Modeling of inhomogeneous compression effects of porous GDL on transport phenomena and performance in PEM fuel cells

A comprehensive, three‐dimensional model of a proton exchange membrane (PEM) fuel cell based on a steady state code has been developed. The model is validated and further be applied to investigate the effects of various porosity of the gas diffusion layer (GDL) below channel land areas, on thermal diffusivity, temperature distribution, oxygen diffusion coefficient, oxygen concentration, activation loss and local current density. The porosity variation of the GDL is caused by the clamping force during assembling, in terms of various compression ratios, that is, 0%, 10%, 20%, 30% and 40%. The simulation results show that the higher compression ratio on the GDL leads to lower porosity, and this is helpful for the heat removal from the cell. The compression effects of the GDL below the land areas have a contrary impact on the oxygen diffusion coefficient, oxygen concentration, cathode activation loss, local current density and cell performance. Generally, a lower porosity leads to a smaller oxygen diffusion coefficient, a less uniform oxygen concentration, a higher activation loss, a smaller local current density and worse cell performance. In order to have a better cell performance, the clamping force on the cell should be as low as possible but ensure gas sealing. Copyright © 2016 John Wiley & Sons, Ltd.     

Visualization of unstable water flow in a fuel cell gas diffusion layer

Modeling two-phase flow in proton exchange membrane (PEM) fuel cells is hampered by a lack of conceptual understanding of flow patterns in the gas diffusion layer (GDL). In this paper, pore-scale visualizations of water in different types of GDLs were used to improve current understanding of flow and transport phenomena in PEM fuel cells. Confocal microscopy was used to capture the real-time transport of water, and pressure micro-transducers were installed to measure water breakthrough pressures. Three types of fuel cell GDLs were examined: TO series (Toray Corp., Tokyo, Japan), SGL series (SGL Carbon Group, Wiesbaden, Germany), and MRC series (Mitsubishi Rayon Corp., Otake City, Japan). The visualizations and pressure measurements revealed that despite difference in “pore” structures in the three types of GDLs, water followed distinct flow paths spanning several pores with characteristics similar to the “column flow” phenomena observed previously in hydrophobic or coarse-grained hydrophilic soils. The results obtained from this study can aid in the construction of theories and models for optimizing water management in fuel cells.     

Effects of gas diffusion layer deformation on the transport phenomena and performance of PEM fuel cells with interdigitated flow fields

In this study, a three-dimensional, non-isothermal, two-phase flow mathematical model is developed and applied to investigate the effect of the GDL deformation on transport phenomena and performance of proton exchange membrane (PEM) fuel cells with interdigitated flow fields. The thickness and porosity of the GDL is decreased after compression, and the corresponding transport parameters (permeability, mass diffusivity, thermal conductivity and electrical conductivity) are affected significantly. The alterations in geometry and transport parameters of the GDL are considered in the mathematical model. The oxygen concentration, temperature, liquid water saturation and volumetric current density distributions of PEM fuel cells without compression are investigated and then compared to the PEM fuel cells with various assembly forces. The numerical results show that the cell performance is considerably improved with increasing assembly forces. However, the pressure drops in the gas flow channels are also substantially increased. It is concluded that the assembly force should be as small as possible to decrease the parasitic losses with consideration of gas sealing concern.     

Liquid water breakthrough pressure through gas diffusion layer of proton exchange membrane fuel cell

The dynamic behavior of liquid water transport through the gas diffusion layer (GDL) of the proton exchange membrane fuel cell is studied with an ex-situ approach. The liquid water breakthrough pressure is measured in the region between the capillary fingering and the stable displacement on the drainage phase diagram. The variables studied are GDL thickness, PTFE/Nafion content within the GDL, GDL compression, the inclusion of a micro-porous layer (MPL), and different water flow rates through the GDL. The liquid water breakthrough pressure is observed to increase with GDL thickness, GDL compression, and inclusion of the MPL. Furthermore, it has been observed that applying some amount of PTFE to an untreated GDL increases the breakthrough pressure but increasing the amount of PTFE content within the GDL shows minimal impact on the breakthrough pressure. For instance, the mean breakthrough pressures that have been measured for TGP-060 and for untreated (0 wt.% PTFE), 10 wt.% PTFE, and 27 wt.% PTFE were 3589 Pa, 5108 Pa, and 5284 Pa, respectively.     

