Performance Enhancement of Ionic Polymer-Metal Composite Actuators with Polyethylene Oxide

Current ionic polymer-metal composite (IPMC) always proves inadequate in terms of large attenuation and short working time in air due to water leakage. To address this problem, a feasible and effective solution was proposed in this study to enhance IPMC performance operating in air by doping polyethylene oxide (PEO) with superior water retention capacity into Nafion membrane. The investigation of physical characteristics of membranes blended with varying PEO contents revealed that PEO/Nafion membrane with 20 wt% PEO exhibited a homogeneous internal structure and a high water uptake ratio. At the same time, influences of PEO contents on electromechanical properties of IPMCs were studied, showing that the IPMCs with 20 wt% PEO presented the largest peak-to-peak displacement, the highest volumetric work density, and prolonged stable working time. It was demonstrated that doping PEO reinforced electromechanical performances and restrained displacement attenuation of the resultant IPMC.

Numerical Simulation on Impacts of Thickness of Nafion Series Membranes and Relative Humidity on PEMFC Operated at 363 K and 373 K

The purpose of this study is to understand the impact of the thickness of Nafion membrane, which is a typical polymer electrolyte membrane (PEM) in Polymer Electrolyte Membrane Fuel Cells (PEMFCs), and relative humidity of supply gas on the distributions of H2, O2, H2O concentration and current density on the interface between a Nafion membrane and anode catalyst layer or the interface between a Nafion membrane and cathode catalyst layer. The effect of the initial temperature of the cell (Tini) is also investigated by the numerical simulation using the 3D model by COMSOL Multiphysics. As a result, the current density decreases along with the gas flow through the gas channel irrespective of the Nafion membrane thickness and Tini, which can be explained by the concentration distribution of H2 and O2 consumed by electrochemical reaction. The molar concentration of H2O decreases when the thickness of Nafion membrane increases, irrespective of Tini and the relative humidity of the supply gas. The current density increases with the increase in relative humidity of the supply gas, irrespective of the Nafion membrane thickness and Tini. This study recommends that a thinner Nafion membrane with well-humidified supply gas would promote high power generation at the target temperature of 363 K and 373 K.

Studying Corrosion Using Miniaturized Particle Attached Working Electrodes and the Nafion Membrane

We developed a new approach to attach particles onto a conductive layer as a working electrode (WE) in a microfluidic electrochemical cell with three electrodes. Nafion, an efficient proton transfer molecule, is used to form a thin protection layer to secure particle electrodes. Spin coating is used to develop a thin and even layer of Nafion membrane. The effects of Nafion (5 wt% 20 wt%) and spinning rates were evaluated using multiple sets of replicates. The electrochemical performance of various devices was demonstrated. Additionally, the electrochemical performance of the devices is used to select and optimize fabrication conditions. The results show that a higher spinning rate and a lower Nafion concentration (5 wt%) induce a better performance, using cerium oxide (CeO2) particles as a testing model. The WE surfaces were characterized using atomic force microscopy (AFM), scanning electron microscopy-focused ion beam (SEM-FIB), time-of-flight secondary ion mass spectrometry (ToF-SIMS), and X-ray photoelectron spectroscopy (XPS). The comparison between the pristine and corroded WE surfaces shows that Nafion is redistributed after potential is applied. Our results verify that Nafion membrane offers a reliable means to secure particles onto electrodes. Furthermore, the electrochemical performance is reliable and reproducible. Thus, this approach provides a new way to study more complex and challenging particles, such as uranium oxide, in the future.

Impact of CeO2 Nanoparticle Morphology: Radical Scavenging within the Polymer Electrolyte Membrane Fuel Cell

This paper reports a systematic investigation of the radical scavenging behaviour of ceria with different morphological shapes inside Nafion membrane. All the ceria nanostructure is synthesized using a template-free hydrothermal route. Distinct crystal planes of CeO2 have different numbers of broken bonds and reaction sites having different surface energies. So, the preparation of CeO2 with various uncovered planes may enhance its scavenging activity. The crystal structure, morphology, and lattice structure are investigated using transmission electron microscopy (TEM), and X-ray diffraction (XRD). The results show that the radical scavenging efficiency of ceria strongly depends on the active surface plane, and decreases in the following order: nanorods > nanocube > nanosphere. Furthermore, the concentrations of surface oxygen vacancies and lattice cerium (III) are correlated with the morphology of the nanoparticles. This relationship clarifies the vital scavenging mechanism of CeO2 that mitigates degradation inside the polymer electrolyte membrane. This is because the inherent lattice strain on the active planes of nanosized ceria with different shapes affects their surficial reactions. The existence of prominent concentration of oxygen vacancy in the nanometric dimension of ceria leading to greater Ce3+ generation by exposed active phase CeO2 nanoparticles is key to achieve a durable hybrid Nafion membrane.