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首页> 外文期刊>Analytical chemistry >Scanning electrochemical microscopy. 60. Quantitative calibration of the SECM substrate generation/tip collection mode and its use for the study of the oxygen reduction mechanism
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Scanning electrochemical microscopy. 60. Quantitative calibration of the SECM substrate generation/tip collection mode and its use for the study of the oxygen reduction mechanism

机译:扫描电化学显微镜。 60. SECM基质生成/吸头收集模式的定量校准及其在研究氧还原机理中的用途

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The substrate generation/tip collection (SG/TC) mode of scanning electrochemical microscopy (SECM) coupled with linear voltammetry is proposed as a way to quantify reaction intermediates generated in the solution at small substrates (100 mu m diameter). The collection efficiency (CE) for SG/TC mode depends on the collector tip radius (a), the tip/substrate distance (d), and the size of the insulating glass sheath surrounding the collector tip (RG). In this work, we present experimental and simulated calibration CE values for different SG/TC geometries. Results of digital simulations in axial 2-D symmetry with the tip approaching a planar substrate are shown and fit experimental results obtained using ferrocenemethanol as a redox mediator very well. This model assumes that the mediator reacts under stationary-state conditions and undergoes diffusion-controlled electron transfer without any heterogeneous or homogeneous kinetic complications. Empirical equations for all SG/TC geometries reported here are provided as a convenient way to predict the maximum CE value for any given distance within the calibration range. Hydrogen peroxide quantification during the oxygen reduction reaction (ORR) at a Hg on Au electrode in acid pH was carried out using the SG/TC mode of SECM to demonstrate the utility of this technique in determining the number of electrons transferred (n) in the ORR. The results (n = 2.12-2.19) clearly point out the predominance of the two-electron pathway over the four-electron pathway when ORR takes place at this electrode material. Therefore, this work presents a powerful alternative to the rotating ring-disk electrode (RRDE) as means of obtaining mechanistic information by calculating the number of electrons transferred during an electrochemical reaction.
机译:提出了结合线性伏安法的扫描电化学显微镜(SECM)的底物生成/吸头收集(SG / TC)模式,作为定量在小底物(直径为100μm)上溶液中生成的反应中间体的一种方法。 SG / TC模式的收集效率(CE)取决于收集器尖端半径(a),尖端/基底距离(d)以及围绕着收集器尖端的绝缘玻璃护套的尺寸(RG)。在这项工作中,我们介绍了针对不同SG / TC几何形状的实验和模拟校准CE值。示出了轴向二维对称性的数字仿真结果,其中尖端接近平面基板,并且很好地拟合了使用二茂铁甲醇作为氧化还原介体获得的实验结果。该模型假定介体在稳态条件下发生反应,并进行扩散控制的电子转移,而没有任何异质或均质的动力学复杂性。提供此处报告的所有SG / TC几何形状的经验公式,作为预测校准范围内任何给定距离的最大CE值的便捷方法。使用SECM的SG / TC模式在Au电极上的汞在酸性pH值下的Hg上进行氧还原反应(ORR)时对过氧化氢进行定量,以证明该技术在确定电子转移数量(n)中的实用性ORR。结果(n = 2.12-2.19)清楚地指出了当在该电极材料上发生ORR时,两电子途径比四电子途径的优势。因此,这项工作为旋转环盘电极(RRDE)提出了强大的替代方案,作为通过计算电化学反应过程中转移的电子数来获得机械信息的手段。

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