Coolant induced variable temperature flow field for improved performance of proton exchange membrane fuel cells

The objective of the coolant induced variable temperature flow field concept is to maintain high membrane water content along the entire flow field without external humidification and without occurrence of liquid water inside the cell at higher currents. This is achieved by imposing a temperature gradient in the cathode downstream direction in such manner that the product water is just sufficient to maintain close to 100% relative humidity along the entire flow field. The concept must be feasible for stack applications and flexible to enable efficient operation under significantly different operating conditions. The concept is investigated via interactive combination of computational fluid dynamics modeling and experimental validation for two membranes, namely Nafion^® 212 and Nafion^® 115. Additional calculations are also carried out for a five-cell stack with Nafion^® 212 membranes. The results of the computational fluid dynamics model are compared with the experimental data. Calculated and measured current density and relative humidity distributions along the cell give insight in the membrane water content and membrane water flux. With the coolant induced variable temperature flow field concept it is possible to achieve close to 100% relative humidity along the entire flow field without the requirement for external humidification, and to minimize the occurrence of liquid water inside the cell, resulting in improved performance of the cell in comparison with commonly used isothermal operation.     

Reactants flow behavior and water management for different current densities in PEMFC

Computational fluid dynamics analysis was carried out to investigate the reactants flow behavior and water management for proton exchange membrane fuel cell (PEMFC). A complete three-dimensional model was chosen for single straight channel geometry considering both anode and cathode humidification. Phase transformation was included in the model to predict the water vapor and liquid water distributions and the overall performance of the cell for different current densities. The simulated results showed that for fully humidified conditions hydrogen mole fraction increases along the anode channel with increasing current density, however, at higher current densities it decreases monotonically. Different anode and cathode humidified conditions results showed that the cell performance was sufficiently influenced by anode humidification. The reactants and water distribution and membrane conductivity in the cell depended on anode humidification and the related water management. The cathode channel–GDL (Gas Diffusion Layer) interface experiences higher temperature and reduces the liquid water formation at the cathode channel. Indeed, at higher current densities the water accumulated in the shoulder area and exposed higher local current density than the channel area. Higher anode with lower cathode humidified combination showed that the cell had best performance based on water and thermal management and caused higher velocity in the cathode channel. The model was validated through the available literature.     

An approach to measuring spatially resolved water crossover coefficient in a polymer electrolyte fuel cell

This paper reports on an experimental approach to measuring the water crossover coefficient distribution for the first time. A straight-channel PEFC of 6 cm² segmented into 10 pieces along the reactant flow direction has been developed. The instrumented cell, combining the functions of current collection and gas sampling with one pin for each segment, is capable of measuring current and species distributions simultaneously from a single experiment. The two distribution data are subsequently combined in a material balance analysis to yield the net water transport coefficient distribution through the membrane. For fully humidified anode and partially humidified cathode, the net water transport coefficient is found to range from 0.47 to 0.025, and the electro-osmotic drag dominates water transport through the membrane. For partially humidified anode and cathode, the net water transport coefficient lies between 0.19 and −0.24, with the negative value indicating dominant back diffusion.     

Effects of humidification temperatures on local current characteristics in a PEM fuel cell

It is well known that water plays a very important role in the performance of proton exchange membrane (PEM) fuel cells. Non-uniform water content in the membrane leads to non-uniform ionic resistance, and non-uniform liquid water fraction in the porous electrode causes varied mass transfer resistances. The objective of this work is to study the effects of different anode and cathode humidification temperatures on local current densities of a PEM fuel cell with a co-flow serpentine flow field. The method used is the current distribution measurement gasket technique [H. Sun, G.S. Zhang, L.J. Guo, H. Liu, J. Power Sources 158 (2006) 326–332]. The experimental results show that both air and the hydrogen need to be humidified to ensure optimal cell performance, and too high or too low humidification temperature can cause severe non-uniform distribution of local current density. From the experimental results of local current density distributions, the local membrane hydration, the optimal humidification temperature, and if flooding occurs can be obtained. Such detailed local measurement results could be very valuable in fuel cell design and operation optimizations.     

