Chem. J. Chinese Universities ›› 2016, Vol. 37 ›› Issue (3): 435.doi: 10.7503/cjcu20150808

• Articles: Inorganic Chemistry • Previous Articles     Next Articles

Hydrothermal Synthesis and Characterization of Sb2Te3 Nanoplates

CHAI Zhenzhen, ZHENG Wenjun*()   

  1. Key Laboratory of Advanced Energy Materials Chemistry, Ministry of Education, College of Chemistry, Collaborative Innovation Center of Chemical Science and Engineering(Tianjin), Nankai University, Tianjin 300071, China
  • Received:2015-10-22 Online:2016-03-10 Published:2016-01-24
  • Contact: ZHENG Wenjun E-mail:zhwj@nankai.edu.cn
  • Supported by:
    † Supported by the National Natural Science Foundation of China(No.21371101, 21421001), the Programme of Introducing Talents of Discipline to Universities, China(No;B12015) and the Innovation Team of the Ministry of Education of China(No;IRT13022)

Abstract:

Under hydrothermal conditions and with ethanolamine acting as the reducing agent, fractional reduction of TeO32- was realized, and Sb2Te3 nanoplates were synthesized in situ with the newly generated Te nanorods acting as tellurium source. The as-prepared product was characterized by X-ray powder diffractometer(XRD), field emission scanning electron microscope(SEM), and transmission electron microscope(TEM). Results showed that the product presents the hexastyle nanoplate structure with the thickness of about 100—200 nm and the diameter of about 0.6—1.5 μm, and has a uniform morphology and good dispersibility. The suitable conditions were that the volume ratio of water to ethanolamine was 8∶12, and the reaction lasted for 24 h at 180 ℃. By comparing the crystal structures of the elemental Te and hexagonal Sb2Te3 as well as some experimental results, that the hexagonal phase Sb2Te3 grew epitaxially on the lateral sides of newly generated Te nanorods was discussed preliminarily, and their crystal orientations were (003)Te//(003)Sb2Te3, and [110]Te//[110]Sb2Te3.

Key words: Hydrothermal synthesis, Sb2Te3 nanoplates, Morphology, Reaction mechanism

CLC Number: 

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