First-principles calculations of structural and bonding properties of Li-doped tetrahedrite thermoelectrics

TL;DR

This study uses first-principles DFT calculations to explore how lithium doping affects the structural, electronic, and bonding properties of tetrahedrite, aiming to develop n-type thermoelectric materials.

Contribution

It provides detailed insights into lithium doping effects on tetrahedrite's stability, electronic structure, and potential for n-type thermoelectric applications, which was previously unexplored.

Findings

Li doping is energetically favorable in tetrahedrite.

For x>2.0, the material becomes n-type.

Li addition increases bond strain and reduces stability.

Abstract

Tetrahedrite (copper antimony sulfosalt) is promising p-type themoeletric material due to very low intrinsic thermal conductivity and moderately-high power factor, with one of the limitations being lack of n-type variant to create thermoelectric generator. In this paper, DFT calculations have been carried out to study tetrahedrite doped with Li into structural voids, LixCu12Sb4S13 (0 <= x <= 3). Enthalpies of formation shows that introduction of Li into both 6b and 24g sites is energetically favorable. Dopants in those positions differently affect rattling Cu(12e) behaviour, as well as vary in magnitude of induced local disorder. Topological analysis of charge density classifies tetrahedrite as closed-shell, ionic system of interactions with some degree of covalency. Addition of Li increases bond strain and decreases structure stability. Electronic band structure shows that for x>2.0, material becomes n-type, however results are not precisely conclusive on whether structure will be synthesizable, which should be determined experimentally.