期刊文献+

BiOBr/BiVO_4异质结薄膜的制备及其光催化性能研究

Study of Synthesis and Photocatalytic Properties of BiOBr/BiVO_4 Heterojunction Films
下载PDF
导出
摘要 通过浸渍法在普通玻璃上制备了纯BiVO_4薄膜和BiOBr/BiVO_4异质结薄膜,运用X射线衍射仪(XRD)、扫描电子显微镜(SEM)对其晶体结构及形貌进行表征.薄膜光催化剂的XRD图谱显示:纯BiVO_4薄膜为单斜白钨矿结构,BiVO_4与BiOBr复合后,BiVO_4的晶体结构未发生改变,BiOBr为四方氟氯铅矿型,且均具有较高的结晶度和纯度.在模拟太阳光的辐射下,以亚甲基蓝染料为目标污染物,对薄膜光催化剂的光催化性能进行评价.光催化降解结果表明,在光下照射3 h后,纯BiVO_4和BiOBr/BiVO_4异质结薄膜对亚甲基蓝的光催化降解率分别为63.33%和85.14%.与纯BiVO_4薄膜相比,BiOBr/BiVO_4异质结薄膜具有更高的光催化性能. The pure BiVO4 film and BiOBr/BiVO4 heterojunction films on glass substrate have been synthesized by impregnation method. X-ray diffraction (XRD) and scanning electron microscopy (SEM) are used to characterize the crystal structure and morphology of the film photocatalysts. The XRD patterns of the film photocatalysts indicate that the crystal structure of BiVO4 is still monoclinic scheelite type after construction of BiVO4 based composite with BiOBr, and BiOBr is tetragonal matlockite type. Moreover, the samples have high crystallinity and purity. The photo- catalytic performance of the film photocatalysts are evaluated for degradation of methylene blue (MB) under simulated sunlight irradiation. The results of photocatalytic degradation show that under light irradiation after 3 h, the pho- tocatalytic degradation rate of pure BiVO, film and BiOBr/BiVO4 heterojunction film for MB is 63.33% and 85.14%, respectively. Compared with pure BiVO4 films, the BiOBr/BiVO4 heterojunction film exhibits a higher photocatalytic performance.
机构地区 昌吉学院物理系
出处 《伊犁师范学院学报(自然科学版)》 2017年第2期37-41,共5页 Journal of Yili Normal University:Natural Science Edition
基金 国家级大学生创新创业训练计划项目(201510997001) 昌吉学院研究生自主创新项目(2015YJSYB04) 国家自然科学基金地区项目(21463002)
关键词 BiOBr/BiVO4 薄膜 浸渍法 光催化 BiOBr/BiVO4 films impregnation method photocatalysis
  • 相关文献

参考文献4

二级参考文献75

  • 1刘晶冰,汪浩,张慧明,张文熊,严辉.化学浴沉积法制备高取向钒酸铋薄膜[J].无机化学学报,2007,23(7):1299-1302. 被引量:14
  • 2Stoltzfus M W, Woodward P M, Seshadri R, et al. Structure and bonding in SnWO4, PbWO4, and BiVO4: lone pairs vs inert pairs. Inorg. Chem., 2007, 46(10): 3839-3850.
  • 3Kudo A, Kato H, Tsuji I. Strategies for the development of visible-light-driven photocatalysts for water splitting. Chem. Lett., 2004, 33(12): 1534-1539.
  • 4Ricote J, Pardo L, Castro A, et al. Study of the process of mechanochemical activation to obtain aurivillius oxides with n=1. J. Solid State Chem., 2001, 160(1): 54-61.
  • 5Kudo A, Hijii S. H2 or O2 evolution from aqueous solutions on layered oxide photocatalysts consisting of Bi3+ with 6s2 configuration and d0 transition metal ions. Chem. Lett., 1999, 28(10): 1103-1104.
  • 6Tang J W, Zou Z G, Ye J H. Photocatalytic decomposition of organic contaminants by Bi2WO6 under visible light irradiation. Catal. Lett., 2004, 92(1/2): 53-56.
  • 7Fu H B, Pan C S, Yao W Q, et al. Visible-light-induced degradation of rhodamine B by nanosized Bi2WO6, J. Phys. Chem. B, 2005, 109(47): 22432-22439.
  • 8Tang J W, Zou Z G, Ye J H. Efficient photocatalytic decomposition of organic contaminants over CaBi2O4 under visible-light irradiation. Angew. Chem. Int. Edit., 2004, 43(34): 4463-4466.
  • 9Zhang C, Zhu Y F. Synthesis of square Bi2WO6 nanoplates as high-activity visible-light-driven photocatalysts. Chem. Mater., 2005, 17(13): 3537-3545.
  • 10Zhu S B, Xu T G, Fu H B, et al. Synergetic effect of Bi2WO6 photocatalyst with C60 and enhanced photoactivity under visible irradiation. Environ. Sci. Technol., 2007, 41(17): 6234-6239.

共引文献101

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部