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Intimate Coupling AgI/AgIO<sub>3</sub> Heterojunction Photocatalysts with Excellent Visible-Light-Driven Photocatalytic Activity

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journal contribution
posted on 2021-08-27, 15:42 authored by Chao Zeng, Haojia Ding, Linping Bao, Yujing Su, Zhipeng Wang
Photodegrading toxic organic pollutants in effluents over semiconductor photocatalysts is friendly and promising. The key is to develop a universally powerful and stable photocatalyst. In this work, highly efficient AgIO<sub>3</sub>@<i>X</i> heterojunction photocatalysts, composed of AgI and AgIO<sub>3</sub> two phases, are fabricated via a facile in situ reduction method. AgIO<sub>3</sub> is reduced and then AgI is generated on the surface of AgIO<sub>3</sub>, so the interfacial interaction between AgI and AgIO<sub>3</sub> is very intimate. Introduction of AgI on the surface of AgIO<sub>3</sub> extends the photoabsorption from an ultraviolet region to a visible region and also greatly improves charge transfer, giving rise to the remarkedly enhanced photocatalysis activity under visible-light excitation over AgIO<sub>3</sub>@<i>X</i> samples relative to the pristine AgIO<sub>3</sub>. The methyl orange (MO) photodegradation rate constant of the optimal AgIO<sub>3</sub>@20% photocatalyst reaches 0.175 min<sup>–1</sup> under visible-light illumination (λ > 420 nm), about 86.5-fold enhanced compared with the pristine counterpart, outperforming most of previously reported state-of-the-art photocatalysts. Particularly, after 20 min of natural sunlight irradiation with a light intensity of 13.8 mW/cm<sup>2</sup>, the AgIO<sub>3</sub>@20% sample can rapidly decompose 81.1% of MO. The as-obtained composite photocatalysts also exhibit excellent photocatalytic activity against rhodamine B (RhB) and 2,4-dichlorophenol (2,4-DCP) under the illumination of visible light. The possible reaction pathways and the MO degradation mechanism have been systematically investigated and illustrated. The study paves a new way for designing and developing efficient visible-light-driven photocatalysts with an intimate interfacial interaction.

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