Ti1 and Ti3, respectively, (ⅲ) the two TM atoms are located at the sites of Ti1 and Ti4, respectively. The value of the distance between the two TM atoms located at the sites of Ti1 and Ti5 is too large (more than 9 Å), and the magnetic coupling effect is very weak. Therefore, the case of two TM atoms located at the sites of Ti1 and Ti5 is not meaningful to discuss here.

After absolutely optimized, as shown in Table Ⅰ, the distances between TM (TM=V, Cr, Mn, Fe, and Co) atoms for the three cases are almost the same. In order to deal with the effect of the magnetic coupling between the two isolated TM atoms, we evaluate the relative energies between ferro-and antiferromagnetically ordered states by LDA+$U$ calculation. Table Ⅱ provides the energy differences between ferromagnetic state (FM) and antiferromagnetic state (AFM) as well as magnetic moments of two TM atoms doping. Here, $\Delta E_\textrm{m}$=$E_{\textrm{AFM}}$-$E_{\textrm{FM}}$ represents energy difference between antiferromagnetic state and ferromagnetic state after optimization, which enables us to estimate stable states of magnetism coupling. $\Delta E_\textrm{m} >$0 indicates that the ferromagnetic state is more stable than the antiferromagnetic state, while $\Delta E_\textrm{m} < $0 indicates that the antiferromagnetic state is more stable than the ferromagnetic state. The energy differences $\Delta E$ of structures with different distance between the two TM atoms substitution for Ti atoms in Na$_{0.5}$Bi$_{0.5}$TiO$_3$ are also listed in Table Ⅱ. By comparing the total energies of the above three cases for Na$_{0.5}$Bi$_{0.5}$Ti$_{0.67}$TM$_{0.33}$O$_3$ (TM=V, Cr, Mn, Fe, and Co), we find that the type of preferential magnetic coupling of system depends upon both the doped transition-metal atoms and the distributions of the Ti atoms substituted.

Table Ⅰ Distance between two Ti atoms substituted by TM (TM=V, Cr, Mn, Fe, and Co) for the three cases of Na$_{0.5}$Bi$_{0.5}$Ti$_{0.67}$TM$_{0.33}$O$_3$.
Table Ⅱ The relative energies of the states FM and AFM ($\Delta E_\textrm{m}$=$ E_{\textrm{AFM}}$-$E_{\textrm{FM}}$), values of the relative stabilities $\Delta E$, calculated for the Na$_{0.5}$Bi$_{0.5}$Ti$_{0.67}$TM$_{0.33}$O$_3$ (TM=V, Cr, Mn, Fe, and Co).

For the Na$_{0.5}$Bi$_{0.5}$Ti$_{0.67}$TM$_{0.33}$O$_3$ (TM=Fe and Co) system, when the two Fe/Co atoms are located at the sites of Ti1 and Ti2, the system with antiferromagnetic coupling has the lowest energy among the three cases; For the Na$_{0.5}$Bi$_{0.5}$Ti$_{0.67}$TM$_{0.33}$O$_3$ (TM=Cr and Mn) system, when the two Cr/Mn atoms are located at the sites of Ti1 and Ti3, the system with antiferromagnetic coupling has the lowest energy among the three cases. Wang et al. reported experimentally that, as Mn ions doping concentration was increased to 20%, the Mn-doped Na$_{0.5}$Bi$_{0.5}$TiO$_3$ sample shows a strong ferromagnetism at room temperature. However, with further increasing the doping concentration of Mn ions up to 30%, the paramagnetic component becomes stronger [15]. Duan et al. found the ferromagnetism disappeared at 10 K and indicated that inside the Na$_{0.5}$Bi$_{0.5}$Ti$_{1-x}$Mn$_x$O$_3$ particles, the antiferromagnetic coupling between the Mn ions can be formed [23], which conformed our calculation results. For the Na$_{0.5}$Bi$_{0.5}$Ti$_{0.67}$V$_{0.33}$O$_3$ system, when the two V atoms are located at the sites of Ti1 and Ti2, the system with ferromagnetic coupling has the lowest energy among the three cases and produces a magnetic moment of 2.00 $\mu _\textrm{B}$, indicating that low temperature ferromagnetism materials could be made by introducing V atoms in Na$_{0.5}$Bi$_{0.5}$TiO$_3$. This may be a new way to produce multiferroic materials.

