Peltier devices utilizing thermoelectric (TE) materials are expected to be used for precise temperature management in 5G and next-generation communication technologies. This demand has driven efforts to develop high-TE-performance Bi2Te3-based...
GeTe is a promising mid-temperature thermoelectric compound but inevitably contains excessive Ge vacancies hindering its performance maximization. This work reveals that significant enhancement in the dimensionless figure of merit (ZT) could be realized by defect structure engineering from point defects to line and plane defects of Ge vacancies. The evolved defects including dislocations and nanodomains enhance phonon scattering to reduce lattice thermal conductivity in GeTe. The accumulation of cationic vacancies toward the formation of dislocations and planar defects weakens the scattering against electronic carriers, securing the carrier mobility and power factor. This synergistic effect on electronic and thermal transport properties remarkably increases the quality factor. As a result, a maximum ZT > 2.3 at 648 K and a record-high average ZT (300-798 K) were obtained for Bi0.07Ge0.90Te in lead-free GeTe-based compounds. This work demonstrates an important strategy for maximizing the thermoelectric performance of GeTe-based materials by engineering the defect structures, which could also be applied to other thermoelectric materials.
Pores in a solid can effectively reduce thermal conduction, but they are not favored in thermoelectric materials due to simultaneous deterioration of electrical conductivity. Conceivably, creating a porous structure may endow thermoelectric performance enhancement provided that overwhelming reduction of electrical conductivity can be suppressed. This work demonstrates such an example, in which a porous structure is formed leading to a significant enhancement in the thermoelectric figure of merit (zT). By a unique BiI3 sublimation technique, pore networks can be introduced into tetrahedrite Cu12Sb4S13‐based materials, accompanied by changes in their hierarchical structures. The addition of a small quantity of BiI3 (0.7 vol%) results in a ≈72% reduction in the lattice thermal conductivity, whereas the electrical conductivity is improved due to unexpected enhanced carrier mobility. As a result, an enhanced zT of 1.15 at 723 K in porous tetrahedrite and a high conversion efficiency of 6% at ΔT = 419 K in a fabricated segmented single‐leg based on this porous material are achieved. This work offers an effective way to concurrently modulate the electrical and thermal properties during the synthesis of high‐performance porous thermoelectric materials.
GeMnTe2 adopts a cubic rock salt structure
and is a
promising mid-temperature thermoelectric material. The pair distribution
function analysis of neutron total scattering data, however, indicates
that GeMnTe2 is locally distorted from the ideal rock salt
structure with Ge2+ cations being discordant and displaced
∼0.3 Å off the octahedron center. By alloying GeMnTe2 with SbTe, the carrier concentration can be tuned in GeMnTe2-x%SbTe (x = 15.1), leading
to converged multiple broad valence bands and a high Seebeck coefficient
of >200 μV K–1 from 300 to 823 K. The system
exhibits a large density-of-state effective mass of >10 m
e and a high weighted mobility of 80 cm2 V–1 s–1, leading to a
power factor
of 15 μWcm–1 K–2 at 823 K. The composition GeMnTe2-15.1%SbTe exhibits
very low lattice thermal conductivity of ∼0.5 Wm–1 K–1 at 823 K, attributed to the combination of
off-centering cations in the rock salt structure, Ge/Mn positional
disorder, dislocations, and abundant Ge-rich and Mn-rich nanoparticles.
A ZT value of ∼1.5 can be achieved for GeMnTe2-15.1%SbTe with a ZT
ave of 0.96
in the temperature range of 400–823 K.
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