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Research Article | Open Access

Volume 2022 |Article ID 9857631 | https://doi.org/10.34133/2022/9857631

Haidi Wang, Qingqing Feng, Xingxing Li, Jinlong Yang, "High-Throughput Computational Screening for Bipolar Magnetic Semiconductors", Research, vol. 2022, Article ID 9857631, 8 pages, 2022. https://doi.org/10.34133/2022/9857631

High-Throughput Computational Screening for Bipolar Magnetic Semiconductors

Received09 Dec 2021
Accepted20 Feb 2022
Published15 Mar 2022

Abstract

Searching ferromagnetic semiconductor materials with electrically controllable spin polarization is a long-term challenge for spintronics. Bipolar magnetic semiconductors (BMS), with valence and conduction band edges fully spin polarized in different spin directions, show great promise in this aspect because the carrier spin polarization direction can be easily tuned by voltage gate. Here, we propose a standard high-throughput computational screening scheme for searching BMS materials. The application of this scheme to the Materials Project database gives 11 intrinsic BMS materials (1 experimental and 10 theoretical) from nearly ~40000 structures. Among them, a room-temperature BMS (mp-771246) is discovered with a Curie temperature of 478 K. Moreover, the BMS feature can be maintained well when cutting the bulk into (001) nanofilms for realistic applications. This work provides a feasible solution for discovering novel intrinsic BMS materials from various crystal structure databases, paving the way for realizing electric-field controlled spintronics devices.

1. Introduction

In the era of big data, information transmission, processing, and storage are under spotlight in the research field. The development and utilization of the freedom of spin of electrons in this new era are the epitome of the so-called spintronics [14]. Its outstanding features, such as faster data processing speed, higher circuit integration, lower energy consumption, and nonvolatility, make it particularly advantageous in information transmission and storage [5]. As a foundation of spintronics, functional spintronics materials such as half metallic ferromagnets (HMF), half semiconductors (HSC), and spin gapless semiconductors (SGS) have been widely investigated [69]. At the same time, we have previously proposed a new conceptual material, namely, bipolar magnetic semiconductor (BMS) [10], which is considered to be a promising spintronics material with tunable feature. Specifically, thanks to its special band structure, the current passing through this kind of material can be totally spin polarized on the one hand, and the spin polarization direction of the current can be directly tuned by simply applying gate voltage on the other hand.

Considering that BMS is deemed as an ideal material for electric control of spin polarization, it has become a hot spot in the field of physical chemistry in recent years. Although BMS has broad application prospects and some BMS materials have been proposed [1118], there is still a long way to go from theoretical study to experiment implementation. The primary obstacle is that the existing BMS materials are problematic in reality in the following aspects: (1) most theoretically designed BMS materials are extrinsic [19, 20], i.e., based on chemical or physical modifications, which makes the experimental synthesizing difficult; (2) magnetic orders are only stable at very low temperatures [21], making it unfeasible for room-temperature devices. In addition, the experimental available BMS candidates are far from sufficient on account of the low efficiency of traditional trial and error method. Therefore, it is necessary to unveil more potential BMS materials with the help of new technical means, thereby paving the way for the synthesis and application of spintronics devices.

In recent years, with the proposal of the “Material Genome Project” [22, 23], high-throughput screening technology has been widely used in the field of material design, and a series of important research results have been achieved. For example, Urban et al. [24] successfully predicted one high-energy-density lithium battery material Li through high-throughput screening within the compound structure space, which has been proved by experiments; Yan et al. [25], by integrating high-throughput theory and experimental technology, discovered 8 ternary vanadates that can be used for photocatalysis and revealed the significance of unit in the structure. Recently, Chen et al. [26] screened 40,000 compounds from the Materials Project and discovered a ferromagnetic half semiconductor with a Curie temperature of about 130 K. In view of the abundant achievements of high-throughput screening, we believe that it should also be adapted to search for BMS materials more effectively.

In this work, we propose a standard high-throughput computational screening scheme for exploring BMS materials from nowadays crystal structure databases based on six filters, i.e., initialization filter, magnetic filter, stability filter, band gap filter, doping filter, and refinement filters. The validity of the proposed scheme is confirmed by its successful application to the Materials Project (MP) [27, 28] database, which contains about one hundred thousand experimentally synthesized and also theoretically predicted inorganic compounds with calculated electronic, magnetic, elastic, and piezoelectric properties. After large-scale computational screening, we obtain 11 candidate BMS materials for spintronics application, among which one BMS material with room-temperature ferromagnetism has been predicted.

