About: Rotating disk electrode is a research topic. Over the lifetime, 3707 publications have been published within this topic receiving 146312 citations. The topic is also known as: Rotating disk electrode , RDE.
TL;DR: In this paper, the authors present a comprehensive overview of electrode processes and their application in the field of chemical simulation, including potential sweep and potential sweep methods, coupled homogeneous chemical reactions, double-layer structure and adsorption.
Abstract: Major Symbols. Standard Abbreviations. Introduction and Overview of Electrode Processes. Potentials and Thermodynamics of Cells. Kinetics of Electrode Reactions. Mass Transfer by Migration and Diffusion. Basic Potential Step Methods. Potential Sweep Methods. Polarography and Pulse Voltammetry. Controlled--Current Techniques. Method Involving Forced Convention--Hydrodynamic Methods. Techniques Based on Concepts of Impedance. Bulk Electrolysis Methods. Electrode Reactions with Coupled Homogeneous Chemical Reactions. Double--Layer Structure and Adsorption. Electroactive Layers and Modified Electrodes. Electrochemical Instrumentation. Scanning Probe Techniques. Spectroelectrochemistry and Other Coupled Characterization Methods. Photoelectrochemistry and Electrogenerated Chemiluminescence. Appendix A: Mathematical Methods. Appendix B: Digital Simulations of Electrochemical Problems. Appendix C: Reference Tables. Index.
TL;DR: In this article, the Butler-Volmer equation was fitted to the HOR/HER exchange current densities on polycrystalline platinum and high surface area carbon-supported platinum nanoparticles using rotating disk electrode (RDE) measurements.
Abstract: The kinetics of the hydrogen oxidation reaction (HOR) and hydrogen evolution reaction (HER) on polycrystalline platinum [Pt(pc)] and high surface area carbon-supported platinum nanoparticles (Pt/C) were studied in 0.1 M KOH using rotating disk electrode (RDE) measurements. After corrections of noncompensated solution resistance from ac impedance spectroscopy and of hydrogen mass transport in the HOR branch, the kinetic current densities were fitted to the Butler-Volmer equation using a transfer coefficient of α = 0.5, from which HOR/HER exchange current densities on Pt(pc) and Pt/C were obtained, and the HOR/HER mechanisms in alkaline solution were discussed. Unlike the HOR/HER rates on Pt electrodes in alkaline solution, the HOR/HER rates on a Pt electrode in 0.1 M HClO 4 were limited entirely by hydrogen diffusion, which renders the quantification of the HOR/HER kinetics impossible by conventional RDE measurements. The simulation of the hydrogen anode performance based on the specific exchange current densities of the HOR/HER at 80°C illustrates that in addition to the oxygen reduction reaction cell voltage loss on the cathode, the slow HOR kinetics are projected to cause significant anode potential losses in alkaline fuel cells for low platinum loadings (> 130 mV at 0.05 Mg pt /CM 2 anode and 1.5 A/cm 2 anode ), contrary to what is reported for proton exchange membrane fuel cells.
TL;DR: In this paper, a thin-film rotating disk electrode method and its application in a rotating ring disk configuration (RRDE) to the investigation of the oxygen reduction reaction (orr) on a supported catalyst powder (Pt/Vulcan XC 72 carbon).
TL;DR: In this paper, the effect of pH on the hydrogen oxidation and evolution reaction (HOR/HER) rates is addressed for the first time for the three most active monometallic surfaces: Pt, Ir, and Pd carbon-supported catalysts.
Abstract: The effect of pH on the hydrogen oxidation and evolution reaction (HOR/HER) rates is addressed for the first time for the three most active monometallic surfaces: Pt, Ir, and Pd carbon-supported catalysts. Kinetic data were obtained for a proton exchange membrane fuel cell (PEMFC; pH ≈ 0) using the H2-pump mode and with a rotating disk electrode (RDE) in 0.1 M NaOH. Our findings point toward: (i) a similar ≈100-fold activity decrease on all these surfaces when going from low to high pH; (ii) a reaction rate controlled by the Volmer step on Pt/C; and (iii) the H-binding energy being the unique and sole descriptor for the HOR/HER in alkaline electrolytes. Based on a detailed discussion of our data, we propose a new mechanism for the HOR/HER on Pt-metals in alkaline electrolytes.
TL;DR: In this article, a method for the characterization of the electrocatalytic properties of highly dispersed electro catalysts in a true rotating disk electrode configuration by attaching the catalyst powder on a glossy carbon electrode via a thin Nafion film is presented.
Abstract: A newly developed method is presented which allows the characterization of the electrocatalytic properties of highly dispersed electrocatalysts in a true rotating disk electrode (RDE) configuration by attaching the catalyst powder on a glossy carbon electrode via a thin Nafion film. Complete utilization and high reproducibility of both the electrode preparation and the catalyst loading could be shown via voltammetry and CO stripping voltammetry. Furthermore RDE measurements on the electro‐oxidation of hydrogen on Pt/Vulcan showed that the effect of diffusion through the Nation film can be avoided by proper electrode preparation. Therefore, the electrode kinetics for fuel cell relevant reactions under continuous flow conditions can be measured directly without mathematical modeling.