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基于废用 S 型异质结光催化剂 BiOI/PCN/茶渣生物炭的可见光驱动光降解亚甲基蓝和盐酸多西环素。

Visible-light-driven photodegradation of methylene blue and doxycycline hydrochloride by waste-based S-scheme heterojunction photocatalyst BiOI/PCN/tea waste biochar.

机构信息

School of Advanced Chemical Sciences, Shoolini University, Solan, Himachal Pradesh, 173212, India.

Department of Organic Chemistry, Bioorganic Chemistry and Biotechnology, Silesian University of Technology, B. Krzywoustego 4, 44-100, Gliwice, Poland.

出版信息

Chemosphere. 2024 Jan;347:140694. doi: 10.1016/j.chemosphere.2023.140694. Epub 2023 Nov 15.

Abstract

Herein, we have reported a photocatalytic BiOI, protonated g-CN heterojunction with directional charge transfer channels provided by tea waste biochar to achieve effective e/h pair isolation for the improved degradation of Methylene blue (MB) and Doxycycline hydrochloride (DCHCl). An S-scheme heterojunction was fabricated via the novel method that combined hydrothermal and ultrasonic dispersion, followed by an electrostatic self-assembly route. The as-fabricated BiOI/protonated g-CN/Tea waste biochar heterojunction formed a strong contact at the interface, as supported by the electron microscopic results. As per the adsorption and photocatalytic degradation kinetics study, BiOI/Tea waste biochar/protonated g-CN (40 wt%) heterojunction showed a higher adsorption rate of 41.56% and 32% for MB and DCHCl within 30 min in the dark. Also, 92.02% MB and 90.21% DCHCl degradation rates in 60 and 90 min, respectively, are approximately 43 and 32 times higher than bare BiOI and protonated g-CN photocatalysts. The highest adsorption and degradation rate was achieved owing to the addition of Tea waste biochar and protonated g-CN in a controlled ratio, and the sufficient interfacial contact between BiOI and protonated g-CN is for the improved isolation rate of e/h pairs as evidenced by zeta potential values photoluminescence spectra as well as from scanning and transmission electron microscopy. Moreover, BiOI/Tea waste biochar/protonated g-CN (40 wt%) possessed high stability and recyclability after four consecutive cycles without much altering the degradation ability. Therefore, we believe that the as-fabricated BiOI/Tea waste biochar/protonated g-CN (40 wt%) provides new insight into the highly efficient S-scheme mechanisms significant for accelerating multicomponent photocatalytic redox reactions; while forming an effective visible light responsive candidate for treating wastewater.

摘要

在此,我们报道了一种光催化 BiOI 与质子化 g-CN 的异质结,其中提供了由茶废料生物炭构成的定向电荷转移通道,以实现有效的 e/h 对隔离,从而有效降解亚甲基蓝(MB)和盐酸多西环素(DCHCl)。通过将水热法和超声分散法相结合,然后采用静电自组装的方法,制备了 S 型异质结。电子显微镜结果表明,所制备的 BiOI/质子化 g-CN/茶废料生物炭异质结在界面处形成了牢固的接触。根据吸附和光催化降解动力学研究,BiOI/茶废料生物炭/质子化 g-CN(40wt%)异质结在黑暗中 30 分钟内对 MB 和 DCHCl 的吸附率分别为 41.56%和 32%。此外,60 和 90 分钟时,MB 和 DCHCl 的降解率分别高达 92.02%和 90.21%,分别约为 bare BiOI 和质子化 g-CN 光催化剂的 43 倍和 32 倍。之所以能够实现最高的吸附和降解速率,是由于在受控比例下添加了茶废料生物炭和质子化 g-CN,并且 BiOI 和质子化 g-CN 之间具有充分的界面接触,从而提高了 e/h 对的分离速率,这一点可以从 Zeta 电位值、光致发光光谱以及扫描和透射电子显微镜得到证明。此外,BiOI/茶废料生物炭/质子化 g-CN(40wt%)在经过四个连续循环后仍具有很高的稳定性和可回收性,而不会大大改变其降解能力。因此,我们相信,所制备的 BiOI/茶废料生物炭/质子化 g-CN(40wt%)为高效 S 型机制提供了新的见解,这对于加速多组分光催化氧化还原反应非常重要;同时为处理废水提供了一种有效的可见光响应候选物。

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