School of Chemistry, The University of New South Wales, Sydney NSW 2052, Australia.
Chemphyschem. 2010 Sep 10;11(13):2807-13. doi: 10.1002/cphc.201000250.
Physical and electrochemical properties of gold nanoparticle-based electrodes are highlighted. Polycrystalline gold electrodes are passivated by a self-assembled monolayer, then the immobilization of gold nanoparticles "switch on" the electrochemical reactivity of ruthenium. Herein, gap-mode Raman studies show that the location of the nanoparticles is on the top of the monolayer, meaning that the "switching on" cannot be attributed to a direct electrical contact between nanoparticles and the gold support. This "switching on" feature is also not affected by the size of the gold nanoparticles with a range of diameters between 4 and 67 nm. Further, the charge of the nanoparticles is investigated by grafting chemical groups onto the nanoparticles which is observed to alter the electron-transfer kinetics. The variation in rate constant however is insufficient to attribute the "switching on" phenomenon to a possible adsorption of the redox species onto the nanoparticles.
基于金纳米粒子的电极的物理和电化学性质得到了强调。多晶金电极被自组装单分子层钝化,然后金纳米粒子的固定“开启”了钌的电化学反应性。在此,间隙模式拉曼研究表明,纳米粒子的位置在单层的顶部,这意味着“开启”不能归因于纳米粒子与金载体之间的直接电接触。这种“开启”特性也不受金纳米粒子直径在 4 至 67nm 之间的大小的影响。此外,通过将化学基团接枝到纳米粒子上研究了纳米粒子的电荷,观察到这会改变电子转移动力学。然而,速率常数的变化不足以将“开启”现象归因于可能的氧化还原物种吸附在纳米粒子上。