光催化
异质结
纳米团簇
甲苯
材料科学
矿化(土壤科学)
光化学
化学工程
辐照
纳米技术
化学
光电子学
有机化学
催化作用
物理
氮气
工程类
核物理学
作者
Lei Wu,Sujing Zou,Xiqiang Mao,Jun Li,Ruiting Xue,Yang Li,Shaobo Cao,Jian Yang,Ximei Fan
标识
DOI:10.1016/j.colsurfa.2024.135011
摘要
The energy band structure and corresponding carrier transfer efficiency are crucial roles in photocatalysis performance, especially involving the volatile organic compounds (VOCs) degradation in gas-solid phase photocatalytic systems. Herein, we reported a S-scheme heterojunction photocatalyst of Ag@WO 3 /TiO 2 . The photocatalytic experiments display that Ag@WO 3 /TO 2 (denoted as Ag@h-WT) possesses almost 94 % of toluene removal rate and nearly 90 % mineralization after 60 min irradiation under simulated sunlight, superior to those of pure TiO 2 and h-WO 3 as well as binary WO 3 /TO 2 heterojunction. The improved photocatalytic activity is mainly ascribed to i) the formation of S-scheme heterojunction. ii) The Ag nanoclusters promotes the carrier separation and broadens the light absorption region. ● The oxidation capacity of WO 3 /TiO 2 (S-scheme) is better retained. ● The deep mineralization of toluene is achieved by further promoting carrier separation through Ag NPs. ● Ag NPs broadens the photo-response region of the catalyst. ● The degradation mechanism of toluene was investigated.
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