Rare earth oxide Y2O3 modified g-C3N4 for efficient photocatalytic hydrogen production: Photocatalytic performance and electron transfer channels

F. Niu, Ziyang Zhang, W. Lei, Jiashuang Li, Baoxiang Wang, Yi Shen
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Abstract

This work used a one-step calcination process to prepare g-C3N4 composites with varying Y2O3 loading. XRD, TEM and XPS verified the structure and morphology of the composite photocatalyst, and its photoelectrochemical and hydrogen production performance were studied. According to the experimental results, it is found that the composite structure between Y2O3 and g-C3N4 effectively suppresses the photoelectron-hole complex and enhances the photocatalytic hydrogen production properties of g-C3N4. Under the irradiation of a 300W xenon lamp, YCN-3 had superior photocatalytic hydrogen generation performance, achieving a rate of 1079.61 μ mol g-1 h-1, which was 2.3 times greater than that of g-C3N4 in its unmodified state. After three consecutive photocatalytic operations, satisfactory stability and reusability were obtained. Finally, the possibility of a mechanism for the photocatalytic charges transfer pathway is discussed, which provides an effective way for g-C3N4 photocatalytic hydrogen production.
稀土氧化物 Y2O3 改性 g-C3N4 用于高效光催化制氢:光催化性能和电子传递通道
本研究采用一步煅烧工艺制备了不同 Y2O3 负载的 g-C3N4 复合材料。XRD、TEM和XPS验证了复合光催化剂的结构和形貌,并研究了其光电化学和制氢性能。实验结果表明,Y2O3 与 g-C3N4 的复合结构有效抑制了光电子-空穴复合,提高了 g-C3N4 的光催化制氢性能。在 300 瓦氙灯的照射下,YCN-3 具有优异的光催化制氢性能,制氢率达到 1079.61 μ mol g-1 h-1,是未改性状态 g-C3N4 的 2.3 倍。经过连续三次光催化操作,获得了令人满意的稳定性和可重复使用性。最后,讨论了光催化电荷转移途径机制的可能性,为 g-C3N4 光催化制氢提供了一条有效途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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