Solar light-driven photocatalytic degradation potential of g-C3N4 based binary chalcogenides (AgBiS2/g-C3N4)

光催化 降级(电信) X射线光电子能谱 傅里叶变换红外光谱 扫描电子显微镜 材料科学 带隙 可见光谱 化学工程 核化学 打赌理论 热液循环 亚甲蓝 化学 光化学 催化作用 计算机科学 光电子学 复合材料 有机化学 电信 工程类
作者
Noreen Akhtar,Nimra Nadeem,Muhammad Yaseen,Asim Jilani,Asif Mahmood,Usman Zubair,Rizwan Haider,Xianxia Yuan,Muhammad Zahid
出处
期刊:Materials Chemistry and Physics [Elsevier BV]
卷期号:316: 129067-129067 被引量:5
标识
DOI:10.1016/j.matchemphys.2024.129067
摘要

Fabrication of the AgBiS2 loaded on g-C3N4 was achieved via a hydrothermal route. The novel composite photocatalyst was successfully characterized using Scanning electron microscopy (SEM), Fourier transform infrared (FTIR), Energy dispersive X-ray (EDX), X-ray diffraction (XRD) techniques, and XPS analysis. The synthesized composite (AgBiS2/g-C3N4) was employed for the photocatalytic degradation of methylene blue (MB) under sunlight. The composition of cheaper and visible light active photocatalyst i.e. g-C3N4, with AgBiS2 was advantageous in terms of effective charge separation -due to heterojunction-, and surface morphology. Besides, the energy band gap reduction (owing to the addition of g-C3N4 in AgBiS2) facilitates sunlight-driven photocatalysis. The influencing parameters such as pH, oxidant dose, AgBiS2/g-C3N4 dose, dye concentration, and irradiation time were analyzed for the selection of the well-suited reaction conditions. The interaction of pollutant molecules with the catalyst surface was investigated based on the pHpzc results. Under preferred conditions (such as dye = 10 ppm, pH = 8, catalyst = 40 mg/100 mL, H2O2 = 12 mM, and time = 180 min) the AgBiS2/g-C3N4 exhibited ∼93% photocatalytic degradation of MB. The key radicals were determined using a radical trapping experiment. The reaction kinetic of the proposed study was also studied using 1st and 2nd order kinetic models. The combined influences of effecting parameters were checked by Response surface methodology.

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