| Summary: | We have investigated thermodynamic behaviors of dilute Mg-Zn-Y ternary alloys to form a unique solute-enriched stacking-fault (SESF), which is an intrinsic-II type stacking-fault (I2-SF) enriched by the Zn and Y atoms and represents the structural-unit of the long-period stacking/order (LPSO) phase. SESF in the hexagonal-close-packed (hcp) Mg matrix forms a local face-centered-cubic (fcc) environment, and hence our thermodynamic analysis is based on the Gibbs energy comparison between hcp and fcc phases over the Mg-Zn-Y ternary composition ranges, using the calculation of phase diagrams (CALPHAD) method aided by the first principles calculations. We find that the Zn/Y co-segregations at the SESF provide a remarkable condition that the fcc layers become more stable than the hcp-Mg matrix. Furthermore, within the SESF, the following spinodal-like decomposition into the Mg-rich solid-solution and the Zn/Y-rich L12-type order phase causes a significant reduction of the total Gibbs energy of the system. These spontaneous thermodynamic behaviors explain why the fault layers can be remarkably stabilized in the LPSO-forming ternary Mg alloys, and also support a phenomenological origin of the Zn-Y clustering with the L12-type short-range order, which is known to occur for the LPSO phases and has been confirmed for the present SESF by electron microscopy experiments. Keywords: Magnesium alloys, Thermodynamic analysis, Calculation of phase diagrams (CALPHAD), Solute-atom clustering, Scanning transmission electron microscopy
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