Google Search

A3: High temperature materials

Priyanka Jood1, Michihiro Ohta1, Hirotaka Nishiate1, Atsushi Yamamoto1, Oleg I. Lebedev2, David Berthbaud2, Suekuni Koichiro3, Masaru Kunii1
1National Institute of Advanced Industrial Science and Technology (AIST)2Laboratoire CRISMAT3Hiroshima University

Materials with phonon-glass electron-crystal (PGEC) behaviour are becoming popular in the thermoelectric field as they are capable of having the electrical conductivity of a crystalline material and the thermal conductivity of an amorphous or a glass like material [1]. Misfit layered compounds obey perfectly this kind of PGEC behaviour and are potential candidates for thermoelectric applications [2]. (LaS)1+mTS2 (T = Cr, Nb) belongs to the misfit layered compound family with a general formula (MX)1+mTX2 (M = Sn, Pb, Bi, Sb, rare earths; X = S, Se; T = Ti, V, Cr, Nb, Ta; and m = 0.07 – 0.28) [3]. In this study we investigated the high-temperature thermoelectric properties of misfit layered n-type (LaS)1.20CrS2 and p-type (LaS)1.14NbS2. The samples were prepared by CS2 sulfurization of 6 h or 12 h duration and then consolidated using pressure-assisted sintering to produce highly and randomly oriented samples with tunable microstructures. The randomly and highly oriented natural superlattices provided ultralow lattice thermal conductivities (as low as ~0.9 W K−1 m−1 and ~0.5 W K−1 m−1, respectively, at 950 K) perpendicular to the pressing axis. The highly oriented texture produced the highest ZT of 0.14 at 950 K among the (LaS)1.20CrS2 system, whereas the weakly/randomly oriented texture produced the highest ZT of 0.15 at 950 K among the (LaS)1.14NbS2 system [4].  The ratio 1+m was also varied for both the systems and it was determined that for m=0.197, a higher ZT of 0.2 can be obtained for the Nb system at 950 K.

References

[1] G.A. Slack, CRC handbook of thermoelectrics (Ed: D.M. Rowe), CRC Press, Boca Raton, 1995, pp. 407–440.

[2] M. Ohta, S. Satoh, T. Kuzuya, S. Hirai, M. Kunii, A. Yamamoto, Acta Mater., 60, 7232 (2012).

[3] G.A. Wiegers, Prog. Solid St. Chem., 24, 1 (1996).

[4] P. Jood, M. Ohta, H. Nishiate, A. Yamamoto, O. Lebedev, D. Berthebaud, K. Suekuni, M. Kunii, Chem. Mater. (DOI: 10.1021/cm5004559)