Bi2ZnOB2O6晶体生长的高温拉曼光谱分析

IF 1.1 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Ji Zhang, Daojun Liu
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引用次数: 0

摘要

晶体生长的微观机理作为一门基础学科受到了广泛的关注。然而,晶体生长过程的原位观察仍然具有挑战性。在本研究中,利用高温拉曼光谱通过原位探测晶体-溶液界面附近的起始溶液结构来研究Bi2ZnOB2O6晶体的生长模式。实验结果表明,溶液主要由370、539、664和1293 cm-1振动频率对应的ZO4和BO3单元组成。这些单元相互连接,在靠近晶体的区域形成更长的链,它们与拉曼光谱中低波数振动的存在有关。此外,由于形成了Bi-O键,在晶体-溶液界面附近观察到Bi2ZnOB2O6晶体松散的胚胎结构。因此,本研究成功地为Bi2ZnOB2O6晶体的形成机制提供了清晰的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High temperature Raman spectroscopic analysis of the crystal growth of Bi2ZnOB2O6
Micromechanism of crystal growth has received considerable attention as a fundamental subject. However, in situ observation of the crystal growth process remains challenging. In this study, high-temperature Raman spectroscopy has been utilized to investigate the growth pattern of Bi2ZnOB2O6 crystals via in situ exploration of the starting solution structure near the crystal-solution interface. The experimental results show that the solution primarily consists of ZO4 and BO3 units corresponding to 370, 539, 664, and 1293 cm-1 vibration frequencies. These units connect with each other forming longer chains in the area close to the crystal, and they are related to the presence of low-wavenumber vibrations in the Raman spectrum. Furthermore, a loose embryonic structure of the Bi2ZnOB2O6 crystal is observed near the crystal-solution interface owing to the formation of Bi-O bonds. Therefore, this study successfully provides a clear understanding of the formation mechanism of Bi2ZnOB2O6 crystals.
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来源期刊
Canadian Journal of Chemistry
Canadian Journal of Chemistry 化学-化学综合
CiteScore
1.90
自引率
9.10%
发文量
99
审稿时长
1 months
期刊介绍: Published since 1929, the Canadian Journal of Chemistry reports current research findings in all branches of chemistry. It includes the traditional areas of analytical, inorganic, organic, and physical-theoretical chemistry and newer interdisciplinary areas such as materials science, spectroscopy, chemical physics, and biological, medicinal and environmental chemistry. Articles describing original research are welcomed.
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