Crystalline Structure-Dependent Mechanical and Thermoelectric Performance in Ag2Se1‐xSx System

Abstract

Self-powered wearable electronics require thermoelectric materials simultaneously with a high dimensionless figure of merit (<i>zT</i>) and good flexibility to convert the heat discharged by the human body into electricity. Ag₂(S,Se)-based semiconducting materials can well satisfy these requirements, and thus, they are attracting great attention in thermoelectric society recently. Ag₂(S,Se) crystalizes in an orthorhombic structure or monoclinic structure, depending on the detailed S/Se atomic ratio, but the relationship between its crystalline structure and mechanical/thermoelectric performance is still unclear to date. In this study, a series of Ag₂Se_1-<i>x</i> S _<i>x</i> (<i>x</i> = 0, 0.1, 0.2, 0.3, 0.4, and 0.45) samples were prepared and their mechanical and thermoelectric performance dependence on the crystalline structure was systematically investigated. <i>x</i> = 0.3 in the Ag₂Se_1-<i>x</i> S _<i>x</i> system was found to be the transition boundary between orthorhombic and monoclinic structures. Mechanical property measurement shows that the orthorhombic Ag₂Se_1-<i>x</i> S _<i>x</i> samples are brittle while the monoclinic Ag₂Se_1-<i>x</i> S <i>_x</i> samples are ductile and flexible. In addition, the orthorhombic Ag₂Se_1-<i>x</i> S _<i>x</i> samples show better electrical transport performance and higher <i>zT</i> than the monoclinic samples under a comparable carrier concentration, most likely due to their weaker electron-phonon interactions. This study sheds light on the further development of flexible inorganic TE materials.