+Advanced Search
High Pressure Synthesis and Thermoelectric Performance of CoSbS1-xSex(x=0~0.3)
DOI:
Author:
Affiliation:

Clc Number:

Fund Project:

  • Article
  • |
  • Figures
  • |
  • Metrics
  • |
  • Reference
  • |
  • Related
  • |
  • Cited by
  • |
  • Materials
  • |
  • Comments
    Abstract:

    Paracostibite (CoSbS), as a thermoelectric material, has attracted much attention recently. It has many advantages such as low cost and environment-friendly. However, the thermoelectric performance is limited by the high thermal conductivity. In addition, the preparation of this material need a long-duration heating process and a complicated process by conventional method. In this paper, CoSbS1-xSex based solid solution alloys were facile and rapidly prepared by one-step high pressure method. Their structures and thermoelectric properties were investigated. The results show that high pressure can accelerate the reaction rate and fabricate single-phase CoSbS quickly. Alloying with a small amount of Se can simultaneously optimize three thermoelectric parameters: increasing Seebeck coefficient, reducing resistivity and thermal conductivity. CoSbS0.8Se0.2 has the largest figure of merit ZT~0.25 at 673 K, which is about four times as much as that of the parent material CoSbS. Moreover, the ZT of high-pressure synthesized samples at the same temperature is higher than that of CoSbS1-xSex prepared by the traditional solid-state reaction combined with spark plasma sintering method. These results indicate that high pressure method is an effective method for preparing CoSbS based thermoelectric materials.

    Reference
    Related
    Cited by
Get Citation

[Zhu Hongyu, Yang Manman, Li Hongtao, Du Jingyang, Li Shangsheng, Hu Meihua, Hu Qiang, Du Baoli, Su taichao. High Pressure Synthesis and Thermoelectric Performance of CoSbS1-xSex(x=0~0.3)[J]. Rare Metal Materials and Engineering,2020,49(4):1422~1426.]
DOI:[doi]

Copy
Article Metrics
  • Abstract:
  • PDF:
  • HTML:
  • Cited by:
History
  • Received:December 28,2018
  • Revised:April 09,2019
  • Adopted:April 10,2019
  • Online: May 07,2020
  • Published: