Semiconductors are increasingly relied upon in modern society. Prototypical elemental semiconductors, Si and Ge, play principal roles in electronics and photovoltaics. Compound semiconductors including GaAs, GaP and GaN have not only enhanced these applications, but also paved the way to optoelectronic devices, such as light-emitting diodes1. Current electronics also utilize oxide semiconductors in thin-film transistors2, and semiconductor-based photocatalysts and photoelectrochemical cells are being developed, particularly for the electrolysis of water3,4. With such a variety of applications, the exploration of novel semiconducting materials has been a fundamentally and technologically important issue. Among the compound semiconductors, nitrides are attractive due to the abundant and environmentally benign nitrogen constituent. Many nitrides possess relatively high chemical stability at high temperature, which is advantageous for applications under severe environments such as power electronics. Moreover, bulk crystal and film growth techniques are well established, especially for group III nitrides. However, the currently commercialized nitride semiconductors are mostly limited to GaN and its based AlxGa1−xN and InxGa1−xN alloys with tuned bandgaps. This situation has stimulated experimental and computational searches of novel nitrides, for instance, spinel-Si3N4 (ref. 5), cubic-Zr3N4 (ref. 6), ZnSnN2 (ref. 7), CuNbN2 (ref. 8) and LaWN3 (ref. 9). In particular, recent developments of high-throughput first-principles screening based on prototype crystal structures and evolutionary algorithm structure searches have enabled the accelerated identification of a variety of previously unreported or uncharacterized semiconductors, including nitrides8,9,10,11,12,13,14,15,16,17,18,19,20.

High carrier mobility is desirable or even mandatory, in most applications of semiconductors, and the effective mass is a relevant fundamental physical parameter. Group III nitrides in the wurtzite structure, especially GaN and InN, have small electron effective masses due to spatially diffuse cation s-orbital contributions to their conduction bands. Moderate hole effective masses are also attained in the valence bands with mainly N-2p characteristics. Technological uses for nitride semiconductors could be expanded if alternative materials with similar desirable electronic properties were found. Ideally, such alternatives should be environmentally benign and comprised of earth-abundant constituents. A chemical analogy to GaN and InN suggests that the nitrides composed of Zn, Ge or Sn would be good candidates. In particular, hybridization between closed-shell Zn-3d and N-2p states in the valence band is expected to reduce hole effective masses in Zn nitrides. Indeed, a Zn binary nitride, Zn3N2, possesses such a band structure21, but the fabrication of its high-quality film is still challenging, partly due to its small exothermic formation enthalpy (−22.6 kJ mol−1 or −47 meV per atom)22. In addition, well-known ternary zinc nitride semiconductors are limited to a small number of systems, such as LiZnN (ref. 23), ZnGeN2 (ref. 24) and ZnSnN2 (ref. 7).

Here we report computational screening of ternary zinc nitrides using a combination of the prototype-based and evolutionary algorithm structure searches. Twenty-one promising semiconductors with small carrier effective masses are identified via systematic first-principles calculations of stability and electronic structure. The proposed nitrides include previously unreported CaZn2N2 with earth-abundant components and a direct bandgap, which is synthesized by high-pressure methods. Alloy calculations indicate a bandgap capable of covering most of the visible light range. Native defect and dopant calculations also predict p- and n-type dopability for CaZn2N2 and the related Ca2ZnN2.


Theoretical identification of ternary zinc nitride semiconductors

Systems of interest have been selected from 583 existing and hypothetical ternary zinc nitrides, which consist of various polymorphs of 125 chemical formulae. These candidate compounds are constructed using 52 prototype crystal structures, either reported in the Inorganic Crystal Structure Database (ICSD)25 or previously predicted theoretically15 (Supplementary Table 1). The considered structures are taken by N3− compounds, that is, nitrides, involving two kinds of cations, at least one of that is divalent; those taken by azides, diazenides and pernitrides are excluded. The divalent cation is replaced with Zn(II) and the other is replaced with a cation of the same valence (Supplementary Table 2), which is expected to yield a closed-shell electronic structure and therefore exhibit a quantifiable bandgap. The cation species are not restricted to abundant elements at this stage because the electronic structure of compounds involving any element can provide useful information on the design of novel semiconductors. Subsequently, an evolutionary algorithm12,26 is used to validate or update the most stable crystal structures. This allows us to overcome the limitations associated with relying on already reported crystal structures in the ICSD.

