Solid-State Synthesis and Thermoelectric Properties of CuFeSe2-CuFeS2 Solid Solutions.

Thermoelectric technology, which converts heat and electricity into each other, has been attracting attention from the perspective of efficient energy utilization. Recently, eco-friendly and cost-effective Cu-based thermoelectric materials have been actively studied. In particular, efforts have been made to improve thermoelectric properties and enhance performance through the formation of solid solutions. This study examines the formation and thermoelectric properties of Cu-chalcogenide solid solutions between eskebornite (tetragonal CuFeSe₂) and chalcopyrite (tetragonal CuFeS₂), synthesized as CuFeSe_2-yS_y (y = 0-2) using solid-state synthesis. These compounds share similar crystal structures, which enable the formation of solid solutions that enhance phonon scattering and may potentially improve thermoelectric performance. As the S content (y) increased, the lattice parameters a and c decreased, attributed to the smaller ionic radius of S^2- compared to Se^2-, as X-ray diffraction analysis identified single-phase regions for 0 ≤ y ≤ 0.4 and 1.6 ≤ y ≤ 2, respectively. However, for 0.8 ≤ y ≤ 1.2, a composite phase of eskebornite and chalcopyrite formed, indicating incomplete solid solution behavior in the intermediate range. Thermoelectric measurements showed a sharp increase in electrical conductivity with increasing S content, alongside a transition in the Seebeck coefficient from positive (p-type) to negative (n-type), attributed to the intrinsic semiconducting nature of the end-member compounds. Eskebornite behaves as a p-type semiconductor, whereas chalcopyrite is n-type, and their combination affects the carrier type and concentration. Despite these changes, the power factor did not show significant improvement due to the inverse relationship between electrical conductivity and the Seebeck coefficient. The thermal conductivity decreased significantly with solid solution formation, with CuFeSe_0.4S_1.6 exhibiting the lowest value of 0.97 Wm^-1K^-1 at 623 K, a result of enhanced phonon scattering at lattice imperfections and the mass fluctuation effect. This value is lower than the thermal conductivity values of single-phase eskebornite or chalcopyrite. However, the reduction in thermal conductivity was insufficient to compensate for the modest power factor, resulting in no substantial enhancement in the thermoelectric figure of merit.