2. Results

As is shown in Figure 1, the high-throughput screening process of BMS materials includes two groups of descriptors: primary descriptors (Figure 1(a)) and secondary descriptors (Figure 1(c)). The primary descriptors consist of five filters, including initialization (I) filter, magnetic (M) filter, stability (S) filter, band gap (G) filter, and doping (D) filter. The function of five filters is described as follows: (1) I filter: this filter is used to build the repository for screening. Considering the requirements of magnetic semiconductors, we select all structures with one or more elements in the set of , where the metal and alloy structures are excluded. (2) M filter: according to band theory, one spin-polarized band has one electron. The fractional magnetic moment must have fractional occupation, which corresponds to metals. Therefore, the M filter selects the structures that only has nonzero integer magnetic moment, which, to some extent, can guarantee that the candidates are magnetic semiconductor materials. At the same time, to reduce the computational complexity, we only select the structures with ferromagnetic (FM) order. (3) S filter: for stability of a compound, two important factors are considered here, including formation energy () and the energy above convex hull (). The formation energy [29] of a compound is the energy required to produce the system from the most stable crystal structures of the individual components, which is defined as where is the total energy of the material , and and are the average energies of the elements and in their stable crystal at 0 K. For , it measures the energy for a material to decompose into the set of the most stable materials. A positive indicates that this material is unstable with respect to such decomposition. A zero indicates that this is the most stable material at its composition [29, 30]. Generally speaking, those compounds with negative are easy to be synthesized. However, considering the error of DFT calculations, we use an appropriate standard to select the candidate structures, namely, less than 0.01 eV/atom. In addition, it is generally believed that structures with less than 0.1 eV/atom can be synthesized experimentally [29, 30]. In short, the standard for the S filter is { eV/atom, eV/atom}. (4) G filter: to make sure the candidate structures are semiconductors, the band gaps should be positive values. As we all know, the PBE-based band gap values of the Materials Project database are underestimated. To ensure that every potential BMS candidate structure is included, the structures with a band gap greater than 0.01 eV are all passed to next filter. (5) D filter: due to the special electronic structure of BMS, the magnetic moment will increase or decrease at the same time when it is doped with electrons or holes. Therefore, we use it as an important filter to screen BMS materials. In this work, the candidate structures are doped by 0.1 electron and 0.1 hole to calculate its magnetic moment.

According to the statistic chart of the number of candidate structures in primary screening stages (see Figure 1(b)), it can be found that the number of candidate structures is quickly reduced to an acceptable number, specifically speaking, 781 compounds. Assuming that the data quality of Materials Project is perfect, all 781 compounds should be BMS materials. However, according to our test, it shows that some of the magnetic ground states of compounds are wrongly predicted, especially those compounds with Co elements, which unusually have two spin states: high spin and low spin [31]. For example, the total energy and magnetic moment of entry mp-1174644 in the MP database are -5.8252 eV/atom and 11.0, respectively. However, our further calculation shows that the Co of this system should be high spin. The real total energy and magnetic moment should be -5.8466 eV/atom and 12.0 , respectively. These validated results indicate that our screening in this work may miss some BMS candidate materials in the MP database, which cannot be solved before the MP database is updated. At the same time, we cannot guarantee all of 781 candidate structures are technically BMS materials. To tackle this problem, we further use the secondary descriptors to refine our results.

