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首页> 外文期刊>Journal of Materials Science >Surfactant-assisted hydrothermal preparation of submicrometer-sized two-dimensional BiFeO3 plates and their photocatalytic activity
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Surfactant-assisted hydrothermal preparation of submicrometer-sized two-dimensional BiFeO3 plates and their photocatalytic activity

机译:表面活性剂辅助水热法制备亚微米级二维BiFeO3 板及其光催化活性

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摘要

2-Dimensional bismuth ferrite (BiFeO3) plates were hydrothermally synthesized starting from Bi(NO3)3 and Fe(NO3)3 in the presence of cetyltrimethylammonium bromide (CTAB) as a morphology directing template. The amount of CTAB was altered to study their effects on the final results. The average diameter and thickness of BiFeO3 plates were about 1.3–2 μm and 200–300 nm. X-ray diffraction (XRD), scanning electron microscopy (SEM), UV–visible diffuse reflection spectrum (UV–vis DRS) were used to investigate the samples’ crystallinity, purity, morphology, spectral features. Furthermore, the effect of the morphology on photocatalysis was also evaluated by photodecolorization of orange II under a blended-light mercury fluorescent lamp (λ ≥ 410 nm). As a result, BiFeO3 plates showed a much higher photocatalytic activity than bulk BiFeO3 for photodecolorization of orange II, suggesting potential application in photocatalysis.
机译:在十六烷基三甲基铵存在下,由Bi(NO3 )3 和Fe(NO3 )3 水热合成二维铋铁氧体(BiFeO3 )板。溴化物(CTAB)作为形态指导模板。改变CTAB的量以研究其对最终结果的影响。 BiFeO3 板的平均直径和厚度约为1.3–2μm和200–300 nm。使用X射线衍射(XRD),扫描电子显微镜(SEM),紫外可见漫反射光谱(UV-vis DRS)来研究样品的结晶度,纯度,形态,光谱特征。此外,还通过在混合光汞荧光灯(λ≥410 nm)下对橙II进行光脱色来评估形态对光催化的影响。结果表明,BiFeO3 板对橙Ⅱ的光脱色具有比块状BiFeO3 更高的光催化活性,表明其在光催化中的潜在应用。

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  • 来源
    《Journal of Materials Science 》 |2007年第16期| 6824-6827| 共4页
  • 作者单位

    School of Chemistry ampampChemical Engineering Jiangsu University Zhenjiang Jiangsu 212013 P.R. China;

    School of Chemistry ampampChemical Engineering Jiangsu University Zhenjiang Jiangsu 212013 P.R. China;

    School of Chemistry ampampChemical Engineering Jiangsu University Zhenjiang Jiangsu 212013 P.R. China;

    School of Chemistry ampampChemical Engineering Jiangsu University Zhenjiang Jiangsu 212013 P.R. China;

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