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In Situ Reaction Induced Core–Shell Structure to Ultralow κlat and High Thermoelectric Performance of SnTe

机译:原位反应诱导的核壳结构对超低κlat和SnTe的高热电性能

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摘要

Lead‐free chalcogenide SnTe has been demonstrated to be an efficient medium temperature thermoelectric (TE) material. However, high intrinsic Sn vacancies as well as high thermal conductivity devalue its performance. Here, β‐Zn Sb is incorporated into the SnTe matrix to regulate the thermoelectric performance of SnTe. Sequential in situ reactions take place between the β‐Zn Sb additive and SnTe matrix, and an interesting “core–shell” microstructure (Sb@ZnTe) is obtained; the composition of SnTe matrix is also tuned and thus Sn vacancies are compensated effectively. Benefitting from the synergistic effect of the in situ reactions, an ultralow κ ≈0.48 W m K at 873 K is obtained and the carrier concentrations and electrical properties are also improved successfully. Finally, a maximum ZT ≈1.32, which increases by ≈220% over the pristine SnTe, is achieved in the SnTe‐1.5% β‐Zn Sb sample at 873 K. This work provides a new strategy to regulate the TE performance of SnTe and also offers a new insight to other related thermoelectric materials.
机译:无铅硫属元素化物SnTe已被证明是一种有效的中温热电(TE)材料。然而,高的固有锡空位以及高的热导率降低了其性能。在这里,β-ZnSb被掺入SnTe基质中以调节SnTe的热电性能。在β-ZnSb添加剂和SnTe基质之间发生顺序的原位反应,并获得了有趣的“核-壳”微结构(Sb @ ZnTe)。 SnTe基体的组成也被调整,从而有效地补偿了Sn空位。得益于原位反应的协同作用,在873 K处获得了超低κ≈0.48W m K,并且载流子浓度和电性能也得到了成功改善。最后,在873 K的SnTe-1.5%β-ZnSb样品中,最大ZT≈1.32,比原始SnTe高出≈220%。这项工作为调节SnTe和TE的TE性能提供了新的策略。也为其他相关的热电材料提供了新的见解。

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