From Figure 1(c), it can be found that there are three steps for the secondary descriptors: magnetic order: the magnetic ground state of 781 candidate structures is carefully investigated to search for those structures with FM order. To be specific, firstly, the FM order of all candidates is calculated to find the magnetic atom and corresponding energy . Then, the antiferromagnetic (AFM) orders are set according to the number of magnetic atoms. Theoretically, the magnetic ground-state calculation is a tedious task that needs to consider all combinations of magnetic order and symmetry of structure [32]. To simplify the calculation, we use the following scheme. Specifically, if the number of magnetic atom is equal to 2, 3, 4, 5, and 6 in a unit cell, the number of AFM orders is 1, 2, 3, , and , respectively. The corresponding energies are labeled as . If the number of magnetic atom is equal to 1 or is larger than 6, then we build three types of supercell (,, and ) to decide the magnetic ground state, where the FM order is applied for unit cell and AFM order is used between unit cells. The corresponding energies are labeled as . Besides, considering the high spin and low spin of Co element, all of structures with Co element adopt 1.3  and 5.5  as initial magnetic moment, which can be assigned by label “MAGMOM” in the VASP input file. According to energy difference between and (or ), the magnetic ground state is then decided. Exchange energy: the Curie temperature is closely related to magnetic exchange energy (). According to the above label, the is defined as =max(/2-) or =max(-). Band gap: according to the refined magnetic ground state, the band gap of selected structures is recalculated by HSE06 functional to identify those structures with positive band gap and BMS feature.

Based on the screening scheme as described in Figure 1, we finally obtain 11 candidate BMS materials for spintronics, among which 1 structure (, MP-ID: mp-556492, ICSD: 37447) is experimentally synthesized and 10 structures are theoretically predicted. Properties of obtained BMS materials are listed in Table 1, which are sorted by the exchange energy per magnetic atom. According to the statistic, the number of entries for V-, Cr-, Mn-, Fe-, Co-, and Ni-based BMS is 1, 1, 2, 3, 3, and 1, respectively. Although 10 of 11 candidate BMS candidates are theoretically predicted structures, all of them have negative and zero or small positive , which indicates that these structures may be synthesized by experiments in future. It is worth noting that the of mp-771246 is larger than 100 meV/atom, indicating it may have a high Curie temperature and be promising in spintronics application. For the rest of the structures, all of are less than 100 meV/atom and show a general tendency: the larger the magnetic atom distance is, the smaller the is. In order to have a clear understanding, we present the crystal structure of first 8 materials (the structures of left BMSs are supplied in SI Figure S1) in Figure 2 due to their relatively large . It can be found that all of the structures have high symmetry and most of the unit cells of structures have at least 2 magnetic atoms.


MP-IDFormulaSymmetry

mp-771246Li2V3TeO8-2.2700.04563.0213180R-3m0.8551.2590.254
mp-1177989Li2Fe3F8-2.8630.034133.168671Cmce1.2420.4143.124
mp-773037Mn3BiO8-1.6730.06082.89812490.0682.1790.613
mp-1247148Mg2Cr3GaS8-1.2520.04193.622321R-3 m0.4500.5070.366
mp-1208920Sm2CoPtO6-2.5660.00545.4272190.1270.0251.627
mp-1222351LiFeF6-2.2650.00044.738230.1211.3651.124
mp-755811Na3CoO3-1.5620.03855.101430.6630.3401.803
mp-849528Li3FeO4-1.8720.01533.08242I-43 m0.1151.7690.231
mp-867641Li4Ni7(OF7)2-2.2640.062152.97572C2/m0.4400.3082.815
mp-556492CoPtF6-1.9970.00045.19212R-30.0400.0201.841
mp-754966Li2MnF6-2.8880.00044.667210.0731.4182.617

In addition, according to our screening results, the energy of FM state and AFM is nearly degenerate for 6 entries, including , , , , , and (see SI Table S1). A previous study shows that strain or doping can be an effective way to tune AFM state to FM state [17]. As a test case, we use 2% strain for to check its strain response. The results based on GGA+U method show that the ground-state magnetic order of under this small strain is FM state and also presents BMS feature (the corresponding DOS is supplied in SI Figure S2).

Then, the basic electronic structure properties of obtained BMSs are investigated. In Figure 3, we plotted the DOS for the first 8 structures by using HSE06-based first-principle calculations (the corresponding HSE06-based DOS for left entries are supplied in SI Figure S3). We can find that all of the 8 compounds possess completely spin-polarized DOS with opposite spin orientations around the Fermi level. Due to the unique electronic structure, the spin direction of these BMS systems can be easily tuned by the electrical gating technique. A positive/negative gate voltage will inject electrons/holes into the BMS system, which causes a controllable half-metallic conducting behaviour [10]. Previous studies [33, 34] show that in certain cases, HSE06 may underscreen the exchange interaction for transition metal elements and does not predict an accurate electronic structure. To provide a quantitative prediction to experimentalists, we also calculated the high-level GW-based DOS for . The result shows that GW gives the similar BMS feature as HSE06, but the spin-flip gap in valence band is largely reduced (see details in Figure S4).

