Université Paris Diderot, ITODYS Laboratory, NanoElectroChemistry Group, CNRS, UMR 7086, Bâtiment Lavoisier, 15 Rue Jean de Baïf, 75205 Paris Cedex 13 France.
Langmuir. 2010 Dec 7;26(23):18542-9. doi: 10.1021/la103000u. Epub 2010 Nov 9.
The electrochemical reduction of 4-nitrophenyl diazonium, NPD, in different ionic liquids presenting different viscosities has been investigated. The electrochemical studies show that the reduction of diazonium leading to the formation of its corresponding radical occurs whatever the viscosity of the grafting media. Following that, the presence of an organic layer attached to the electrode after electrochemical treatment was evidenced by cyclic voltammetry (CV) in acidic media thanks to the presence of nitro groups. Moreover, infrared spectroscopy (IR), X-ray photoelectron spectroscopy (XPS), and atomic force microscopy (AFM) confirm the presence of a nitrophenyl (NP) layer attached to the electrode material. Next, the examination of the electrochemical data through the measurement of the charge, corresponding to the reduction of the attached nitrophenyl (NP) moieties, shows that the surface concentration of NP, Γ(NP), decreases when the viscosity, η, of the grafting media increases. Additionally, in the case of the more viscous ionic liquid, N-tributyl-N-methylammonium bis(trifluoromethylsulfonyl)imide [Bu(3)MeN] [NTf(2)], a cosolvent has been added leading to fine decrease of the viscosity. The IR and CV investigations of the modified electrodes demonstrate the decrease of the amount of the attached molecules when the viscosity of the grafting media increases. In addition, a correlation between Γ(NP) as function of 1/η was observed. Finally, XPS and AFM experiments lead to an estimate of the thickness of the attached layer. As a result, both methods are in perfect agreement and thicknesses of 4 and 1 nm are measured after grafting in acetonitrile and in pure ionic liquid [Bu(3)MeN] [NTf(2)], respectively. By comparison with classical solvent, the use of viscous ionic liquid for the grafting leads to a decrease in the amount of the attached molecules and conduce to the formation of thinner or less dense layer.
已研究了不同粘度的离子液体中 4-硝基苯重氮盐(NPD)的电化学还原。电化学研究表明,重氮盐的还原导致其相应自由基的形成,无论接枝介质的粘度如何。之后,通过在酸性介质中的循环伏安法(CV),由于硝基基团的存在,证明了在电化学处理后电极上附着有有机层。此外,红外光谱(IR)、X 射线光电子能谱(XPS)和原子力显微镜(AFM)证实了电极材料上附着有硝基苯(NP)层。接下来,通过测量对应于附着的硝基(NP)部分还原的电荷来检查电化学数据,表明当接枝介质的粘度η增加时,NP 的表面浓度Γ(NP)降低。此外,在粘性较大的离子液体 N-三丁基-N-甲基铵双(三氟甲烷磺酰基)亚胺[Bu(3)MeN] [NTf(2)]中,添加了一种共溶剂,导致粘度进一步降低。修饰电极的 IR 和 CV 研究表明,当接枝介质的粘度增加时,附着分子的数量减少。此外,观察到Γ(NP)与 1/η的关系。最后,XPS 和 AFM 实验导致附着层厚度的估计。结果,两种方法完全一致,在乙腈中接枝后分别测量到 4nm 和 1nm 的厚度,在纯离子液体[Bu(3)MeN] [NTf(2)]中接枝后分别测量到 4nm 和 1nm 的厚度。与经典溶剂相比,粘性离子液体用于接枝会导致附着分子数量减少,并导致形成更薄或更稀疏的层。