首页|WO2/Ag3VO4 Z型异质结的构建及其光催化性能

WO2/Ag3VO4 Z型异质结的构建及其光催化性能

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利用水热法和超声辅助沉淀法制备了 Z型异质结WO2/Ag3VO4复合光催化剂。采用多种表征手段对其晶体结构、形貌和性能进行了表征,并以盐酸四环素(TCH)为降解对象考察了 WO2/Ag3VO4复合催化剂的光催化活性。结果表明:简单斜方的WO2负载在单斜相的Ag3VO4表面,形成Z型异质结结构,这种结构以及Ag3VO4光腐蚀产生的Ag0,能加速无效电子-空穴对的复合,促进有效光生载流子的分离,提升WO2/Ag3VO4复合催化剂的可见光催化活性;WO2/Ag3VO4复合催化剂对TCH的降解效果明显优于纯WO2和Ag3VO4,其中5 wt%WO2/Ag3VO4的效果最好,可见光下3 h对TCH的降解率可达85。8%,且降解过程符合一级动力学反应模型。
Construction and Photocatalytic Performance of Z-scheme WO2/Ag3VO4 Heterojunction
The Z-scheme heterojunction WO2/Ag3VO4 composite photocatalyst was prepared by hydrothermal and ultrasonic assisted precipitation methods.Various characterization techniques were employed to analyze its crystal structure,morphology,and performance.The photocatalytic activity of the WO2/Ag3VO4 composite catalyst was evaluated using tetracycline hydrochloride(TCH)as the degradation target.The results revealed that simple orthorhombic WO2 was deposited onto the surface of monoclinic Ag3VO4,creating a Z-scheme heterojunction structure.This structure and the Ag0 generated by the photocorrosion of Ag3VO4 accelerated the recombination of ineffective electron-hole pairs,promoted the separation of effective photogenerated carriers,and enhanced the visible light catalytic activity of the WO2/Ag3VO4 composite catalyst.The degradation effect of the catalyst on TCH was noticeably superior to that of pure WO2 and Ag3VO4,with 5 wt%WO2/Ag3VO4 having the best performance,achieving a degradation rate of 85.8%for TCH under visible light for 3 hours.The degradation process conformed to the first-order kinetic reaction model.

Ag3VO4WO2HeterojunctionPhotocatalysisTetracycline hydrochloride

叶红勇、杜佳、刘月、王弈帆、韦怡羽、左广玲

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南阳理工学院生物与化学工程学院,南阳 473000

河南省工业微生物资源与发酵利用重点实验室,南阳 473000

Ag3VO4 WO2 异质结 光催化 盐酸四环素

国家自然科学基金

22201146

2024

中国陶瓷
中国轻工业陶瓷研究所

中国陶瓷

北大核心
影响因子:0.376
ISSN:1001-9642
年,卷(期):2024.60(8)