Li Runmei, Wang Zhuorui, Gu Xuefan, Chen Cong, Zhang Yaya, Hu Daodao
Engineering Research Center of Historical and Cultural Heritage Protection, Ministry of Education, School of Materials Science and Engineering, Shaanxi Normal University, Xi'an 710062, China.
College of Chemistry and Chemical Engineering, Xi'an Shiyou University, Xi'an 710065, China.
ACS Omega. 2020 Mar 4;5(10):4943-4952. doi: 10.1021/acsomega.9b03823. eCollection 2020 Mar 17.
In this work, the self-assembly behavior of cetyltrimethylammonium bromide (CTAB) on the surface of citrate-capped gold nanoparticles (AuNPs) in solution has been studied by UV-vis absorption spectroscopy, fluorescence probe techniques, ζ potentiometric methods, transmission electron microscopy, etc. The UV-vis spectra show that the color with the increase of CTAB for the mixture containing CTAB and a given amount of AuNPs changes from red to blue and then to red. The absolute value of ζ potential corresponding to this color change decreases initially and then increases. Specially, the reversible color change, from red to blue and then to red, could be observed only in the case of a gradual addition of a AuNP solution to a CTAB solution; however, this reversible change is not suitable for the mixture formed in a reverse order of mixing. The results from pyrene used as the fluorescence probe indicate that the features in the fluorescence spectrum (including fluorescence quenching, / , and the excimer) well correspond to those from the UV-vis spectrum mentioned above. Based on the experimental results, the mechanism of the assembly structure variation of CTAB on the surface of negatively charged AuNPs was proposed. For a given amount of AuNPs, the assembly structure of CTAB on the surface of AuNPs undergoes the transformation from a monolayer to a bilayer with the increase of CTAB. In the case of the concentration of CTAB far beyond its critical micelle concentration (CMC) and the higher ratio of CTAB and AuNPs, there is a possibility of the formation of an extra micellar structure only after the formation of a double-layer structure.
在本工作中,通过紫外可见吸收光谱、荧光探针技术、ζ电位测定法、透射电子显微镜等手段,研究了十六烷基三甲基溴化铵(CTAB)在溶液中柠檬酸盐包覆的金纳米粒子(AuNPs)表面的自组装行为。紫外可见光谱表明,对于含有CTAB和一定量AuNPs的混合物,随着CTAB的增加,颜色从红色变为蓝色,然后又变为红色。对应于这种颜色变化的ζ电位绝对值最初减小,然后增大。特别地,只有在将AuNP溶液逐渐加入到CTAB溶液中的情况下,才能观察到从红色到蓝色再到红色的可逆颜色变化;然而,这种可逆变化不适用于以相反混合顺序形成的混合物。以芘作为荧光探针的结果表明,荧光光谱中的特征(包括荧光猝灭、/ 以及激基缔合物)与上述紫外可见光谱中的特征很好地对应。基于实验结果,提出了CTAB在带负电的AuNPs表面组装结构变化的机理。对于一定量的AuNPs,随着CTAB的增加,AuNPs表面CTAB的组装结构从单层转变为双层。在CTAB浓度远超过其临界胶束浓度(CMC)且CTAB与AuNPs比例较高的情况下,只有在形成双层结构后才有可能形成额外的胶束结构。