评价聚吡咯增强Bi₂WO₆/g-C₃N₅纳米复合材料对有效降解有机污染物的光催化效率

K.S Pushpa Valli , A. Antony Christian Raja , V. Selvam , S. Mary Jelastin Kala , A.S.I Joy Sinthiya , B. Malathi
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引用次数: 0

摘要

通过将石墨氮化碳和Bi2WO6纳米颗粒结合在一起,并以聚吡咯(Ppy)增强,实现了先进的Z-scheme光催化体系g-C3N5@/Bi2WO6/Ppy的有效开发。在Z-scheme体系中,PPy作为导电聚合物起到欧姆接触的作用,从而实现g-C3N5和Bi2WO6之间的电荷转移。XRD证实了Bi2WO6和光催化剂的结晶性质。通过UV-DRS测定,光催化剂的带隙增强。BET研究证实,在g-C3N5@/Bi2WO6中加入吡咯可以显著增加光催化剂的表面积。具体来说,1:10 g-C3N5@/Bi2WO6在可见光下表现出优异的光催化活性,在60 分钟内破坏了96% %的罗丹明B (RhB)和98% %的亚甲基蓝(MB)。根据光电化学测试和清除实验,参与光催化过程的主要物质是超氧自由基(O2•−)和空穴(h+)。在循环光催化研究中,光催化剂表现出优异的稳定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluating the photocatalytic efficiency of polypyrrole-enhanced Bi₂WO₆/g-C₃N₅ nanocomposites for effective organic pollutant degradation
The effective development of an advanced Z-scheme photocatalytic system, denoted as g-C3N5@/Bi2WO6/Ppy, was achieved by incorporating graphitic carbon nitride and Bi2WO6 nanoparticles, which were reinforced with polypyrrole (PPy). In the Z-scheme system, PPy functions as an Ohmic contact as a conductive polymer, thereby enabling the transfer of charge between g-C3N5 and Bi2WO6. The XRD confirms the crystalline nature of the Bi2WO6 and photocatalyst. The bandgap of the photocatalyst was enhanced, as determined through UV-DRS. BET studies confirms that adding pyrrole to g-C3N5@/Bi2WO6 significantly increases the surface area of the photocatalyst. Specifically, the 1:10 g-C3N5@/Bi2WO6 with PPy composition demonstrated exceptional photocatalytic activity, destroying over 96 % of Rhodamine B (RhB) and 98 % of Methylene Blue (MB) in 60 minutes under visible light. The primary species involved in the photocatalytic process are superoxide radicals (O2•−) and holes (h+), according to photoelectrochemical tests and scavenging experiments. In recycling photocatalytic studies, the photocatalysts showed outstanding stability.
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