Espen Vinge Fanavoll , David A. Harrington , Svein Sunde , Frode Seland
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引用次数: 0
摘要
介绍了微流控通道中多电极电化学电池的结构和实验验证。给出了利用软光刻技术制备电极和聚二甲基硅氧烷通道的详细方法。电极之间的收集效率和传输时间的校准验证了这些电池用于可溶性物质的快速电化学检测。两个电极之间的质量传输时间低至3ms,流速为200 μ L min-1。我们证明了电极宽度与通道高度比的上限取决于电解质的导电性。提出了最大电极宽度与沟道高度比的建议。在0.1 M H2SO4中,电极宽度建议不超过通道高度的4倍。我们还演示了最小化空气中氧气影响的操作策略,优化步进电机注射泵参数,电解质切换,并展示了如何在通道电极上沉积催化剂颗粒。•制造方法给出了与多个电极的微流体流动电池的所有组件•条件给出了改进的操作,包括几何形状,泵送和电气参数。
Fabrication and optimization of a multielectrode microfluidic electrochemical flow cell for fast and dynamic detection of reaction products
Construction and experimental validation of electrochemical cells with multiple electrodes in a microfluidic channel is described. Details of the fabrication of the electrodes and polydimethylsiloxane channel using soft lithography methods are given. Calibration of the collection efficiencies and transit times between electrodes validate the use of these cells for fast electrochemical detection of soluble species. Mass transit times between two electrodes down to 3 ms with a flow rate of 200 µL min-1 are demonstrated. We demonstrate that there is an upper limit in the electrode width to channel height ratio depending on the electrolyte conductivity. A recommendation for the maximum electrode width to channel height ratio is presented. The electrode width is recommended to not exceed four times the height of the channel in 0.1 M H2SO4. We also demonstrate operating strategies to minimize the impact of oxygen in air, optimization of stepping motor syringe pump parameters, electrolyte switching, and show how to deposit catalyst particles on a channel electrode.
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Fabrication methods are given for all components of microfluidic flow cells with multiple electrodes
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Conditions are given for improved operation, including geometry, pumping, and electrical parameters.