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用于去除碱性染料的g-CN/Ce(WO)纳米复合材料的研究

Investigation of g-CN/Ce(WO) Nanocomposites for the Removal of Basic Dyes.

作者信息

Subramanian Keerthana, Rathinam Yuvakkumar, Ganesan Ravi, Venkatasamy Ravi Sankar

机构信息

Department of Physics, Alagappa University, Karaikudi, Tamil Nadu 630 003, India.

Department of Physics, Chandigarh University, Mohali, Punjab 140 413, India.

出版信息

ACS Omega. 2024 Feb 22;9(9):10110-10118. doi: 10.1021/acsomega.3c06147. eCollection 2024 Mar 5.

DOI:10.1021/acsomega.3c06147
PMID:38463307
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10918798/
Abstract

Herein, we have synthesized pristine and g-CN-assisted Ce(WO) via a facile hydrothermal method. The structure was confirmed with the standard JCPDS card. g-CN encapsulated the crystal and reduced the size. The Raman spectra revealed the presence of Ce-O, W-O stretching and bending vibrations. Electron hole transfer facilitation and controllable recombination were altered by g-CN heterojunction with cerium tungstate. Ce(WO) possessed a larger band gap. As g-CN was assisted, the band gap was reduced which facilitates Ce(WO) to utilize more visible light. The prepared photocatalysts were used to investigate the model pollutant removal with visible light. The pure Janus Green B sample showed lesser efficiency, as it does not show self-degradation under light. As Ce(WO) was added, it slightly improved the efficiency as it possesses lower electron hole transfer and high recombination. Thus, g-CN was composited with Ce(WO) to make heterojunctions which will enhance the photo-excited electron and hole transfer and decrease e/h recombination. The rate constant values of the photocatalysts were calculated, and the system follows the first-order pseudo-kinetic model. Ciprofloxacin, a well-known antibiotic, was also used to degrade under visible light. The pure sample showed lower efficiency, and the antibiotic was reduced well with the addition of prepared photocatalysts. The modification of Ce(WO) with the optimum-level g-CN facilitated electron hole charge transfer, and numerous adsorbed dye molecules on the photocatalyst surface made 0.1 g g-CN-Ce(WO) a plausible photocatalyst for the water remediation process.

摘要

在此,我们通过简便的水热法合成了原始的和g-CN辅助的Ce(WO₄)₂。结构通过标准的JCPDS卡片得以确认。g-CN包裹了晶体并减小了其尺寸。拉曼光谱揭示了Ce-O、W-O的伸缩振动和弯曲振动的存在。g-CN与钨酸铈的异质结改变了电子空穴转移的促进作用和可控复合。Ce(WO₄)₂具有较大的带隙。在g-CN的辅助下,带隙减小,这有利于Ce(WO₄)₂利用更多的可见光。所制备的光催化剂用于研究可见光下对模型污染物的去除。纯的Janus Green B样品效率较低,因为它在光照下不会发生自降解。加入Ce(WO₄)₂后,效率略有提高,因为它具有较低的电子空穴转移和较高的复合率。因此,将g-CN与Ce(WO₄)₂复合制成异质结,这将增强光激发电子和空穴的转移并减少e/h复合。计算了光催化剂的速率常数,该体系遵循一级伪动力学模型。环丙沙星,一种知名的抗生素,也用于可见光下降解。纯样品效率较低,加入所制备的光催化剂后抗生素得到了很好的降解。用最佳水平的g-CN对Ce(WO₄)₂进行改性促进了电子空穴电荷转移,并且光催化剂表面大量吸附的染料分子使得0.1 g g-CN-Ce(WO₄)₂成为水修复过程中一种可行的光催化剂。

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