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首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Design and facile one-step synthesis of FeWO4/Fe2O3 di-modified WO3 with super high photocatalytic activity toward degradation of quasi-phenothiazine dyes
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Design and facile one-step synthesis of FeWO4/Fe2O3 di-modified WO3 with super high photocatalytic activity toward degradation of quasi-phenothiazine dyes

机译:用超高光催化活性朝向准吩噻嗪染料降解的少量高光催化活性的设计与舒适的一步合成

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For most of WO3, a visible-light-driven photocatalyst, its barrier in photocatalytic degradation is the low conduction band (CB) potential that can not reduce O-2 to O-2(-) center dot and HO2 center dot radicals and thus results in fast recombination of electron/hole. With this in mind, a new active FeWO4/Fe2O3 di-modified WO3 was designed and prepared via by a straightforward but effective strategy by introducing of FeWO4 and Fe2O3 clusters (or nanoparticles) on WO3. The performance of di-modified WO3 showed super high photocatalytic activity in degrading quasi-phenothiazine dyes of Methylene blue (MB), Toluidine blue (TB), Azure I (AI) and Acridine orange (AO) under visible light irradiation, and the corresponding k values are 5.3, 4.4, 3.8 and 5.8 times larger than that of pure WO3, respectively. This improvement was mainly due to the fact that photoexcited electrons can migrate to the matching CB of firmly and highly dispersed FeWO4 and Fe2O3, then be consumed rapidly by a valence decrease from Fe3+ to Fe2+ and Fenton reaction between Fe2+ and H2O2. And the strong adsorption of Fe species toward N and S (or N) elements in quasi-phenothiazine dyes, also positively promoted the efficiency of degradation.
机译:对于大多数WO3,光催化降解中的可见光触发光催化剂是不能降低O-2( - )中心点和HO2中心点基团的低导电带(CB)电位,因此导致电子/孔的快速重组。考虑到这一点,通过在WO3上引入少量4和Fe 2 O 3簇(或纳米颗粒),通过直接但有效的策略设计和制备新的活性器的少量4 / FE2O3 Di-Demified WO3。 Di-Temified WO3的性能显示出可见光照射下亚甲基蓝(Mb),甲苯胺蓝(Tb),甲苯胺蓝(Tb),Azure I(AI)和吖啶橙(AO)的亚甲硫噻嗪染料中的超高光催化活性,并相应的K值分别比纯WO3的5.3,4.4,3.8和5.8倍。这种改进主要是由于光屏蔽的电子可以迁移到牢固和高度分散的匹配Cb的事实,然后通过Fe3 +至Fe2 +和Fe2 +和H 2 O 2之间的FENTON反应快速消耗。并且强烈吸附Fe物种在准吩噻嗪染料中的N和S(或N)元素,也促进了降解效率。

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