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Highly improved visible light photocatalytic activity of BiPO4 through fabricating a novel p-n heterojunction BiOI/BiPO4 nanocomposite

机译:通过制造新型的p-n异质结BiOI / BiPO4纳米复合材料,极大地提高了BiPO4的可见光光催化活性。

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摘要

Novel BiOI/BiPO4 photocatalyst with a p-n heterojunction was fabricated via a facile deposition-precipitation method. The phase structures, morphologies and optical properties of the obtained samples were studied by several characterization tools including XRD, SEM, HRTEM, BET, EDS and UV-Vis DRS. BiOI/ BiPO4 photocatalyst displayed much higher photocatalytic performance for the methyl orange (MO) degradation than the single BiPO4 and BiOI under visible light (λ >400 nm). The best photocatalytic activity of BiOI/BiPO4 with nearly 98% MO degradation located at molar percentage ratio of 40% after 2 h irradiation. Moreover, BiOI/BiPO4 could also decompose 50% of colorless phenol solution after 8 h irradiation. The enhanced photocatalytic performance can be mainly ascribed to the formation of p-n heterojunction interface in BiOI/BiPO4 which facilitates the transfer and separation of photogenerated electron-hole pairs, as well as the strong visible light absorption originating from the sensitization role of BiOI to BiPO4.
机译:通过简便的沉积-沉淀法制备了具有p-n异质结的新型BiOI / BiPO4光催化剂。用XRD,SEM,HRTEM,BET,EDS和UV-Vis DRS等多种表征工具研究了所得样品的相结构,形貌和光学性质。在可见光(λ> 400 nm)下,BiOI / BiPO4光催化剂对甲基橙(MO)的降解表现出比单一BiPO4和BiOI高得多的光催化性能。 BiOI / BiPO4的最佳光催化活性(MO降解近98%)在2 h照射后的摩尔百分比为40%。此外,BiOI / BiPO4还可在辐照8小时后分解50%的无色酚溶液。增强的光催化性能主要归因于BiOI / BiPO4中p-n异质结界面的形成,这促进了光生电子-空穴对的转移和分离,以及源自BiOI对BiPO4的敏化作用的强烈可见光吸收。

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