The screening is performed from various aspects: (i) the electronic structure, that is, bandgaps and effective masses; (ii) dynamic stability against lattice vibration; and (iii) thermodynamic stability against competing phases in the phase diagram. Here, not only thermodynamically stable phases, but also metastable phases with small positive formation energies (<50 meV per atom) are selected. This tolerance partly accommodates errors associated with the approximations used in first-principles calculations and the omission of temperature effects (Supplementary Method 1). Although metastable phases with higher formation energies may be grown by the use of high pressure, high temperature and/or non-equilibrium conditions, we prioritize the predictions of thermodynamically stable or slightly metastable compounds for the ease of the fabrication. Furthermore, the energetics of relevant native point defects and dopants is assessed to identify the dopability into p type, n type or both for promising compounds. Details of the screening and computational procedures are described in the Methods section and Supplementary Method 1.

Identified from the computational screening are 21 nitrides that are dynamically stable and thermodynamically stable/slightly metastable against competing phases (with formation energies that are <50 meV per atom), possess bandgaps and exhibit small effective masses for holes, electrons or both (smaller than 2m0, where m0 denotes the free-electron rest mass); their crystal structures, phonon densities of states, phase diagrams and electronic band structures are presented in Supplementary Figs 1–4 and Supplementary Table 3. Here, heavy holes are considered when the valence band maximum (VBM) is degenerate or nearly degenerate, as their dominant contributions to the electronic density of states near the VBM mean that heavy holes are most relevant to hole conduction. The bandgaps and effective masses of these nitrides are shown in Fig. 1, alongside those of Zn3N2 and GaN. Our screening identifies 11 nitrides that have not been reported in the ICSD, Be2ZnN2, Mg2ZnN2, CaZn2N2, Zn3LaN3, ZnTiN2, ZnZrN2, ZnHfN2, Zn2VN3, Zn2NbN3, Zn2TaN3 and Zn3WN4. It has also selected 10 already known nitrides, validating our computational methods and screening criteria: LiZnN (ref. 23), Ca2ZnN2 (ref. 27), Sr2ZnN2 (ref. 28), Ba2ZnN2 (ref. 28), ZnSiN2 (ref. 24), ZnGeN2 (ref. 24), ZnSnN2 (ref. 7) and Zn2PN3 (ref. 29) reported experimentally, and NaZnN and KZnN predicted theoretically15. We note that four of these known nitrides, that is, Ca2ZnN2, Sr2ZnN2, Ba2ZnN2 and Zn2PN3 have not, to our knowledge, been considered as semiconductors previously and their appealing band structures are unveiled in the present study. In addition, the majority of the identified nitrides consist solely of abundant elements.

Figure 1: Electronic properties of theoretically identified ternary zinc nitrides.
figure 1

(a) Bandgaps. Filled and open circles denote the values for direct and indirect gaps, respectively. Available experimental values are shown with bars (see Supplementary Table 4 for tabulated values and references). (b) Effective masses for holes and electrons normalized by the free-electron rest mass, m0. The values for the directions that provide the smallest effective masses are shown (see Supplementary Table 5 for tabulated values). Heavy holes are considered when the valence band maximum is degenerate or nearly degenerate (<0.1 eV differences in band energies). The values for Zn3N2 and GaN are also shown as references. As-yet-unreported nitrides are indicated with a bold purple font.

Among the known nitrides, ZnSiN2, ZnGeN2 and ZnSnN2 are found to favour a wurtzite-derived crystal structure in consistency with previous experiments7,24. ZnTiN2 is predicted to take this crystal structure among the newly identified Zn–IV–N2 compounds, whereas ZnZrN2 and ZnHfN2 are energetically more favourable with an alternate, P3m1 crystal structure obtained using the evolutionary algorithm. The present results extend the wurtzite derivatives from Zn–IV–N2 to those involving group V and VI elements. Zn2PN3 can be regarded as a prototype of such kind with a group V element. Our calculations suggest that Zn2VN3, Zn2NbN3 and Zn2TaN3 are stable in this Zn2PN3 structure. In addition, Zn3WN4 is predicted to take a wurtzite-derived structure as well. In total, 10 unique structure types are observed for the 21 identified nitrides (Supplementary Table 3; Supplementary Fig. 1).

