BiOI/BiOBr异质结催化剂的制备及光催化降解罗丹明B
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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(PT092013);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


Preparation of BiOI/BiOBr heterojunction catalyst and its photocatalytic degradation of rhodamine B
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    摘要:

    采用水热法合成异质结复合光催化材料BiOI/BiOBr,探究其对罗丹明B的降解能力,并与纯的BiOBr以及BiOI的降解情况进行比较。通过X射线衍射XRD、场发射扫描电子显微镜FESEM、紫外-可见漫反射光谱DRS以及稳态、瞬态荧光光谱PL等表征方法对合成的异质结复合光催化剂BiOI/BiOBr样品进行了结构、形貌、光学性质的表征。采用分光光度法分析罗丹明B的降解率,结果显示,BiOI/BiOBr异质结光催化材料对100 mg/L的罗丹明B有很好的降解能力,在40 min内对罗丹明B的降解率为100%,明显高于纯的BiOBr(80%)和BiOI(72%);其一级动力学速率常数为0.102 8 min-1,分别为BiOBr(0.040 3 min-1)和BiOI(0.034 4 min-1)的2.6倍和3倍。这种异质结光催化剂不仅可以有效促进光生电荷分离而且可以保持复合材料的强氧化还原能力,这可能是BiOI/BiOBr异质结高效降解罗丹明B的内在原因。

    Abstract:

    BiOI/BiOBr heterojunction composite catalytic material was synthesized with solvothermal method. Its degradation ability of rhodamine B was investigated. The photocatalytic performance of the BiOI/BiOBr heterojunction,BiOBr and BiOI was compared. The structure,morphology and optical properties of the samples were characterized by X- ray diffraction (XRD),field emission scanning electron microscopy (FESEM),UV-vis diffuse reflection spectrum (UV-vis DRS),steady-state and transient-state PL spectra. The degradation rate of rhodamine B was analyzed by spectrophotometry. The results showed that the BiOI/BiOBr heterojunction photocatalytic materials had good degradation ability to 100 mg/L rhodamine B,indicating that the degradation rate of rhodamine B was 100% in forty minutes,significantly higher than that of pure BiOBr (80%) and BiOI (72%). The first order kinetic rate constant was 0.102 8 min-1,2.6 times of BiOBr (0.040 3 min-1) and 3 times of BiOI (0.034 4 min-1),respectively. This heterojunction photocatalyst can both effectively promote the photogenerated charge separation and maintain the strong redox ability of the composites,which may be the internal reason for efficient degradation of Rhodamine B by BiOI/BiOBr heterostructures.

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谭海燕,张世龙,吴德勇,杨艳,胡卫兵. BiOI/BiOBr异质结催化剂的制备及光催化降解罗丹明B[J].华中农业大学学报,2021,40(3):187-194

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  • 收稿日期:2021-01-21
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  • 在线发布日期: 2021-06-07
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