Abdelrahman Ahmed I, Mohammad Ahmad M, Okajima Takeyoshi, Ohsaka Takeo
Department of Electronic Chemistry, Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, Midori-ku, Yokohama 226-8502, Japan.
J Phys Chem B. 2006 Feb 16;110(6):2798-803. doi: 10.1021/jp056238x.
Multilayers film of nanostructured citrate-stabilized gold particles (AuNPs) has been fabricated based on the layer-by-layer (LBL) technique using a self-assembled monolayer of 1,4-benzenedimethanethiol (BDMT). The formation of AuNPs and BDMT self-assemblies as alternative multilayers was confirmed by transmission electron microscopy (TEM), X-ray photoelectron spectroscope (XPS), and quartz crystal microbalance (QCM). The formation of uniform AuNP layers with an average monolayer thickness of 5-6 nm was obvious in the TEM images. The existence of BDMT molecules as cross linkers for the AuNPs' layers was proved by XPS measurements. The greater affinity of AuNPs' layers to bind BDMT molecules in comparison with the bare Au bulk electrode was revealed by QCM measurements. Electrochemically, the AuNPs' layers on the electrode surface did not only catalyze the reduction of oxygen (ca. 100-mV positive shift of the reduction peak potential compared with that at the bare Au bulk electrode) but also showed a fascinating nature of working as a renewed activated-electrode surface; a zigzag response was observed for oxygen reduction during alternative immobilization of BDMT and the AuNP layer. The self-assembly of a new AuNPs layer restored the catalytic activity that was entirely blocked by the preceding BDMT layer.
基于层层(LBL)技术,使用1,4-苯二甲硫醇(BDMT)的自组装单分子层制备了纳米结构柠檬酸盐稳定的金颗粒(AuNP)多层膜。通过透射电子显微镜(TEM)、X射线光电子能谱仪(XPS)和石英晶体微天平(QCM)确认了AuNP和BDMT自组装作为交替多层膜的形成。在TEM图像中,平均单层厚度为5-6nm的均匀AuNP层的形成很明显。XPS测量证明了BDMT分子作为AuNP层交联剂的存在。QCM测量揭示了与裸金本体电极相比,AuNP层对结合BDMT分子具有更大的亲和力。在电化学方面,电极表面的AuNP层不仅催化氧的还原(与裸金本体电极相比,还原峰电位正移约100mV),而且还表现出作为新的活化电极表面的迷人特性;在交替固定BDMT和AuNP层期间,观察到氧还原的锯齿形响应。新的AuNP层的自组装恢复了被先前BDMT层完全阻断的催化活性。