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Codoping in SnTe: Enhancement of Thermoelectric Performance through Synergy of Resonance Levels and Band Convergence

机译:SnTe中的共掺杂:通过共振能级和能带收敛的协同作用提高热电性能

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摘要

We report a significant enhancement of the thermoelectric performance of p-type SnTe over a broad temperature plateau with a peak ZT value of ~1.4 at 923 K through In/Cd codoping and a CdS nanostructuring approach. Indium and cadmium play different but complementary roles in modifying the valence band structure of SnTe. Specifically, In-doping introduces resonant levels inside the valence bands, leading to a considerably improved Seebeck coefficient at low temperature. Cd-doping, however, increases the Seebeck coefficient of SnTe remarkably in the mid- to high-temperature region via a convergence of the light and heavy hole bands and an enlargement of the band gap. Combining the two dopants in SnTe yields enhanced Seebeck coefficient and power factor over a wide temperature range due to the synergy of resonance levels and valence band convergence, as demonstrated by the Pisarenko plot and supported by first-principles band structure calculations. Moreover, these codoped samples can be hierarchically structured on all scales (atomic point defects by doping, nanoscale precipitations by CdS nanostructuring, and mesoscale grains by SPS treatment) to achieve highly effective phonon scattering leading to strongly reduced thermal conductivities. In addition to the high maximum ZT the resultant large average ZT of ~0.8 between 300 and 923 K makes SnTe an attractive p-type material for high-temperature thermoelectric power generation.
机译:我们报道了通过In / Cd共掺杂和CdS纳米结构化方法,在宽温度范围内p型SnTe的热电性能有了显着提高,在923 K时ZT峰值为1.4。铟和镉在修饰SnTe的价带结构中起着不同但互补的作用。具体而言,In掺杂在价带内部引入了共振能级,从而导致低温下的塞贝克系数大大提高。但是,Cd掺杂会通过轻,重空穴带的会聚以及带隙的扩大,在中高温区域显着提高SnTe的塞贝克系数。由于共振能级和价带收敛的协同作用,在宽温度范围内将两种掺杂剂结合在SnTe中可产生更高的塞贝克系数和功率因数,这一点由Pisarenko图证明并得到第一性原理带结构计算的支持。而且,这些共掺杂样品可以在所有尺度上进行分层结构(通过掺杂实现原子点缺陷,通过CdS纳米结构实现纳米尺度的沉淀以及通过SPS处理实现中尺度晶粒),从而实现高效声子散射,从而大大降低热导率。除了较高的最大ZT外,所得的300至923 K之间的〜0.8的较大平均ZT使SnTe成为用于高温热电发电的有吸引力的p型材料。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2015年第15期|5100-5112|共13页
  • 作者单位

    Department of Chemistry, Northwestern University, Evanston, Illinois 60208, United States;

    Department of Materials Science and Engineering, Northwestern University, Evanston, Illinois 60208, United States;

    Department of Materials Science and Engineering, Northwestern University, Evanston, Illinois 60208, United States;

    Department of Physics, University of Michigan, Ann Arbor, Michigan 48109, United States;

    Department of Chemistry, Northwestern University, Evanston, Illinois 60208, United States;

    Department of Physics, University of Michigan, Ann Arbor, Michigan 48109, United States;

    Department of Materials Science and Engineering, Northwestern University, Evanston, Illinois 60208, United States;

    Department of Materials Science and Engineering, Northwestern University, Evanston, Illinois 60208, United States;

    Department of Chemistry, Northwestern University, Evanston, Illinois 60208, United States,Materials Science Division, Argonne National Laboratory, Argonne, Illinois 60439, United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:09:38

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