Jiang Jiao-lai, Zhang Jing, Jia Jian-ping, Wang Shao-fei, Wu Hao-xi, Yun Wen, Wang Xiao-lin, Liao Jun-sheng
Guang Pu Xue Yu Guang Pu Fen Xi. 2016 Nov;36(11):3563-7.
Uranium is one of the important nuclear materials to nuclear industry. Because of the direct disposal of spent fuel, there is still a huge possibility that uranium migrates into the groundwater, causing water contamination. It is of great importance to understand the concentration and their species distribution in aqueous solutions. Surface-Enhanced Raman Scattering (SERS) technique has been widely used for the detection of uranium (Ⅵ). However, the interactions between uranium (Ⅵ) and SERS substrate cause the symmetric stretching vibration peak of uranium (Ⅵ) shift to low wave number direction, which is unfavorable for confirming the species of uranium (Ⅵ) in aqueous solution. For instance, the normal Raman bands of uranyl in nitric acid solution are 871 cm-1, which belongs to the symmetric stretching mode of UO2+2. However, it moves to 710 cm-1 on the surface of silver nanorods SERS substrtate. What’s more, different SERS substrate causes different number of shift. Graphene has advantages of inertness and integrity as well as 2-dimensional thickness. In this paper, graphene-isolated SERS substrate which is silver nanoparticles (AgNPs)/graphene complex substrate, was designed to prevent the interaction between SERS substrate and it was analyzed by using the inert graphene layer. First of all, according to our previous work, AgNPs SERS substrate was fabricated on silicon wafer by using an ascorbic acid-actived self-assembly method. Then, AgNPs/graphene complex substrate was prepared by transfering monolayer graphene onto the self-assembly AgNPs substrate. The morphology of complex substrate was obtained by SEM. Some AgNPs link together closely to form nanochain structures. Nanochain structures were distributed evenly on the surface of silicon wafer. The 2-dimensional thickness of graphene did not affect the morphology of AgNPs. When using the complex substrate to detect uranyl nitrate (5×10-4 mol·L-1),the Raman peak that appeared around 771 cm-1 is considered to be the symmetric stretching mode of UO2+2, shifting back about 52 cm-1 to high wave number direction when compared with AgNPs substrate, which was about ~719 cm-1. The result indicates that graphene layer isolates the interaction between AgNPs substrate and uranyl in some degree.
铀是核工业重要的核材料之一。由于乏燃料的直接处置,铀仍有极大可能迁移至地下水中,造成水体污染。了解其在水溶液中的浓度及物种分布至关重要。表面增强拉曼散射(SERS)技术已被广泛用于检测铀(Ⅵ)。然而,铀(Ⅵ)与SERS基底之间的相互作用会导致铀(Ⅵ)的对称伸缩振动峰向低波数方向移动,这不利于确定水溶液中铀(Ⅵ)的物种。例如,硝酸溶液中铀酰的正常拉曼谱带为871 cm-1,属于UO2+2的对称伸缩模式。然而,在银纳米棒SERS基底表面,它移至710 cm-1。此外,不同的SERS基底导致的位移数量不同。石墨烯具有惰性、完整性以及二维厚度的优势。本文设计了石墨烯隔离的SERS基底,即银纳米颗粒(AgNPs)/石墨烯复合基底,通过使用惰性石墨烯层来防止SERS基底之间的相互作用并对其进行分析。首先,根据我们之前的工作,采用抗坏血酸活化自组装法在硅片上制备AgNPs SERS基底。然后,通过将单层石墨烯转移到自组装的AgNPs基底上制备AgNPs/石墨烯复合基底。通过扫描电子显微镜(SEM)获得复合基底的形貌。一些AgNPs紧密连接在一起形成纳米链结构。纳米链结构均匀分布在硅片表面。石墨烯的二维厚度并未影响AgNPs的形貌。当使用复合基底检测硝酸铀酰(5×10-4 mol·L-1)时,出现在约771 cm-1处的拉曼峰被认为是UO2+2的对称伸缩模式,与AgNPs基底相比,向高波数方向回移约52 cm-1,约为~719 cm-1。结果表明,石墨烯层在一定程度上隔离了AgNPs基底与铀酰之间的相互作用。