用于光催化降解水中曙红黄染料的掺杂钆氧化锆-石墨氮化碳异质结构

Charles Kwame Bandoh , Moro Haruna , David Adu-Poku , Bernice Yram Danu , Mandela Toku , Francis Kofi Ampong , Robert Kwame Nkum , Eric Selorm Agorku
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引用次数: 0

摘要

本文研究了钆(Gd)对氧化锆-石墨化氮化碳(ZrO2-g-C3N4)纳米复合材料的结构、光吸收和光催化活性的影响,用于分解合成废水中的曙红黄(EY)染料。光催化剂采用化学共沉淀法合成,然后进行煅烧。对合成样品的结构检测表明,裸 ZrO2 具有氧化锆的单斜相。然而,当掺杂剂浓度相对较高时,纳米复合材料发生了从单斜相到立方相的完全转变。此外,光学吸光度测量显示带隙从 3.82 eV 减小到 3.17 eV,这归因于引入钆和 g-C3N4 后在金属氧化物的禁带隙内产生了缺陷态。降解结果表明,在 ZrO2-g-C3N4 系统中加入 Gd 大大提高了其降解活性。降解效率从 30% 显著提高到 97%,相应的速率常数(k)分别为 5.7×10-4min-1 和 17.1×10-2min-1。光降解结果表明,最佳掺杂百分比浓度为 0.8%,超过这一浓度,光催化效率就会下降。Gd-ZrO2-g-C3N4 异质结构的光降解性能增强归因于多种因素,如光吸收能力增强、电荷分离效率高和表面积增大。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gadolinium doped-zirconium oxide-graphitic carbon nitride heterostructures for photocatalytic degradation of eosin yellow dye in water
In this paper, we present the impact of gadolinium (Gd) on the structure, optical absorption, and photocatalytic activities of zirconium oxide-graphitic carbon nitride (ZrO2-g-C3N4) nanocomposites for the decomposition of eosin yellow (EY) dye in synthetic wastewater. Chemical co-precipitation was used to synthesize the photocatalysts, which was then followed by calcination. The structural examination of the synthesized samples showed that the bare ZrO2 possesses the monoclinic phase of zirconium oxide. However, a complete monoclinic to cubic phase transformation occurred in the nanocomposites at a relatively higher dopant concentration. Additionally, optical absorbance measurement exhibited a reduction in bandgap from 3.82 to 3.17 eV which was attributed to the creation of defect states within the forbidden gap of the metal oxides, brought about by the introduction of both the Gd and the g-C3N4. The degradation outcome indicated that incorporating Gd into the ZrO2-g-C3N4 system substantially improved its degradation activities. The tremendous degradation efficiency was confirmed to rise remarkably from 30 % to 97 %, with a corresponding rate constant (k) of 5.7×104min1 and 17.1×102min1. The photodegradation results of this study showed that the optimum dopant percentage concentration was found to be 0.8 % Gd, beyond which a decline in the photocatalytic efficiency was realized. The enhanced photodegradation performances of the Gd-ZrO2-g-C3N4 heterostructures were attributed to numerous factors such as enhanced light absorption, efficient charge separation, and enhanced surface area.
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