Novel FeVO4/Bi7O9I3 nanocomposite with enhanced photocatalytic dye degradation and photoelectrochemical properties

光催化 纳米复合材料 光电流 材料科学 罗丹明B 甲基橙 可见光谱 线性扫描伏安法 光化学 异质结 亚甲蓝 化学工程 降级(电信) 循环伏安法 核化学 纳米技术 化学 电化学 光电子学 电极 催化作用 有机化学 电信 物理化学 计算机科学 工程类
作者
Auttaphon Chachvalvutikul,Jaroon Jakmunee,Somchai Thongtem,Sila Kittiwachana,Sulawan Kaowphong
出处
期刊:Applied Surface Science [Elsevier BV]
卷期号:475: 175-184 被引量:80
标识
DOI:10.1016/j.apsusc.2018.12.214
摘要

Novel FeVO4/Bi7O9I3 nanocomposites with different weight percentages (3, 6.25, 12.5, and 25%wt) of FeVO4 were successfully synthesized by cyclic microwave irradiation, followed by wet impregnation. The applications for photocatalytic dye degradation and photoelectrochemical (PEC) were investigated. The 6.25%wt-FeVO4/Bi7O9I3 nanocomposite exhibited excellent photocatalytic degradation of methylene blue, rhodamine B, and methyl orange with decolorization efficiencies of 81.3%, 98.9%, and 94.9% within 360 min, respectively. Moreover, this nanocomposite possessed excellent reusability and stability during the photocatalytic degradation process. PEC performance in water oxidation of the 6.25%wt-FeVO4/Bi7O9I3 photoanode was evaluated by linear sweep voltammetry (LSV) measurement. Enhanced PEC performance with photocurrent density of 0.029 mA cm−2 at 1.23 V (vs. RHE) was observed under visible-light irradiation, which was ca. 3.7 times higher than that of the pure Bi7O9I3. Based on the optical characterization, energy band positions, and active species trapping experiments, a possible photocatalytic mechanism of the FeVO4/Bi7O9I3 heterojunction was discussed. The enhancement in the photocatalytic and the PEC performance ascribed to synergistic effects of visible-light absorption and a favorable “type II heterojunction” structure of the FeVO4/Bi7O9I3 nanocomposite. These were the main effects that promoted the photogenerated electrons and holes transfer across the contact interface between FeVO4 and Bi7O9I3, as well as suppressed the recombination of photogenerated electron-hole pairs and facilitated charge separation and transportation.
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