Phase evolution in preparing ZnSnO3 powders by precipitation method

• Published in: Applied physics. A, Materials science & processing Vol. 127; no. 2
• Main Authors: Ge, Qing, Liu, Chaoqian, Zhao, Yu, Wang, Nan, Zhang, Xiaoyang, Feng, Chuce, Zhang, Shuang, Wang, Hualin, Jiang, Weiwei, Liu, Shimin, Ding, Wanyu, Dong, Chuang
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 2021; Springer Nature B.V
• Subjects: Applied physics; Characterization and Evaluation of Materials; Condensed Matter Physics; Crystal structure; Crystallization; Decomposition reactions; Evolution; First principles; Ilmenite; Lithium niobates; Machines; Manufacturing; Materials science; Morphology; Nanotechnology; Optical and Electronic Materials; Physics; Physics and Astronomy; Precursors; Processes; Raman spectra; Raman spectroscopy; Roasting; Spectrum analysis; Surfaces and Interfaces; Thermal stability; Thin Films; Tin dioxide; Zinc stannate; Phase evolution; powder; Precipitation method; Raman spectrum; Morphology; ZnSnO
• ISSN: 0947-8396; 1432-0630
• DOI: 10.1007/s00339-020-04244-4

Previous studies on the preparation of ZnSnO 3 under normal pressure and non-epitaxy conditions are ambiguous and contradictory. Therefore, the phase evolution in preparing ZnSnO 3 powder with different calcination temperatures was systematically studied by precipitation method under normal pressure in the present work. The phase of the samples was characterized by XRD and Raman spectroscopy. Due to lacking the reliable Raman data of ZnSnO 3 in previous literatures, the Raman spectra of ZnSnO 3 with LiNbO 3 -type structure and ilmenite-type structure were simulated by first principle based on CASTEP module of Materials Studio. Moreover, the TG-DSC analysis was carried out for the as-dried precursor powder to further clarify the phase evolution. The results indicated that the phase of the as-dried precursor powder was ZnSn(OH) 6 with cubic structure and a series of decomposition reactions occurred with increasing calcination temperature. Wherein, ZnSn(OH) 6 began to decompose into ZnSnO 3 at about 170 °C, and then ZnSnO 3 began to decompose into Zn 2 SnO 4 and SnO 2 at about 320 °C. Namely, the thermal stability temperature of ZnSnO 3 should be lower than 320 °C under normal pressure. Furthermore, the beginning crystallization temperature for the decomposition-achieved Zn 2 SnO 4 and SnO 2 was about 670 °C. In addition, the morphologies of all the samples were detected by SEM, and mainly determined by the crystal structures of the phases in the samples.