Enhanced photocatalytic activity of BaTiO3@g-C3N4 for the degradation of methyl orange under simulated sunlight irradiation

光催化 激进的 甲基橙 光化学 光致发光 辐照 对苯二甲酸 煅烧 羟基自由基 材料科学 降级(电信) 化学 催化作用 复合材料 有机化学 电信 聚酯纤维 物理 光电子学 核物理学 计算机科学
作者
Tao Xian,Hua Yang,Lijing Di,Jianfeng Dai
出处
期刊:Journal of Alloys and Compounds [Elsevier BV]
卷期号:622: 1098-1104 被引量:187
标识
DOI:10.1016/j.jallcom.2014.11.051
摘要

BaTiO3@g-C3N4 composites were prepared by a simple mixing–calcining method. SEM observation indicates that BaTiO3 nanoparticles are uniformly assembled onto the surface of g-C3N4 platelets. The photocatalytic activity of as-prepared BaTiO3@g-C3N4 composites were evaluated by the degradation of methyl orange (MO) under simulated sunlight irradiation, revealing that the composites exhibit enhanced photocatalytic activity compared to bare BaTiO3 and g-C3N4. This can be explained by the efficient separation of the photogenerated electron–hole pairs due to the migration of the carriers between g-C3N4 and BaTiO3; as a result, electrons and holes are increasingly available for the photocatalytic reaction. Hydroxyl radicals were detected by the photoluminescence technique using terephthalic acid as a probe molecule and are found to be produced equally on the irradiated BaTiO3 particles and BaTiO3@g-C3N4 composites. The effect of benzoquinone, ammonium oxalate and ethanol on the photocatalytic efficiency was also investigated. According to the experimental results, superoxide radicals and photogenerated holes are suggested to be the main active species responsible for the dye degradation, while hydroxyl radicals play a relatively small role in the photocatalytic reaction.
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