Atomic Level Defect Structure Engineering for Unusually High Average Thermoelectric Figure of Merit in n-Type PbSe Rivalling PbTe

Abstract

Realizing high average thermoelectric figure of merit (ZT(ave)) and power factor (PFave) has been the utmost task in thermoelectrics. Here the new strategy to independently improve constituent factors in ZT is reported, giving exceptionally high ZT(ave) and PFave in n-type PbSe. The nonstoichiometric, alloyed composition and resulting defect structures in new Pb1+xSe0.8Te0.2 (x = 0-0.125) system is key to this achievement. First, incorporating excess Pb unusually increases carrier mobility (mu(H)) and concentration (n(H)) simultaneously in contrast to the general physics rule, thereby raising electrical conductivity (sigma). Second, modifying charge scattering mechanism by the authors' synthesis process boosts a magnitude of Seebeck coefficient (S) above theoretical expectations. Detouring the innate inverse proportionality between n(H) and mu(H); and sigma and S enables independent control over them and change the typical trend of PF to temperature, giving remarkably high PFave approximate to 20 mu W cm(-1) K-2 from 300 to 823 K. The dual incorporation of Te and excess Pb generates unusual antisite Pb at the anionic site and displaced Pb from the ideal position, consequently suppressing lattice thermal conductivity. The best composition exhibits a ZT(ave) of approximate to 1.2 from 400 to 823 K, one of the highest reported for all n-type PbQ (Q = chalcogens) materials.