Vu Quoc Trung, Nguyen Dang Phu, Pham Van Hai, Chung-Li Dong, Ta Thi Thuy Nga, Wu-Ching Chou, Nguyen Thi Ngoc Hue, Pham Thi Hue, Luu Anh Tuyen, Nguyen Quang Hung, Luc Huy Hoang
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引用次数: 0
Abstract
High-quality two-dimensional Bi₂WO₆ nanolayers were synthesized via hydrothermal processes, with oxygen vacancies introduced through an ultrasound-assisted alkali etching treatment. Comprehensive characterization using Raman spectroscopy, X-ray absorption spectroscopy (XAS), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and positron annihilation spectroscopy (PAS) confirmed the presence and effects of these vacancies on the structural and electronic properties of the nanolayers. Raman spectroscopy revealed shifts in vibrational modes, particularly a blue shift in the WO₆ octahedral vibration modes, indicative of oxygen vacancy formation. XPS analysis showed a reduction in the binding energies of the Bi 4 f and W 4 f orbitals, confirming an altered electronic environment. TEM images demonstrated significant lattice distortions in the oxygen-vacancy-rich regions, particularly disordered WO₆ octahedra and disrupted Bi-O bond lengths. These distortions are consistent with the structural disorder observed in XAS measurements, which highlighted a reduction in the coordination number of W atoms and a corresponding contraction of W-O bond lengths. This charge redistribution between Bi and W atoms due to oxygen vacancies leads to localized structural perturbations, as further evidenced by PAS, which showed increased positron lifetimes associated with vacancy clusters, particularly around the Bi and W atoms. These vacancies create defective sites that trap photogenerated electrons, preventing their recombination with holes, thereby significantly enhancing photocatalytic performance. The enhanced photocatalytic activity was demonstrated by the nearly 98% degradation of Rhodamine B dye under visible-light irradiation, a substantial improvement over the 70% degradation achieved by the untreated sample. This work presents an innovative approach for generating stable oxygen vacancies in Bi₂WO₆ nanolayers and offers an in-depth understanding of the mechanisms that enhance photocatalytic performance, providing valuable insights for advancing photocatalysts designed for environmental remediation.
通过水热法合成了高质量的二维 Bi₂WO₆纳米层,并通过超声辅助碱蚀刻处理引入了氧空位。利用拉曼光谱、X 射线吸收光谱(XAS)、透射电子显微镜(TEM)、X 射线光电子能谱(XPS)和正电子湮灭光谱(PAS)进行的综合表征证实了这些空位的存在及其对纳米层结构和电子特性的影响。拉曼光谱显示了振动模式的变化,特别是 WO₆ 八面体振动模式的蓝移,表明了氧空位的形成。XPS 分析表明,Bi 4 f 和 W 4 f 轨道的结合能降低,证实电子环境发生了改变。TEM 图像显示氧空位富集区的晶格发生了明显的畸变,尤其是 WO₆ 八面体的无序和 Bi-O 键长度的中断。这些畸变与 XAS 测量中观察到的结构紊乱一致,XAS 测量突出显示了 W 原子配位数的减少和 W-O 键长度的相应收缩。氧空位导致的 Bi 原子和 W 原子间的电荷再分布导致了局部结构扰动,PAS 进一步证明了这一点,它显示了与空位簇相关的正电子寿命延长,尤其是在 Bi 原子和 W 原子周围。这些空位形成了缺陷位点,可捕获光生电子,阻止它们与空穴重组,从而显著提高光催化性能。在可见光照射下,罗丹明 B 染料的降解率接近 98%,与未经处理的样品 70% 的降解率相比有了大幅提高,这证明了光催化活性的增强。这项研究提出了一种在 Bi₂WO₆ 纳米层中产生稳定氧空位的创新方法,并深入揭示了提高光催化性能的机制,为推进环境修复光催化剂的设计提供了宝贵的见解。
期刊介绍:
The Journal of Alloys and Compounds is intended to serve as an international medium for the publication of work on solid materials comprising compounds as well as alloys. Its great strength lies in the diversity of discipline which it encompasses, drawing together results from materials science, solid-state chemistry and physics.