Experimental study of water transport in a polybenzimidazole-based high temperature PEMFC

The present work reports a systematic experimental analysis on water transport in a phosphoric acid doped polybenzimidazole-based high temperature PEM fuel cell. Two sets of polarization curves are run with dry and alternatively humidified reactants, covering a wide range of fuel cell operating temperatures and stoichiometries. With dry feed streams, up to 18% of water produced by electrochemical reaction is found on anode side proving the presence of water transport from cathode electrode. Under the investigated conditions, water transport across the membrane is independent of fuel cell temperature but strongly dependent on reactants stoichiometry and humidification. Such parameters can even determine a change in water transport direction. Humidification causes a limited drop in membrane proton resistivity (around 6 mΩ cm²); conversely a slight decrease in fuel cell performances (−5 to −20 mV) is measured.     

Analyses of heat and water transport interactions in a proton exchange membrane fuel cell

A two-phase non-isothermal model is developed to explore the interaction between heat and water transport phenomena in a PEM fuel cell. The numerical model is a two-dimensional simulation of the two-phase flow using multiphase mixture formulation in a single-domain approach. For this purpose, a comparison between non-isothermal and isothermal fuel cell models for inlet oxidant streams at different humidity levels is made. Numerical results reveal that the temperature distribution would affect the water transport through liquid saturation amount generated and its location, where at the voltage of 0.55 V, the maximum temperature difference is 3.7 °C. At low relative humidity of cathode, the average liquid saturation is higher and the liquid free space is smaller for the isothermal compared with the non-isothermal model. When the inlet cathode is fully humidified, the phase change will appear at the full face of cathode GDL layer, whereas the maximum liquid saturation is higher for the isothermal model. Also, heat release due to condensation of water vapor and vapor-phase diffusion which provide a mechanism for heat removal from the cell, affect the temperature distribution. Instead in the two-phase zone, water transport via vapor-phase diffusion due to the temperature gradient. The results are in good agreement with the previous theoretical works done, and validated by the available experimental data.     

Numerical studies of liquid water behaviors in PEM fuel cell cathode considering transport across different porous layers

In this paper, a two-phase two-dimensional PEM fuel cell model, which is capable of handling liquid water transport across different porous materials, is employed for parametric studies of liquid water transport and distribution in the cathode of a PEM fuel cell. Attention is paid particularly to the coupled effects of two-phase flow and heat transfer phenomena. The effects of key operation parameters, including the outside cell boundary temperature, the cathode gas humidification condition, and the cell operation current, on the liquid water behaviors and cell performance have been examined in detail. Numerical results elucidate that increasing the fuel cell temperature would not only enhance liquid water evaporation and thus decrease the liquid saturation inside the PEM fuel cell cathode, but also change the location where liquid water is condensed or evaporated. At a cell boundary temperature of 80 °C, liquid water inside the catalyst layer and gas diffusion media under the current-collecting land would flow laterally towards the gas channel and become evaporated along an interface separating the land and channel. As the cell boundary temperature increases, the maximum current density inside the membrane would shift laterally towards the current-collecting land, a phenomenon dictated by membrane hydration. Increasing the gas humidification condition in the cathode gas channel and/or increasing the operating current of the fuel cell could offset the temperature effect on liquid water transport and distribution.     

Sensitivity analysis of a polybenzimidazole‐based polymer fuel cell and insight into the effect of humidification

The present work describes a systematic investigation of the effect of operating temperature, cathode stoichiometry, anode stoichiometry and reactants humidification rate on the behavior of a polybenzimidazole‐based high temperature polymer fuel cell. The effect of reactants humidification was also considered; actually, in real applications, the syngas holds great amounts of water. Furthermore, water diffuses through the membrane and reaches the cathode side where it adds to the water produced by the electrochemical reaction. The investigation is based on the analysis of polarization curves measured under different operating conditions. Anode stoichiometry has no impact on the fuel cell voltage, while cathode stoichiometry and fuel cell temperature are relevant. When the anode stream is humidified, negligible effects take place; conversely, when the cathode stream is humidified, a consistent drop in the fuel cell voltage is observed, with a consequent drop in the power output. When air is saturated at 70 °C, a power loss of 8% and 27% takes place at 0.55 A cm^?2 and 0.9 A cm^?2, respectively. Such a finding might represent an issue when high power densities are pursued. The effect of cathode humidification was further investigated by means of electrochemical impedance spectroscopy and cyclic voltammetry. Thanks to dedicated tests, the effect of water in the cathode feed stream was clarified. Cathode humidification increases the electrode catalyst active area due to the dilution of the phosphoric acid retained in the electrode. Conversely, the presence of water hinders the oxygen mass transport to the catalyst active sites. Copyright © 2013 John Wiley & Sons, Ltd.     

