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Exploring the thermoelectric behavior of spark plasma sintered Fe7-xCoxS8 compounds

Sulfide-based materials are emerging as viable alternatives for the current state-of-the-art thermoelectric materials, which usually are composed of toxic, expensive and scarce elements. Here, a systematic study of one such inexpensive and environmentally friendly sulfide-based system, i.e. Fe7-xCox...

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Bibliographic Details
Published in:Journal of alloys and compounds 2020-04, Vol.819, p.152999, Article 152999
Main Authors: Simon, Juliette, Guélou, Gabin, Srinivasan, Bhuvanesh, Berthebaud, David, Mori, Takao, Maignan, Antoine
Format: Article
Language:English
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Summary:Sulfide-based materials are emerging as viable alternatives for the current state-of-the-art thermoelectric materials, which usually are composed of toxic, expensive and scarce elements. Here, a systematic study of one such inexpensive and environmentally friendly sulfide-based system, i.e. Fe7-xCoxS8 pyrrhotite-type compounds that were synthesized by solid-state reaction and densified by Spark Plasma Sintering are investigated for their structural and thermoelectric properties. We report that substitution of Co for Fe in pyrrhotites: (i) induces structural transition from monoclinic 4C superstructure to trigonal 3C superstructure; (ii) modifies the magnetic behavior by decreasing the magnetic ordering temperature and magnetization; (iii) alters the type of dominant charge carriers (from p-to n-type) and enhances their electrical transport properties; (iv) mitigates the phonon contribution to the thermal conductivity; and (v) amplifies the thermoelectric figure of merit when compared with that of pristine pyrrhotites. •Thermoelectric behavior of Fe7-xCoxS8 compounds are explored for the first time.•Highly densified samples are obtained after SPS (∼97% of the theoretical density).•Co-doping improves the power factor and suppresses the thermal transport (phonons).•Structural, magnetic transitions are corroborated with experimental evidences.
ISSN:0925-8388
1873-4669
DOI:10.1016/j.jallcom.2019.152999