4.7 Article

SnS2-covalent organic framework Z-scheme van der Waals heterojunction for enhanced photocatalytic reduction of uranium (VI) in rare earth tailings wastewater

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 460, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2023.141756

Keywords

Covalent organic frameworks; Semiconductor; Photocatalytic reduction; Uranium; Z-scheme heterojunction

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Uranium removal by photocatalytic reduction is effectively achieved using a Z-scheme van der Waals heterojunction photocatalyst (SnS2COF) synthesized by combining covalent organic frameworks (COF) with semiconductor (SnS2). The SnS2COF heterojunction exhibits superior U (VI) reduction capacity in rare earth tailings wastewater due to wider light absorption range, more active sites, and higher electron-hole separation and transfer efficiency. Under photoexcitation, the heterojunction maintains high reducibility and avoids photocorrosion of SnS2. The organic-inorganic heterojunction design concept provides an alternative strategy to enhance photocatalytic performance.
Uranium removal by photocatalytic reduction is one of the most promising methods to reduce radioactive contamination in wastewater. Herein, a Z-scheme van der Waals heterojunction photocatalyst (SnS2COF) was synthesized in situ by combining covalent organic frameworks (COF) with semiconductor (SnS2) for U (VI) reduction in rare earth tailings wastewater. The synthesis method of van der Waals heterojunction is simple and solves the problem of no hanging bond in composite components. In this heterojunction, large areas of van der Waals interaction form high-speed electron transport channels. In addition, it is deduced that SnS2COF fits the Z-scheme heterojunction electron transport mode through the theoretical calculation of the ground state and excited state electron density difference and the related band structure. Under the photoexcitation, the direction of electron flow is reversed, which further promotes the separation of the photogenerated electron (e(-))-hole (h+) under the action of the built-in electric field, maintains the high reducibility of the conduction band, and avoids the photocorrosion of SnS2. Compared with inorganic-inorganic heterojunction, SnS2COF has a wider light ab-sorption range, more active sites, and higher e(-)-h+ separation and transfer efficiency. Therefore, it had a higher U (VI) reduction removal capacity, up to 1123.3 mg g(-1), far surpassing the SnS2 and COF counterparts under ultraviolet/visible light. And the U (VI) removal rate reached 98.5 % in rare earth tailings wastewater. The design concept of organic-inorganic heterojunction materials provides an alternative strategy for improving the photocatalytic performance.

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