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可见光活性 Z 型 g-CN/MoS 异质结中的高界面电荷分离:柳氮磺胺吡啶的降解机制。

High interfacial charge separation in visible-light active Z- scheme g-CN/MoS heterojunction: Mechanism and degradation of sulfasalazine.

机构信息

College of Materials Science and Engineering, Shenzhen Key Laboratory of Polymer Science and Technology, Guangdong Research Center for Interfacial Engineering of Functional Materials, Nanshan District Key Lab. for Biopolymers and Safety Evaluation, Shenzhen University, Shenzhen, 518060, PR China; International Research Centre of Nanotechnology for Himalayan Sustainability (IRCNHS), Shoolini University, Solan, 173212, Himachal Pradesh, India.

Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh, 11451, Saudi Arabia.

出版信息

Chemosphere. 2022 Dec;308(Pt 1):136162. doi: 10.1016/j.chemosphere.2022.136162. Epub 2022 Aug 26.

Abstract

Examination of highly proficient photoactive materials for the degradation of antibiotics from the aqueous solution is the need of the hour. In the present study, a 2D/2D binary junction GCM, formed between graphitic-carbon nitride (g-CN) and molybdenum disulphide (MoS), was synthesized using facile hydrothermal method and its photo-efficacy was tested for the degradation of sulfasalazine (SUL) from aqueous solution under visible-light irradiation. Morphological analysis indicated the nanosheets arrangement of MoS and g-CN. The visible-light driven experiments indicated that 97% antibiotic was degraded by GCM-30% within 90 min which was found to be quite high than pristine g-CN and MoS at solution pH of 6, GCM-30% dose of 20 mg, and SUL concentration of 20 mgL. The degradation performance of GCM-30% was selectively improved due to enhanced visible-light absorption, high charge carrier separation, and high redox ability of the photogenerated charges which was induced by the effective Z-scheme 2D/2D heterojunction formed between g-CN and MoS. The reactive radicals as determined by the scavenging study were •O, and h. A detailed degradation mechanism of SUL by GCM-30% was also predicted based on the detailed examination of the band gaps of g-CN and MoS.

摘要

研究高效光活性材料以降解水溶液中的抗生素是当前的需求。在本研究中,通过简便的水热法合成了一种二维/二维二元结 GCM,由石墨相氮化碳 (g-CN) 和二硫化钼 (MoS) 组成,并测试了其在可见光照射下从水溶液中降解柳氮磺胺吡啶 (SUL) 的光催化性能。形貌分析表明 MoS 和 g-CN 呈纳米片排列。可见光驱动实验表明,在溶液 pH 为 6、GCM-30%剂量为 20mg、SUL 浓度为 20mg/L 的条件下,GCM-30%在 90min 内可降解 97%的抗生素,这明显优于原始的 g-CN 和 MoS。GCM-30%的降解性能因有效 Z 型 2D/2D 异质结的形成而得到了选择性的提高,该异质结在 g-CN 和 MoS 之间形成,增强了可见光吸收、提高了载流子分离效率,并增强了光生载流子的氧化还原能力。通过清除实验确定的反应自由基为 •O 和 h。还根据 g-CN 和 MoS 的能带隙的详细检查,预测了 GCM-30%降解 SUL 的详细机制。

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