The hole and electron effective masses of many of the identified nitrides are comparable to or even smaller than those of Zn3N2 and GaN. In particular, much smaller hole effective masses than that of GaN (2.0m0) are recognized for a number of ternary zinc nitrides. This is partly attributed to the hybridization of the Zn-3d orbitals near the VBM and is appealing in view of potential applications utilizing p-type conductivity. Especially, Zn3LaN3 shows a non-degenerate VBM with an exceedingly small hole effective mass of 0.2m0 (Fig. 1b; Supplementary Fig. 4). Moreover, some of the identified nitrides have direct bandgaps that are advantageous for light emission and harvesting. Indirect-gap compounds with slightly larger direct gaps can also be good candidates for photoabsorbers in solar cells13,15. Identified nitrides having such indirect or direct band structures and exhibiting good matching with the solar spectrum (bandgaps of 0.8 to 1.9 eV) include LiZnN, KZnN, CaZn2N2, Sr2ZnN2, Ba2ZnN2, Zn3LaN3 and ZnSnN2 (Fig. 1a). In particular, the present study reveals the properties of Ba2ZnN2 with a theoretical indirect gap of 1.3 eV and a high absorption coefficient of 5 × 104 cm−1 near the absorption threshold at 1.5 eV, which are suited for thin-film photovoltaics (Supplementary Fig. 5). Compounds with rather wide gaps (>4 eV) together with small effective masses are of interest for potential applications in power electronics, where wider gaps allow for higher breakdown voltages. Promising systems in this respect are ZnSiN2 and Zn2PN3.

Among the identified nitrides, Ca2ZnN2 and CaZn2N2 are especially attractive due to their earth-abundant constituents, and small hole and electron effective masses. The synthesis of Ca2ZnN2 has been reported27, but the electronic properties have not thus far been established experimentally. Electronic density of states from a first-principles calculation has been reported in ref. 30 and our result shown in Fig. 2c is similar in the shape of the valence and conduction bands. Ca2ZnN2 is predicted to have an indirect-type band structure with a minimum bandgap of 1.7 eV (Figs 1a and 2b, left of panel). Ca-3d states mainly constitute electronic states near the conduction band minimum (CBM) (Fig. 2c, left of panel); nevertheless, the electron effective mass is as small as 0.5m0 for a particular direction (Σ–Γ), and a small hole effective mass of 1.0m0 is also appealing (Fig. 1b). The optical absorption spectrum shows a threshold of 2.0 eV, which is 0.3 eV above the indirect-gap (Fig. 2d, left of panel).

Figure 2: Theoretically predicted characteristics of Ca2ZnN2 and CaZn2N2.
figure 2

(a) Ca–Zn–N ternary phase diagram at 0 K and 0 GPa, showing the stable region of Ca2ZnN2 and CaZn2N2 in the chemical potential space. The chemical potentials Δμi (i=Ca, Zn and N) are relative to those at the standard states, which are taken to be the Ca and Zn metals, and the N2 molecule. The Zn3N2 phase is metastable and indicated in parenthesis. Chemical potential conditions I–IV are considered in the discussion of point-defect energetics. On the left and right sides of panel are the crystal structures of Ca2ZnN2 and CaZn2N2, respectively. The frames represent the conventional unit cells (I4/mmm (tetragonal) and (trigonal), respectively). The Ca atoms (green) and Zn atoms (white) are coordinated by five and two N atoms (yellow), respectively, in Ca2ZnN2, whereas by six and four N atoms in CaZn2N2; only Zn–N bonds are illustrated for easy visualization. (b) Electronic band structures. (c) Total and site-projected electronic densities of states per formula unit. (d) Absorption spectra (α: absorption coefficient; : photon energy). For bd, the left and right sides of each panel show results for Ca2ZnN2 and CaZn2N2, respectively.

The other ternary phase, CaZn2N2, has not been reported previously to the best of our knowledge. Our calculations predict that this phase is stable against the known competing elementary, binary and ternary phases, including Ca2ZnN2 (Fig. 2a). It takes a relatively simple trigonal structure, where the Ca and Zn atoms are coordinated by six and four N atoms, respectively (Fig. 2a). The highest valence states have an N-2p characteristic with sizable contributions of Zn and Ca orbitals (Fig. 2c, right of panel). The cation s orbitals mainly constitute electronic states near the CBM in stark contrast to the case of Ca2ZnN2. These bands show large dispersions (Fig. 2b, right of panel) and thereby yield small effective masses of 0.9m0 and 0.2m0 for heavy holes and electrons, respectively (Fig. 1b); the heavy hole effective mass is about half the value of GaN and the electron effective mass is comparable to that of GaN. The symmetrically allowed electronic transitions over the direct gap lead to a steep optical absorption threshold and slightly above that, the absorption coefficient reaches as high as 5 × 104 cm−1 (Fig. 2d, right of panel). The direct bandgap of 1.8 eV (Figs 1a and 2b, right of panel) corresponds to a red region in visible light when light emission is considered. It would also be suitable as a solar cell photoabsorber, given the theoretical photovoltaic energy conversion efficiency at the Shockley–Queisser limit is 27% for this bandgap under the air mass 1.5 G sunlight31. The bandgap can be narrowed via alloying towards a higher theoretical efficiency, as discussed later.