Maintaining desired level of relative humidity throughout a fuel cell with spatially variable heat removal rates

A concept of using the product water to internally humidify the air stream in a PEM fuel cell without external humidification is investigated by a simple, pseudo 2-D model along a single channel. This model takes into account the mass and energy balance, water and heat generation rates, heat removal, and water transport through the membrane. The model and thus the concept were confirmed experimentally using a 5-segment fuel cell. The temperature of each segment could be individually controlled, and the temperature and humidity of air could be measured between each segment. A temperature profile has been established, by applying spatially variable heat removal rates along the cathode channel, that results in relative humidity being close to 100% throughout the cell without any external humidification. The concept may be applied to a fuel cell stack resulting in simplification of the suporting system by avoiding external humidification.     

Effect of humidification on distribution and uniformity of reactants and water content in PEMFC

Restricted by experimental conditions, it is difficult to analyze reactants distribution and uniformity through experiment. A simulation model is established by experiment fuel cell. Hydrogen humidification has a great impact on hydrogen distribution and concentrates in inlet and serpentine sections. At anode side membrane water content increases significantly when hydrogen relative humidity is over 50%. Air humidification has little effect on air distribution and water content. The oxygen mass fraction only decreases with relative humidity increase. Hydrogen humidification has greater influence on the distribution of reactants and membrane water content than air humidification, but hydrogen humidification needs to control the relative humidity of hydrogen within a suitable range. According to the simulation results in this article, the relative humidity of hydrogen should be controlled at 25%–50%. This paper proposes mass fraction difference coefficient, as uniformity evaluation index. When hydrogen relative humidity is 50%, uniformity of reactants distribution is the best.     

Electrical/flow heterogeneity of gas diffusion layer and inlet humidity induced performance variation in polymer electrolyte fuel cells

A three-dimensional single-flow channel computational model is used to investigate the performance characteristics of polymer electrolyte fuel cells (PEFC). The combined influence of non-uniform interfacial contact resistance (ICR) and inlet relative humidity (RH), along with the heterogeneous flow properties of the gas diffusion layer (GDL) on the PEFC performance is evaluated. The study considers combinations of full and partial humidification of anode and cathode reactants. Results reveal heterogeneous GDL with non-uniform ICR distribution results in a slight ∼4.4% reduction in current density at 0.3V compared to the homogeneous case. However, under same electrical/flow heterogeneities, the current density is observed to increase by ∼19% to ∼1.3A/cm² under fully humidified anode and partially humidified cathode (i.e., RH_a|RH_c = 100%|60%) as compared to ∼1.1A/cm² under symmetric RH_a|RH_c = 100%|100%. Interesting observations are made on the temperature distribution and cathodic water fractions. The variation in anodic inlet humidity is observed to have no impact on temperature distribution in the membrane, whereas variation in cathodic inlet humidity is effective in reducing the temperature in the channel regime with a 4K (kelvin) difference among all the cases. It is noted here that the overpotential map is not an indicator for performance loss, at least at full inlet humidity. This parameter is observed to depend on water concentration in the cathode. The study provides a detailed analysis of the distribution of reactant mass fraction, water concentration, current density, temperature, cathodic overpotential, and cell performance for all the simulated cases.     

A comprehensive,consistent and systematic mathematical model of PEM fuel cells

This paper presents a comprehensive, consistent and systematic mathematical model for PEM fuel cells that can be used as the general formulation for the simulation and analysis of PEM fuel cells. As an illustration, the model is applied to an isothermal, steady state, two-dimensional PEM fuel cell. Water is assumed to be in either the gas phase or as a liquid phase in the pores of the polymer electrolyte. The model includes the transport of gas in the gas flow channels, electrode backing and catalyst layers; the transport of water and hydronium in the polymer electrolyte of the catalyst and polymer electrolyte layers; and the transport of electrical current in the solid phase. Water and ion transport in the polymer electrolyte was modeled using the generalized Stefan–Maxwell equations, based on non-equilibrium thermodynamics. Model simulations show that the bulk, convective gas velocity facilitates hydrogen transport from the gas flow channels to the anode catalyst layers, but inhibits oxygen transport. While some of the water required by the anode is supplied by the water produced in the cathode, the majority of water must be supplied by the anode gas phase, making operation with fully humidified reactants necessary. The length of the gas flow channel has a significant effect on the current production of the PEM fuel cell, with a longer channel length having a lower performance relative to a shorter channel length. This lower performance is caused by a greater variation in water content within the longer channel length.     

