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Probing charge screening dynamics and electrochemical processes at the solid–liquid interface with electrochemical force microscopy

机译:用电化学力显微镜探测固-液界面上的电荷筛选动力学和电化学过程

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The presence of mobile ions complicates the implementation of voltage-modulated scanning probe microscopy techniques such as Kelvin probe force microscopy (KPFM). Overcoming this technical hurdle, however, provides a unique opportunity to probe ion dynamics and electrochemical processes in liquid environments and the possibility to unravel the underlying mechanisms behind important processes at the solid–liquid interface, including adsorption, electron transfer and electrocatalysis. Here we describe the development and implementation of electrochemical force microscopy (EcFM) to probe local bias- and time-resolved ion dynamics and electrochemical processes at the solid–liquid interface. Using EcFM, we demonstrate contact potential difference measurements, consistent with the principles of open-loop KPFM operation. We also demonstrate that EcFM can be used to investigate charge screening mechanisms and electrochemical reactions in the probe–sample junction. We further establish EcFM as a force-based imaging mode, allowing visualization of the spatial variability of sample-dependent local electrochemical properties.
机译:流动离子的存在使电压调制扫描探针显微镜技术(例如开尔文探针力显微镜(KPFM))的实现复杂化。然而,克服这一技术障碍为在液体环境中探查离子动力学和电化学过程提供了独特的机会,并有可能揭示固液界面上重要过程背后的潜在机理,包括吸附,电子转移和电催化。在这里,我们描述了电化学力显微镜(EcFM)的开发和实施,以探测固-液界面处的局部偏置和时间分辨离子动力学以及电化学过程。使用EcFM,我们证明了接触电势差的测量结果与开环KPFM操作的原理一致。我们还证明了EcFM可用于研究探针-样品连接处的电荷筛选机制和电化学反应。我们进一步将EcFM建立为基于力的成像模式,从而可以可视化样本依赖的局部电化学特性的空间变异性。

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