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有序光电化学纳米孔径阵列处远程荧光成像的电化学调制

Electrochemical modulation of remote fluorescence imaging at an ordered opto-electrochemical nanoaperture array.

作者信息

Chovin Arnaud, Garrigue Patrick, Servant Laurent, Sojic Neso

机构信息

Laboratoire d'Analyse Chimique par Reconnaissance Moléculaire Université Bordeaux I, ENSCPB, 33607 Pessac, France.

出版信息

Chemphyschem. 2004 Aug 20;5(8):1125-32. doi: 10.1002/cphc.200400015.

Abstract

An array of nanometer-sized apertures capable of electrochemically modulating the fluorescence of a model analyte is presented. The device, which combines near-field optical methods and ultramicroelectrode properties in an array format, is based on an etched coherent optical fiber bundle. Indeed, the fabrication steps produced an ordered array where each optical nanoaperture is surrounded by a ring-shaped gold nanoelectrode. The chronoamperometric behavior of the array shows stable diffusion-limited quasi-steady-state response. The model analyte, tris(2,2'-bipyridine) ruthenium, emits fluorescence in the Ru(II) state, but not in the oxidized Ru(III) state. Fluorescence is excited by visible light exiting from each nanoaperture since light is confined to the tip apex by the gold coating. A fraction of the isotropically emitted luminescence is collected by the same nanoaperture, transmitted by the corresponding fiber core and eventually detected by a charge-coupled device (CCD) camera. The array format provides a fluorescence image resolved at the nanometric scale which covers a large micrometric area. Therefore the high-density array plays a bridging role between these two fundamental scales. We established that the opto-electrochemical nanoapertures are optically independent. Fluorescence of the sample collected by each nanoaperture is modulated by changing the potential of the nanoring electrodes. Reversible electrochemical switching of remote fluorescence imaging is performed through the opto-electrochemical nanoaperture array itself. Eventually this ordered structure of nanometer light sources which are electrochemically manipulated provides promising photonic or electro-optical devices for various future applications. For example, such an array has potential in the development of a combined SNOM-electrochemical nanoprobe array to image a real sample concomitantly at the nanometer and micrometer scale.

摘要

本文展示了一种能够对模型分析物的荧光进行电化学调制的纳米尺寸孔径阵列。该装置以阵列形式结合了近场光学方法和超微电极特性,基于蚀刻的相干光纤束制成。实际上,制造步骤产生了一种有序阵列,其中每个光学纳米孔径被环形金纳米电极包围。该阵列的计时电流行为显示出稳定的扩散限制准稳态响应。模型分析物三(2,2'-联吡啶)钌在Ru(II)状态下发射荧光,但在氧化的Ru(III)状态下不发射。由于光被金涂层限制在尖端顶点,可见光从每个纳米孔径射出时激发荧光。各向同性发射的一部分发光由同一个纳米孔径收集,通过相应的光纤芯传输,最终由电荷耦合器件(CCD)相机检测。阵列形式提供了在纳米尺度上分辨的荧光图像,覆盖了较大的微米区域。因此,高密度阵列在这两个基本尺度之间起到了桥梁作用。我们确定光电化学纳米孔径在光学上是独立的。通过改变纳米环电极的电位来调制每个纳米孔径收集的样品的荧光。通过光电化学纳米孔径阵列本身进行远程荧光成像的可逆电化学切换。最终,这种经电化学操纵的纳米光源有序结构为未来各种应用提供了有前景的光子或电光器件。例如,这样的阵列在开发组合式扫描近场光学显微镜 - 电化学纳米探针阵列以同时在纳米和微米尺度上对真实样品成像方面具有潜力。

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