Experimental verification of Ca2ZnN2 and CaZn2N2

The theoretical phase diagram of the Ca–Zn–N ternary system indicates that the stable region of the newly identified CaZn2N2 phase is limited to high nitrogen chemical potential conditions. The corresponding nitrogen partial pressure is much higher than 0.1 MPa at, for instance, 800 K and above (Fig. 2a; Supplementary Figs 6 and 7; Supplementary Note 1). Therefore, we have utilized high-pressure synthesis that can allow access to such conditions. Conventional synthesis without applying external pressure successfully forms the previously reported Ca2ZnN2 (Fig. 3a) and predominantly yields this phase even with the starting composition corresponding to CaZn2N2 (Supplementary Fig. 8). Using high pressure, trigonal CaZn2N2 is obtained as the primary component with a minority presence of Zn metal (Fig. 3b; Supplementary Fig. 9; Supplementary Tables 6 and 7); the origin of Zn metal segregation is a chemical reaction between the Ca component and BN in the high-pressure cell. This result demonstrates that high-pressure synthesis is effective to realize complex nitrides that are stable only under high nitrogen partial pressure conditions. The experimentally determined lattice parameters of CaZn2N2 are a=3.46380(11) Å and c=6.00969(30) Å. These values are close to theoretically predicted lattice parameters of a=3.454 Å and c=5.990 Å, with 0.3% differences between experiment and theory for both a and c. The Ca to Zn ratio measured for a CaZn2N2 region using the electron probe micro-analyzer is 1.00(1):1.97(3), which is almost exactly the target composition.

Figure 3: Experimental verification of the Ca2ZnN2 and CaZn2N2 phases.
figure 3

Schematics of experimental set-ups and X-ray diffraction profiles for (a) a polycrystalline sample with a starting composition of Ca:Zn:N=2:1:2 aiming at the formation of the Ca2ZnN2 phase, which was encapsulated in a sealed steel tube and annealed at 680 °C for 40 h, and (b) a polycrystalline sample treated at 1200 °C and 5.0 GPa for 1 h with a starting composition of 1:2:2 corresponding to CaZn2N2. Also shown are simulated profiles that were obtained on the basis of the theoretically predicted crystal structure of CaZn2N2 and the reported crystal structures of Ca2ZnN2 and Zn. The broad peaks around 2θ=20° originate from sample capsules used in the measurements. (c) Absorption spectra of Ca2ZnN2 and CaZn2N2 derived from diffuse reflectance spectra at 300 K and the Kubelka–Munk relation (α: absorption coefficient; S: scattering factor; and : photon energy). (d) Photoluminescence (PL) from CaZn2N2: PL spectra at 10, 100, 200 and 300 K (left of panel), the temperature dependence of the PL peak position (middle of panel) and a photograph of red PL at 10 K (right of panel).

As mentioned above, our calculations predict that the previously reported Ca2ZnN2 is an indirect-type semiconductor, whereas the newly identified CaZn2N2 is direct-type. Corresponding to such differences in theoretical band structures and absorption spectra between the two phases (Fig. 2b,d), CaZn2N2 exhibits a steeper absorption threshold, with an energy of 1.9 eV at 300 K (Fig. 3c). Furthermore, red photoluminescence originating from a band-to-band transition is observed (Fig. 3d). The band-edge luminescence peak is located at 1.98 eV at 10 K and gradually shifts to lower energies with increasing temperature, down to 1.92 eV at 300 K. It should be noted that the red luminescence is visible even at room temperature (Supplementary Fig. 10) and no deep-level emissions are observed despite the polycrystalline nature. Therefore, this nitride is a promising candidate not only for a photoabsorber, but also a red light emitter. The diffuse reflectance and photoluminescence results indicate that the direct bandgap of CaZn2N2 is 1.9 eV at room temperature. This value is close to the theoretically predicted direct gap of 1.83 eV. The bandgap of the Ca2ZnN2 phase has not been reported either, and we estimate its indirect and direct gaps to be 1.6 and 1.9 eV from the diffuse reflectance, respectively, again in good agreement with the corresponding theoretical values of 1.65 and 1.92 eV. The theoretically proposed earth-abundant nitride, CaZn2N2, is thus verified experimentally, as well as Ca2ZnN2 whose fundamental properties have not been well established previously.

