X射线光电子能谱
化学状态
辐照
铀
铀酰
分析化学(期刊)
化学
氧化态
X射线
半导体
谱线
材料科学
金属
核磁共振
光学
物理
环境化学
冶金
光电子学
核物理学
有机化学
天文
作者
Shirong Qiang,Jingjing Wang,Yun Wang,Longmiao Yuan,Leiping Shi,Zhe Ding,Wei Wang,Jianjun Liang,Ping Li,Qiaohui Fan
标识
DOI:10.1016/j.apsusc.2021.151886
摘要
X-ray photoelectron spectroscopy (XPS) is an efficient technique for recognizing the state of elements. However, the effects of X-ray irradiation on change in the chemical state are sometimes ignored, which may impair the understanding of the environmental behavior of these elements. This study determined the change in the U 4f spectra induced by X-ray irradiation during XPS detection. For U(VI) on non-semiconductors, X-ray irradiation led to a negative shift of U 4f7/2 to ∼ 380.8 eV due to the break of the uranyl molecules, but not resulting in U(IV) species. However, owing to the photocatalytic reduction of U(VI), the irradiation of U(VI) loaded semiconductors rapidly induced the negative shift of U 4f7/2 peak to ∼ 379.8 eV, which is the characteristic of U(IV). Moreover, apparent photo-reduction occurred even if the samples were far from the center of the X-ray beam (>3971 μm). Based on these findings, methods for reducing potential error due to X-ray irradiation are suggested, including using the minimum scan time, measuring uranium-containing samples first or independent of other samples, and using X-ray of lower intensity. The results indicated that X-ray induced alteration to the chemical states must be considered when using X-ray techniques.
科研通智能强力驱动
Strongly Powered by AbleSci AI