Chemical bonding and thermodynamic properties of gallium and indium monochalcogenides. (January 2019)

• Record Type: Journal Article
• Authors: Sedmidubský, David; Sofer, Zdeněk; Huber, Štěpán; Luxa, Jan; Točík, Radek; Mahnel, Tomáš; Růžička, Květoslav
• Is Part Of: Journal of chemical thermodynamics. Volume 128(2019)
• Page Start: 97
• Page End: 102
• Publication Date: 2019-01
• Subjects: In -- Ga mohochalcogenides -- Electronic structure -- Enthalpy of formation -- Entropy -- Heat capacity; Thermodynamics -- Periodicals; Thermochemistry -- Periodicals; Thermodynamique -- Périodiques; Thermochimie -- Périodiques; Thermochemistry; Thermodynamics; Periodicals; 541.369
• DOI: 10.1016/j.jct.2018.08.013
• Languages: English
• ISSNs: 0021-9614

Abstract

Graphical abstract: Highlights: Ga and In (AIII) monochalcogenides exhibit layered structures with direct metal-metal bonding. Cohesive energies and enthalpies of formation reveal a decreasing stability downwards the AIII and chalcogen group. Entropies at 298 K show an increasing trend downwards both groups as a result of lowering of Debye and Einstein temperatures. Abstract: Monochalcogenides of heavier Group 13 (AIII) elements represent a unique family of compounds which, unlike the corresponding sesquichalcogenides, do not follow the classical valence concept. Their low-dimensional structures and semiconducting transport characteristics make them prospective candidates for various applications such as nanoelectronics, photonics and thermoelectric conversion. On the other hand, the variety of the respective phase diagrams involving several coexisting phases in narrow compositional ranges and high volatility of the components represent a challenge for their reproducible synthesis. In this study we explore the thermodynamic properties of In and Ga monochalcogenides by ab-initio density functional theory calculations of enthalpies of formation, low temperature heat capacity measurement to assess the standard entropies and differentials scanning calorimetry to obtain the temperature dependence of heat capacity above the reference temperature.