Laboratory of Biosensors and Bioelectronics, Department of Information Technology and Electrical Engineering, ETH Zürich, Zürich, Switzerland.
Langmuir. 2010 May 18;26(10):7619-26. doi: 10.1021/la9042342.
The optical signal of a localized surface plasmon resonance (LSPR)-based sensor combined with electrochemistry was investigated. Gold nanoparticles were immobilized on an indium tin oxide (ITO) substrate, which functioned as working electrode. Using cyclic voltammetry synchronized with LSPR sensing, surface reactions on gold were detected both electrically and optically. In the capacitive charging regime, optical signals linear to the applied potential were detected. Gold was found to be dissolved above the oxidation potential and partially redeposited during the reduction, which changed size and conformation of the gold nanoparticles. In kinetic measurements, slower potential establishment was observed at lower salt concentrations. Simulations by multiple multipole program (MMP) suggested the formation of a lossy layer by combination of charge depletion of gold and negative ion adsorption even below the reaction potential. We consider the results presented here of importance for any future sensors based on combined plasmonics and electrochemistry.
研究了结合电化学的局域表面等离子体共振(LSPR)传感器的光学信号。将金纳米粒子固定在氧化铟锡(ITO)基底上,作为工作电极。通过与 LSPR 传感同步的循环伏安法,在电化学和光学上检测金表面的反应。在电容充电状态下,检测到与施加电位成正比的光学信号。金在氧化电位以上被溶解,并在还原过程中部分再沉积,这改变了金纳米粒子的大小和构象。在动力学测量中,在较低的盐浓度下观察到较慢的电位建立。多极矩程序(MMP)的模拟表明,即使在反应电位以下,通过金的电荷耗尽和负离子吸附的组合,也会形成一个有损耗的层。我们认为这里提出的结果对任何基于等离子体和电化学结合的未来传感器都很重要。