Concentration and ohmic losses in free-breathing PEMFC

Non-isothermal and three-dimensional simulations were carried out to study concentration and ohmic losses in free-breathing PEMFC under diverse conditions. Flow fields, species transport, transport of water in polymer membrane and movement of liquid water in cathode and anode porous layers were determined. Numerical results were obtained under different hydrating conditions, cell temperatures, cathode catalyst loadings and channel lengths. Current density and polymer electrolyte water content distributions as well as average power density were used as main output variables to study effects of operative conditions on performance. Results show that slow oxygen transport to active sites constitutes the most limiting factor to consider. Dehydrating conditions slightly affect free-breathing PEMFC performance. The numerical model showed to be suitable to study diverse phenomenon involved in free-breathing PEMFC performance.     

Numerical simulation of exchange membrane fuel cells in different operating conditions

A two-dimensional, steady state model for proton exchange membrane fuel cell (PEMFC) is presented. The model is used to describe the effect operation conditions (current density, pressure and water content) on the water transport, ohmic resistance and water distribution in the membrane and performance of PEMFC. This model considers the transport of species and water along the porous media: gas diffusion layers (GDL) anode and cathode, and the membrane of PEMFC fuel cell.     

Three-dimensional modeling of water transport in PEMFC

A three dimensional two phase flow model is proposed to study transport phenomena in a PEMFC. In order to capture the effects of liquid water on the performance of the fuel cell, all regions are modeled from the anode to the cathode as having finite thickness. The geometry of the bipolar plate is modeled in detail to capture the effect of liquid water accumulation under the channel rib. This model takes into account the effect of temperature and inlet RH of both the anode and cathode. The three-dimensional model uses the finite volume method to solve the equations of mass conservation, momentum, energy, species transfer and protonic potential. These equations include the effect of liquid water on the transport properties as well as the electrochemical source. The effects of water on ohmic losses are presented for different humidity conditions of the anode and cathode at various fuel cell temperatures.     

Parameter sensitivity examination for a complete three-dimensional,two-phase,non-isothermal model of polymer electrolyte membrane fuel cell

Parameter sensitivity analysis is carried out for a complete three-dimensional, two-phase, non-isothermal model of polymer electrolyte membrane (PEM) fuel cell with a parallel flow field design. The model couples the two-phase flow of the multi-component reactants and liquid water, species transport, electrochemical reactions, proton and electron transport, and the electro-osmosis transport, back diffusion of water in the membrane, and energy transport. Twenty nine parameters, which are classified into the structural or transport parameters of porous layers (tortuosity, porosity, permeability, proton conductivity, electron conductivity, and thermal conductivity) as well as the electrochemical parameters (anodic and cathodic exchange current densities, anodic and cathodic transfer coefficients for anode and cathode reactions), are used to implement individual parameter investigation. The results show the parameters can be divided in to strongly sensitive, conditional sensitive and weak sensitive parameters according to its effect on the cell polarization curve. The optimization of parameters of cathode gas diffusion layer (GDL) and catalyst layer (CL) is more important to improve cell performance than that of anode GDL and CL because liquid water transport and removal affect significantly membrane hydration and reactant transport. Electrochemical parameters determine the activation potential and the slope of ohmic polarization hence these parameters can be used to fit experimental polarization curve more effectively than the other parameters.     

Performance analysis of a PEM fuel cell cathode with multiple catalyst layers

The cathode catalyst layer (CL) of a PEM fuel cell (PEMFC) plays an important role in the performance of the cell because of the rate limiting mechanisms that take place in it. For enhancing the performance of a PEMFC, the use of multiple, ultra thin CLs instead of a single CL is considered in the present work. Since the concentration of oxygen decreases in a CL from the diffusion medium-CL interface towards the polymer membrane, the CL adjacent to the diffusion medium should be of higher porosity than the other CLs. Similarly, the CL adjacent to the polymer membrane should contain more ionomer than the other CLs. Furthermore, liquid water should be removed without causing significant mass transport and/or ohmic losses. Therefore, the design parameters of a CL can be varied spatially to minimize losses in a PEMFC. However, such a continuously graded CL is difficult to manufacture due to lack of commercially available techniques and associated costs. As an alternative, a combination of layers can be synthesized where each layer is manufactured with different design parameters. This approach provides the opportunity to optimize the design parameters of each layer. With this objective in mind, a detailed steady state model of a PEMFC cathode with multiple layers is developed. The model considers liquid water in all the layers. The catalyst layer microstructure is modeled as a network of spherical agglomerates. For improved water management, a thin micro-porous layer is considered between the gas diffusion layer (GDL) and the first catalyst layer. The performance curves for various combinations of the design parameters are shown and the results are analyzed. The results show that there exists an optimum combination of design parameters for each catalyst layer that can significantly improve the performance of a PEMFC.     

