New frontier in printed thermoelectrics: formation of β-AgSe through thermally stimulated dissociative adsorption leads to high

Printed thermoelectrics (TE) could significantly reduce the production cost of energy harvesting devices by large-scale manufacturing. However, developing a high performance printable TE material is a substantial challenge. In this work, a new one-pot synthesis and processing of high performance Ag...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2020-08, Vol.8 (32), p.16366-16375
Hauptverfasser: Mallick, Md Mofasser, Rösch, Andres Georg, Franke, Leonard, Gall, Andre, Ahmad, Sarfraz, Geßwein, Holger, Mazilkin, Andrey, Kübel, Christian, Lemmer, Uli
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Zusammenfassung:Printed thermoelectrics (TE) could significantly reduce the production cost of energy harvesting devices by large-scale manufacturing. However, developing a high performance printable TE material is a substantial challenge. In this work, a new one-pot synthesis and processing of high performance Ag 2 Se based n-type printed TE materials is reported. Structural analyses reveal that orthorhombic β-Ag 2 Se is the dominant phase in the n-type printed material compounds. For a printed material at room temperature, a breakthrough power-factor of ∼17 μW cm −1 K −2 with a record high figure-of-merit ZT ∼ 1.03 is achieved. A high average ZT , an important parameter for device applications, of ∼0.85-0.60 has been realized in the temperature range of 300 K to 400 K. Using this material for n-type legs in combination with commercially available PEDOT:PSS for p-type legs, a printed TE generator (print-TEG) of two thermocouples has been fabricated. An output voltage of 17.6 mV and a high maximum power output P max of 0.19 μW are achieved using the print-TEG at Δ T = 75 K. High figure-of-merit achieved in Ag-Se-based n-type printed film due to the formation of the β-Ag 2 Se phase via thermally stimulated dissociative adsorption.
ISSN:2050-7488
2050-7496
DOI:10.1039/d0ta05859a