School of Metallurgical Engineering, Xi'an University of Architecture and Technology, Xi'an, 710055, China.
Photochem Photobiol Sci. 2018 Aug 8;17(8):1084-1090. doi: 10.1039/c8pp00078f.
Bi2WO6 nanosheets were synthesized by a hydrothermal method with H2WO4 for the first time. The band structure of Bi2WO6 was investigated on the basis of density functional theory calculations. Bi2WO6 photocatalysts showed photocatalytic activity for the degradation of methylene blue under visible light irradiation. Kinetic studies using radical scavenger technologies suggested that holes were the dominant photo-oxidants. After hybridization with C3N4, the photocatalytic activity of Bi2WO6 was obviously enhanced. The enhanced photocatalytic activity of the C3N4/Bi2WO6 photocatalysts could be attributed to the effective separation of photogenerated e-/h+ pairs. The photogenerated holes on the valence band of Bi2WO6 can transfer to the highest occupied molecular orbital of C3N4via the well-developed interface, causing a reduction in the probability of e-/h+ recombination; consequently, large numbers of photogenerated holes led to the enhancement of the photocatalytic activity.
采用水热法首次以 H2WO4 合成了 Bi2WO6 纳米片。基于密度泛函理论计算研究了 Bi2WO6 的能带结构。Bi2WO6 光催化剂在可见光照射下表现出对亚甲基蓝的光催化降解活性。使用自由基清除剂技术的动力学研究表明,空穴是主要的光氧化剂。与 C3N4 杂交后,Bi2WO6 的光催化活性明显增强。C3N4/Bi2WO6 光催化剂增强的光催化活性可归因于光生电子-空穴对的有效分离。Bi2WO6 价带上的光生空穴可以通过发达的界面转移到 C3N4 的最高占据分子轨道,从而降低 e-/h+复合的概率;因此,大量的光生空穴导致光催化活性增强。