Surface effects of monolayer-protected gold nanoparticles on the redox reactions between ferricyanide and thiosulfate
Surface effects of monolayer-protected gold nanoparticles on the redox reactions between ferricyanide and thiosulfate作者机构:State Key Laboratory of Electroanalytical Chemistry Changchun Institute of Applied Chemistry Chinese Academy of Sciences Changchun China Department of Chemistry Tsinghua University Beijing China Department of Chemistry University of California Santa Cruz Santa Cruz USA
出 版 物:《Science China Chemistry》 (中国科学(化学英文版))
年 卷 期:2005年第48卷第5期
页 面:424-430页
核心收录:
学科分类:081704[工学-应用化学] 07[理学] 08[工学] 0817[工学-化学工程与技术] 0703[理学-化学] 070301[理学-无机化学]
基 金:financially supported by the National Natural Science Foundation of China(Outstanding Youth Fund Grant No.20125513) a research fellowship from the K.C.Wong Educational Foundation
主 题:electron transfer, three-dimensional self-assembled monolayers, redox reaction, electron transfer mediator, surface effect.
摘 要:Electron transfer through the self-assembled monolayers (SAMs) on gold nanopar-ticles is investigated by using the monolayer protected gold nanoclusters (MPCs) as elec-tron-transfer mediators. 3-Mercaptopropionic acid (MPA) and 11-meraptoundecanoic acid (MUA) MPCs were employed to catalyze the redox reaction between potassium ferricyanide and sodium thiosulfate. The catalytic mechanism was proposed that the MPCs act as diffusing elec-tron-mediators and electron transfers to and from the MPCs surface. Therefore the electron transfer rate through the capping layers would be proportional to the MPCs catalyzed reaction rate, which was monitored by the UV absorbance of ferricyanide. The calculated apparent rate constant was orders of magnitude smaller than that of the maximum of tunneling current, which was attributed to the splited energy level of the nanoscale particles.