A study of water transport as a function of the micro-porous layer arrangement in PEMFCs

Electrochemical losses as a function of the micro-porous layer (MPL) arrangement in Proton Exchange Membrane Fuel Cells (PEMFCs) are investigated by electrochemical impedance spectroscopy (EIS). Net water flux across the polymer membrane in PEMFCs is investigated for various arrangements of the MPL, namely with MPL on the cathode side alone, with MPL on both the cathode and the anode sides and without MPL. EIS and water transport are recorded for various operating conditions, such as the relative humidity of the hydrogen inlet and current density, in a PEMFC fed by fully-saturated air. The cell with an MPL on the cathode side alone has better performance than two other types of cells. Furthermore, the cell with an MPL on only the cathode increases the water flux from cathode to anode as compared to the cells with MPLs on both electrodes and cells without MPL. Oxygen-mass-transport resistances of cells in the presence of an MPL on the cathode are lower than the values for the other two cells, which indicates that the molar concentration of oxygen at the reaction surface of the catalyst layer is higher. This suggests that the MPL forces the liquid water from the cathode side to the anode side and decreases the liquid saturation in GDL at high current densities. Consequently, the MPL helps in maintaining the water content in the polymer membrane and decreases the cathode charge transfer and oxygen-mass transport resistances in PEMFCs, even when the hydrogen inlet has a low relative humidity.     

Modeling of water transport through the membrane electrode assembly for direct methanol fuel cells

In this work, a one-dimensional, isothermal two-phase mass transport model is developed to investigate the water transport through the membrane electrode assembly (MEA) for liquid-feed direct methanol fuel cells (DMFCs). The liquid (methanol–water solution) and gas (carbon dioxide gas, methanol vapor and water vapor) two-phase mass transport in the porous anode and cathode is formulated based on classical multiphase flow theory in porous media. In the anode and cathode catalyst layers, the simultaneous three-phase (liquid and vapor in pores as well as dissolved phase in the electrolyte) water transport is considered and the phase exchange of water is modeled with finite-rate interfacial exchanges between different phases. This model enables quantification of the water flux corresponding to each of the three water transport mechanisms through the membrane for DMFCs, such as diffusion, electro-osmotic drag, and convection. Hence, with this model, the effects of MEA design parameters on water crossover and cell performance under various operating conditions can be numerically investigated.     

Novel in situ measurements of relative humidity in a polymer electrolyte membrane fuel cell

Miniature temperature/humidity sensors are incorporated into the graphite flowplates of a single cell polymer electrolyte membrane fuel cell (PEMFC) in order to measure the humidity profile along the serpentine channels of both anode and cathode in real time. The sensors show robust performance and importantly are able to recover after saturation. The key observation is a significant increase in relative humidity along the anode gas channel due to back diffusion of water from cathode to anode. Such measurements may be used to determine the water balance in the cell under a range of operating conditions to facilitate model validation and system optimisation.     

Calculations of transport phenomena and reaction distribution in a polymer electrolyte membrane fuel cell

The performance of Polymer Electrolyte Membrane fuel cells depends on the design of the cell as well as the operating conditions. The design of the cell influences the complex interaction of activation effects, ohmic losses, and transport limitations, which in turn determines the local current density. Detailed models of the electrochemical reactions and transport phenomena in Polymer Electrolyte Membrane fuel cells can be used to determine the current density distribution for a given fuel cell design and operating conditions. In this work, three-dimensional, multicomponent and multiphase transport calculations are performed using a computational fluid dynamics code. The computational results for a full-scale fuel cell design show that ohmic effects due to drying of polymer electrolyte in the anode catalyst layer and membrane, and transport limitations of air and flooding in the cathode cause the current density to be a maximum near the gas channel inlets where ohmic losses and transport limitations are a minimum. Elsewhere in the cell, increased ohmic losses and transport limitations cause a decrease in current density, and the performance of the fuel cell is significantly lower than that which could be attained if the ohmic losses and transport limitations throughout the cell were the same as those near the gas channel inlets. Thus overall fuel cell design is critical in maximizing unit performance.     

Water balance simulations of a polymer-electrolyte membrane fuel cell using a two-fluid model

A previously published computational multi-phase model of a polymer-electrolyte membrane fuel cell cathode has been extended in order to account for the anode side and the electrolyte membrane. The model has been applied to study the water balance of a fuel cell during operation under various humidification conditions. It was found that the specific surface area of the electrolyte in the catalyst layers close to the membrane is of critical importance for the overall water balance. Applying a high specific electrolyte surface area close to the membrane (a water-uptake layer) can prevent drying out of the anode and flooding at the cathode while the average membrane water content is only weakly affected. The results also indicate that in contrast to common presumption membrane dehydration may occur at either anode or cathode side, entirely depending on the direction of the net water transport because the predominant transport mechanism is diffusion. Consequently, operating conditions with a high net water transport from anode to cathode should be avoided as it is important to keep the cathode catalyst layer well humidified in order to prevent high protonic losses. Addition of the micro-porous layer did not affect the overall water balance or membrane water content in our study.     

