The fundamental challenge for enhancing
the thermoelectric performance
of n-type PbTe to match p-type counterparts is to eliminate the Pb
vacancy and reduce the lattice thermal conductivity. The Cu atom has
shown the ability to fill the cationic vacancy, triggering improved
mobility. However, the relatively higher solubility of Cu2Te limits the interface density in the n-type PbTe matrix, leading
to a higher lattice thermal conductivity. In particular, a quantitative
relationship between the precipitate scattering and the reduction
of lattice thermal conductivity in the n-type PbTe with low solubility
of Cu2Te alloys still remains unclear. In this work, trivalent
Sb atoms are introduced, aiming at decreasing the solubility of Cu
in PbTe for improving the precipitate volumetric density and ensuring
n-type degenerate conduction. Benefiting from the multiscale hierarchical
microstructures by Sb and Cu codoping, the lattice thermal conductivity
is considerably decreased to 0.38 W m–1 K–1. The Debye–Callaway model quantifies the contribution from
point defects and nano/microscale precipitates. Moreover, the mobility
increases from 228 to 948 cm2 V–1 s–1 because of the elimination of cationic vacancies.
Consequently, a high quality factor is obtained, enabling a superior
peak figure of merit ZT of ∼1.32 in n-type Pb0.975Sb0.025Te by alloying with only ∼1.2% Cu2Te. The present finding demonstrates the significant role of low-solubility
Cu2Te in advancing thermoelectrics in n-type PbTe.