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Ultrasensitive spectroelectrochemistry of monolayer and submonolayer thin films using an electroactive integrated optical waveguide

机译:使用电活性集成光波导的单层和亚单层薄膜的超灵敏光谱电化学

摘要

To increase the applicability of spectroelectrochemistry to ultrathin films at a transparent semiconductor electrode, a single-mode, step-index electroactive integrated optical waveguide (the EA-IOW) incorporating an indium tin oxide top layer as an electrode was developed. The EA-IOW is much more sensitive to absorbance by molecular adlayer species than previous electroactive waveguide designs; a sensitivity increase of ca. 4000 relative to a single-pass transmission experiment has been measured by monitoring the reduction of a surface-adsorbed dye molecule. An important characteristic of the present three-layer EA-IOW structure is that its design is close to being optimized in terms of maximizing sensitivity while maintaining acceptable optical losses, as determined by theoretical modeling. Before the EA-IOW can be applied to measure absorbance changes arising from electron transfer in ultrathin films, the background optical changes that occur as a function of potential must be understood. There is a linear decrease in outcoupled intensity as the EA-IOW is scanned negative which is a result of an increase in the number of free carriers inside the ITO, a highly reproducible effect. There is also a poorly reproducible non-linear component to the optical background, accompanied by a hysteresis between the forward and reverse potential scans, that disappears after conditioning the EA-IOW in electrolyte solution for a period of several days. It is hypothesized that his effect is due to hydroxylation of the ITO network. To test the EA-IOW experimentally, the reduction of surface-adsorption methylene blue was monitored, along with the formation of Prussian blue during the electrochemistry of ferricyanide. Two experimental applications of the EA-IOW will be reviewed; first, the EA-IOW was used to measure the spectroelectrochemistry of submonolayer films of phthalocyanine polymeric assemblies to compare the electrochemistry at submonolayer and multilayer coverages. Finally, the use of the EA-IOW in protein electrochemistry will be discussed. The dichroic ratio of cytochrome c adsorbed to indium tin oxide was measured as a function of potential, and found to be consistent with an orientation of the heme ligand that is almost parallel to the electrode surface. Also, a change in heme orientation was detected during reduction of the protein.
机译:为了增加光谱电化学在透明半导体电极上对超薄膜的适用性,开发了一种以铟锡氧化物顶层作为电极的单模,阶跃折射率电活性集成光波导(EA-IOW)。与以前的电活性波导设计相比,EA-IOW对分子吸收层物种的吸收更为敏感。灵敏度增加约通过监测表面吸附的染料分子的减少,已经测量了相对于单次通过实验的4000。当前的三层EA-IOW结构的一个重要特征是,如理论模型所确定的,就其设计而言,在最大程度地提高灵敏度,同时保持可接受的光学损耗方面,其设计已接近优化。在将EA-IOW用于测量超薄膜中电子转移引起的吸光度变化之前,必须了解作为电势函数而发生的背景光学变化。当EA-IOW被扫描为负值时,外耦合强度呈线性下降,这是ITO内部自由载流子数量增加的结果,具有高度可复制的效果。光学背景中还存在可重现的非线性成分,伴有正向和反向电位扫描之间的滞后现象,在电解质溶液中将EA-IOW调节几天后,该滞后现象消失了。假设他的作用是由于ITO网络的羟基化。为了通过实验测试EA-IOW,监测了表面吸附亚甲基蓝的减少以及铁氰化物电化学过程中普鲁士蓝的形成。 EA-IOW的两个实验应用将得到审查;首先,EA-IOW用于测量酞菁聚合物组件的亚单层膜的光谱电化学,以比较亚单层和多层覆盖率的电化学。最后,将讨论EA-IOW在蛋白质电化学中的用途。测量了吸附到铟锡氧化物上的细胞色素c的二向色比,作为电位的函数,发现与几乎平行于电极表面的血红素配体的取向一致。同样,在蛋白质还原过程中检测到血红素方向的变化。

著录项

  • 作者

    Dunphy Darren Robert;

  • 作者单位
  • 年度 1999
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  • 原文格式 PDF
  • 正文语种 en_US
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