Modulating Electrocatalysis on Graphene Heterostructures: Physically Impermeable Yet Electronically Transparent Electrodes.

The electronic properties and extreme thinness of graphene make it an attractive platform for exploring electrochemical interactions across dissimilar environments. Here, we report on the systematic tuning of the electrocatalytic activity toward the oxygen reduction reaction (ORR) via heterostructures formed by graphene modified with a metal underlayer and an adlayer consisting of a molecular catalyst. Systematic voltammetric testing and electrochemical imaging of patterned electrodes allowed us to confidently probe modifications on the ORR mechanisms and overpotential. We found that the surface configuration largely determined the ORR mechanism, with adlayers of porphyrin molecular catalysts displaying a higher activity for the 2e- pathway than the bare basal plane of graphene. Surprisingly, however, the underlayer material contributed substantially to lower the activation potential for the ORR in the order Pt > Au > SiO x, strongly suggesting the involvement of the solution-excluded metal on the reaction. Computational investigations suggest that ORR enhancements originate from permeation of metal d-subshell electrons through the graphene layer. In addition, these physically impermeable but electronically transparent electrodes displayed tolerance to cyanide poisoning and stability toward long-term cycling, highlighting graphene as an effective protection layer of noble metal while enabling electrochemical interactions. This work has implications in the mechanistic understanding of 2D materials and core-shell-type heterostructures for electrocatalytic reactions.

Cyclic Voltammetry Probe Approach Curves with Alkali Amalgams at Mercury Sphere-Cap Scanning Electrochemical Microscopy Probes.

We report a method of precisely positioning a Hg-based ultramicroelectrode (UME) for scanning electrochemical microscopy (SECM) investigations of any substrate. Hg-based probes are capable of performing amalgamation reactions with metal cations, which avoid unwanted side reactions and positive feedback mechanisms that can prove problematic for traditional probe positioning methods. However, prolonged collection of ions eventually leads to saturation of the amalgam accompanied by irreversible loss of Hg. In order to obtain negative feedback positioning control without risking damage to the SECM probe, we implement cyclic voltammetry probe approach surfaces (CV-PASs), consisting of CVs performed between incremental motor movements. The amalgamation current, peak stripping current, and integrated stripping charge extracted from a shared CV-PAS give three distinct probe approach curves (CV-PACs), which can be used to determine the tip-substrate gap to within 1% of the probe radius. Using finite element simulations, we establish a new protocol for fitting any CV-PAC and demonstrate its validity with experimental results for sodium and potassium ions in propylene carbonate by obtaining over 3 orders of magnitude greater accuracy and more than 20-fold greater precision than existing methods. Considering the timescales of diffusion and amalgam saturation, we also present limiting conditions for obtaining and fitting CV-PAC data. The ion-specific signals isolated in CV-PACs allow precise and accurate positioning of Hg-based SECM probes over any sample and enable the deployment of CV-PAS SECM as an analytical tool for traditionally challenging conditions.

Fabrication and Demonstration of Mercury Disc-Well Probes for Stripping-Based Cyclic Voltammetry Scanning Electrochemical Microscopy.

Scanning electrochemical microscopy (SECM) is a rising technique for the study of energy storage materials. Hg-based probes allow the extension of SECM investigations to ionic processes, but the risk of irreversible Hg amalgam saturation limits their operation to rapid timescales and dilute analyte solutions. Here, we report a novel fabrication protocol for Hg disc-well ultramicroelectrodes (UMEs), which retain access to stripping information but are less susceptible to amalgam saturation than traditional Hg sphere-caps or thin-films. The amalgamation and stripping behaviors of Hg disc-well UMEs are compared to those of traditional Hg sphere-cap UMEs and corroborated with data from finite element simulations. The improved protection against amalgam saturation allows Hg disc-wells to operate safely in highly concentrated environments at long timescales. The utility of the probes for bulk measurements extends also to SECM studies, where the disc geometry facilitates small tip-substrate gaps and improves both spatial and temporal resolution. Because they can carry out slow, high-resolution anodic stripping voltammetry approaches and imaging in concentrated solutions, Hg disc-well electrodes fill a new analytical niche for studies of ionic reactivity and are a valuable addition to the electrochemical toolbox.

