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復合光催化劑Bi12O17Cl2/TiO2制備及其性能研究

28 Chen Y., Mao G.B., Tang Y.W., et al. Synthesis of core-shell nanostructured Cr2O3/C@TiO2 for photocatalytic hydrogen production J. Chinese Journal of Catalysis, 2021, 42(1): 225-234.

  • 摘要: 在室溫條件下,利用五水合三氯化鉍、氫氧化鈉、乙醇作原料合成了Bi12O17Cl2光催化劑。把TiO2與Bi12O17Cl2通過機械混合法進行復合,制備Bi12O17Cl2/TiO2復合光催化劑。通過改變Bi12O17Cl2在Bi12O17Cl2/TiO2中的質量百分含量,分別考察Bi12O17Cl2/TiO2、TiO2在紫外光和可見光條件下,對甲基橙的光催化降解效率。研究發現,當用紫外光照射1.25h時,3% Bi12O17Cl2/TiO2催化劑的紫外光催化活性最高,3% Bi12O17Cl2/TiO2光催化降解甲基橙的降解效率為100%。當用可見光照射2h時,3% Bi12O17Cl2/TiO2催化劑的可見光催化活性最高,3% Bi12O17Cl2/TiO2光催化降解甲基橙的降解率為90%。當用可見光照射2 h時,3% Bi12O17Cl2/TiO2光催化降解甲基橙溶液的COD去除率最高,其COD去除率為75%。通過對Bi12O17Cl2/TiO2光催化反應機理研究表明,二氧化鈦具有比Bi12O17Cl2更負的導帶值,TiO2也具有比Bi12O17Cl2更正的價帶值。在光照條件下,位于二氧化鈦導帶上的電子,可以向Bi12O17Cl2的導帶上遷移.。與此同時,位于二氧化鈦價帶上的空穴,可以向Bi12O17Cl2的價帶上遷移,以便使得TiO2中光生電子與空穴的復合率獲得有效降低,也就提高了Bi12O17Cl2/TiO2光催化降解率。

     

    Abstract: At room temperature,the photocatalyst of Bi12O17Cl2 was synthesized with bismuth trichloride pentahydrate, sodium hydroxide and ethanol as raw materials.Bi12O17Cl2/TiO2 of composite photocatalyst was prepared to composite TiO2 and Bi12O17Cl2 by mechanical mixing method.By changing the mass percentage content of Bi12O17Cl2 in Bi12O17Cl2/TiO2, the photocatalytic degradation efficiencies of Bi12O17Cl2/TiO2 ,TiO2 under ultraviolet and visible light conditions were investigated,respectively.By researching and finding, the UV photocatalytic activity of 3% Bi12O17Cl2/TiO2 was the highest when UV light illuminated for 1.25h, and the photocatalytic degradation efficiency of methyl orange was 100% with 3% Bi12O17Cl2/TiO2 as catalyst.When visible light illuminated for 2h, the visible light catalytic activity of 3% Bi12O17Cl2/TiO2 was the highest, and the photocatalytic degradation rate of methyl orange was 90% with 3%Bi12O17Cl2/TiO2 as catalyst.When visible light illuminated for 2 h, the COD removal rate of photocatalytic degradation of methyl orange solution was the highest by 3% Bi12O17Cl2/TiO2, and its COD removal rate was 75%.The study on the photocatalytic reaction mechanism of Bi12O17Cl2/TiO2 shows that titanium dioxide has a more negative conduction value than Bi12O17Cl2, and TiO2 also has a more corrected valence band value than Bi12O17Cl2.Under light conditions, electrons locating in the conduct band of titanium dioxide can migrate to the conduct band of Bi12O17Cl2 . At the same time, the holes locating in the valence band of titanium dioxide can migrate to the valence band of Bi12O17Cl2, so that the recombination rate of photogenerated electrons and holes in TiO2 can be effectively reduced, and the photocatalytic degradation rate of Bi12O17Cl2/TiO2 can be improved.

     

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