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g-C3N4/Bi/Bi2WO6光催化材料的协同改性研究
引用本文:黄曦瑶,李明春,郭银彤.g-C3N4/Bi/Bi2WO6光催化材料的协同改性研究[J].无机盐工业,2022,54(12):133-138.
作者姓名:黄曦瑶  李明春  郭银彤
作者单位:沈阳工业大学材料科学与工程学院,辽宁 沈阳 110870
基金项目:国家自然科学基金项目(51874200)
摘    要:以五水合硝酸铋Bi(NO33·5H2O]为铋源、二水合钨酸钠(Na2WO4·2H2O)为钨源通过水热法制备出多孔钨酸铋(Bi2WO6),并以纳米板条堆叠形成椭球结构的类石墨相氮化碳(g-C3N4)为基底通过溶剂热法在原位还原金属铋(Bi)的同时制备出具有Z型异质结构的g-C3N4/Bi/Bi2WO6(CN/B/BWO)复合光催化材料。采用X射线衍射(XRD)、扫描电镜(SEM)、透射电镜(TEM)、氮气吸附-脱附等温线(BET)、紫外-可见吸收光谱(UV-Vis)和光致发光(PL)光谱等检测手段对制备的样品进行了表征。结果表明,金属铋可以作为类石墨相氮化碳和钨酸铋之间的电荷转移媒介,其产生的表面等离子体共振(SPR)效应可协同增强光生电子-空穴对的分离效率和载流子的迁移率,从而提升样品的光催化活性。采用350 W氙灯照射30 min,样品CN/B/BWO-0.7对盐酸四环素(TC-H)的降解率达到99.94%,并对其降解机理进行了探讨。

关 键 词:钨酸铋  异质结构  光催化  盐酸四环素  
收稿时间:2022-05-17

Study on synergistic modification of g-C3N4/Bi/Bi2WO6 photocatalyst
HUANG Xiyao,LI Mingchun,GUO Yintong.Study on synergistic modification of g-C3N4/Bi/Bi2WO6 photocatalyst[J].Inorganic Chemicals Industry,2022,54(12):133-138.
Authors:HUANG Xiyao  LI Mingchun  GUO Yintong
Affiliation:School of Materials Science and Engineering,Shenyang University of Technology,Shenyang 110870,China
Abstract:By using Bi(NO33·5H2O as the bismuth source and Na2WO4·2H2O as the tungsten source,porous Bi2WO6 was prepared by hydrothermal method,and g-C3N4/Bi/Bi2WO26(CN/B/BWO) composite photocatalyst with Z-type heterostructure was prepared by solvothermal method with g-C3N4 with ellipsoidal structure formed by stacking nano strips as substrate and in situ reduction of metal Bi.The prepared samples were characterized by X-ray diffraction(XRD),scanning electron microscopy(SEM),transmission electron microscopy(TEM),nitrogen adsorption desorption isotherm(BET),ultraviolet visible absorption spectrum(UV-vis) and photoluminescence spectrum(PL).The results showed that the metal Bi could be used as the charge transfer medium between g-C3N4 and Bi2WO6.The surface plasmon resonance(SPR) effect generated by metal Bi could synergistically enhance the separation efficiency of photogenerated electron-hole pairs and the mobility of carriers,thereby improving the photocatalytic activity of the samples.Under the irradiation of 350 W xenon lamp for 30 min,the degradation rate of tetracycline hydrochloride(TC-H) by sample CN/B/BWO-0.7 was 99.94%,and the degradation mechanism was discussed.
Keywords:Bi2WO6  heterostructure  photocatalysis  tetracycline hydrochloride  
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