Operation of a proton-exchange membrane fuel cell under non-humidified conditions using thin cast Nafion membranes with different gas-diffusion media

Thin membranes in polymer electrolyte membrane fuel cells (PEMFCs) enhance the back diffusion of water from cathode to anode and allow operation of the PEMFC under dry conditions. In this work, thin cast Nafion membranes are prepared to operate the PEMFC under non-humidified conditions at various temperatures. Also, the effect of gas-diffusion media (GDM) on cell performance is examined using two different GDM that have distinct physical properties. Single cells with thin cast membranes provide better performance than those with commercially available Nafion 112. This improvement is due to better back-diffusion of water and lower membrane resistance. The performance of cell using GDM with low porosity is superior to that of a cell using GDM with high porosity. The fuel cell can be operated successfully under non-humidified conditions with a thin cast membrane and low porosity GDM.     

Water transport characteristics in a passive liquid-feed DMFC

A two-dimensional, two-phase, non-isothermal model was developed to investigate the water transport characteristics in a passive liquid-feed direct methanol fuel cell (DMFC). The liquid–gas two-phase mass transport in the porous anode and cathode was formulated based on multi-fluid model in porous media, and water and methanol crossover through the membrane were considered with the effect of diffusion, electro-osmotic drag, and convection. The model enabled numerical investigation of the effects of various operating parameters, such as current density, methanol concentration, and air humidity, as well as the effect of the cathode hydrophobic air filter layer, on the water transport and cell performance. The results showed that for the free-breathing cathode, gas species concentration and temperature showed evident differences between the cell and the ambient air. The use of a hydrophobic air filter layer at the cathode helped to achieve water recovery from the cathode to the anode, although the oxygen transport resistance was increased to some extent. It was further revealed that the water transport can be influenced by the ambient relative humidity.     

Assisted water management in a PEMFC with a modified flow field and its effect on performance

This work designed and tested innovative flow channels in order to improve water management in a polymer electrolyte membrane fuel cell (PEMFC). The design employed slanted channels with an angle of 20° in a flow plate to collect the liquid water that permeated from the gas diffusion layers. The effects of orientations of the slanted channels in up-slanted and down-slanted directions and relative humidity levels on the cell performance were investigated. The experimental results showed that modifying the anode flow field using down-slanted channels provided higher cell performance. Water concentration at the gas diffusion layer is reduced resulting in more back diffusion of water from the cathode to anode, thus inducing membrane hydration and improving the conductivity. Promotion of water removal by applying down-slanted channels in the cathode side did not improve the performance. This work has demonstrated that channel cross-section design alone could improve the PEM fuel cell performance. The anode down-slanted cell indeed improved the performances at extremely wet condition and the power was equally good as that without modified flow channel at less wet condition.     

The experimental analysis of a dead-end H2/O2 PEM fuel cell stack with cascade type design

Proton exchange membrane fuel cells (PEMFCs) with a dead-ended anode and cathode can reach high hydrogen and oxygen utilization by a relatively simple system. Nevertheless, the accumulation of the water in the anode and cathode channels can lead to a local fuel starvation deteriorating the performance and the durability of PEMFCs. In this study, a novel design for a polymer electrolyte membrane (PEM) fuel-cell stack was presented which could achieve higher fuel utilization without using hydrogen and oxygen recirculation devices such as hydrogen pumps or ejectors that consume parasitic power and require additional control schemes. The basic concept of the innovatively proposed design was to divide the cells of a stack into several stages by conducting the outlet gas of each stage to a separator and reentering it into the next stage; thereby, a multistage anode and cathode system was prepared. In this relatively ingenious design, a higher gaseous flow rate was maintained at the cell outlet, even under dead-end conditions resulted in a reduced purge-gas emission by avoiding the accumulation of liquid water in the cells. The results revealed that proposed design had the same polarization curve as the open-end mode, leading to an enhanced PEMFC performance.     

