煅烧
降级(电信)
氧化铟锡
电极
亚甲蓝
电化学
光催化
化学
基质(水族馆)
涂层
化学工程
材料科学
核化学
催化作用
有机化学
电信
物理化学
计算机科学
工程类
海洋学
地质学
作者
Yanxi Gong,Jianbing Wang,Zikun Cheng,Zhiyuan Han,Xu Zhao,Buyu Chai,Yuanchun Han
标识
DOI:10.1016/j.cclet.2022.05.049
摘要
Developing a high-quality photoelectrode for photoelectrochemical applications is still an ongoing challenge. In this study, we prepared the g-C3N4 film on the indium tin oxide (ITO) glass through conventional coating, liquid-based growth, in-situ calcination, and vapor deposition methods, respectively. These electrodes were characterized and used as photoanodes to degrade methylene blue (MB) in water. Among these methods, the in-situ calcination method was most appropriate for preparing the continuous and organized g-C3N4 film electrodes with uniform g-C3N4 coverage and strong adhesion to the ITO substrate. It also had the highest activity in the photocatalytic (PC), electrochemical (EC), and photoelectrocatalytic (PEC) degradation processes of MB. In the PEC reaction, at an applied potential of 1.0 V and a light intensity of 0.96 W/cm2, the removal rate of MB was 62.5%, which was much higher than those in the PC and EC reactions. The high degradation rate was due to the synergistic effect of PEC degradation, wherein the PC and EC reactions promote and optimize each other. In the PC reaction, MB was degraded by −CH3 elimination, while the EC degradation pathway mainly included the conversion of sulfhydryl into sulfoxide and the opening of the central aromatic ring. Both methyl loss and aromatic ring opening occurred in the PEC reaction. Moreover, some monocyclic compounds were formed, and MB showed more complete degradation in the PEC reaction.
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