Anode water removal and cathode gas diffusion layer flooding in a proton exchange membrane fuel cell

Anode water removal (AWR) is studied as a diagnostic tool to assess cathode gas diffusion layer (GDL) flooding in PEM fuel cells. This method uses a dry hydrogen stream to remove product water from the cathode, showing ideal fuel cell performance in the absence of GDL mass transfer limitations related to water. When cathode GDL flooding is limiting, the cell voltage increases as the hydrogen stoichiometry is increased. Several cathode GDLs were studied to determine the effect of microporous layer (MPL) and PTFE coating. The largest voltage gains occur with the use of cathode GDLs without an MPL since these GDLs are prone to higher liquid water saturation. Multiple GDLs are studied on the cathode side to exacerbate GDL flooding conditions to further confirm the mechanism of the AWR process. Increased temperature and lower cathode RH allow for greater overall water removal so the voltage improvement occurs faster, though this leads to quicker membrane dehydration.     

Measurement of water transport rates across the gas diffusion layer in a proton exchange membrane fuel cell,and the influence of polytetrafluoroethylene content and micro-porous layer

Water management in a proton exchange membrane (PEM) fuel cell is one of the critical issues for improving fuel cell performance and durability, and water transport across the gas diffusion layer plays a key role in PEM fuel cell water management. In this work, we investigated the effects of polytetrafluoroethylene (PTFE) content and the application of a micro-porous layer (MPL) in the gas diffusion layer (GDL) on the water transport rate across the GDL. The results show that both PTFE and the MPL play a similar role of restraining water transport. The effects of different carbon loadings in the MPL on water transport were also investigated. The results demonstrate that the higher the carbon loading in the MPL, the more it reduces the water transport rate. Using the given cell hardware and components, the optimized operation conditions can be obtained based on a water balance analysis.     

Two-phase transport in the cathode gas diffusion layer of PEM fuel cell with a gradient in porosity

Two-phase transport in the cathode gas diffusion layer (GDL) of a proton exchange membrane fuel cell (PEMFC) is studied with a porosity gradient in the GDL. The porosity gradient is formed by adding micro-porous layers (MPL) with different carbon loadings on the catalyst layer side and on the flow field side. The multiphase mixture model is employed and a direct numerical procedure is used to analyze the profiles of liquid water saturation and oxygen concentration across the GDL as well as the resulting activation and concentration losses. The results show that a gradient in porosity will benefit the removal rate of liquid water and also enhance the transport of oxygen through the cathode GDL. The present study provides a theoretical support for the suggestion that a GDL with porosity gradient will improve the cell performance.     

Surface treatments with perfluoropolyether derivatives for the hydrophobization of gas diffusion layers for PEM fuel cells

In the present work, preliminary results of different hydrophobic surface treatments for gas diffusion layer (GDL) for PEM fuel cells are presented. This hydrophobic coating consists of new perfluoropolyether (PFPE) derivatives, in comparison to standard polytetrafluoroethylene (PTFE) dispersions. Experimental conditions for an efficient coating of fluoropolymers onto carbon clothes were explored by wet chemical methods.The GDLs obtained were tested in a single fuel cell at the lab scale. The cell testing was run at two temperatures (60 °C and 80 °C) with a relative humidity (RH) of the feeding gases of 80/100%, hydrogen/air respectively.The new PFPE coatings measurably improve the cell performances, and this effect is more evident at 60 °C with respect to 80 °C.     

Measurement of the water transport rate in a proton exchange membrane fuel cell and the influence of the gas diffusion layer

Water management in a PEM fuel cell significantly affects the fuel cell performance and durability. The gas diffusion layer (GDL) of a PEM fuel cell plays a critical role in the water management process. In this short communication, we report a simple method to measure the water transport rate across the GDL. Water rejection rates across a GDL at different cathode air-flow rates were measured. Based on the measurement results, the fuel cell operating conditions, such as current density, temperature, air stoichiometry and relative humidity, corresponding to membrane drying and flooding conditions were identified for the particular GDL used. This method can help researchers develop GDLs for a particular fuel cell design with specific operating conditions and optimize the operation conditions for the given PEM fuel cell components.     

A comprehensive assessment on the durability of gas diffusion electrode materials in PEM fuel cell stack

Polymer electrolyte membrane (PEM) fuel cell is the most promising among the various types of fuel cells. Though it has found its applications in numerous fields, the cost and durability are key barriers impeding the commercialization of PEM fuel cell stack. The crucial and expensive component involved in it is the gas diffusion electrode (GDE) and its degradation, which limits the performance and life of the fuel cell stack. A critical analysis and comprehensive understanding of the structural and functional properties of various materials involved in the GDE can help us to address the related durability and cost issues. This paper reviews the key GDE components, and in specific, the root causes influencing the durability. It also envisages the role of novel materials and provides a critical recommendation to improve the GDE durability.     

