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Bi2O2CO3 Growth at Room Temperature: In Situ X-ray Diffraction Monitoring and Thermal Behavior

机译:Bi 2 O 2 CO 3 在室温下的生长:原位X射线衍射监测和热行为

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The room-temperature formation of bismuth oxycarbonate (Bi_(2)O_(2)CO_(3)) from Bi_(2)O_(3) in sodium carbonate buffer was investigated with in situ powder X-ray diffraction (PXRD) in combination with electron microscopy and vibrational spectroscopy. Time-resolved PXRD measurements indicate a pronounced and rather complex pH dependence of the reaction mechanism. Bi_(2)O_(2)CO_(3) formation proceeds within a narrow window between pH 8 and 10 via different mechanisms. Although a zero-dimensional nucleation model prevails around pH 8, higher pH values induce a change toward a diffusion-controlled model, followed by a transition to regular nucleation kinetics. Ex situ synthetic and spectroscopic studies confirm these trends and demonstrate that in situ monitoring affords vital parameter information for the controlled fabrication of Bi_(2)O_(2)CO_(3) materials. Furthermore, the β → α bismuth oxide transformation temperatures of Bi_(2)O_(2)CO_(3) precursors obtained from different synthetic routes differ notably (by min 50 °C) from commercially available bismuth oxide. Parameter studies suggest a stabilizing role of surface carbonate ions in the as-synthesized bismuth oxide sources. Our results reveal the crucial role of multiple preparative history parameters, especially of pH value and source materials, for the controlled access to bismuth oxide-based catalysts and related functional compounds.
机译:结合粉末X射线衍射(PXRD)研究了碳酸钠缓冲液中Bi_(2)O_(3)在室温下由碳酸铋(Bi_(2)O_(2)CO_(3))的形成。电子显微镜和振动光谱法。时间分辨的PXRD测量表明反应机理对pH的依赖性很强。 Bi_(2)O_(2)CO_(3)的形成通过不同的机理在pH 8和10之间的狭窄窗口内进行。尽管零维成核模型在pH值8左右普遍存在,但较高的pH值会导致向扩散控制模型的转变,然后过渡到规则成核动力学。异位合成和光谱研究证实了这些趋势,并证明了原位监测为Bi_(2)O_(2)CO_(3)材料的受控制造提供了重要的参数信息。此外,从不同合成途径获得的Bi_(2)O_(2)CO_(3)前体的β→α氧化铋转变温度与市售氧化铋有显着差异(至少50°C)。参数研究表明表面碳酸根离子在合成的氧化铋源中具有稳定作用。我们的研究结果揭示了多种制备历史参数(尤其是pH值和原料)的关键作用,对于受控获取基于氧化铋的催化剂和相关功能化合物至关重要。

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