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Noise Phenomena Caused by Reversible Adsorption in Nanoscale Electrochemical Devices

机译:纳米级电化学装置中可逆吸附引起的噪声现象

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We theoretically investigate reversible adsorption in electrochemical devices on a molecular level. To this end, a computational framework is introduced, which is based on 3D random walks including probabilities for adsorption and desorption events at surfaces. We demonstrate that this approach can be used to investigate adsorption phenomena in electrochemical sensors by analyzing experimental noise spectra of a nanofluidic redox cycling device. The evaluation of simulated and experimental results reveals an upper limit for the average adsorption time of ferrocene dimethanol of ~200 μs. We apply our model to predict current noise spectra of further electrochemical experiments based on interdigitated arrays and scanning electrochemical microscopy. Since the spectra strongly depend on the molecular adsorption characteristics of the detected analyte, we can suggest key indicators of adsorption phenomena in noise spectroscopy depending on the geometric aspect of the experimental setup.
机译:我们从理论上在分子水平上研究电化学装置中的可逆吸附。为此,引入了一种基于3D随机游动的计算框架,其中包括表面吸附和解吸事件的概率。我们证明了该方法可用于通过分析纳米流体氧化还原循环装置的实验噪声谱来研究电化学传感器中的吸附现象。模拟和实验结果的评估表明,二茂铁二甲醇的平均吸附时间上限为〜200μs。我们将我们的模型应用于基于叉指阵列和扫描电化学显微镜的进一步电化学实验的当前噪声谱。由于光谱在很大程度上取决于检测到的分析物的分子吸附特性,因此我们可以根据实验装置的几何形状,提出噪声光谱中吸附现象的关键指标。

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