Predictions on the bandgap engineering of CaZn2N2

The applications of semiconductors often require tuning of bandgaps, typically via alloying. This is explored for CaZn2N2 theoretically. CaMg2N2 (ref. 32), which is a known phase isostructural to CaZn2N2, is found to be a good alloying agent (Fig. 4a). As expected from a relatively small lattice mismatch (+2.1 and +1.0% against CaZn2N2 for lattice parameters a and c, respectively), our cluster expansion and grand canonical Monte Carlo simulations predict alloy formation for the whole composition range of CaMg2xZn2(1−x)N2 (0≤x≤1) even at room temperature (Supplementary Fig. 11). The bandgap of the CaMg2xZn2(1−x)N2 alloy increases almost linearly with the Mg composition from 1.8 eV to the bandgap of CaMg2N2, 3.3 eV, preserving the direct-type band structure (Fig. 4b). This covers most of the visible light range. The hole and electron effective masses of CaMg2N2 are 1.8m0 and 0.2m0, respectively (Supplementary Table 5). These values, coupled with the similarity in valence and conduction band structures between CaZn2N2 and CaMg2N2 (Fig. 2b, right of panel; Supplementary Fig. 4v), imply that the electron effective mass does not change significantly by alloying, whereas the hole effective mass increases up to 1.8m0. We note that this value is still comparable to the hole effective mass of GaN (2.0m0).

Figure 4: Theoretical bandgaps of nitrides relevant to CaZn2N2 and its alloys.
figure 4

(a) Bandgaps of CaZn2N2 and relevant isostructural ternary nitrides versus lattice parameter a, alongside those of GaN and InN. Theoretical and experimental values are shown with open and filled symbols, respectively; the experimental gap and lattice parameter of CaZn2N2 are obtained in the present study, whereas the other experimental values are from literature (see Supplementary Tables 4 and 8 for tabulated values and references). (b) Theoretical bandgaps of CaMg2xZn2(1−x)N2 and SrxCa1−xZn2N2 (0≤x≤1) alloys. The curves are quadratic fittings to , where Eg, and are the bandgaps of the alloy and alloy components A and B, respectively. Band bowing parameters b are 0.24 and 0.17 eV for CaMg2xZn2(1−x)N2 and SrxCa1−xZn2N2, respectively.

The bandgap of CaZn2N2 can also be narrowed towards the near-infrared range. Isostructural SrZn2N2, which is previously unreported and found to be metastable with respect to decomposition into competing phases (Supplementary Fig. 3f), shows a theoretical bandgap of 1.6 eV (Fig. 4a) and the substitution of Sr for Ca reduces the bandgap of CaZn2N2 (Fig. 4b). Given the similarity in band structures and carrier effective masses between CaZn2N2 and SrZn2N2 (Fig. 2b, right of panel; Supplementary Fig. 4x; Supplementary Table 5), the changes in the effective masses by alloying are expected to be small. The predicted mutual solubility of CaZn2N2 and SrZn2N2 is limited at low temperature, compared with the CaZn2N2–CaMg2N2 system (Supplementary Fig. 12). Still, quenching from a moderate temperature (1,000 K or above) or non-equilibrium growth would allow for bandgap tuning via alloying in a wide composition range. Isostructural BaZn2N2 was also considered as an alloying agent, but is found to be unstable against lattice vibration (Supplementary Fig. 2y). Another option for bandgap narrowing is the substitution of Cd for Zn. This is expected to reduce the bandgap of CaZn2N2 substantially, given the theoretical bandgap of 0.4 eV for CaCd2N2; however, replacing too much Zn with Cd is likely to result in an excessive relaxation that leads to the breakdown of the CaZn2N2 structure (Supplementary Method 2). In addition, the use of Cd would ideally be avoided in view of the toxicity of many of Cd compounds. The bandgap of CaZn2N2 is thus most readily tuned via alloying with CaMg2N2 towards higher energies. We note that the lattice mismatch in the CaZn2N2–CaMg2N2 system (2%) is much smaller than that of the GaN–InN system (10%), as shown in Fig. 4a. This, in turn, allows for the stable alloy formation as discussed above.

