Hierarchical Bi2Te3 Nanostrings: Green Synthesis and Their Thermoelectric Properties

Bi2Te3 hierarchical nanostrings have been synthesized through a solvothermal approach with the assistance of sucrose. The hierarchical Bi2Te3 was supposed to be fabricated through a self‐assembly process. Te nanorods first emerge with the reduction of TeO32− followed by heterogeneous nucleation of B...

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Veröffentlicht in:Chemistry : a European journal 2018-07, Vol.24 (39), p.9765-9768
Hauptverfasser: Liu, Yu, Wang, Qishun, Pan, Jing, Sun, Yabin, Zhang, Lingling, Song, Shuyan
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Sprache:eng
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Zusammenfassung:Bi2Te3 hierarchical nanostrings have been synthesized through a solvothermal approach with the assistance of sucrose. The hierarchical Bi2Te3 was supposed to be fabricated through a self‐assembly process. Te nanorods first emerge with the reduction of TeO32− followed by heterogeneous nucleation of Bi2Te3 nanoplates on the surface and tips of Te nanorods. Te nanorods further transform into Bi2Te3 nanorods simultaneously with the nanoplates’ growth leading to a hierarchical structure. By controlling the reaction kinetics by adding different amount of ethylene glycol, the length of nanorods and the number of nanoplates could be tailored. The use of sucrose is vital to the formation of hierarchical structure because it not only serves as a template for the well‐defined growth of Te nanorods but also promotes the heterogeneous nucleation of Bi2Te3 in the self‐assembly process. The Bi2Te3 nanomaterial shows a moderate thermoelectric performance because of its hierarchical structure. This study shows a promising way to synthesize Bi2Te3‐based nanostructures through environmental friendly approach. A Bi2Te3 nanomaterial with hierarchical structure was synthesized through a green solvothermal method with the assistance of sucrose. The morphologies vary from the amount of water and ethylene glycol added. The increased grain–grain interfaces caused by hierarchical structure leading to moderate figure‐of‐merit values.
ISSN:0947-6539
1521-3765
DOI:10.1002/chem.201801611