ABSTRACT
Oxygen evolution reaction (OER) represents the efficiency-limiting reaction in water electrolyzers, metal-air batteries, and unitized regenerative fuel cells. To achieve high-efficiency OER in alkaline media, we fabricated three novel electrocatalysts by the assembly of as-prepared Co45Pt55 alloy nanoparticles (NPs) on three different carbon-based support materials: reduced graphene oxide (CoPt/rGO), mesoporous graphitic carbon nitride (CoPt/mpg-CN), and commercial Ketjenblack carbon (CoPt/KB). Voltammetry studies revealed that CoPt/rGO electrocatalyst provided lower OER overpotentials accompanied by higher currents and specific current density values than the other two studied materials. Moreover, CoPt/rGO outperformed commercial CoPt/C electrocatalysts in terms of notably higher specific current densities. Additionally, it was found that CoPt/rGO electrocatalyst activity increases with increasing temperature up to 85°C, as suggested by the increase in the exchange current density. Electrochemical impedance spectroscopy studies of three electrocatalysts in OER revealed similar charge transfer resistance, although CoPt/rGO provided a higher current density. The main issue observed during long-term chronoamperometry and chronopotentiometry studies is the materials' instability under OER polarization conditions, which is still to be tackled in future work.
ABSTRACT
Electrochemical exfoliation is an efficient and scalable method to obtain liquid-phase graphene. Graphene in solution, obtained through electrochemical exfoliation or other methods, is typically polydisperse, containing particles of various sizes, which is not optimal for applications. We employed cascade centrifugation to select specific particle sizes in solution and prepared thin films from those graphene particles using the Langmuir-Blodgett assembly. Employing centrifugation speeds of 3, 4, and 5 krpm, further diluting the solutions in different volumes of solvent, we reliably and consistently obtained films of tunable thickness. We show that there is a limit to how thin these films can be, which is imposed by the percolation threshold. The percolation threshold is quantitatively compared to results found in literature that are obtained using other, more complex graphene film fabrication methods, and is found to occur with a percolation exponent and percolative figure of merit that are of the same order as results in literature. A maximum optical transparency of 82.4% at a wavelength of 660 nm is obtained for these films, which is in agreement with earlier works on Langmuir-Blodgett assembled ultrasonic-assisted liquid-phase exfoliated graphene. Our work demonstrates that films that are in all respects on par with films of graphene obtained through other solution-based processes can be produced from inexpensive and widely available centrifugal post-processing of existing commercially available solutions of electrochemically exfoliated graphene. The demonstrated methodology will lower the entry barriers for new research and industrial uses, since it allows researchers with no exfoliation experience to make use of widely available graphene materials.
ABSTRACT
Humidity sensing is important to a variety of technologies and industries, ranging from environmental and industrial monitoring to medical applications. Although humidity sensors abound, few available solutions are thin, transparent, compatible with large-area sensor production and flexible, and almost none are fast enough to perform human respiration monitoring through breath detection or real-time finger proximity monitoring via skin humidity sensing. This work describes chemiresistive graphene-based humidity sensors produced in few steps with facile liquid phase exfoliation followed by Langmuir-Blodgett assembly that enables active areas of practically any size. The graphene sensors provide a unique mix of performance parameters, exhibiting resistance changes up to 10% with varying humidity, linear performance over relative humidity (RH) levels between 8% and 95%, weak response to other constituents of air, flexibility, transparency of nearly 80%, and response times of 30 ms. The fast response to humidity is shown to be useful for respiration monitoring and real-time finger proximity detection, with potential applications in flexible touchless interactive panels.
