Abstract

Derivatives of synthetic tetrahedrite, Cu12Sb4S13, are receiving increasing attention in the thermoelectric community due to their exploitation of plentiful, relatively nontoxic elements, combined with a thermoelectric performance that rivals that of PbTe-based compounds. However, traditional synthetic methods require weeks of annealing at high temperatures (450-600 °C) and periodic regrinding of the samples. Here we report a solvothermal method to produce tetrahedrite that requires only 1 day of heating at a relatively low temperature (155 °C). This allows preparation of multiple samples at once and is potentially scalable. The solvothermal material described herein demonstrates a dimensionless figure of merit (ZT) vs temperature curve comparable to that of solid-state tetrahedrite, achieving the same ZT of 0.63 at ∼720 K. As with the materials from solid-state synthesis, products from this rapid solvothermal synthesis can be improved by mixing in a 1:1 molar ratio with the Zn-containing natural mineral, tennantite, to achieve 0.9 mol equiv of Zn. This leads to a 36% increase in ZT at ∼720 K for solvothermal tetrahedrite, to 0.85.

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