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Precursor-Led Grain Boundary Engineering for Superior Thermoelectric Performance in Niobium Strontium Titanate

[Image: see text] We present a novel method to significantly enhance the thermoelectric performance of ceramics in the model system SrTi(0.85)Nb(0.15)O(3) through the use of the precursor ammonium tetrathiomolybdate (0.5–2% w/w additions). After sintering the precursor-infused green body at 1700 K f...

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Detalles Bibliográficos
Autores principales: Zhu, Yibing, Azough, Feridoon, Liu, Xiaodong, Zhong, Xiangli, Zhao, Minghao, Margaronis, Kalliope, Kar-Narayan, Sohini, Kinloch, Ian, Lewis, David J., Freer, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10020962/
https://www.ncbi.nlm.nih.gov/pubmed/36854123
http://dx.doi.org/10.1021/acsami.2c22712
Descripción
Sumario:[Image: see text] We present a novel method to significantly enhance the thermoelectric performance of ceramics in the model system SrTi(0.85)Nb(0.15)O(3) through the use of the precursor ammonium tetrathiomolybdate (0.5–2% w/w additions). After sintering the precursor-infused green body at 1700 K for 24 h in 5% H(2)/Ar, single-crystal-like electron transport behavior developed with electrical conductivity reaching ∼3000 S/cm at ∼300 K, almost a magnitude higher than that in the control sample. During processing, the precursor transformed into MoS(2), then into MoO(x), and finally into Mo particles. This limited grain growth promoted secondary phase generation but importantly helped to reduce the grain boundary barriers. Samples prepared with additions of the precursor exhibited vastly increased electrical conductivity, without significant impact on Seebeck coefficients giving rise to high power factor values of 1760 μW/mK(2) at ∼300 K and a maximum thermoelectric figure-of-merit zT of 0.24 at 823 K. This processing strategy provides a simple method to achieve high charge mobility in polycrystalline titanate and related materials and with the potential to create “phonon-glass-electron-crystal” oxide thermoelectric materials.