Effects of cathode gas diffusion layer design on polymer electrolyte membrane fuel cell water management and performance

The effects of a microporous layer (MPL) on performance and water management of polymer electrolyte fuel cells are investigated. The presence of an MPL on the cathode side is found to slightly improve performance, although the voltage gain is less significant than that obtained by wetter reactants. The effect of the MPL on water management depends on the cathode inlet-gas humidity. Differences in water crossover rate are insignificant for wet cathode feed (RH = 75%), while they are significant for dry feed (RH = 25%). A model based on transport resistance of the MPL is proposed to explain the experimental trends observed. Modeling results suggest that the presence of the MPL on the cathode side causes a reduction of the water flux from the cathode catalyst layer to the flow channels, effectively promoting water back diffusion through the membrane. Higher cathode humidity reduces the driving force for water transport from the electrode to the gas channels, also reducing the importance of the water transport resistance due to the presence of the MPL.     

Experimental investigation on the performance and durability of hydrogen AEMFC with electrochemical impedance spectroscopy

In situ experimental tests and scanning electron microscope (SEM) observations are done to explore the impact of geometry structure and operating conditions on the performance and durability of alkaline electrolyte membrane fuel cell (AEMFC) accompanied by electrochemical diagnosis. The results show that low anode and cathode polarization resistances can be achieved by selecting a proper ionomer mass fraction (IMF) of the catalyst layer (CL). Increasing the IMF can improve the tolerance to inlet gas humidity. The presence of the anode microporous layer (MPL) greatly improves the cell performance, but cathode MPL plays a reverse effect. After the durability test, the homogeneity of CL is seriously deformed, leading to a great increment of anode and cathode polarization resistances, verified by the electrochemical impedance spectroscopy (EIS) and SEM results. An enhancement of fuel cell durability is achieved by adding nanoscale polytetrafluoroethylene (PTFE) into CL. This work can provide some guidance for the structural and operating parameter optimization of the AEMFC researches in the future.     

Effects of a microporous layer on the performance degradation of proton exchange membrane fuel cells through repetitive freezing

The gas diffusion layer (GDL) covered with a microporous layer (MPL) is being widely used in proton exchange membrane fuel cells (PEMFCs). However, the effect of MPL on water transport is not so clear as yet; hence, many studies are still being carried out. In this study, the effect of MPL on the performance degradation of PEMFCs is investigated in repetitive freezing conditions. Two kinds of GDL differentiated by the existence of MPL are used in this experiment. Damage on the catalyst layer due to freezing takes place earlier when GDL with MPL is used. More water in the membrane and catalyst layer captured by MPL causes permanent damage on the catalyst layer faster. More detailed information about the degradation is obtained by electrochemical impedance spectroscopy (EIS). From the point of view that MPL reduces the ohmic resistance, it is effective until 40 freezing cycles, but has no more effect thereafter. On the other hand, from the point of view that MPL enhances mass transport, it delays the increase in the mass transport resistance.     

Modeling of hydrogen alkaline membrane fuel cell with interfacial effect and water management optimization

In this study, a whole-cell 3D multiphase non-isothermal model is developed for hydrogen alkaline anion exchange membrane (AAEM) fuel cell, and the interfacial effect on the two-phase transport in porous electrode is also considered in the model. The results show that the insertion of anode MPL, slight anode pressurization and reduction of membrane thickness generally improve the cell performance because the water transport from anode to cathode is enhanced, which favors both the mass transport and membrane hydration. The effect of cathode MPL is generally insignificant because liquid water rarely presents in cathode. It is demonstrated that slight pressurization of anode, which might not lead to apparent damage to the membrane, can effectively solve the anode flooding and cathode dryout issues.     

