Stability, thermodynamic, electronic, and thermoelectric properties of triclinic Cu[formula omitted]Se structure

Abstract

The conversion of heat into electricity using the thermoelectric effect is a crucial issue to tackle the ever-increasing global energy consumption. Cu2Se is one of the high-performance thermoelectric materials due to its liquid-like atomic structure, which minimizes the phonon-derived thermal conductivity. Nevertheless, the unambiguous atomic structure of the low-temperature phase, α-Cu2Se, remains controversial. By employing a combination of theoretical approaches including an evolutionary algorithm for structural searching, density functional theory, and lattice dynamics, the α-Cu2Se phase is proposed to crystalize in the dynamically stable triclinic Cu2Se structure (s.g. P1) which can be regarded as a monoclinic polymorph (s.g. P21/c†) through slight distortion. The corresponding heat capacity (CV) and Debye temperature (ΘD) are 0.37 J/g K and 276 K, respectively, indicating low thermal conductivity in the material. The semiconducting P1 phase possesses an indirect gap of 1.0 eV. Additionally, based on the Boltzmann transportation theory, fundamental thermoelectric parameters around the transition temperature (300–500 K) are investigated. Beyond the semiconducting phase, a novel metallic phase identified as the triclinic P1̄ phase is also discovered, exhibiting a two-dimensional (2D) crystal geometry.