梯形异质结Bi2O3/BiOI的制备及降解四环素的机制研究
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国家自然科学基金项目(21769009);超轻弹性体材料绿色制造国家民委重点实验室开放项目(PT092101);广西林产化学与工程重点实验室开放项目(GXFK1904);广西科技基地和人才专项(桂科AD 18126005);湖北省“双一流”建设专项;湖北民族大学博士启动基金(MY2018B022)


Preparation of Bi2O3/BiOI step-scheme heterojunction photocatalyst and its degradation mechanism of tetracycline
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    摘要:

    以绿色焙烧方法制备梯形异质结复合材料Bi2O3/BiOI,将复合材料Bi2O3/BiOI/BiOI用于抗生素生产废水中四环素的降解,并与纯的Bi2O3/BiOI与BiOI的降解效果进行对比。以X射线衍射(XRD)、X射线光电子能谱(XPS) 对Bi2O3/BiOI/BiOI样品物相组成和形貌进行表征分析,采用分光光度法测试并计算Bi2O3/BiOI/BiOI样品降解四环素,结果显示:降解率为92.4%,一级动力学常数为0.018 59 min-1。密度泛函理论计算显示,Bi2O3/BiOI与BiOI的功函数分别为3.0、6.0 eV。梯形异质结复合材料Bi2O3/BiOI/BiOI在光催化反应时,在内建电场和能带弯曲的共同作用下,BiOI中导带上还原能力较弱的电子将与Bi2O3/BiOI价带中氧化能力较弱的空穴部分复合,从而保留较强还原以及氧化能力的光生电子和空穴,这可能是梯形异质结复合材Bi2O3/BiOI/BiOI具有较高光催化活性的原因。

    Abstract:

    Bi2O3/BiOI step-scheme heterojunction photocatalyst was synthesized with green calcination method and its degradation ability of tetracycline was investigated.The photocatalytic performance of the Bi2O3/BiOI heterojunction,Bi2O3 and BiOI was compared.The structure and morphology of the samples were characterized with X-ray diffraction (XRD),X-ray photoelectron spectrograph (XPS).The degradation rate of tetracycline was analyzed with spectrophotometry.The result of calculation showed that the degradation rate of tetracycline was 92.4% in two hours.The first order kinetic rate constant was 0.018 59 min-1.The result of calculation with density functional theory showed that the work function of Bi2O3 and BiOI was 3.0 eV and 6.0 eV,respectively.When this step-scheme heterojunction was used as a photocatalyst,the weaker electrons in the conduction band of BiOI were combined with the weaker holes in the Bi2O3 valence band under the combined effect with built-in electric field and band bending,retaining strong reducing and oxidizing ability of photoelectrons and holes,which may be the reason why Bi2O3/BiOI step-scheme heterojunction has higher photocatalytic activity.

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谭海燕,石新雨,程新华,吴德勇,江雪超,胡卫兵.梯形异质结Bi2O3/BiOI的制备及降解四环素的机制研究[J].华中农业大学学报,2021,40(6):84-90

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  • 收稿日期:2021-06-18
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  • 在线发布日期: 2021-11-30
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