Considerations for dual barrel electrode fabrication and experimentation.

New electrochemical probes offer the opportunity to investigate new systems. A dual barrel electrode can be laser pulled to produce micron-sized platinum disk electrodes. Here, we detail several important considerations for both the fabrication process and for experimental implimentation of the probe. We provide parameters for a Sutter P-2000 laser puller, methods for optical and electrochemical characterization, tips for how to successfully bevel the microelectrodes, and how salt concentrations and electrostatic discharge affect the voltammetry. This paper serves as a guide for how to successfully implement dual barrel electrodes from fabrication to experimentation.

Triple-Barrel Ultramicroelectrodes for Multipurpose, Submilliliter Electroanalysis.

Here, we have developed and applied a triple-barrel microelectrode. This device incorporates a platinum disk working electrode, a platinum disk counter electrode, and a low-leakage Ag/AgCl reference electrode into a small probe. We demonstrate that the incorporated low-leakage reference electrode shows similar voltammetry, potentiometry, and drift when compared to a commercial reference electrode in bulk solution. We also demonstrate the versatility of such a small three-channel system via voltammetry in nanoliter droplets and through electroanalysis of captured aerosols. Finally, we demonstrate the probe's potential utility in single-cell electroanalysis by making measurements within salmon eggs.

A troubleshooting guide for laser pulling platinum nanoelectrodes.

While there are numerous publications on laser-assisted fabrication and characterization of Pt nanoelectrodes, the exact replication of those procedures is not as straightforward as following a single recipe across laboratories. Often, the working procedures vary by day, by laser puller, or by person. Only a handful of nanoelectrode fabrication papers record their parameters, and even fewer offer troubleshooting advice. Here, we provide a step-by-step guide for laser-assisted Pt nanoelectrode fabrication using low-cost equipment including a laser puller, voltammetry, and simple microscope images captured via cell phone. We also offer solutions for common failures experienced throughout the process to guide beginners as they troubleshoot their own fabrication procedures.

Detecting Methamphetamine in Aerosols by Electroanalysis in a Soap Bubble Wall.

We present a facile method to detect methamphetamine in aerosols by trapping aerosols in a soap bubble wall for electroanalysis. A microwire was placed through a soap bubble wall as a sensing electrode along with a 1 mm diameter platinum wire as the counter/reference electrode. The resulting electrochemical cell and electrode geometry are unique and allow for reproducible electrochemistry between bubble walls. We first provide a thorough investigation of the cell and electrode geometry and an electrochemical characterization of ferrocene methanol in a soap bubble wall composed of 0.1 M KCl and 0.1% Triton X-100 (v/v). To visualize the boundary where the bubble wets the microwire (the effective electrode area) with tens of nanometer resolution, we electrodeposited platinum on carbon microwire. Scanning electron microscopy and energy dispersive X-ray spectroscopy revealed the bubble contact (i.e., cylindrical electrode height) is 157 ± 30 µm. Correlated digital microscopy suggests that the wetting reaches r ∼ 125 µm along the bubble wall laterally from the microwire. Beyond the wetting region, the bubble thickness is 18 ± 1 µm, as indicated by ultraviolet-visible spectroscopy experiments probing dissolved bis(bipyridine)ruthenium(II) chloride. We illustrate that the voltammetric character in this system is highly dependent on the bubble wetting parameters, which are tuned by changing the microwire material. We then applied this system to the collection and electrochemical detection of methamphetamine in liquid aerosols, where the bubble wall acts as a low volume collector.

Mapping Solvent Entrapment in Multiphase Systems by Electrogenerated Chemiluminescence.

The interfacial properties of multiphase systems are often difficult to quantify. We describe the observation and quantification of immiscible solvent entrapment on a carbonaceous electrode surface using microscopy-coupled electrogenerated chemiluminescence (ECL). As aqueous microdroplets suspended in 1,2-dichloroethane collide with a glassy carbon electrode surface, small volumes of the solvent become entrapped between the electrode and aqueous phase, resulting in an overestimation of the true microdroplet/electrode contact area. To quantify the contribution of solvent entrapment decreasing the microdroplet contact area, we drive an ECL reaction within the microdroplet phase using tris(bipyridine)ruthenium(II) chloride ([Ru(bpy)3]Cl2) as the ECL luminophore and sodium oxalate (Na2C2O4) as the co-reactant. Importantly, the hydrophilicity of sodium oxalate ensures that the reaction proceeds in the aqueous phase, permitting a clear contrast between the aqueous and 1,2-dichloroethane present at the electrode interface. With the contrast provided by ECL imaging, we quantify the microdroplet radius, apparent microdroplet contact area (aqueous + entrapped 1,2-dichloroethane), entrapped solvent contact area, and the number of entrapped solvent pockets per droplet. These data permit the extraction of the true microdroplet/electrode contact area for a given droplet, as well as a statistical assessment regarding the probability of solvent entrapment based on microdroplet size.

Aerosol Electroanalysis by PILSNER: Particle-into-Liquid Sampling for Nanoliter Electrochemical Reactions.

Particle-into-liquid sampling (PILS) has enabled robust quantification of analytes of interest in aerosol particles. In PILS, the limit of detection is limited by the factor of particle dilution into the liquid sampling volume. Thus, much lower limits of detection can be achieved by decreasing the sampling volume and increasing the surface area-to-volume ratio of the collection substrate. Unfortunately, few analytical techniques can realize this miniaturization. Here, we use an ultramicroelectrode in a microliter or smaller sampling volume to detect redox active species in aerosols to develop the technique of Particle-into-Liquid Sampling for Nanoliter Electrochemical Reactions (PILSNER). As a proof-of-concept to validate this technique, we demonstrate the detection of K4Fe(CN)6 in aerosol particles (diameter ∼0.1-2 µm) and quantify the electrochemical response. To further explore the utility of the method to detect environmentally relevant redox molecules, we show PILSNER can detect 1 ng/m3 airborne Pb in aerosols. We also demonstrate the feasibility of detecting perfluorooctanesulfonate (PFOS), a persistent environmental contaminant, using this technique. PILSNER is shown to represent a significant advancement toward simple and effective detection of a variety of emerging contaminants with an easily miniaturizable and tunable electroanalytical platform.