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溶液处理的 SnSe 热电薄膜中组成变化驱动的织构化和掺杂。

Composition change-driven texturing and doping in solution-processed SnSe thermoelectric thin films.

机构信息

School of Materials Science and Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan, 44919, Republic of Korea.

School of Chemical and Biological Engineering, Institute of Chemical Processes, Seoul National University, Seoul, 08826, Republic of Korea.

出版信息

Nat Commun. 2019 Feb 20;10(1):864. doi: 10.1038/s41467-019-08883-x.

Abstract

The discovery of SnSe single crystals with record high thermoelectric efficiency along the b-axis has led to the search for ways to synthesize polycrystalline SnSe with similar efficiencies. However, due to weak texturing and difficulties in doping, such high thermoelectric efficiencies have not been realized in polycrystals or thin films. Here, we show that highly textured and hole doped SnSe thin films with thermoelectric power factors at the single crystal level can be prepared by solution process. Purification step in the synthetic process produced a SnSe-based chalcogenidometallate precursor, which decomposes to form the SnSe phase. We show that the strong textures of the thin films in the b-c plane originate from the transition of two dimensional SnSe to SnSe. This composition change-driven transition offers wide control over composition and doping of the thin films. Our optimum SnSe thin films exhibit a thermoelectric power factor of 4.27 μW cm K.

摘要

具有沿 b 轴记录高热电效率的 SnSe 单晶体的发现,导致了寻求合成具有类似效率的多晶 SnSe 的方法。然而,由于弱织构和掺杂困难,这种高热电效率在多晶或薄膜中尚未实现。在这里,我们表明,可以通过溶液法制备具有单晶级热电功率因子的高织构和空穴掺杂 SnSe 薄膜。合成过程中的净化步骤产生了基于 SnSe 的硫属化物金属酸盐前体,该前体分解形成 SnSe 相。我们表明,薄膜在 b-c 平面内的强织构源于二维 SnSe 向 SnSe 的转变。这种由组成变化驱动的转变为薄膜的组成和掺杂提供了广泛的控制。我们的最佳 SnSe 薄膜表现出 4.27 μW cm K 的热电功率因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f08a/6382880/4709ded5190c/41467_2019_8883_Fig1_HTML.jpg

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