Fabrication of 2D/2D Bi2MoO6/Sx@g-C3N(4−y) type-II heterojunction photocatalyst for enhanced visible-light-mediated degradation of tetracycline in wastewater†

IF 3.3 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR Dalton Transactions Pub Date : 2024-12-17 DOI:10.1039/D4DT02334J
Soorya K. K., Adarsh Singh, Suneel Kumar Srivastava, Animesh Bhattacharya, Amit Bhatnagar and Ashok Kumar Gupta
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Abstract

Aquatic biota and human health are seriously threatened by the dramatic rise in antibiotics in environmental matrices. In this regard, the present study aims to improve knowledge of the combined effects of heterojunction design and defect engineering on the photocatalytic degradation of pharmaceuticals in aqueous matrices. Advantageously, the positioning of the valence band (VB) and conduction band (CB) levels of Sx@g-C3N(4−y), being higher than those of Bi2MoO6, demonstrates the feasibility of forming a type-II heterojunction between these materials. Initially, S and N defects were inserted in S-doped g-C3N4 through an alkali-assisted calcination method (referred to as Sx@g-C3N(4−y)), as affirmed by the reduced concentrations of S and N in the end product. Thereafter, the Bi2MoO6/Sx@g-C3N(4−y) photocatalysts (referred to as BSxNy) were synthesized via a solvothermal method followed by calcination. Among the prepared samples, the integration of 10% Sx@g-C3N(4−y) with Bi2MoO6 (referred to as BSxNy (II)) demonstrated superior photocatalytic performance. Under optimal conditions, BSxNy (II) achieved a remarkable 92.4% degradation efficiency of tetracycline (TCL) in an aqueous solution after 60 min. The degradation rate of BSxNy (II) transcended that of pristine Sx@g-C3N(4-y) and Bi2MoO6 by 4.86 and 3.41 times, respectively. The higher number of active sites and the greater electron–hole pair separation are responsible for this improvement in the rate of TCL degradation. The photocatalyst also exhibited remarkable thermal/chemical stability and possessed reusability, as noted by 84% TCL degradation TCL up to 5 cycles. The radical scavenging experiment indicated O2˙ as the primary contributor towards TCL degradation, with h+ and ˙OH playing a secondary role. Additionally, a seed germination experiment used to measure phytotoxicity determined that the treated effluent was non-phytotoxic, making it suitable for irrigation.

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制备二维/二维 Bi2MoO6/Sx@g-C3N(4-y) II 型异质结光催化剂,增强可见光介导的废水中四环素降解能力
环境基质中抗生素的急剧增加严重威胁着水生生物群和人类健康。在这方面,本研究旨在提高对异质结设计和缺陷工程对水基质中药物光催化降解的综合影响的认识。有利的是,Sx@g-C3N(4-y)的价带(VB)和导带(CB)水平的定位高于Bi2MoO6,证明了在这些材料之间形成ii型异质结的可行性。最初,通过碱辅助煅烧法(Sx@g-C3N(4-y))将S和N缺陷插入到S掺杂的g-C3N4中,最终产物中S和N的浓度降低了。然后,通过溶剂热法煅烧合成Bi2MoO6/Sx@g-C3N(4-y)光催化剂(简称BSxNy)。在所制备的样品中,10% Sx@g-C3N(4-y)与Bi2MoO6(简称BSxNy (II))的整合表现出优异的光催化性能。在最佳条件下,60 min后BSxNy (II)对四环素(TCL)的降解效率达到了92.4%,其降解率分别是原始Sx@g-C3N(4-y)和Bi2MoO6的4.86倍和3.41倍。较高的活性位点数目和较大的电子空穴对分离是导致TCL降解率提高的原因。该光催化剂还表现出了显著的热/化学稳定性,并具有可重复使用性,在5次循环中,TCL的降解率为84%。自由基清除实验表明,“O”_“2”^“•-”是TCL降解的主要贡献者,h+和•OH起次要作用。此外,用于测量植物毒性的种子发芽实验确定处理后的废水无植物毒性,使其适合灌溉。
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来源期刊
Dalton Transactions
Dalton Transactions 化学-无机化学与核化学
CiteScore
6.60
自引率
7.50%
发文量
1832
审稿时长
1.5 months
期刊介绍: Dalton Transactions is a journal for all areas of inorganic chemistry, which encompasses the organometallic, bioinorganic and materials chemistry of the elements, with applications including synthesis, catalysis, energy conversion/storage, electrical devices and medicine. Dalton Transactions welcomes high-quality, original submissions in all of these areas and more, where the advancement of knowledge in inorganic chemistry is significant.
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