光电流
电极
单层
激发态
部分
电化学
材料科学
吸收光谱法
光化学
自组装单层膜
化学
纳米技术
光电子学
立体化学
物理化学
光学
原子物理学
物理
作者
Hiroshi Imahori,Takayuki Azuma,Anawat Ajavakom,Hiroyuki Norieda,Hiroko Yamada,Yoshiteru Sakata
摘要
Three different kinds of C60 alkanethiols have been prepared by changing systematically the linking positions, ortho, meta, and para, at a phenyl group on a pyrolidine ring fused to the C60 moiety. Electrochemical measurements showed that well-ordered structures are formed in self-assembled monolayers of these C60 alkanethiols on gold electrodes. Photoelectrochemical studies were carried out using gold electrodes modified with self-assembled monolayers of the C60. A stable anodic photocurrent was observed in the presence of an electron sacrificer when the modified gold electrode was illuminated with a monochromic light. Dependence of the photocurrents on the applied potential together with the agreement of the action spectra with the absorption spectra support the following photocurrent generation mechanism: the generation of a vectorial electron flow from the electron sacrificer to the gold electrode via the excited triplet state of the C60. The quantum yields vary from 7.5% to 9.8%, depending on the linking positions.
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