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首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >One-pot fabrication of Bi3O4Cl/BiOCl plate-on-plate heterojunction with enhanced visible-light photocatalytic activity
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One-pot fabrication of Bi3O4Cl/BiOCl plate-on-plate heterojunction with enhanced visible-light photocatalytic activity

机译:一锅法制备Bi3O4Cl / BiOCl板对板异质结具有增强的可见光光催化活性

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摘要

Bi3O4Cl/BiOCl (B3O4C/BOC) heterojunction photocatalyst with high visible-light photocatalytic activity was synthesized by one-pot hydrothermal method. The morphology, crystal, structure, optical and photo catalytic property of the synthesized samples were characterized by XRD, SEM, HRTEM, EDX, BET, UV-vis DRS, photocurrent, PL, and etc. The B3O4C/BOC heterojunction photocatalyst exhibited higher photocatalytic activity than pure BiOCl (BOC) and Bi3O4Cl (B3O4C) for the degradation of Orange II under visible light (lambda >= 420 nm). The 0.50B(3)O(4)C/BOC-1 heterojunction exhibited the highest photocatalytic activity and its photocatalytic efficiency was 4.4-fold more than those of pure BOC. In addition, the 0.50B(3)O(4)C/BOC-1 synthesized by one-pot hydrothermal method exhibited higher photocatalytic activity than that prepared by two-step traditional synthesis method. The enhanced photocatalytic activity of the B3O4C/BOC heterostructure photocatalyst was predominantly attributed to the efficient separation of photoinduced electrons and holes. Ultimately, the results also reveal that (OH)-O-center dot and center dot O2- radicals are primarily reactive species in the photocatalytic system, which are the key factors responsible for the nearly complete mineralization of Orange II. (C) 2015 Elsevier B.V. All rights reserved.
机译:通过一锅水热法合成了具有高可见光光催化活性的Bi3O4Cl / BiOCl(B3O4C / BOC)异质结光催化剂。用XRD,SEM,HRTEM,EDX,BET,UV-vis DRS,光电流,PL等对合成样品的形貌,晶体,结构,光学和光催化性能进行了表征。B3O4C / BOC异质结光催化剂表现出较高的光催化性能。在可见光(λ> = 420 nm)下,其降解活性比纯BiOCl(BOC)和Bi3O4Cl(B3O4C)强。 0.50B(3)O(4)C / BOC-1异质结表现出最高的光催化活性,其光催化效率是纯BOC的4.4倍。此外,一锅水热法合成的0.50B(3)O(4)C / BOC-1的光催化活性高于两步传统合成法。 B 3 O 4 C / BOC异质结构光催化剂的增强的光催化活性主要归因于光致电子和空穴的有效分离。最终,结果还表明(OH)-O-中心点和O2-中心点自由基是光催化系统中的主要反应物种,这是导致Orange II几乎完全矿化的关键因素。 (C)2015 Elsevier B.V.保留所有权利。

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