Ⅳ CONCLUSION

We explore the structural, electronic and magnetic properties of TM-doped (TM=V, Cr, Mn Fe and Co) Na$_{0.5}$Bi$_{0.5}$TiO$_3$ alloys via the first-principles PAW potential within DFT, employing the exchange-correlation potential provided by the LDA+$U$. The results demonstrate that, for Na$_{0.5}$Bi$_{0.5}$TiO$_3$ system, magnetic moments can be induced when one Ti atom is substituted by a TM atom. On the electronic structures, the analyses of total DOSs indicate that V-, Cr-, Fe-and Co-doped Na$_{0.5}$Bi$_{0.5}$TiO$_3$ alloys are all half-metals and magnetic with 100% spin polarization. It also can be found that the magnetic phase is energetically preferred to the nonmagnetic phase for all the Na$_{0.5}$Bi$_{0.5}$Ti$_{0.84}$TM$_{0.16}$O$_3$ (TM=V, Cr, Mn, Fe and Co) systems. For V-, Cr-, Fe-and Co-doped Na$_{0.5}$Bi$_{0.5}$TiO$_3$ alloys, the results of spin-projected DOS show that the spin splitting mainly comes from TM3d states. Small magnetic moments are also observed for the O atoms, which are due to the small spin polarization of p-states of O atoms. We also compared the energies of ferromagnetic and antiferromagnetic couplings between two TM (TM=V, Cr, Mn, Fe and Co) atoms substitutions in Na$_{0.5}$Bi$_{0.5}$TiO$_3$ supercell, in which we investigate three distributions. For Cr-/Mn-/Fe-/Co-doped Na$_{0.5}$Bi$_{0.5}$TiO$_3$ system, antiferromagnetic coupling is more stable. The results can successfully explain the experimental phenomenon that, in Mn/Fe doped Na$_{0.5}$Bi$_{0.5}$TiO$_3$ system, the ferromagnetism disappears at low temperature and the paramagnetic component becomes stronger with the increase of doping concentration of Mn/Fe/Co ions. Furthermore, we find the Na$_{0.5}$Bi$_{0.5}$Ti$_{0.67}$V$_{0.33}$O$_3$ system with ferromagnetic coupling is favorable and produces a magnetic moment of 2.00 $\mu _\textrm{B}$, which indicating that low temperature ferromagnetism materials could be made by introducing V atoms in Na$_{0.5}$Bi$_{0.5}$TiO$_3$. This may be a new way to produce low temperature multiferroic materials.

Ⅴ Acknowledgments

This work was supported by National Natural Science Foundation of China (No.11547176) and Henan College Key Research Project (No.15A140017).

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过渡金属掺杂在Na0.5Bi0.5TiO3体系中诱导产生磁性的第一性原理研究
鞠林a, 徐同帅a, 张雍家b, 孙礼b     
a. 安阳师范学院物理与电气工程学院, 安阳 455000;
b. 太原理工大学物理系, 太原 030024
摘要: 用从头算研究了在Na0.5Bi0.5TiO3体系中,采用过渡金属掺杂从而诱导出磁性的可能性.计算结果表明,用一个过渡金属原子置换一个钛原子之后,可以在该体系中产生磁矩.所产生的磁矩主要是由于过渡金属原子的3d轨道电子的自旋极化导致的.通过交换关联能的计算,我们发现在铬、锰、铁、钴掺杂的Na0.5Bi0.5TiO3体系中,反铁磁耦合状态比铁磁耦合状态稳定.印证了实验中,随着锰、铁掺杂量的增加,Na0.5Bi0.5TiO3体系在低温下铁磁性消失,顺磁性增强.在钒掺杂的Na0.5Bi0.5Ti0.67O3体系中,铁磁耦合比反铁磁耦合稳定,并且带有2μB的磁矩.这就意味着,可以通过钒掺杂制备Na0.5Bi0.5Ti0.67O3低温铁磁材料.
关键词: 过渡金属     掺杂     磁性     第一性原理计算