A Micropore Nanoband Electrode Array for Enhanced Electrochemical Generation/Analysis in Flow Systems

IF 3.3 3区 化学 Q2 CHEMISTRY, PHYSICAL Faraday Discussions Pub Date : 2024-07-26 DOI:10.1039/d4fd00125g
Fiona Moore, Ilka Schmueser, Jonathan G Terry, Andrew R Mount
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Abstract

Our previous work has established that micron resolution photolithography can be employed to make microsquare nanoband edge electrode (MNEE) arrays. The MNEE configuration enables systematic control of the parameters (electrode number, cavity array spacing, and nanoelectrode dimensions and placement) which control geometry, conferring consistent high-fidelity electrode response across the array (e.g. high signal, high signal-to-noise, low limits of detection and fast, steady-state, reproducible and quantitative response) and allowing the tuning of individual and combined electrode interactions. Building on this, in this paper we now produce and characterise a Micropore Nanoband Electrode (MNE) Array designed for flow-through detection, where an MNEE edge electrode configuration is used to form a nanotube electrode embedded in the wall of each micropore, formed as an array of pores of controlled pore size and placement through an insulating membrane of sub-micrometer thickness. The success of this approach is established by the close correspondence between experiment and simulation and the enhanced and quantitative detection of redox species flowing through the micropores over the very wide range of flow rates relevant e.g. to (bio)sensing and chromatography. Quantitative electrochemical reaction with low conversion, suitable for analysis, is demonstrated at high flow, whilst quantitative electrochemical reaction with high conversion, suitable for electrochemical product generation, is enabled at lower flow. The fundamental array response is analysed in terms of established flow theories, demonstrating the additive contributions of within pore enhanced diffusional (nanoband edge) and advective (Levich-type) currents, the control of the degree of diffusional overlap between pores through pore spacing and flow rate, the control by design across length scales ranging from nanometer through micrometer to a centimetre array and the ready determination of physicochemical parameters, enabling discussion of the potential of this breakthrough technology to addresses unmet needs in generation and analysis.
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用于增强流动系统中电化学生成/分析的微孔纳米带电极阵列
我们之前的工作已经证实,微米分辨率光刻技术可用于制造微方形纳米带边缘电极(MNEE)阵列。MNEE 配置可对控制几何形状的参数(电极数量、空腔阵列间距以及纳米电极尺寸和位置)进行系统控制,使整个阵列具有一致的高保真电极响应(例如,高信号、高信噪比、低检测限以及快速、稳态、可重现和定量响应),并可对单个和组合电极的相互作用进行调整。在此基础上,我们在本文中制作了微孔纳米带电极(MNE)阵列,并对其进行了表征,该阵列设计用于流过式检测,其中 MNEE 边缘电极配置用于在每个微孔壁中嵌入纳米管电极,形成孔径大小可控的孔阵列,并通过亚微米厚度的绝缘膜放置。这种方法的成功之处在于实验与模拟之间的紧密联系,以及在非常宽的流速范围内对流经微孔的氧化还原物种进行增强和定量检测,例如与(生物)传感和色谱法相关的检测。在高流量条件下,可实现适合分析的低转化率定量电化学反应,而在低流量条件下,可实现适合电化学产品生成的高转化率定量电化学反应。根据已建立的流动理论对基本阵列反应进行了分析,证明了孔内增强扩散(纳米带边缘)和平流(列维奇型)电流的叠加贡献、通过孔间距和流速控制孔间扩散重叠程度、通过设计控制从纳米到微米再到厘米阵列的长度尺度以及随时确定物理化学参数,从而讨论了这项突破性技术的潜力,以满足生成和分析方面的未满足需求。
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来源期刊
Faraday Discussions
Faraday Discussions 化学-物理化学
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期刊介绍: Discussion summary and research papers from discussion meetings that focus on rapidly developing areas of physical chemistry and its interfaces
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