Structural properties and phase transformations under pressure of XTe compounds (X = Be, Mg, and Ca): The role of the exchange–correlation potential

We have performed first principles total energy calculations to investigate the structural properties and possible phase transitions under pressure of IIA–VI compounds: BeTe, MgTe and CaTe. We have considered the following possible structures: rock-salt, nickel arsenide, cesium chloride, zinc-blende, and in some cases wurtzite. Calculations are done using the periodic density functional theory. We employ the full potential linearized augmented plane wave method as implemented in the wien2k code. The exchange and correlation potential energies are treated according to the generalized gradient approximation (GGA) using the Perdew, Burke, Ernzerhof (PBE) parameterization, and the local density approximation (LDA). Our results show that the GGA calculations correctly predict the ground state structure of all three binary compounds: zinc-blende for BeTe, wurtzite/zinc-blende for MgTe, and rock-salt for CaTe. Under pressure, BeTe and MgTe transform to the nickel arsenide structure, while CaTe transforms from rock-salt to cesium chloride. Slightly different results are found using the LDA approximation. We discuss the role of the ionicity in the difference between the LDA and GGA results.

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