Predictions on the dopability of Ca2ZnN2 and CaZn2N2

We now discuss the dopability of Ca2ZnN2 and CaZn2N2 into p and/or n type, including the effect of alloying of CaZn2N2 with CaMg2N2, based on the defect chemistry, that is, whether carrier compensation by native defects can be sufficiently suppressed and whether dopants that act as shallow accepters or donors exist. The theoretical defect energetics indicates that dominant donor-type native defects are N vacancies (VN) in both Ca2ZnN2 and CaZn2N2 (Fig. 5a,b). They form shallow donor levels, which are associated with host CBM states perturbed by the N vacancies. The formation energies of the N vacancies are relatively low under N-poor conditions, such as condition II for Ca2ZnN2 and IV for CaZn2N2. In particular, the N vacancy shows quite low formation energy in Ca2ZnN2 even with the Fermi level near the CBM, implying its native n-type characteristic when prepared under N-poor conditions. Turning to N-rich conditions, as represented by condition I, allows for the suppression of the N vacancy formation. In connection with this relatively large chemical potential dependence, our Ca2ZnN2 sample exhibits a semiconducting behaviour with an activation energy of 20 meV (Supplementary Fig. 15), whereas a previous study obtained an insulating sample27. Among acceptor-type defects, the Ca and Zn vacancies (VCa and VZn) are dominant in both nitrides. Interstitial defects (Cai, Zni and Ni) generally show high formation energies. Cation antisites are often major defects in ternary compounds, while the formation energies of Ca-on-Zn and Zn-on-Ca antisites (CaZn and ZnCa) are not significantly low (>1.2 eV) in both Ca2ZnN2 and CaZn2N2. This is presumably because of a relatively large-size mismatch between Ca(II) and Zn(II) ions. More importantly, the isovalence of Ca and Zn results in neutral and, therefore, electrically inactive antisite defects. This leads to a design principle of ternary compound semiconductors: a large-size mismatch and/or the isovalence of two types of cations are desirable to suppress the charge compensation by antisite defects.

Figure 5: Theoretical defect energetics in Ca2ZnN2, CaZn2N2 and CaMg2N2.
figure 5

The formation energies of native point defects as a function of the Fermi level for (a) Ca2ZnN2, (b) CaZn2N2 and (c) CaMg2N2 under N-rich and N-poor chemical potential conditions, corresponding to I–VI indicated in Fig. 2a and Supplementary Fig. 13. The range of the Fermi level is given by the valence band maximum, which is set to zero, and the conduction band minimum. V in defect species denotes vacancies. The subscripts designate defect sites, where i means interstitial sites. The results for two interstitial sites in Ca2ZnN2 are shown with solid and broken lines (Supplementary Fig. 14). The charge states of defects, which correspond to the gradients as defined by equation (1) in the Methods section, are described; only the most energetically favourable charge state at a given Fermi level is shown for each defect. Positive and negative charge states mean donor and acceptor behaviour of defects, respectively. The Fermi level at which the favourable charge state changes corresponds to the positions of donor or acceptor levels, which are designated by filled circles; shallow donor or acceptor levels associated with electronic states inheriting host orbital characteristics are designated by open circles. The controllable ranges of the Fermi level, in which carrier compensation by spontaneous formation of native defects is avoidable, are indicated by arrows.

The controllable range of the Fermi level is restricted by the spontaneous formation of charged native defects that compensate carriers, that is, their negative formation energies33. All defects show positive formation energies in Ca2ZnN2 under N-rich conditions as represented by condition I, irrespective of the Fermi level position. Similarly in CaZn2N2, positive formation energies are recognized for almost whole range of the Fermi level under both N-rich (III) and N-poor (IV) conditions. Therefore, electron and hole densities are not significantly limited in terms of native defect compensation, when the Fermi level is controlled towards the VBM or CBM via doping. In other words, both n- and p-type doping is feasible in both Ca2ZnN2 and CaZn2N2. The defect energetics in CaMg2N2 (Fig. 5c), in contrast, indicates that electron carrier density is limited by the compensation by cation vacancies in CaMg2xZn2(1−x)N2 alloys with a high Mg content.

The above assessment of the dopability assumes the availability of dopants that act as shallow acceptors or donors. Our calculations indeed found such dopants having small size mismatches with host ions: Na and K at the Ca site as shallow acceptors and Ga at the Zn site as a shallow donor in Ca2ZnN2, where Al at the Zn site acts as a deep donor; and Na and K at the Ca site as shallow acceptors, and Al and Ga at the Zn or Mg site as shallow donors in CaZn2N2 and CaMg2N2. Another assumption made is a thermodynamic equilibrium. The use of non-equilibrium growth and/or doping conditions can allow for the Fermi level control over the aforementioned limits.