质子交换膜燃料电池建模及水热传输特性分析

针对质子交换膜燃料电池(PEMFC)水管理开展了研究,建立了一维非等温两相流解析模型,研究了不同电流密度、微孔层接触角和不同加湿方案对电池内部水分布和温度分布的影响,提出了更好的进气加湿方案。结果表明:电流密度增大会导致阳极拖干、阴极水淹加剧,导致电池各部分温度上升。因各层材料亲水性不同,在交界面处能观察到液态水阶跃现象。增大微孔层接触角促进阴极液态水反扩散到阳极,一定程度上缓解阳极变干,但过大的接触角可能导致阴极水淹加剧。通过采取"阳极充分加湿、阴极低加湿"的进气加湿方案可以有效提高电池性能,并且能在一定程度改善电池内部受热,提高电池使用寿命。     

Experimental study of gas humidification with injectors for automotive PEM fuel cell systems

A scaled gas humidification system using injectors for PEM fuel cell vehicles was developed and the humidification performance was evaluated under various operating conditions. The humidification system consists of an injector, a duplex enthalpy mixer and a water management apparatus. A dew point meter of the chilled mirror type was used to measure the humidity of the air and the hydrogen. Humidification performance was evaluated by measuring the dew point temperature of the humidified gases. Humidification performance was observed to be critically affected by the temperature of injected water and the gas flow rate in this study. The dew point of the humidified gas rose when the temperature of injected water increased, however, it dropped when the gas flow rate was increased. Experimental results show that the outlet temperature was 58.4 °C, dew point temperature of the humidified air reached 54.0 °C when the injection water temperature was 69.5 °C with the room temperature air flow rate of 200 L min⁻¹. Inlet gas temperature also affected the humidification performance and response time. In addition, a 50 cm² PEM fuel cell was tested to verify the effectiveness of the devised humidifier. When operated at 65 °C, the fuel cell showed an operating voltage of 0.5 V at a current density of 600 mA cm⁻².     

Influences of gas relative humidity on the temperature of membrane in PEMFC with interdigitated flow field

A fundamental understanding of the water balance of a fuel cell during operation is crucial for improving the cell performance and durability. The humidification in the anode or cathode has an important effect on the flow characteristics and cell efficiency. Three-dimensional steady mathematical model based on the electrochemical, current distribution, fluid motion continuity equation, momentum and energy equation, boundary layer theory has been developed to simulate PEMFC with interdigitated flow field using the computational fluid dynamics (CFD). Effects on the current density and temperature differences have been simulated and analyzed respectively, when the humidification in the anode or cathode is from 0% to 100% respectively. The numerical results show that the humidification strongly influences the current density and temperature difference so as to affect the cell efficiency. Under the same operation conditions and low humidification conditions, anode humidification can better enhance the performance of the battery and improve the extent of PEM humidification.     

Comparison of current distributions in proton exchange membrane fuel cells with interdigitated and serpentine flow fields

Current distributions in a proton exchange membrane fuel cell (PEMFC) with interdigitated and serpentine flow fields under various operating conditions are measured and compared. The measurement results show that current distributions in PEMFC with interdigitated flow fields are more uniform than those observed in PEMFC with serpentine flow fields at low reactant gas flow rates. Current distributions in PEMFC with interdigitated flow fields are rather uniform under any operating conditions, even with very low gas flow rates, dry gas feeding or over-humidification of reactant gases. Measurement results also show that current distributions for both interdigitated and serpentine flow fields are significantly affected by reactant gas humidification, but their characteristics are different under various humidification conditions, and the results show that interdigitated flow fields have stronger water removal capability than serpentine flow fields. The optimum reactant gas humidification temperature for interdigitated flow fields is higher than that for serpentine flow fields. The performance for interdigitated flow fields is better with over-humidification of reactant gases but it is lower when air is dry or insufficiently humidified than that for serpentine flow fields.     

