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Thermoelectric performance of Cu2Se doped with rapidly synthesized gel-like carbon dots

  • Cagri Y. Oztan
  • , Bejan Hamawandi
  • , Yiqun Zhou
  • , Sedat Ballikaya
  • , Muhammet S. Toprak
  • , Roger M. Leblanc
  • , Victoria Coverstone
  • , Emrah Celik*
  • *Corresponding author for this work
  • University of Miami
  • KTH Royal Institute of Technology
  • Istanbul University

Research output: Contribution to journalArticlepeer-review

34 Citations (Scopus)

Abstract

As an earth-abundant, inexpensive and non-toxic compound, Copper Selenide (Cu2Se) is a frequently investigated material for thermoelectric (TE) conversion applications. In this research, stoichiometric Cu2Se compounds were systematically doped with gel-like Carbon Dots (CDs), that were fabricated using a rapid and straightforward solvothermal method, at weight ratios of 2, 5 and 10%. The resultant ingots were spark plasma sintered and their TE performance was characterized. Scanning electron microscopy (SEM), energy dispersive X-Ray spectroscopy (EDX) and powder X-ray diffraction (PXRD) were used to correlate the microstructure to the TE properties. Based on these measurements, CD doping strategy on Cu2Se yielded highly compacted, single phase grains with minimal oxidation. Characterization demonstrated a continuous enhancement of TE figure of merit (ZT) to a maximum of 2.1 at the optimum dopant ratio of 2 wt %. This enhancement was mainly due to the energy filtering effect of CD interfaces along the grain boundaries, and phonon scattering which increased the Seebeck coefficient and reduce the thermal conductivity. Doping beyond 2 wt% was recorded to inhibit this improvement. This research paved the path towards broader utilization of rapidly fabricated CDs to enhance TE conversion performance.

Original languageEnglish
Article number157916
JournalJournal of Alloys and Compounds
Volume864
DOIs
Publication statusPublished - 25 May 2021
Externally publishedYes

Keywords

  • Carbon dots
  • Copper selenide
  • High efficiency
  • Thermoelectric

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