To estimate the Curie temperatures of obtained BMS materials, three methods are available, including mean-field approximation (MFA), random-phase approximation (RPA), and Monte Carlo simulation (MC) [35]. Compared with RPA and MC, MFA usually overestimates the Curie temperature. In this work, we use the MC method based on the classical Heisenberg Hamiltonian to estimate the Curie temperature: where is the exchange parameter and is the spin of magnetic atoms. Here, we consider two exchange parameters and (labeled in Figure 4(a)), which represent the intralayer and interlayer nearest-neighbor exchange parameter, respectively. The spin density of FM and AFM states is shown in Figures 4(a)–4(c), where the local magnetic moments are all contributed by V atoms. For MC simulation, the supercell for is set to be . According to the in Table 1, we deduce that the of is 33.3 meV and 15.7 meV. Then, the simulated spin magnetic moment and susceptibility as a function of temperature are plotted in Figure 4(d). For , all the spins of V atoms point in the same direction at 0 K, forming a strict FM order, while the magnetic moment decreases rapidly when heated. The critical point for FM to paramagnetic transition occurs at about 478 K, as indicated by an abrupt increase in the magnetic susceptibility curve.

As discussed above, the bulk is predicted to be a potential candidate for BMS. However, to design modern nanosized devices, a thin film (slab) structure is required. Due to the surface states and quantum-size effect, the properties of two-dimensional (2D) slab structures are generally different from their bulk counterpart and depend on the slab thickness. Therefore, it is necessary to answer the following questions: can the 2D slab of maintain the BMS feature? What is the smallest thickness required for maintaining stable BMS feature? For simplicity, we here only consider the (001) oriented slabs. According to the symmetry of , 5 slabs with different surface terminations are selected, namely, O1-, O2-, Te-, V-, and Li-termination (see Figure S5). The calculation based on the GGA+U method shows that the O1 termination has the lowest formation energy. Then, the electronic properties of O1 termination with different numbers of V atom layers are tested. Considering that FM order will finally be the ground state as the number of V atom layers increases, here, we only calculate the DOS of O1-terminated slabs with FM order to reduce the workload. According to DOS based on the GGA+U method (Figure S6), it can be found that as the number of V atom layers increases, the electronic structure gradually converges. Specifically, when the number of V atom layers is greater than or equal to 6, the total magnetic moment will increase by 5  for each additional V atom layer. At the same time, when the number of V atom layers reaches to 11, the slab structure shows BMS feature and the structure with 12 V atom layers also has the same feature and a similar DOS. That is to say, a minimum number of 11 V atom layers (corresponding to 5.34 nm) are required for spintronics application. The detailed properties of 2D slabs with different thicknesses are summarized in Table S2.

Despite its potential application in spintronics devices design, is still not synthesized yet. However, according to the query results from the MP database (see Table S3), it can be found that the formation energy and energy above hull are all lower than those of experimental phases (ICSD: 21012) and (ICSD: 249325) when the stable phases LiTe3 (ICSD: 935), VTe2 (ICSD: 38369), and TeO2 (ICSD: 26844 and 30222) are selected as references. At the same time, the theoretically proposed reaction of has the largest reaction enthalpy change (exothermic reaction) compared with LiVTeO5 and LiV3(TeO6)2. Therefore, Li2V3TeO8 would have possibility to be synthesized experimentally.

3. Discussion

Based on initialization filter, magnetic filter, stability filter, band gap filter, doping filter, and refinement filters, we propose a standard high-throughput computational screening scheme for exploring an important class of ferromagnetic semiconductors with electrically controllable spin polarization, namely, BMS. Compared with the traditional trial and error method, the present scheme is direct and efficient. By using the present scheme, a total number of 11 BMS materials are obtained via screening a comprehensive quantum material repository containing 44703 magnetic compounds. Among them, Li2V3TeO8 is predicted to be a room-temperature BMS with a Curie temperature of about 478 K. Meanwhile, the corresponding slab structure of Li2V3TeO8 with 11 or more V atom layers can maintain the bulk’s BMS feature well. Besides, the low formation energy and energy above convex hull make the experimental synthesis of Li2V3TeO8 feasible.

However, some drawbacks also exist for the current scheme. For example, the DFT calculation is very expensive, which limits us to search for BMS materials with larger unit cell. In the initialization filter, we only consider the structures with V, Cr, Mn, Fe, Co, and Ni transition metals, which may lead to missing some ferromagnetic-order candidates, such as Si-deficient silicon carbide [36]. In addition, the current MP database is not adequately qualified, which will result in the missing of some potential BMS candidates. To solve these problems, a highly qualified database is needed. At the same time, based on existing BMS materials to build structure-property relationship, use machine learning method to predict new BMS is a feasible way. We will leave these problems in our future work and also wish our current work can guide experiments and theories for developing BMS materials.

4. Methods

The first-principle calculations of electronic structure are conducted by using the Vienna ab initio simulation package (VASP) software package [37, 38]. The generalized gradient approximation (GGA) of Perdew, Burke, and Ernzerhof (PBE) exchange correlation functional [39] with collinear spin polarization is employed. The plane wave basis set is used to describe the valence electrons with the cutoff set to 520 eV. The convergence criteria for electronic SCF iterations and ionic step iterations were set to be  eV and  eV, respectively. The reciprocal space grid was set to 8000 according to Pymatgen method [28]. To better describe onsite Coulomb repulsion among or electrons, we adopt the GGA+U scheme [40] during the screening stage, where the effective onsite Coulomb interaction parameter () and exchange interaction parameter () for different structures are set according to Pymatgen default values. To fix semilocal PBE calculations of electronic structures, the density of states (DOS) of final candidate materials is calculated based on screened hybrid HSE06 functional [41, 42] with 20% Hartree-Fock exchange. The accurate DOS of most promising BMS Li2V3TeO8 is further calculated by the GW method as implemented in the VASP. The energy cutoff for response function is set to 200 eV, and the total band number is set to 400.

In order to ensure that the large-scale BMS screening tasks run on the HPC cluster in an efficient, stable, and automated manner, we use DPDispatcher (see Code Availability) to create, manage, and collect tasks. To generate input files of static and density of state calculation and to analyze output files, Pymatgen and MapTool (see Code Availability) are used. The visualization of crystal structure is implemented by VESTA software [43].

Data Availability

The authors confirm that the data supporting the findings of this study are available within the article and its supplementary materials. All of the structures and related information can be downloaded online (https://gitee.com/haidi-hfut/bms).

Additional Points

Code Availability. DPDispatcher can be found at https://github.com/deepmodeling/dpdispatcher. MapTool can be found at https://github.com/haidi-ustc/maptool.

Conflicts of Interest

The authors declare that there are no competing interests.

Authors’ Contributions

Haidi Wang, Xingxing Li, and Jinlong Yang conceived the idea. Haidi Wang and Qingqing Feng performed the calculations. All authors helped to write, modify, and analyze this manuscript.

Acknowledgments

This work is financially supported by the Fundamental Research Funds for the Central Universities, by the National Natural Science Foundation of China (Grant No. 21688102), by the National Key Research & Development Program of China (Grant No. 2016YFA0200604), by Anhui Initiative in Quantum Information Technologies (Grant No. AHY090400), by the Youth Innovation Promotion Association CAS (2019441), and by University of Science and Technology of China Research Funds of the Double First-Class Initiative (YD2060002011). The authors thank the Supercomputer platform of USTC, Beijing, and HFUT for the computational resources.

Supplementary Materials

Table for properties of entries mp-24105, mp-1036443, mp-1190177, mp-759690, mp-560127, and mp-776070; crystal structure and density of states for Li4Ni7(OF7)2 (mp-867641), CoPtF6 (mp-556492) and Li2MnF6 (mp-754966); density of states for MnH8(NF3)2 under strain; density of states for Li4Ni7(OF7)2 (mp-867641), CoPtF6 (mp-556492), and Li2MnF6 (mp-754966); table for properties of Li2V3TeO8 of (001) oriented O1-termination slabs with different numbers of V atom layers; (001) oriented slabs of Li2V3TeO8 with different surface terminations; density of states of Li2V3TeO8 of (001) oriented O1-termination slabs; table for properties of Li-V-Te-O quaternary compounds Li2V3TeO8, LiVTeO5 and LiV3(TeO6)2. (Supplementary Materials)

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