X射线光电子能谱
光催化
光降解
异质结
材料科学
拉曼光谱
热重分析
漫反射红外傅里叶变换
光谱学
高分辨率透射电子显微镜
扫描电子显微镜
光致发光
光化学
分析化学(期刊)
透射电子显微镜
化学工程
化学
纳米技术
光电子学
光学
有机化学
催化作用
物理
工程类
量子力学
复合材料
作者
Osmando F. Lopes,Kele T. G. Carvalho,Waldir Avansi,D. M. B. P. Milori,Cauê Ribeiro
出处
期刊:RSC Advances
[Royal Society of Chemistry]
日期:2018-01-01
卷期号:8 (20): 10889-10897
被引量:31
摘要
This paper describes the synthesis of Bi2O2CO3/BiVO4 heterostructures through a one-step method based on the difference in solubility between two semiconductors that possess a metal in common. The as-synthesized Bi2O2CO3/BiVO4 heterostructures were characterized by X-ray diffraction (XRD), thermogravimetric analysis (TGA), Raman spectroscopy, ultraviolet-visible diffuse reflectance spectroscopy (UV-vis DRS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), N2 physisorption, X-ray photoelectron spectroscopy (XPS) and time resolved photoluminescence spectroscopy (TRPL). The role of the heterojunction formed was evaluated by methylene blue (MB) dye and amiloride photodegradation. The formation of the heterostructure was observed indirectly by the great increase in the thermal stability of the Bi2O2CO3 phase when compared to its pure phase. The amount of heterojunctions formed between the Bi2O2CO3 and BiVO4 was tuned by vanadium precursor concentration. The proposed strategy was efficient for obtaining Bi2O2CO3/BiVO4 heterostructures with enhanced photocatalytic performance when compared to their isolated phases, MB and amiloride photodegradation occurred mainly by the action of ˙OH radicals, i.e. by an indirect mechanism. Based on TRPL spectroscopy and VB-XPS results, an enhancement of photoactivity related to an increase in the spatial separation of photo-generated electron/hole pairs was observed due to the formation of a type-II heterostructure.
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