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Application of integrated SECM ultra-micro-electrode and AFM force probe to biosensor surfaces

机译:集成式SECM超微电极和AFM力探头在生物传感器表面的应用

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摘要

The integration of scanning electrochemical ultra-micro-electrode (UME) with atomic force microscope cantilever probe have been achieved by using a homemade photolithography system. A gold-film-coated AFM cantilever was insulated with photo resist coating and a pointed end of the AFM probe was opened by illuminating with maskless arbitrary optical micro-pattern generator. To realize precise control of probe sample distance constantly, the resulting scanning electrochemical microscopy (SECM)–AFM probe was operated using a dynamic force microscopy (DFM) technique with magnetic field excitation. From a steady-state voltammetric experiment, the effective electrode diameters of the probes thus prepared were estimated to be from 0.050 to 6.2 m. The capability of this SECM–AFM probe have been tested using gold comb in the presence of Fe(CN)_6~(3-). The simultaneous imaging of the topography and electrochemical activity of the strip electrode was successfully obtained. We also used the SECM–AFM to examine in situ topography and enzymatic activity measurement. Comparison of topography and oxidation current profiles above enzyme-modified electrode showed active parts distribution of biosensor surface.
机译:通过使用自制的光刻系统,已将扫描电化学超微电极(UME)与原子力显微镜悬臂探针集成在一起。用光致抗蚀剂涂层使涂有金膜的AFM悬臂绝缘,并通过用无掩模的任意光学微图案发生器照射来打开AFM探针的尖端。为了不断实现对探针样品距离的精确控制,所产生的扫描电化学显微镜(SECM)–AFM探针是使用带有磁场激励的动态力显微镜(DFM)技术进行操作的。根据稳态伏安法实验,由此制备的探针的有效电极直径估计为0.050至6.2m。已经使用金梳在Fe(CN)_6〜(3-)存在下测试了SECM–AFM探针的功能。成功获得带状电极的形貌和电化学活性的同时成像。我们还使用了SECM–AFM来检查原位形貌和酶活性测量结果。酶修饰电极上方的形貌和氧化电流曲线的比较显示了生物传感器表面的活性部分分布。

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