Development of small polymer electrolyte fuel cell stacks

The results on the research and development of small polymer electrolyte fuel cell stacks, including the assembly of single cell. 6-cell and 21-cell modules, are described. The important characteristics of the systems are: (i) membrane and electrode assemblies were made with Nafion^® 115 and 117 membranes and particularly low catalyst loading electrodes presenting a geometric area of 20 cm² and a catalyst loading of 0.4 mg Pt/cm²: (ii) bipolar plates were fabricated using a nonporous graphite material in which a series/parallel flow field was machined out: (iii) external distribution of gases to the cells was done using parallel manifolding; (iv) cooling systems were tested employing water/air cooling plates distributed every three cells throughout the stack; (v) the reactant gases were externally humidified using temperature controlled humidification bottles. Testing of the stacks was conducted in a specially designed test station employing nonpressurized H₂/O₂ reactants and measuring the individual and the overall cell voltage vs. current under several conditions for the overall system operation.     

Three dimensional,two phase flow mathematical model for PEM fuel cell: Part II. Analysis and discussion of the internal transport mechanisms

The internal transport mechanisms, which were acquired from the modeling results in Part I of this series, are discussed and compared for PEM fuel cells with a conventional flow field and an interdigitated flow field. The modeling results show that the oxygen concentration fraction in an interdigitated flow field is higher than that in a conventional flow field to increase the reaction rate, and the liquid water saturation in the former flow field is much less than that in the latter one at the cathode side to reduce the concentration overpotential largely. However, if the cathode inlet air in a PEM fuel cell with interdigitated flow field is not humidified, the performance of this fuel cell is inferior to that of a PEM fuel cell with conventional flow field because of a larger ohmic overpotential. As a result, the humidification is important for an interdigitated flow field to acquire a much better performance than a conventional flow field.     

An experimental study on vapor transport of a hollow fiber membrane module for humidification in proton exchange membrane fuel cells

Water management is key in the optimization of proton exchange membrane fuel cell performance and durability. Humidifiers can be used to provide water vapor to cathode air, ensuring the proper operation of proton exchange membrane fuel cells. In this study, water vapor transport characteristics of hollow fiber membrane modules were investigated in shell-tube humidifiers under isothermal conditions, using two different test jig constructions: a convection jig and a diffusion jig. The mass transfer rate of water vapor was evaluated via the impact of various operating parameters, including temperature, flow rate, pressure, and relative humidity of inlet wet air, flow arrangements, and surface area of the tube side. The result was presented by the water vapor transport rate from wet air flow to dry air flow across the hollow fiber membrane. It was found that humidification performance could be improved with higher operating temperature, flow rate, and relative humidity of inlet wet air, lower pressure, larger membrane surface area, higher convection effect, and substituting co-current with counter-current flow configuration.     

Spatially resolved current density measurements and real-time modelling as a tool for the determination of local operating conditions in polymer electrolyte fuel cells

In this contribution a simplified, isothermal, two-phase, one-dimensional model for the calculation of the cathodic gas flow along the flow field channels of a polymer electrolyte fuel cell (PEFC) is presented. The composition of the humidified oxidant gas, average gas velocity, pressure drop, and other quantities can be calculated for any gas distributor structures with one channel. Thereby, the model requires several input parameters which have to be determined solely by experiment and pre-defined operation conditions, e.g. the water content of the feed gas, local current densities, and gas flow rates. In contrast to other models, the cross-section reduction has been taken into account which results from the penetration of the gas diffusion layer into the flow field channels due to the mounting pressure. Beyond this, the model needs no fit-parameters for further adjustment.For close examination of the factors limiting the performance of a PEFC, the DLR has developed several techniques for measuring the current density distribution with spatial resolution. In order to investigate the origin of the corresponding effects, one of these techniques has been improved by implementing the model of the cathodic gas flow as an on-line feature.The combination of a spatially resolved measurement technique with a real-time simulation gives a better understanding of the local processes within the cell and represents a helpful tool for the development of fuel cell components as well as for the optimization of the operating conditions. Exemplarily, the presentation the results for a 25 cm² serpentine flow field at different operation modes are shown in this paper.