Three-dimensional modeling and experimental investigation for an air-breathing polymer electrolyte membrane fuel cell (PEMFC)

An air-breathing polymer electrolyte membrane fuel cell bears many advantages, which are important for portable-power applications. However, several barriers must be overcome before an air-breathing PEMFC achieve commercially wide-scale adoption. In this paper, with emphasis on improving the performance of air-breathing PEMFC, the simulation and experiment has been done simultaneously. Considering the natural convection in the cathode side, electrochemical reaction in the catalyst layer, water transport in the membrane, a coupled three-dimensional complex model has been developed in this work. The parameters which greatly affect the performance of an air-breathing PEMFC have been calculated for the base case such as the distribution of water and reactant, temperature and electrochemical performance. To validate the numerical result, the experiment test system have been designed to investigate the temperature distribution and cell performance. The results from this work show that the performance of air-breathing PEMFCs is strongly affected by natural convection feature. The concentration losses play a major role on the cell performance. The ambient relative humidity also has significant effect on the cell performance. The fields of water, temperature, velocity and electrochemical reaction have strong interaction on each others.     

Water transport characteristics of polymer electrolyte membrane fuel cell

This paper describes the performance of a polymer electrolyte membrane fuel cell (PEMFC) system without humidification of the reactants which consumes a lot of parasitic power, increases the weight of the PEMFC system and thus adds complexity. Such PEMFC systems are preferable for portable applications. The results indicate that dry gas operation depends on various factors like reactant flow field design, area of the electrode and equilibration time for the product water. The performance of the fuel cell can be improved by giving some equilibration time for the product water, produced by the electrochemical reactions, to get transported across the membrane to the anode side, thus increasing the conductivity of the membrane. The water transported through the membrane across the cell was investigated by measuring the amount of product water at the anode side which allows humidification for the anode gas and less condensed water in the fluid flow channels of the cathode.     

质子交换膜燃料电池阴极传质过程的数值模拟

利用CFD方法对采用交指型流道质子交换膜燃料电池阴极的传质过程进行数值模拟,得到了阴极扩散层内氧气和水蒸汽质量浓度的分布特性,探讨了电池结构参数和操作条件对电池性能的影响。     

Detailed analysis of polymer electrolyte membrane fuel cell with enhanced cross‐flow split serpentine flow field design

Most generally used flow channel designs in polymer electrolyte membrane fuel cells (PEMFCs) are serpentine flow designs as single channels or as multiple channels due to their advantages over parallel flow field designs. But these flow fields have inherent problems of high pressure drop, improper reactant distribution, and poor water management, especially near the U‐bends. The problem of inadequate water evacuation and improper reactant distribution become more severe and these designs become worse at higher current loads (low voltages). In the current work, a detailed performance study of enhanced cross‐flow split serpentine flow field (ECSSFF) design for PEMFC has been conducted using a three‐dimensional (3‐D) multiphase computational fluid dynamic (CFD) model. ECSSFF design is used for cathode part of the cell and parallel flow field on anode part of the cell. The performance of PEMFC with ECSSFF has been compared with the performance of triple serpentine flow design on cathode side by keeping all other parameters and anode side flow field design similar. The performance is evaluated in terms of their polarization curves. A parametric study is carried out by varying operating conditions, viz, cell temperature and inlet humidity on air and fuel side. The ECSSFF has shown superior performance over the triple serpentine design under all these conditions.     

Performance enhancement of air-cooled open cathode polymer electrolyte membrane fuel cell with inserting metal foam in the cathode side

In this study, a novel way to improve performance of the air-cooled open cathode polymer electrolyte membrane fuel cell is introduced. We suggest using a metal foam in the cathode side of the planar unit fuel cell for the solution to conventional problems of the open cathode fuel cell such as excessive water evaporation from the membrane and poor transportation of air. We conduct experiment and the maximum power density of the fuel cell with metal foam increases by 25.1% compared with the conventional fuel cell without metal foam. The open cathode fuel cell with metal foam has smaller ohmic losses and concentration losses. In addition, we prove that the open cathode fuel cell with metal foam prevents excessive water evaporation and membrane drying out phenomena with numerical approach. Finally, we apply the metal foam to the air-cooled open cathode fuel cell stack as well as the planar unit cell.     

Effect of the cathode gas diffusion layer on the water transport behavior and the performance of passive direct methanol fuel cells operating with neat methanol

The passive operation of a direct methanol fuel cell with neat methanol requires the water that is produced at the cathode to diffuse through the membrane to the anode to compensate the methanol oxidation reaction (MOR). Hence, the anode performance of this type of fuel cell can be limited by the water transport rate from the cathode to the anode. In this work we theoretically show that the water transport from the cathode to the anode depends primarily on the design of the cathode gas diffusion layer (GDL). We investigate experimentally the effects of the design parameters of the cathode GDL, including the PTFE (polytetrafluoroethylene) content in the backing layer (BL), and the carbon loading and the PTFE content in the microporous layer (MPL) on the water transport and the performance of the passive DMFC with the help of a reference electrode. The results indicate that on one hand, these parameters can be adjusted to decrease the water concentration loss of the anode performance, but on the other hand, they can also cause an increase in the oxygen concentration loss of the cathode performance. Hence, an optimal balance in minimizing the both concentration losses is the key to maximize the cell performance.