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具有高度改善的可见光光催化性能的多孔棒状NiTiO-BiOBr异质结

Porous Rod-like NiTiO-BiOBr Heterojunctions with Highly Improved Visible-Light Photocatalytic Performance.

作者信息

Sun Kaiyue, Li Mengchao, Zhou Hualei, Ma Xiaohui, Li Wenjun

机构信息

Beijing Key Laboratory for Science and Application of Functional Molecular and Crystalline Materials, Department of Chemistry and Chemical Engineering, University of Science and Technology Beijing, Beijing 100083, China.

出版信息

Materials (Basel). 2023 Jul 17;16(14):5033. doi: 10.3390/ma16145033.

Abstract

NiTiO-BiOBr heterostructured photocatalysts were constructed via precipitation, calcination and hydrothermal treatments. Various characterizations demonstrated that BiOBr nanosheets were decorated on NiTiO nanoparticals, forming porous rod-like heterojunctions. Compared with independent NiTiO and BiOBr, the composites with optimal BiOBr content presented highly improved visible-light photocatalytic efficiency. The degradation rates of Rhodamine B (RhB) and tetracycline (TC) reached 96.6% in 1.5 h (100% in 2 h) and 73.5% in 3 h, which are 6.61 and 1.53 times those of NiTiO, respectively. The result is an improved photocatalytic behavior from the formation of heterojunctions with a large interface area, which significantly promoted the separation of photogenerated carriers and strengthened the visible-light absorption. Based on the free radical capture experiments and band position analysis, the photodegradation mechanism of type-II heterojunction was deduced. This study provides a new way to fabricate highly efficient NiTiO-based photocatalysts for degrading certain organics.

摘要

通过沉淀、煅烧和水热法制备了NiTiO-BiOBr异质结构光催化剂。各种表征表明,BiOBr纳米片装饰在NiTiO纳米颗粒上,形成多孔棒状异质结。与单独的NiTiO和BiOBr相比,具有最佳BiOBr含量的复合材料表现出显著提高的可见光光催化效率。罗丹明B(RhB)和四环素(TC)的降解率在1.5小时内分别达到96.6%(2小时内达到100%)和3小时内达到73.5%,分别是NiTiO的6.61倍和1.53倍。这一结果是由于形成了具有大界面面积的异质结,从而改善了光催化性能,显著促进了光生载流子的分离并增强了可见光吸收。基于自由基捕获实验和能带位置分析,推导了II型异质结的光降解机理。本研究为制备用于降解某些有机物的高效NiTiO基光催化剂提供了一种新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27c0/10382046/1d5898889794/materials-16-05033-g001.jpg

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