Electrochemical Imaging of Photoanodic Water Oxidation Enhancements on TiO2 Thin Films Modified by Subsurface Aluminum Nanodimers.

Detecting metal plasmonic enhancements on the activity of semiconducting photoanodes for water oxidation is often obscured by the inherent electroactivity and instability of the metal in electrolyte. Here, we show that thin TiO2 photoanodes modified by subsurface Al nanodimers (AlNDs) display enhancements that are consistent with plasmon modes. We directly observed enhancements by mapping the oxygen evolution rates on TiO2/AlND patterns using scanning electrochemical microscopy (SECM) while exciting the surface plasmons of the nanodimers. This study highlights the importance of sample configuration for the in situ characterization of metal/photoanode interactions and suggests a route for Al-based plasmonics applied to photoelectrochemistry.

Emerging scanning probe approaches to the measurement of ionic reactivity at energy storage materials.

Many modern energy storage technologies operate via the nominally reversible shuttling of alkali ions between an anode and a cathode capable of hosting them. The degradation process that occurs with normal usage is not yet fully understood, but emerging progress in analytical tools may help address this knowledge gap. By interrogating ionic fluxes over electrified surfaces, scanning probe methods may identify features that impact the local cyclability of a material and subsequently help inform rational electrode design for future generations of batteries. Methods developed for identifying ion fluxes for batteries show great promise for broader applications, including biological interfaces, corrosion, and catalysis.

Lithium ion quantification using mercury amalgams as in situ electrochemical probes in nonaqueous media.

We report on the quantitative, spatially resolved study of ionic processes for energy materials in nonaqueous environments by in situ electrochemical means at the micro- and nanoscale. Mercury-capped platinum ultramicroelectrodes (Hg/Pt UMEs) were tested as probes for alkali ions in propylene carbonate (PC) in an oxygen- and water-free environment. Anodic stripping voltammetry (ASV) performed at Hg/Pt UMEs displayed a linear response to Li(+) concentration extending from 20 µM to at least 5 mM. The sensitivities of these probes for ionic lithium are 1.93 and -23.2 pA µM(-1) by the steady-state amalgamation current and the peak stripping current, respectively. These values showed excellent agreement with simulated results as well as to those obtained experimentally for Cd(2+) in H2O. We further explored the interfacial imaging of lithium ion flux at an electrified interface. Scanning electrochemical microscopy (SECM) using Hg/Pt UMEs showed that the steady-state amalgamation of ionic lithium could be used to reliably position a probe close to a substrate. Investigations on a selectively insulated gold electrode in an organic solvent system showcased the response of Hg/Pt UMEs to lithium uptake by an electroactive material. Additionally, lithium stripping voltammetry at Hg deposits on a 120 nm carbon nanoelectrode demonstrated the possibility of implementing the introduced imaging strategy at the nanoscale. This work opens a way to directly correlate material defects and reactive heterogeneity in energy materials with unprecedented spatial and temporal resolution.

Information content in fluorescence correlation spectroscopy: binary mixtures and detection volume distortion.

When properly implemented, fluorescence correlation spectroscopy (FCS) reveals numerous static and dynamic properties of molecules in solution. However, complications arise whenever the measurement scenario is complex. Specific limitations occur when the detection region does not match the ideal Gaussian geometry ubiquitously assumed by FCS theory, or when properties of multiple fluorescent species are assessed simultaneously. A simple binary solution of diffusers, where both mole fraction and diffusion constants are sought, can face interpretive difficulty. In order to better understand the limits of FCS, this study systematically explores the relationship between detection-volume distortion, diffusion constants, species mole fraction, and fitting methodology in analyses that utilize a two-component autocorrelation model. FCS measurements from solution mixtures of dye-labeled protein and free dye are compared to simulations, which predict the performance of FCS under a variety of experimental circumstances. The results reveal a range of conditions necessary for performing accurate measurements and describe experimental scenarios that should be avoided. The findings also provide guidelines for obtaining meaningful measurements when grossly distorted detection volumes are utilized and generally assess the latent information contained in FCS datasets.