Department of Chemical Engineering, University of California, Santa Barbara, California 93106-5080, United States.
Langmuir. 2012 Sep 11;28(36):13080-93. doi: 10.1021/la3018216. Epub 2012 Aug 29.
We present a newly designed electrochemical surface forces apparatus (EC-SFA) that allows control and measurement of surface potentials and interfacial electrochemical reactions with simultaneous measurement of normal interaction forces (with nN resolution), friction forces (with μN resolution), and distances (with Å resolution) between apposing surfaces. We describe three applications of the developed EC-SFA and discuss the wide-range of potential other applications. In particular, we describe measurements of (1) force-distance profiles between smooth and rough gold surfaces and apposing self-assembled monolayer-covered smooth mica surfaces; (2) the effective changing thickness of anodically growing oxide layers with Å-accuracy on rough and smooth surfaces; and (3) friction forces evolving at a metal-ceramic contact, all as a function of the applied electrochemical potential. Interaction forces between atomically smooth surfaces are well-described using DLVO theory and the Hogg-Healy-Fuerstenau approximation for electric double layer interactions between dissimilar surfaces, which unintuitively predicts the possibility of attractive double layer forces between dissimilar surfaces whose surface potentials have similar sign, and repulsive forces between surfaces whose surface potentials have opposite sign. Surface roughness of the gold electrodes leads to an additional exponentially repulsive force in the force-distance profiles that is qualitatively well described by an extended DLVO model that includes repulsive hydration and steric forces. Comparing the measured thickness of the anodic gold oxide layer and the charge consumed for generating this layer allowed the identification of its chemical structure as a hydrated Au(OH)(3) phase formed at the gold surface at high positive potentials. The EC-SFA allows, for the first time, one to look at complex long-term transient effects of dynamic processes (e.g., relaxation times), which are also reflected in friction forces while tuning electrochemical surface potentials.
我们提出了一种新设计的电化学表面力仪(EC-SFA),该仪器允许控制和测量表面电势和界面电化学反应,同时测量法向相互作用力(分辨率为 nN)、摩擦力(分辨率为 μN)以及相互接近表面之间的距离(分辨率为 Å)。我们描述了所开发的 EC-SFA 的三种应用,并讨论了其广泛的潜在其他应用。特别是,我们描述了以下三种应用的测量结果:(1)光滑和粗糙金表面之间以及附着有自组装单分子层的光滑云母表面之间的力-距离曲线;(2)粗糙和光滑表面上以 Å 精度测量阳极生长氧化层的有效变化厚度;(3)金属-陶瓷接触处的摩擦力随施加电化学电势的变化,所有这些都作为应用电化学电势的函数。原子级光滑表面之间的相互作用力可以很好地用 DLVO 理论和用于不同表面之间电双层相互作用的 Hogg-Healy-Fuerstenau 近似来描述,这一近似出人意料地预测了具有相似符号的不同表面之间可能存在吸引力的电双层力,以及具有相反符号的表面之间的排斥力。金电极的表面粗糙度导致力-距离曲线中出现额外的指数排斥力,这可以通过扩展的 DLVO 模型很好地描述,该模型包括排斥水合和空间力。将测量的阳极金氧化层的厚度与生成该层所消耗的电荷进行比较,从而确定其化学结构为在高正电势下在金表面形成的水合 Au(OH)(3)相。EC-SFA 首次允许人们观察动态过程(例如弛豫时间)的复杂长期瞬态效应,同时在调整电化学表面电势时也可以反映在摩擦力中。