Graduate School, Nanchang Institute of Technology, Nanchang 330099, China
| Abstract: | Thermoelectric materials have the advantage of direct interaction between thermal energy and electric energy, which has attracted extensive attention. Among them, Bi2Te3-based thermoelectric materials with medium and low temperature have attracted special attention because of their high thermoelectric figure of merit in the room temperature range. Wet chemical method is widely used as an effective method to synthesize nano thermoelectric materials, which has the advantages of simple process equipment, low reaction temperature, low energy consumption and high yield. Therefore, the wet chemical preparation methods of Bi2Te3-based thermoelectric materials are analyzed and studied in this paper. The main methods are low-temperature and low-pressure wet chemical method (conventional low-temperature wet chemical method, microwave-assisted wet chemical method, ultrasonic-assisted wet chemical method) and high-temperature and high-pressure wet chemical method (hydrothermal method, solvothermal method). The phase analysis and micro-morphology analysis of the synthesized products are carried out by means of XRD, SEM and TEM, and the related chemical reaction mechanism in the synthesis process of Bi2Te3-based thermoelectric materials is explored. By changing the experimental conditions, we hope to further optimize the preparation process and analyze the reaction mechanism of chemical synthesis. In this paper, the influence factors of nano-powder morphology are studied by wet chemical method, which is of great significance to prepare Bi2Te3-based thermoelectric materials with controllable structure, good dispersion and high purity. At the same time, the optimization mechanism of thermoelectric transport performance is discussed, and the application prospect and development trend of nano-thermoelectric materials are prospected. |
| Keywords: | Nanostructure; Thermoelectric Material; Preparation Method; Performance Optimization |
| DOI: | 10.57237/j.se.2023.04.002 |
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