Our high-throughput first-principles screening has identified 10 previously reported and 11 unreported nitrides as promising semiconductors. The latter class of materials includes CaZn2N2, which has a tunable direct bandgap and small effective masses, is comprised of only abundant elements, and is obtainable via high-pressure synthesis. Other predicted rare-element-free nitrides include newly identified Mg2ZnN2, ZnTiN2 and ZnZrN2, as well as Ca2ZnN2, Sr2ZnN2, Ba2ZnN2 and Zn2PN3, for which synthesis has been reported previously, but the applications as semiconductors have not been suggested to the best of our knowledge. The variety in bandgaps of the identified nitrides, coupled with small effective masses, widens the choice of nitride semiconductors that can be used in electronics, optoelectronics and photovoltaics. The present study demonstrates accelerated materials discovery via computational screening followed by targeted experiments, particularly showing high-pressure synthesis to be effective in the realization of as-yet-unreported nitrides.


Calculations of fundamental properties and stability

The first-principles calculations were conducted using the projector augmented-wave method34 and either the Perdew–Burke–Ernzerhof generalized gradient approximation (PBE-GGA) functional35 or the Heyd–Scuseria–Ernzerhof (HSE06) hybrid functional36,37, as implemented in the Vienna Ab initio Simulation Package (VASP)38,39. The PBE-GGA was used for screening in terms of thermodynamic and lattice dynamic stability. The HSE06 hybrid functional was employed for evaluating the bandgaps, carrier effective masses, electronic band structures, electronic densities of states, absorption spectra and point-defect energetics of the identified compounds. Thermodynamic stability was also investigated using HSE06 and such results for the Ca–Zn–N and Ca–Mg–N ternary systems are shown in Fig. 2a and Supplementary Fig. 13 for consistency with point-defect calculations. The phase diagrams were drawn using the CHESTA code40, where competing phases that are reported to be stable in the Materials Project database41 are considered. Plane-wave cutoff energies of 550 and 400 eV were used for the geometry optimization of perfect crystals and for the calculations of fundamental and defect properties, respectively. Even k-point meshes were used in geometry optimization, which were determined on the basis of the convergence of PBE-GGA total energies: the criterion of the total energy change was set at <0.005 meV per atom per the number of incremental k points. For instance, this results in an 8 × 8 × 4 mesh for the wurtzite GaN unit cell. Three times finer meshes were used in the calculations of electronic densities of states and absorption spectra. The bandgaps obtained using the HSE06 hybrid functional are generally close to available experimental values for relevant systems as shown in Supplementary Table 4, alongside comparison with theoretical values from the GW approximation42 to many-body perturbation theory (see also a discussion in Supplementary Note 2). Effective masses were estimated by quadratic fittings of the bands that constitute the VBM and CBM, using fine sampling of k points around the VBM and CBM. The absorption spectra were obtained via the calculations of dielectric functions within the independent particle approximation, where excitonic effects and phonon-assisted absorption were not considered. Details of the screening procedure based on these calculations are described in Supplementary Method 1.

Crystal structure prediction

The crystal structure search was performed using an evolutionary algorithm as implemented in the USPEX code12,26, in conjunction with first-principles calculations using the PBE-GGA as described above. The chemical formula for each system was fixed, but allowed to vary in multiples of between 1 and 4. The calculations were considered converged when no lower energy structure could be found after 20 generations; with each generation containing 20 individual structures.

Alloy property calculations

The phase diagrams of the CaZn2N2–CaMg2N2 and CaZn2N2–SrZn2N2 pseudobinary systems were constructed using the PBE-GGA and the cluster expansion technique43,44 in conjunction with grand canonical Monte Carlo simulations, using the CLUPAN code45. Quasi-random structures46 were employed for predicting band bowing using the HSE06 hybrid functional. More details of the alloy property calculations are given in Supplementary Method 2 and Supplementary Figs 16–21.

Modelling of point defects

Native point defects and dopants in Ca2ZnN2, CaZn2N2 and CaMg2N2 were modelled using 90-atom supercells (Supplementary Fig. 14). Atomic positions were relaxed with the cell parameters fixed at the perfect crystal values. Spin polarization was considered for odd-numbered electron systems. Defect formation energies were evaluated as47

where Ed is the total energy of a supercell containing a defect in charge state q, Ep is that of the perfect crystal supercell and Δni is the difference in the number of constituent atom i between these supercells. μi and ɛF are the chemical potential of atom i and the Fermi level, respectively. Ed and Ep are evaluated using the HSE06 hybrid functional. The finite-size effects of supercells associated with electrostatic interactions between charged defects, their periodic images and the charge compensating background were corrected using the scheme reported in refs 48, 49. Our implementation accounts for the anisotropic screening of defect charges using dielectric tensors. In addition, atomic-site local potential is used as a potential marker, which has been shown to be effective for relaxed atomic configurations49.

