For more than a decade strongly correlated semiconductors and Kondo insulators have been considered as potential thermoelectric materials. Such materials have large d-or f -character of the electronic band structure close to the Fermi level that theoretically leads to Seebeck coefficients (S) with large magnitudes. In this work it is shown for the first time that the strongly correlated semiconductor FeSb2 exhibits a colossal Seebeck coefficient of ∼ −45000 µVK −1 at 10 K. The thermoelectric power factor P F = S 2 • ρ −1 , where ρ is the electrical resistivity, reaches a record high value of ∼ 2300 µWK −2 cm −1 at 12 K and is 65 times larger than that of the state-of-the-art Bi2Te3-based thermoelectric materials. However, due to a large lattice thermal conductivity the dimensionless thermoelectric figure of merit is only 0.005 at 12 K. Nonetheless, the potential of FeSb2 as a future solid-state thermoelectric cooling device at cryogenic temperatures is underlined.

Organic molecules are currently investigated as redox species for aqueous low-cost redox flow batteries (RFBs). The envisioned features of using organic redox species are low cost and increased flexibility with respect to tailoring redox potential and solubility from molecular engineering of side groups on the organic redox-active species. In this paper 33, mainly quinone-based, compounds are studied experimentially in terms of pH dependent redox potential, solubility and stability, combined with single cell battery RFB tests on selected redox pairs. Data shows that both the solubility and redox potential are determined by the position of the side groups and only to a small extent by the number of side groups. Additionally, the chemical stability and possible degradation mechanisms leading to capacity loss over time are discussed. The main challenge for the development of all-organic RFBs is to identify a redox pair for the positive side with sufficiently high stability and redox potential that enables battery cell potentials above 1 V.

Eu 8 Ga 16 Ge 30 is the only clathrate known so far where the guest positions are fully occupied by a rare-earth element. Our investigations show that, in addition to the previously synthesized Eu 8 Ga 16 Ge 30 modification with clathrate-I structure, there exists a second modification with clathrate-VIII structure. Polycrystalline samples of both phases behave as local-moment ferromagnets with relatively low Curie temperatures ͑10.5 and 36 K͒. The charge-carrier concentrations are rather small ͑3.8 and 12.5ϫ10 20 cm Ϫ3 at 2 K͒ and, together with the low Curie temperatures, point to a semimetallic behavior. Both the specific heat and the thermal conductivity are consistent with the concept of guest atoms ''rattling'' in oversized host cages, leading to low thermal conductivities ͑''phonon glasses''͒. However, the electron mobilities are quite low, which, if intrinsic, would question the properties of an ''electron crystal'', commonly presumed in ''filled-cage'' materials. The dimensionless thermoelectric figure of merit reaches values of 0.01 at 100 K.

No abstract