He Ping, Liu Hongtao, Li Zhiying, Liu Yang, Xu Xiudong, Li Jinghong
State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, Jilin 130022, People's Republic of China.
Langmuir. 2004 Nov 9;20(23):10260-7. doi: 10.1021/la048480l.
The use of room-temperature ionic liquids (RTILs) as media for electrochemical application is very attractive. In this work, the electrochemical deposition of silver was investigated at a glassy carbon electrode in hydrophobic 1-n-butyl-3-methylimidazolium hexafluorophosphate (BMIMPF6) and hydrophilic 1-n-butyl-3-methylimidazolium tetrafluoroborate (BMIMBF4) RTILs and in KNO3 aqueous solution by cyclic voltammetric and potentiostatic transient techniques. The voltammograms showed the presence of reduction and oxidation peaks associated with the deposition and dissolution of silver from AgBF4 in both BMIMPF6 and BMIMBF(4), resembling the redox behavior of AgNO3 in KNO3 aqueous solution. A crossover loop was observed in all the cyclic voltammograms of these electrochemical systems, indicating a nucleation process. From the analysis of the experimental current transients, it was shown that the electrochemical deposition process of silver in these media was characteristic of 3D nucleation with diffusion-controlled hemispherical growth, and the silver nucleation closely followed the response predicted for progressive nucleation in BMIMPF6 and instantaneous nucleation in KNO3 aqueous solution, respectively. Compared with these two cases, the electrochemical deposition of silver in BMIMBF4 deviated from both the instantaneous and progressive nucleation models, which could be controlled by mixed kinetics and diffusion. On the basis of the experimental results, it was shown that parameters such as viscosity and water miscibility of RTILs would affect the electrodeposition behavior of silver. Atom force microscopy was employed to probe the surface morphology of the silver deposit, and it showed that the shining electrodeposit of silver was fairly dense and separate nanoclusters of <100 nm were in evidence, corresponding to an island growth model. The strongly enhanced Raman scattering from the monolayer film of 4-mercaptobenzoic acid demonstrated that as-prepared silver nanoparticular film was surface-enhanced Raman scattering (SERS) active. The enhancement factor was calculated to be up to 9.0 x 10(5) and 1.0 x 10(6) for the silver film obtained in BMIMPF6 and BMIMBF4 RTILs, respectively.
将室温离子液体(RTILs)用作电化学应用的介质非常具有吸引力。在这项工作中,通过循环伏安法和恒电位瞬态技术,研究了在疏水的1-正丁基-3-甲基咪唑六氟磷酸盐(BMIMPF6)和亲水的1-正丁基-3-甲基咪唑四氟硼酸盐(BMIMBF4)室温离子液体以及KNO3水溶液中的玻碳电极上银的电化学沉积。伏安图显示在BMIMPF6和BMIMBF4中存在与AgBF4中银的沉积和溶解相关的还原峰和氧化峰,类似于KNO3水溶液中AgNO3的氧化还原行为。在这些电化学系统的所有循环伏安图中都观察到一个交叉环,表明存在成核过程。通过对实验电流瞬变的分析表明,银在这些介质中的电化学沉积过程具有三维成核且扩散控制半球形生长的特征,并且银的成核分别紧密遵循BMIMPF6中渐进成核和KNO3水溶液中瞬时成核的预测响应。与这两种情况相比,银在BMIMBF4中的电化学沉积偏离了瞬时和成核模型,这可能受混合动力学和扩散控制。基于实验结果表明,室温离子液体的粘度和与水的混溶性等参数会影响银的电沉积行为。采用原子力显微镜探测银沉积物的表面形貌,结果表明光亮的银沉积物相当致密,明显存在<100 nm的分离纳米团簇,这对应于岛状生长模型。4-巯基苯甲酸单层膜的强烈增强拉曼散射表明,所制备的银纳米颗粒膜具有表面增强拉曼散射(SERS)活性。对于在BMIMPF6和BMIMBF4室温离子液体中获得的银膜,增强因子分别计算高达9.0×10^5和1.0×10^6。