Exploring multifunctional properties of ternary chalcogenides for advanced energy applications

探索三元硫族化合物的多功能特性及其在先进能源领域的应用

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Abstract

We performed a thorough first-principles study of Mg(2)TeS and Mg(2)TeSe, including structural, electronic, optical, and transport features. Structurally, both compounds have a trigonal R3m structure with different polyhedral designs. Mg(2)TeSe shows a larger equilibrium volume, and thermodynamic parameter (E(coh) ≈ - 3.65 eV/atom for Mg(2)TeS and - 3.79 eV/atom for Mg(2)TeSe; ΔHf ≈ - 2.17 and - 2.53 eV/atom) indicate both are energetically valuable, with Mg(2)TeSe relatively more stable. Electronically, these materials are found as direct band gap semiconductors. The WC-GGA underestimated band gaps with values of (≈ 1.49 eV and 1.83 eV), which were then corrected by SOC + TB-mBJ with values of (≈ 2.64 eV and 2.71 eV) for Mg(2)TeS and Mg(2)TeSe, respectively. Projected density of states indicates valence bands are dominated by Te states and conduction bands by Mg states, and replacing S with Se narrows the band gap while shifting density of states toward the Fermi level. Optically, notable interband responses occur with ε(1)(ω) and refractive index maxima between 5.0 and 5.5 eV, ε(2)(ω) peaks ≈ 5.5-5.8 eV, static refractive index ≈ 2.1, absorption peaking at ≈ 4.0 eV (Mg(2)TeS) and ≈ 3.5 eV (Mg(2)TeSe), low static reflectivity (~ 0.12), and plasmonic loss peaks near 17.0 and 16.0 eV. The transport results demonstrate modest Seebeck at low T, electrical conductivity σ/τ ≈ 2.27 × 10(19) and 2.24 × 10(19) (Ω·m·s)(-1) at 300 K, lower lattice thermal conductivity and a greater power factor for Mg₂TeSe, and ZT increasing with temperature to maxima ≈ 0.32 (Mg(2)TeS) and 0.24 (Mg(2)TeSe) at 1200 K, illustrating Mg(2)TeSe's promise for thermoelectric applications.

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