No abstract

Scanning electrochemical cell microscopy (SECCM) is used to map anodic and cathodic processes on polycrystalline zinc in 10 mM H2SO4, at the nanoscale. Electrochemical maps are correlated directly with structural data from electron backscatter diffraction applied to the same regions of the surface, and density functional theory (DFT) calculations are used to rationalize the data. Preliminary data on droplet stability with SECCM point measurements indicated that there was a significant spreading of the meniscus cell with an air atmosphere, attributed to changes in pH during the oxygen reduction reaction, compromising the lateral resolution of the SECCM measurement. Experiments with an argon atmosphere, as well as the application of a hydrophobic n-dodecane oil layer on the Zn interface, prevented spreading. Electrochemical maps of polycrystalline Zn surface under an Ar atmosphere indicated that the hydrogen evolution reaction (HER) and Zn electrodissolution on individual low-index grains decreased in the order 1 ¯ 2 1 ¯ 0 ≥ 01 1 ¯ 0 > 0001 . DFT calculations revealed a correlation between experimental values of current associated with HER and Zn dissolution reactions and the predicted hydrogen adsorption and Zn dissolution energies on individual facets, respectively. This work further advances SECCM as a technique for probing electrified interfaces and demonstrates its applicability to reactive metals.

The redox activity (Li‐ion intercalation/deintercalation) of a series of individual LiMn2O4 particles of known geometry and (nano)structure, within an array, is determined using a correlative electrochemical microscopy strategy. Cyclic voltammetry (current–voltage curve, I–E) and galvanostatic charge/discharge (voltage–time curve, E–t) are applied at the single particle level, using scanning electrochemical cell microscopy (SECCM), together with co‐location scanning electron microscopy that enables the corresponding particle size, morphology, crystallinity, and other factors to be visualized. This study identifies a wide spectrum of activity of nominally similar particles and highlights how subtle changes in particle form can greatly impact electrochemical properties. SECCM is well‐suited for assessing single particles and constitutes a combinatorial method that will enable the rational design and optimization of battery electrode materials.

To fully elucidate the structural controls on corrosion-related processes at metal surfaces, experimental measurements should correlate and compare directly structure and activity at the scale of surface heterogeneities (e.g., individual grains, grain boundaries, inclusions, etc.). For example, the hydrogen evolution reaction (HER), which usually serves as the cathodic counterpart to anodic metal dissolution in acidic media, may be highly sensitive to surface microstructure, highlighting the need for nanoscale-resolution electrochemical techniques. In this study, we employ scanning electrochemical cell microscopy (SECCM) in conjunction with colocated scanning electron microscopy, electron backscatter diffraction, and energy-dispersive X-ray spectroscopy to elucidate the relationship between surface structure/composition and HER activity on low carbon steel in aqueous sulfuric acid (pH ≈ 2.3). Through this correlative electrochemical multimicroscopy approach, we show that the HER activity of the low index grains (slightly) decreases in the order (100) > (111) > (101), with grain-dependent free energy of hydrogen adsorption (calculated for the low index planes of iron by using density functional theory, DFT) proposed as a tentative explanation for this subtle structural dependence. More significantly, we show that the HER is greatly facilitated by submicrometer surface defects, specifically grain boundaries, and MnS inclusions, directly identifying these heterogeneities as potential “cathodic sites” during (atmospheric) corrosion. This study demonstrates the considerable attributes of correlative SECCM for identifying nanoscale active sites on surfaces, greatly aiding the understanding of corrosion and electrocatalytic processes.