光催化
材料科学
结晶度
拉曼光谱
光致发光
傅里叶变换红外光谱
高分辨率透射电子显微镜
漫反射红外傅里叶变换
纳米棒
单斜晶系
兴奋剂
四方晶系
光化学
分析化学(期刊)
化学工程
透射电子显微镜
纳米技术
化学
相(物质)
晶体结构
光电子学
结晶学
光学
有机化学
催化作用
复合材料
工程类
物理
作者
Manifa Noor,Fahmida Sharmin,Md. Abdullah Al Mamun,Sajjad Hasan,M. A. Hakim,M. A. Basith
标识
DOI:10.1016/j.jallcom.2021.162639
摘要
The development of metal oxide photocatalysts with improved dye degradation efficiency under natural sunlight is in increasing demand due to their superior chemical stability and cost effectiveness. In this context, Gd and Y co-doped BiVO4 having the nominal compositions Bi0.92GdxYyVO4(0.06 ≤ x ≤ 0.08; 0 ≤ y ≤ 0.02) have been synthesized via a surfactant free hydrothermal technique. The structural characterizations by X-ray diffraction, Raman spectroscopy and Fourier transform infrared spectroscopy confirmed a monoclinic to tetragonal phase transition induced by co-doping in BiVO4. High resolution transmission electron microscopy images revealed successful synthesis of Gd and Y co-doped BiVO4 with a very good crystallinity. The steady-state photoluminescence spectroscopy analysis indicated significant suppression of charge carrier recombination in the co-doped samples. Under simulated sunlight, Bi0.92Gd0.07Y0.01VO4 photocatalyst demonstrated 94% degradation of methylene blue dye (MB) within 90 min of irradiation time, which is about 4 times higher than that of pristine BiVO4 photocatalyst. This superior photocatalytic performance may be attributed to the synergistic effect of nanorod like shape of the synthesized materials, negative surface charge, and enhanced charge career lifetime of the Bi0.92Gd0.07Y0.01VO4 photocatalyst.
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