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Structural and Electrical Properties of Na_XCOO_2 Thermoelectric Synthesized via Citric-Nitrate Auto-Combustion Reaction

机译:通过柠檬酸硝酸盐自燃反应合成Na_XCOO_2热电学的结构和电性能

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A series of Na_xCoO_2 thermoelectric has been successfully prepared from nanoparticles powder synthesized via citric-nitrate auto combustion reaction. In this work, the aqueous Co nitrate was mixed with a controlled concentration of aqueous Na nitrate to obtain the mixture solution with Na molar concentration, x from = 0.1 to 0.9. A calculated amount of citric acid and ammonia solutions were added to the mixture as a fuel and ignition agent for the combustion reaction respectively. The drying process at 300 °C on the hotplate with an infrared lamp at the top has turned the mixture solution into precursor gels which yielded fine ashes throughout the auto combustion reaction. The ashes are calcined at 700 °C for 1 h, pelletized by 14.2 MPa of compressive force and sintered at 900°C for 1 h. The TG/DT analysis of the gel samples show that the decomposition reaction of the Na and Co nitrates occurred in a highly exothermic single-step reaction at around 250 °C to 280 °C and left the desirable mass. The XRD analysis revealed that the calcination process has transformed the mass into pure Na_xCoO_2 phase. The atomic percentage obtained from the EDX indicated that the Na in Na_xCoO_2 yielded with expected x in each sample. The FESEM images of the calcined samples depicted two distinct microstructures appeared in samples with x ≤ 0.3 which was recognized as Na_xCoO_2 and CoO_2 phases. Whereas for the Na_xCoO_2 samples with x ≥ 0.5 a single, dense and plate-like microstructure is developed during the calcination process. The pellet sample with x = 0.7 exhibits the highest temperature dependence electrical conductivity around 690 S·cm~(-1) at 330 K compared to other samples due to effective phonon scattering center provided by Na ions by this concentration.
机译:通过纳米颗粒粉末通过柠檬酸硝酸盐自动燃烧反应合成的纳米颗粒成功制备了一系列Na_XCOO_2热电学。在这项工作中,将硝酸水溶液与受控硝酸盐水溶液混合,得到具有Na摩尔浓度的混合物溶液,X来自= 0.1至0.9。将计算出的柠檬酸和氨溶液作为燃料和点火剂加入混合物中,分别用于燃烧反应。在顶部的红外灯的加热板上在300℃下的干燥过程将混合物溶液转化为前体凝胶,其在整个自燃反应中产生细灰。将灰烬在700℃下煅烧1小时,通过14.2MPa的压缩力造粒并在900℃下烧结1小时。凝胶样品的Tg / DT分析表明,Na和硝酸盐的分解反应在高温下的单步反应中发生在约250℃至280℃并留下所需的质量。 XRD分析显示煅烧过程已将质量转化为纯Na_xCOO_2相。从EDX获得的原子百分比表明NA_XCOO_2中的NA在每个样品中产生预期的X.描绘了两个不同微结构的煅烧样品的FeSEM图像出现在具有X≤0.3的样品中,其被识别为Na_xCOO_2和COO_2相。然而,对于Na_xcoO_2样品,X≥0.5,在煅烧过程中开发单一,致密和板状微观结构。由于通过该浓度提供的有效的声子散射中心,具有x = 0.7的颗粒样品在330k上显示出约690 s·cm〜(-1)的最高温度依赖性电导率。

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