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用于光催化去除甲基橙的α-FeO修饰的g-CN异质结构的合成与表征

Synthesis and Characterization of an α-FeO-Decorated g-CN Heterostructure for the Photocatalytic Removal of MO.

作者信息

Khurram Rooha, Nisa Zaib Un, Javed Aroosa, Wang Zhan, Hussien Mostafa A

机构信息

Beijing Key Laboratory for Green Catalysis and Separation, Department of Chemistry and Chemical Engineering, Beijing University of Technology, Beijing 100124, China.

Department of Chemistry, School of Natural Sciences (SNS), National University of Sciences and Technology (NUST), H-12, Islamabad 44000, Pakistan.

出版信息

Molecules. 2022 Feb 21;27(4):1442. doi: 10.3390/molecules27041442.

Abstract

This study describes the preparation of graphitic carbon nitride (g-CN), hematite (α-FeO), and their g-CN/α-FeO heterostructure for the photocatalytic removal of methyl orange (MO) under visible light illumination. The facile hydrothermal approach was utilized for the preparation of the nanomaterials. Powder X-ray diffraction (XRD), Scanning electron microscopy (SEM), Energy dispersive X-ray (EDX), and Brunauer-Emmett-Teller (BET) were carried out to study the physiochemical and optoelectronic properties of all the synthesized photocatalysts. Based on the X-ray photoelectron spectroscopy (XPS) and UV-visible diffuse reflectance (DRS) results, an energy level diagram vs. SHE was established. The acquired results indicated that the nanocomposite exhibited a type-II heterojunction and degraded the MO dye by 97%. The degradation ability of the nanocomposite was higher than that of pristine g-CN (41%) and α-FeO (30%) photocatalysts under 300 min of light irradiation. The formation of a type-II heterostructure with desirable band alignment and band edge positions for efficient interfacial charge carrier separation along with a larger specific surface area was collectively responsible for the higher photocatalytic efficiency of the g-CN/α-FeO nanocomposite. The mechanism of the nanocomposite was also studied through results obtained from UV-vis and XPS analyses. A reactive species trapping experiment confirmed the involvement of the superoxide radical anion (O) as the key reactive oxygen species for MO removal. The degradation kinetics were also monitored, and the reaction was observed to be pseudo-first order. Moreover, the sustainability of the photocatalyst was also investigated.

摘要

本研究描述了石墨相氮化碳(g-CN)、赤铁矿(α-Fe₂O₃)及其g-CN/α-Fe₂O₃异质结构的制备,用于在可见光照射下光催化去除甲基橙(MO)。采用简便的水热法制备纳米材料。进行了粉末X射线衍射(XRD)、扫描电子显微镜(SEM)、能量色散X射线(EDX)和布鲁诺尔-埃米特-泰勒(BET)分析,以研究所有合成光催化剂的物理化学和光电性质。基于X射线光电子能谱(XPS)和紫外-可见漫反射(DRS)结果,建立了相对于标准氢电极(SHE)的能级图。所得结果表明,该纳米复合材料呈现II型异质结,对MO染料的降解率达97%。在300分钟的光照下,该纳米复合材料的降解能力高于原始g-CN(41%)和α-Fe₂O₃(30%)光催化剂。具有理想能带排列和能带边缘位置以实现有效界面电荷载流子分离以及更大比表面积的II型异质结构的形成,共同导致了g-CN/α-Fe₂O₃纳米复合材料具有更高的光催化效率。还通过紫外-可见光谱和XPS分析结果研究了该纳米复合材料的作用机制。活性物种捕获实验证实超氧自由基阴离子(O₂⁻)是去除MO的关键活性氧物种。还监测了降解动力学,观察到该反应为准一级反应。此外,还研究了光催化剂的可持续性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db73/8877162/fa5c234de32e/molecules-27-01442-g001.jpg

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