On the P21/m and Pmmn pathways of the B1-B2 phase transition in NaCl:: a quantum-mechanical study

The monoclinic P2(1)/m and orthorhombic Pmmn (Watanabe et al's-type) mechanisms of the high-pressure phase transition of NaCl between the B1 (rocksalt, Fm (3) over barm) and B2 (CsCl-like, Pm (3) over barm) cubic phases were investigated by ab initio DFT techniques with all-electron localized basis sets. Enthalpy profiles versus the order parameter were computed at constant pressures of 15, 26.3 (equilibrium) and 35 GPa for each pathway. The monoclinic path shows a lower activation enthalpy at the equilibrium pressure, but at different p values (hysteresis effects) the other mechanism becomes competitive. In the P2(1)/m case, sharpjumps of structural parameters are observed along the transformation coordinate, which can be explained by a mechanism based on discontinuous sliding of alternating pairs of (100) atomic layers. This accounts also for the predicted formation of a metastable intermediate Cmcm phase with TlI-like structure, similar to that observed experimentally at high pressure in AgCl, and the relations with the KOH structure are discussed, too. On the other hand, along the Pmmn pathway the structural parameters vary quite smoothly, indicating a continuous motion of neighbouring atomic planes within the constraint of the additional mirror symmetry.