The lamellar structure of (Bi,Sb) 2 (Te,Se) 3 alloys makes it difficult to achieve isotropic thermoelectric properties in the directions along and perpendicular to the c-axis, especially for n-type samples. In this work, by introducing Cu in polycrystalline ntype Cu x Bi 2 Te 2.7 Se 0.3 and applying the traditional synthesis process of high-energy ball milling and hot pressing, substantial enhancement of the thermoelectric figure of merit zT is obtained in both in-plane and out-of-plane directions. The intercalated Cu not only provides electron transport media for mobility improvement but also reduces the lattice thermal conductivity owing to the strain fluctuation. Typically, the van der Waals gap in the out-of-plane direction leads to relatively slower mobility and lower lattice thermal conductivity. Taking into account the same average density-of-state effective mass (m avg * ∼ 1.5m e ) predicted based on a single parabolic model, the obtained quality factor β is comparable in both directions. As a result, a peak zT ∼ 1.05 at 420 K and the average zT approaching to 1.0 in the temperature range 300−500 K are obtained in both directions for the Cu 0. 02 Bi 2 Te 2.7 Se 0.3 sample. The simple synthesis process and isotropic thermoelectric properties in this work make n-type Bi 2 Te 3 more convenient for potential production and application. KEYWORDS: n-type Bi 2 Te 2.7 Se 0.3 , isotropic, Cu doping, quality factor, thermoelectric

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AgCrSe2, which crystallizes in alternative layers of Ag+ and CrSe2− octahedral structure, has shown great potential as good thermoelectric material due to its unique ultralow lattice thermal conductivity. In this work, compound Cr2/3Te is alloyed with the matrix Ag0.97CrSe2 and the carrier concentration ranges within 1018–1020 cm−3, enabling a reliable assessment of transport properties based on single parabolic band model at room temperature. Moreover, homogeneous nanoprecipitate is observed in the matrix for high Cr2/3Te content samples, which leads to the scattering of main heat carrier of long-wavelength phonons, and thus a slight reduction of lattice thermal conductivity (∼0.3 W/m K) compared with intrinsic AgCrSe2. Combined with the optimized carrier concentration and the low lattice thermal conductivity, a figure of merit zT of 0.6 at 650 K is achieved, exceeding other reported AgCrSe2 systems, demonstrating the current Ag0.97CrSe2(Cr2/3Te)x materials as good potential thermoelectrics.

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