紫外激光拉曼光谱法对15mol % ba取代钽酸锶1773 K的原位观察

H. Fujimori, Ippei Kawanishi, N. Matsushita
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引用次数: 2

摘要

用连续波紫外拉曼光谱系统成功地获得了15mol % ba取代的Sr2Ta2O7在1773 K温度下的拉曼光谱。尽管发生了P21Cmcm跃迁,但拉曼光谱并没有随着温度的升高而发生显著变化。目前的结果是用恒压下与温度变化有关的参数来描述的,其定义方式与格鲁尼森参数类似。位于220 cm以上的拉曼波段的参数值小于低频模式,表明这些高频模式被分配给了TaO6内部模式。由于Ta-O化学键较强,Ba取代可以诱导陶6八面体中的偶极矩和整个晶格中的铁电极化,而Ta-O - ta键角在180度范围内不会有较大偏差,从而提高了光催化性能。
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In situ Observation of 15 mol% Ba-Substituted Strontium Tantalate up to 1773 K by Ultraviolet Laser Raman Spectroscopy
Raman spectra of 15 mol% Ba-substituted Sr2Ta2O7 have been successfully obtained at temperatures up to 1773 K by a continuous-wave ultraviolet Raman spectroscopic system. The Raman spectra do not change significantly with an increase in temperature, despite the P21  Cmcm transition. The present result is described in terms of the parameter related to temperature variation at constant pressure, defined in a similar way to the Gruneisen parameter. Raman bands located above 220 cm show smaller values of the parameter than lower frequency modes, suggesting that these higher frequency modes are assigned to TaO6 internal modes. Due to the strong Ta—O chemical bonds, the dipole moments in the TaO6 octahedra and the ferroelectric polarization in the whole crystal lattice can be induced by the Ba substitution without large deviation of the Ta—O—Ta bond angles from 180, which enhances the photocatalytic performance.
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