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Heterogeneous electrocatalytic reactions are believed to occur at a minority of coordination sites through a series of elementary reactions that are balanced by minor equilibria. These features mask changes in reaction sites, making it challenging to directly identify and analyze reaction sites or intermediates while studying reaction mechanisms. Systematic perturbations of a reaction system often yield systematic changes in material properties and behavior. Correlations between measurable changes in parameters describing the structure and behavior, therefore, serve as powerful tools for distinguishing active reaction sites. This review explores structure–property correlations that have advanced understanding of behavior and reaction mechanisms in heterogeneous electrocatalysis. It covers correlations that have advanced understanding of the contributions of the local reaction environment to reactivity, of structure and bonding within solid-state materials, of geometric or mechanical strain in bonding environments, and of the impact of structural defects. Such correlations can assist researchers in developing next generation catalysts by establishing catalyst design principles and gaining control over reaction mechanisms.

The consistent fabrication of high performance α-Fe2O3 photoanodes for the oxygen evolution reaction remains a challenge. We work towards resolving this issue by developing in situ variable temperature Raman spectroscopy as a means to better understand the formation of α-Fe2O3, using the conversion of γ-FeOOH to α-Fe2O3 under varied gaseous environments as a model case. The sensitivity of Raman spectroscopy to structural changes provides mechanistic insights that are not readily available in more conventional approaches, such as thermal gravimetric analysis and differential scanning calorimetry. The Raman spectra are combined with conventional thermal analyses to interpret the photoelectrocatalytic performance of a series of α-Fe2O3 photoanodes prepared by systematic variation of a three-stage annealing protocol. The combined results suggest that protohematite, a form of α-Fe2O3 where trapped hydroxyl ligands are balanced by Fe(III) vacancies, forms between 200 °C and 400 °C in a reaction environment-dependent fashion. This protohematite is shown to be remarkably persistent once formed, degrading photoelectrocatalytic performance. This research advances understanding of the γ-FeOOH to α-Fe2O3 structural transformation, illustrates a powerful method to study solid state phase transitions, and provides guidance for the synthesis of high quality α-Fe2O3 from a convenient precursor.

Single gold particles may serve as room temperature single electron memory units because of their size dependent electronic level spacing. Here, we present a proof-of-concept study by electrochemically controlled scanning probe experiments performed on tailor-made Au particles of narrow dispersity. In particular, the charge transport characteristics through chemically synthesized hexane-1-thiol and 4-pyridylbenzene-1-thiol mixed monolayer protected Au(144) clusters (MPCs) by differential pulse voltammetry (DPV) and electrochemical scanning tunneling spectroscopy (EC-STS) are reported. The pyridyl groups exposed by the Au-MPCs enable their immobilization on Pt(111) substrates. By varying the humidity during their deposition, samples coated by stacks of compact monolayers of Au-MPCs or decorated with individual, laterally separated Au-MPCs are obtained. DPV experiments with stacked monolayers of Au(144)-MPCs and EC-STS experiments with laterally separated individual Au(144)-MPCs are performed both in aqueous and ionic liquid electrolytes. Lower capacitance values were observed for individual clusters compared to ensemble clusters. This trend remains the same irrespective of the composition of the electrolyte surrounding the Au(144)-MPC. However, the resolution of the energy level spacing of the single clusters is strongly affected by the proximity of neighboring particles.