Configurational entropy significantly influences point defect thermodynamics and diffusion in crystalline silicon

JP Luo and CY Zhou and YJ Cheng and QH Li and LJ Liu and JF Douglas and T Sinno, PHYSICAL REVIEW MATERIALS, 6, 064603 (2022).

DOI: 10.1103/PhysRevMaterials.6.064603

It has long been suggested that the familiar intrinsic point defects (vacancies and self-interstitials) encountered in crystals at low temperatures (T ) transform into extended domains characterized by a missing or excess atom compared with the same-sized region in the perfect crystal so that such extended defects may be viewed as dropletlike regions of enhanced or diminished density. However, the implications of such a transformation, or whether it even occurs in crystalline Si, remain uncertain. To address this fundamental problem, we consider a comprehensive thermodynamic analysis of the thermodynamics of vacancy and self-interstitial formation over a broad T range based on thermodynamic integration with a focus on entropic contributions. In cooled liquids, it is well known that the form of the intermolecular potential can greatly influence the configurational entropy S-c, and correspondingly, we analyze several empirical Si potentials to determine how the potential influences both the T dependence of S-c and the enthalpy and entropy of defect formation. We indeed find that the S-c associated with point defects increases significantly upon heating, consistent with the existence of extended defects. Moreover, each type of defect species gives a significantly different contribution to S-c at elevated T and to a qualitive difference in the T dependence of the entropy of defect formation in the extended defect regime. We discuss some potential consequences of these thermodynamic changes of defect formation on the T dependence of diffusion in heated crystals.

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