Dynamic modeling of a PEM fuel cell with temperature effects

With the aim of dynamic simulation and control, a new non-linear state-space dynamic non-isothermal polymer electrolyte membrane fuel cell (PEMFC) model is developed in this paper. This mathematical model is developed based on mass and energy equation. The present model takes in account subsequent factors as the effects of charge double layer capacitance, the geometrical capacity and the effect of temperature gradient. In this paper, the authors propose a combination of several dynamic equations to study the effect of suddenly variation of some operating parameters like load resistance, gas pressure and gas temperature input. The results are compared to those of an isothermal model. This model will be extremely functional for the best possible design and real-time control of PEMFC systems. The present model is executed in MATHCAD software and the fuel cell is symbolized by an equivalent circuit which incorporates gas diffusion layer, membrane and electrodes. The analysis results show that the main elements that influence the performance of the cell are load resistance and functioning temperature.     

Implications of non-uniform porosity distribution in gas diffusion layer on the performance of a high temperature PEM fuel cell

The present study discusses a detailed investigation on the implications of non-uniform porosity distribution in the gas diffusion layer (GDL) on the performance of proton exchange membrane fuel cell (PEMFC). A three-dimensional, single-phase, isothermal model of high-temperature PEMFC is employed to study the effect of non-uniform porosity distribution in GDL. The different porosity configurations with stepwise, sinusoidal, and logarithmic variation in porosity along the streamwise direction of GDL are considered. The numerical experiments are performed, keeping average porosity as constant in the GDL. The electrochemical characteristics such as the oxygen molar concentration, power density, current density, total power dissipation density, average diffusion coefficient, vorticity magnitude, and overpotential are studied for a range of porosity distributions. Furthermore, the variations of oxygen concentration, average diffusion coefficient, and vorticity magnitude are also discussed to showcase the influence of non-uniform porosity distribution. Our study reveals that the PEM fuel cell performance is the best when the porosity of the GDL decreases logarithmically in the streamwise direction. On the contrary, the performance deteriorates when the GDL porosity decreases sinusoidally. Also, it has been observed that the effects of non-uniform porosity distribution are more pronounced, especially at higher current densities. The outcomes of present investigation have potential utility in GDL fabrication and membrane assembly's sintering process for manufacturing high valued PEMFC products.     

A micro-scale model for predicting contact resistance between bipolar plate and gas diffusion layer in PEM fuel cells

Contact resistance between the bipolar plate (BPP) and the gas diffusion layer (GDL) in a proton exchange membrane (PEM) fuel cell constitutes a significant portion of the overall fuel cell electrical resistance under the normal operation conditions. Most current methods for contact resistance estimation are experimental and there is a lack of well developed theoretical methods. A micro-scale numerical model is developed to predict the electrical contact resistance between BPP and GDL by simulating the BPP surface topology and GDL structure and numerically determining the status for each contact spot. The total resistance and pressure are obtained by considering all contact spots as resistances in parallel and summing the results together. This model shows good agreements with experimental results. Influences of BPP surface roughness parameters on contact resistance are also studied. This model is beneficial in understanding the contact behavior between BPP and GDL and can be integrated with other fuel cell simulations to predict the overall performance of PEM fuel cells.     

Performance of a metallic gas diffusion layer for PEM fuel cells

A novel metallic porous medium with improved thermal and electrical conductivities and controllable porosity was developed based on micro/nano technology for its potential application in PEM fuel cells. In this work to demonstrate its applicability, the gas diffusion medium, made of 12.5 μm thick copper foil, was tested in an operational fuel cell. The small thickness and straight-pore feature of this novel material provides improved water management even at low flow rates. The performance does not decline at lower flow rates, unlike conventional gas diffusion layers. It has been shown that the performance can be further enhanced by increasing the in-plane transport. The improvements of such gas diffusion layer, including pore shape, porosity, and surface properties, are fully discussed.     

Experimental investigations on liquid water removal from the gas diffusion layer by reactant flow in a PEM fuel cell

The cross flow from channel to channel through gas diffusion layer (GDL) under the land could play an important role for water removal in proton exchange membrane (PEM) fuel cells. In this study, characteristics of liquid water removal from GDL have been investigated experimentally, through measuring unsteady pressure drop in a cell which has the GDL initially wet with liquid water. The thickness of GDL is carefully controlled by inserting various thicknesses of metal shims between the plates. It has been found that severe compression of GDL could result in excessive pressure drop from channel inlet to channel outlet. Removing liquid water from GDL by cross flow is difficult for GDL with high compression levels and for low inlet air flow rates. However, effective water removal can still be achieved at high compression levels of GDL if the inlet air flow rate is high. Based on different compressed GDL thicknesses, different GDL porosities and permeabilities were calculated and their effects on the characteristics of liquid water removal from GDL were evaluated. Visualization of liquid water transport has been conducted by using transparent flow channel, and liquid water removal from GDL under the land was observed for all the tested inlet air flow rates, which confirms that cross flow is practically effective to remove the liquid water accumulated in GDL under the land area.     