Synthesis of Ca2ZnN2 and CaZn2N2

Polycrystalline Ca2ZnN2 and CaZn2N2 disks and powders were prepared by solid-state reactions. Two kinds of common precursor nitrides, Ca3N2 and Zn3N2, were employed in both cases. Ca3N2 was synthesized by heating dendritic pieces of Ca metal (purity: 99.99%, Sigma-Aldrich Co. LLC.) in an electric furnace, directly connected with a glove box filled with dry inert Ar gas (dew point less than −90 °C, oxygen concentration<1 p.p.m.), at 900 °C for 10 h under N2 gas (purity: >99.9998 vol% (G2)) flow atmosphere. For Zn3N2, a commercially available reagent powder (purity: 99%, Alfa Aesar Co.) was employed.

To obtain high-purity Ca2ZnN2, the precursor powders were mixed in the glove box at the molar ratio of Ca3N2:Zn3N2=2.0:1.0 and then the mixture was uniaxially pressed into a disk (6 mm in diameter and ca. 10 mm in height), which was covered by a BN crucible and sealed in an Ar-filled stainless tube as shown in Fig. 3a. The BN crucible prevents chemical reaction between the pressed disk and the stainless tube. The stainless tube was heated at 680 °C (temperature as used in ref. 27) for 40 h. For the synthesis of CaZn2N2, we employed a belt-type high-pressure apparatus developed by Fukunaga et al.50. The precursor powders were mixed in the glove box at the molar ratio of Ca3N2:Zn3N2=1.0:2.0. The mixture was set up in a high-pressure cell composed of NaCl (10 wt% ZrO2) and BN with a carbon heater as shown in Fig. 3b. Pressure was increased to 5.0 GPa for ca. 20 min at room temperature. Temperature was then elevated to 1,200 °C in 30 min and retained for 1 h. After the high-pressure/temperature treatment, the high-pressure cell was water-cooled to room temperature and then returned to ambient pressure. We slightly polished the sample pellet by a file to obtain an unreacted and fresh bulk region of CaZn2N2 because the top surface of the pellet chemically reacted with a BN surface. The final size of the pellet was 5.5 mm in diameter and ca. 3 mm in height.

CaZn2N2 is air-stable: any decomposed and impurity phases are not observed by X-ray diffraction, when the sample is exposed at room temperature in air for 1 week. It is stable up to at least 300 °C in air and 500 °C in Ar atmosphere; oxidization occurs at 400 °C in air, and CaZn2N2 decomposes into Ca2ZnN2 at 600 °C in Ar atmosphere. On the other hand, Ca2ZnN2 rapidly decomposes into some oxides and hydroxides, such as ZnO and Ca(OH)2 in air.


Crystalline phases were determined by X-ray diffraction using a Cu Kα1+Kα2 source radiated from a rotary anode (45 kV × 360 mA, to detect a small amount of impurity phases) and a θ-coupled 2θ scan with Bragg–Brentano geometry. We used an Ar-filled O-ring-sealed sample holder in the X-ray diffraction measurements for exact assessment of formed crystalline phases. Lattice parameters were determined using the Pawley method. Structure refinement was performed using the Rietveld method. These analyses were made using TOPAS Version 4.2 (Karlsruhe, Germany: Bruker AXS). X-ray diffraction profile simulations were conducted using the RIETAN-FP code51. Chemical composition, that is, atomic ratio of Ca to Zn, was evaluated with an electron probe micro-analyzer employing a wavelength-dispersive spectroscopy mode.

Diffuse reflectance (R) spectra of the polycrystalline samples were measured in the visible–near-infrared wavelength region using a conventional spectrophotometer. To estimate the optical bandgaps, the observed diffuse reflectance spectra were converted by the Kubelka–Munk equation (1–R)2/(2R)=α/S, where α and S denote an absorption coefficient and a scattering factor, respectively. Photoluminescence spectra were measured using excitation by third harmonic generation of Nd:YAG pulsed laser (wavelength: 355 nm) with an energy density of 7 mJ cm−2.

Data availability

The authors declare that the data supporting the findings of this study are available within the article and its Supplementary Information file.

Additional information

How to cite this article: Hinuma, Y. et al. Discovery of earth-abundant nitride semiconductors by computational screening and high-pressure synthesis. Nat. Commun. 7:11962 doi: 10.1038/ncomms11962 (2016).