Enhanced photocatalytic performance of magnetically reclaimable N-doped g-C3N4/Fe3O4 nanocomposites for efficient tetracycline degradation

IF 5.45 Q1 Physics and Astronomy
Paramasivam Shanmugam , Mohan Gopalakrishnan , Siwaporn Meejoo Smith , Apanee Luengnaruemitchai , Soorathep Kheawhom , Supakorn Boonyuen
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引用次数: 0

Abstract

The growing environmental challenge posed by the persistence of tetracycline (TC) antibiotics in natural waters is of increasing concern. To address this, there is an imperative need for advanced methods to mitigate TC residues. Herein, we demonstrate the preparation of nitrogen-doped graphitic carbon nitride integrated with magnetic Fe3O4 (N-g-CN/Fe3O4) composites, showcasing narrow band gaps optimized for TC degradation. These advanced materials, conceived through a thermal poly-condensation approach, utilize citric acid and melamine as precursors for nitrogen and g-CN, respectively. These composites exhibit a face-centered cubic architecture, with particle dimensions between 8 to 12 nm and encompassing both meso and microporous structure. The results of the Brunauer–Emmett–Teller analysis indicated specific surface areas of 6.73 m²/g for g-CN, 69.80 m²/g for N-g-CN, 62.55 m²/g for Fe3O4, and 148.32 m²/g for N-g-CN/Fe3O4. These values demonstrate an increase in surface area upon the incorporation of heteroatom of nitrogen and Fe3O4, into the g-CN matrix, thus influence the photocatalytic performance. Under solar light exposure, the synthesized photocatalysts demonstrated photocatalytic activity with a degradation efficiency of 94.16 % within 120 min. Specifically, the N-g-CN/Fe3O4 (22.5 %) composites exhibited remarkable photocatalytic efficiency due to the narrow band gap energy between N-g-CN and Fe3O4, enhanced light absorption in the visible range, and effective charge carrier separation and transportation to the pollutants. N-g-CN/Fe3O4 (22.5 %) composites demonstrated good recyclability (five cycles), magnetic sustainability, and stability for the degradation of TC and emerging pollutants from wastewater using photocatalysts. Similarly, FGCN composites exhibited good recyclability (five cycles), magnetic retrievability, and stability for degrading organic and emerging pollutants from wastewater through photocatalysis. This efficiency can be attributed to the harmonious combination of nitrogen doping, refined surface area, and the natural heterojunction between N-g-CN and Fe3O4.
增强磁性可回收 N 掺杂 g-C3N4/Fe3O4 纳米复合材料的光催化性能,实现四环素的高效降解
四环素(TC)抗生素在天然水域中的持久性所带来的日益严峻的环境挑战正日益引起人们的关注。为解决这一问题,迫切需要先进的方法来减少四环素类抗生素的残留。在本文中,我们展示了氮掺杂氮化石墨与磁性 Fe3O4(N-g-CN/Fe3O4)复合材料的制备方法,其窄带隙可优化 TC 降解。这些先进材料采用热缩聚方法,分别以柠檬酸和三聚氰胺作为氮和 g-CN 的前体。这些复合材料呈现出面心立方结构,颗粒尺寸在 8 到 12 nm 之间,包含中孔和微孔结构。布鲁瑙尔-艾美特-泰勒分析结果表明,g-CN 的比表面积为 6.73 m²/g,N-g-CN 为 69.80 m²/g,Fe3O4 为 62.55 m²/g,N-g-CN/Fe3O4 为 148.32 m²/g。这些数值表明,氮和 Fe3O4 的杂原子加入 g-CN 基质后,表面积增大,从而影响了光催化性能。在太阳光照射下,合成的光催化剂具有光催化活性,120 分钟内的降解效率达到 94.16%。具体而言,N-g-CN/Fe3O4(22.5%)复合材料表现出显著的光催化效率,这是由于 N-g-CN 和 Fe3O4 之间的带隙能较窄,增强了可见光范围内的光吸收,并有效地将电荷载流子分离和传输到污染物中。N-g-CN/Fe3O4 (22.5%) 复合材料在利用光催化剂降解废水中的三氯甲烷和新污染物方面表现出良好的可回收性(五次循环)、磁性可持续性和稳定性。同样,FGCN 复合材料在通过光催化降解废水中的有机污染物和新污染物方面也表现出良好的可回收性(五个周期)、磁性可回收性和稳定性。这种效率可归因于氮掺杂、细化表面积以及 N-g-CN 和 Fe3O4 之间天然异质结的和谐组合。
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来源期刊
Nano-Structures & Nano-Objects
Nano-Structures & Nano-Objects Physics and Astronomy-Condensed Matter Physics
CiteScore
9.20
自引率
0.00%
发文量
60
审稿时长
22 days
期刊介绍: Nano-Structures & Nano-Objects is a new journal devoted to all aspects of the synthesis and the properties of this new flourishing domain. The journal is devoted to novel architectures at the nano-level with an emphasis on new synthesis and characterization methods. The journal is focused on the objects rather than on their applications. However, the research for new applications of original nano-structures & nano-objects in various fields such as nano-electronics, energy conversion, catalysis, drug delivery and nano-medicine is also welcome. The scope of Nano-Structures & Nano-Objects involves: -Metal and alloy nanoparticles with complex nanostructures such as shape control, core-shell and dumbells -Oxide nanoparticles and nanostructures, with complex oxide/metal, oxide/surface and oxide /organic interfaces -Inorganic semi-conducting nanoparticles (quantum dots) with an emphasis on new phases, structures, shapes and complexity -Nanostructures involving molecular inorganic species such as nanoparticles of coordination compounds, molecular magnets, spin transition nanoparticles etc. or organic nano-objects, in particular for molecular electronics -Nanostructured materials such as nano-MOFs and nano-zeolites -Hetero-junctions between molecules and nano-objects, between different nano-objects & nanostructures or between nano-objects & nanostructures and surfaces -Methods of characterization specific of the nano size or adapted for the nano size such as X-ray and neutron scattering, light scattering, NMR, Raman, Plasmonics, near field microscopies, various TEM and SEM techniques, magnetic studies, etc .
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