Chidsey C E
Science. 1991 Feb 22;251(4996):919-22. doi: 10.1126/science.251.4996.919.
The rate constant of the electron-transfer reaction between a gold electrode and an electroactive ferrocene group has been measured at a structurally well-defined metal-electrolyte interface at temperatures from 1 degrees to 47 degrees C and reaction free energies from -1.0 to +0.8 electron volts (eV). The ferrocene group was positioned a fixed distance from the gold surface by the self-assembly of a mixed thiol monolayer of (eta(5)C(5)H(5))Fe(eta(5)C(5)H(4))CO(2)(CH(2))(16)SH and CH(3)(CH(2))(15)SH. Rate constants from 1 per second (s(-1)) to 2 x 10(4) s(-1) in 1 molar HClO(4) are reasonably fit with a reorganization energy of 0.85 eV and a prefactor for electron tunneling of 7 x 10(4) s(-1) eV(-1). Such self-assembled monolayers can be used to systematically probe the dependence of electron-transfer rates on distance, medium, and spacer structure, and to provide an empirical basis for the construction of interfacial devices such as sensors and transducers that utilize macroscopically directional electron-transfer reactions.
在温度为1摄氏度至47摄氏度、反应自由能为-1.0至+0.8电子伏特(eV)的结构明确的金属-电解质界面上,测量了金电极与电活性二茂铁基团之间电子转移反应的速率常数。通过(η⁵C₅H₅)Fe(η⁵C₅H₄)CO₂(CH₂)₁₆SH和CH₃(CH₂)₁₅SH的混合硫醇单层自组装,将二茂铁基团定位在距金表面固定距离处。在1摩尔HClO₄中,每秒1(s⁻¹)至2×10⁴ s⁻¹的速率常数与0.85 eV的重组能和7×10⁴ s⁻¹ eV⁻¹的电子隧穿前置因子合理拟合。这种自组装单层可用于系统地探究电子转移速率对距离、介质和间隔结构的依赖性,并为构建利用宏观定向电子转移反应的界面器件(如传感器和换能器)提供经验基础。