Non‐isothermal multi‐phase modeling of PEM fuel cell cathode

In this study, numerical simulation has been carried out for the heat transfer and temperature distribution in the cathode of polymer electrolyte membrane fuel cells along with the multi‐phase and multi‐species transport under the steady‐state condition. The commercial software, COMSOL Multiphysics, is used to solve the conservation equations for momentum, mass, species, charge and energy numerically. The conservation equations are applied to the solid, liquid and vapor phases in the bipolar plate and gas diffusion (GDL) and catalyst layers of a two‐dimensional cross section of the cathode. The catalyst layer is assumed to be a finite domain and the water production in the catalyst layer is considered to be in the liquid form. The temperature distribution in the cathode is simulated and then the effects of the relative humidity of the air stream, the permeability of the cathode and the flow channel shoulder to channel width ratio are investigated. It is shown that the highest temperature change, both in the in‐plane and across‐the‐plane directions, occurs in the GDL, while the highest temperature is reached in the catalyst layer. The distribution of temperature in the bipolar plate is shown to be relatively uniform due to the high thermal conductivity of the plate. A decrease in the inlet relative humidity of the air stream results in the decrease of the maximum temperature due to the absorption of heat during the evaporation of liquid water in the GDL and catalyst layer. The non‐uniformity of the temperature distribution, especially in the catalyst layer, is observed with the increase of the permeability of the cathode. Similarly, the decrease of the channel shoulder to channel width ratio leads to a non‐uniform distribution of temperature especially under the channel areas. Copyright © 2009 John Wiley & Sons, Ltd.     

Computational model of a PEM fuel cell with serpentine gas flow channels

A three-dimensional computational fluid dynamics model of a PEM fuel cell with serpentine flow field channels is presented in this paper. This comprehensive model accounts for the major transport phenomena in a PEM fuel cell: convective and diffusive heat and mass transfer, electrode kinetics, and potential fields. A unique feature of the model is the implementation of a voltage-to-current (VTC) algorithm that solves for the potential fields and allows for the computation of the local activation overpotential. The coupling of the local activation overpotential distribution and reactant concentration makes it possible to predict the local current density distribution more accurately. The simulation results reveal current distribution patterns that are significantly different from those obtained in studies assuming constant surface overpotential. Whereas the predicted distributions at high load show current density maxima under the gas channel area, low load simulations exhibit local current maxima under the collector plate land areas.     

Numerical investigation of multi-layered porosity in the gas diffusion layer on the performance of a PEM fuel cell

A mathematical model is developed to investigate the influence of porosity configurations in the gas diffusion layer (GDL) of the cathode on the electrochemical performance characteristics of a 3-D high-temperature proton exchange membrane (PEM) fuel cell. Four different non-uniform porosity configurations are defined through step functions and analyzed with uniform porosity case. The results are presented in terms of the cell performance characteristics viz. Current density, power density, vorticity magnitude, oxygen molar concentration, overpotential, and total power dissipation density. Our study reveals that oxygen molar concentration, current density, power density are found to be maximum when the stepwise porosity in GDL decreases in the streamwise direction. However, these parameters observed to be the least when the stepwise porosity in GDL increases along the streamwise direction. Additionally, the highest total power dissipation density is observed when the porosity in GDL varies across cross-stream wise direction among other configurations considered. However, it is found to be the least when porosity varies in a streamwise direction. The overpotential becomes the least when stepwise porosity decreases in the streamwise direction although the same is found to be maximum when the porosity in GDL increases along the streamwise direction. The performance is found to be optimal when porosity is maximum at cathode gas channel inlet and GDL-cathode gas channel interface.     

Modeling of ion and water transport in the polymer electrolyte membrane of PEM fuel cells

Ion and water transport phenomena in the polymer electrolyte membrane (PEM) play a significant role in the energy conversion process of a PEM fuel cell, as they provide the closure for the electric and mass transport in the PEM fuel cells. A mathematical model for the transport of ion and water in the PEM is formulated in this study, based on the non-equilibrium thermodynamics and the Generalized Stefan–Maxwell equations. The physical constants of the model, such as the binary diffusion coefficients in the Generalized Stefan–Maxwell equations, are determined from experimental data available in literature for membrane-water diffusion and conductivity. The electrolyte transport model is incorporated into a model for the entire PEM fuel cell; water transport in the electrolyte and in the other cell components are coupled and solved in a single computational domain. It is shown that the present generalized formulation is advantageous to other formulations for the macroscopic analysis of transport phenomena through the membrane electrolyte.