CeO2/Bi2MoO6纳米复合材料的制备及其增强光催化降解性能研究

Synthesis of CeO2/Bi2MoO6 nanocomposites and their enhanced photocatalytic degradation performance

  • 摘要: 采用水热法制备了一系列不同的CeO2/Bi2MoO6纳米复合材料,分别考察了pH值(2~9)和Ce/Bi摩尔比(3 %~10 %)等因素对其光催化性能的影响.利用X射线粉末衍射、扫描电镜、红外光谱、紫外-可见漫反射光谱、光致发光光谱、瞬态光电流-时间响应等一系列分析测试手段对催化剂的组成、结构、光电性能等进行表征.结果表明,当pH=6时,所制备的Bi2MoO6(BMO)晶体形貌为细针状,复合CeO2后形貌为厚片状,比表面积减小、晶体颗粒增大.在实验室模拟太阳光条件下(300 W氙灯)进行光催化活性测试,分别以罗丹明B(RhB)、亚甲基蓝(MB)和苯酚为模拟污染物,对复合光催化剂的光催化活性进行考察,结果表明,当CeO2的含量为5 %时呈现出最高的光催化降解活性. 5 % CeO2/BMO对RhB、MB和苯酚的光催化反应的速率常数分别为0.037 min-1、0.016 min-1和0.007 min-1,相对于纯的BMO分别提高了3.19倍、1.70倍和4.58倍.其光催化性能增强主要原因是CeO2与Bi2MoO6复合后形成异质结有利于光生电子-空穴的有效分离,从而提高了活性自由基的含量.在自由基捕获实验中,超氧根离子自由基(·O2-)、羟基自由基(·OH)和空穴(h+)参与了光催化降解,其影响顺序为:·O2->·OH>h+.

     

    Abstract: A series of CeO2/Bi2MoO6 nanocomposites were prepared by hydrothermal method. The effect of pH value (2~9) and Ce/Bi molar ratio (3 %~10 %) on the photocatalytic performance of the prepared composites were investigated. The composition, structure and photoelectric properties of the catalyst were characterized by X-ray powder diffraction, scanning electron microscopy, infrared spectroscopy, ultraviolet-visible diffuse reflectance spectroscopy, photoluminescence spectroscopy and transient photocurrent-time response spectrum, etc. The results showed that the morphology of Bi2MoO6 (BMO) crystals was needle-like at pH 6, and it became thick after recombination with CeO2. At the same time, the specific surface area reduced and the crystal particles enlarged. Photocatalytic activity of the catalyst was tested by photocatalytic degradation of Rhodamine B (RhB), methylene blue (MB) and phenol, respectively, under simulated sunlight irradiation (a 300 W Xenon lamp). The results showed that the optimal composite containing 5 % CeO2 could achieve the maximum photocatalytic degradation rate. Under the same experimental conditions, reaction rate constants of photocatalytic degradation of RhB, MB and phenol by 5 % CeO2/BMO were 0.037, 0.016 and 0.007 min-1, respectively, which were 3.19, 1.70 and 4.58 times higher than pure BMO, respectively. The enhanced photocatalytic performance was attributed to the formation of heterojunctions between CeO2 and Bi2MoO6, which were beneficial to the efficient separation of photogenerated electrons and holes. This, as a result, increased the content of active free radicals. Free radical trapping experiments showed that superoxide ion radical (O2-)、hydroxyl radical (OH) and holes (h+) all participated in the photocatalytic degradation, and their influence was in the order of O2->OH>h+.

     

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