Experimental investigation of liquid water formation and transport in a transparent single-serpentine PEM fuel cell

Liquid water formation and transport were investigated by direct experimental visualization in an operational transparent single-serpentine PEM fuel cell. We examined the effectiveness of various gas diffusion layer (GDL) materials in removing water away from the cathode and through the flow field over a range of operating conditions. Complete polarization curves as well as time evolution studies after step changes in current draw were obtained with simultaneous liquid water visualization within the transparent cell. The level of cathode flow field flooding, under the same operating conditions and cell current, was recognized as a criterion for the water removal capacity of the GDL materials. When compared at the same current density (i.e. water production rate), higher amount of liquid water in the cathode channel indicated that water had been efficiently removed from the catalyst layer.

Visualization of the anode channel was used to investigate the influence of the microporous layer (MPL) on water transport. No liquid water was observed in the anode flow field unless cathode GDLs had an MPL. MPL on the cathode side creates a pressure barrier for water produced at the catalyst layer. Water is pushed across the membrane to the anode side, resulting in anode flow field flooding close to the H₂ exit.     

Experimental study on water transport coefficient in Proton Exchange Membrane Fuel Cell

Water transport within Proton Exchange Membrane Fuel Cell (PEMFC) is investigated by systematic measurements of the water transport coefficient, defined as the net water flux across the membrane divided by the water production. It is recorded for various operating conditions (current density, gas stoichiometry, air inlet relative humidity, temperature, pressure) in a fuel cell stack fed by dry hydrogen. The measurement of the water transport coefficient shows that a significant fraction of water is collected at the anode while water is produced or injected at the cathode. Moreover, in usual operating conditions, liquid water is present at the cell outlet not only in the cathode but also in the anode. Contrary to the electrical performances, ageing has no influence on the water transport coefficient, which allows the comparison between data collected at different periods of the fuel cell lifetime. From this comparison, it was found that the hydrogen flow rate, the amount of vapor injected at cathode inlet, and the temperature are the main parameters influencing the water transport coefficient. It is shown that air and hydrogen stoichiometry present significant effects on water transport but only through these parameters.     

Influence of micro-porous layer and operating conditions on the fluoride release rate and degradation of PEMFC membrane electrode assemblies

In this study, the influence of micro-porous layers (MPL) on polymer electrolyte membrane fuel cell (PEMFC) durability was investigated. Two fuel cells were built, one with a micro-porous layer on the anode side, and a second cell with MPL on both sides. Experiments were conducted by varying operational parameters such as current density, reactant stoichiometry, and inlet relative humidity. Fuel cell degradation was evaluated by measuring fluoride release rates. The largest factor determining fluoride release rate was found to be the presence of MPL; the cell with MPLs on both sides exhibited significantly reduced fluoride release rates compared to that of cell with one MPL. Increasing the current density also reduced the fluoride release rate for cells with only one MPL whereas there was only a moderate effect on cells with two MPLs. Microscopy analysis showed small but significant changes in ionomer layer thickness. Polarization measurements indicated that there was little change in the performance for both cells over the test period.     

Investigation of the effect of microporous layers on water management in a proton exchange membrane fuel cell using novel diagnostic methods

Water management remains a significant challenge for the Proton Exchange Membrane Fuel Cell (PEMFC) with respect to performance, lifetime and operational flexibility. In recent years, microporous layers (MPL) have been widely used on the cathode side of the PEMFC in order to improve fuel cell performance and water management capabilities. Many modeling and experimental studies have with limited success attempted to analyze the underlying mechanisms that are responsible for the performance improvement due to the MPL. In this study, porous inserts along with various in-situ experimental techniques are used to investigate the MPLs. It was observed that the anode pressure drop increased when a cathode MPL was present, indicating water cross-over from the cathode towards the anode side. Further testing identified that the MPL improved cell performance due to the reduction of water saturation in the cathode catalyst layer, which resulted in enhanced oxygen diffusion. The influence of the MPL on the anode side was also studied with the aid of porous inserts and other techniques, and it was observed that the anode MPL improves cell voltage stability and reduces water accumulation in the anode catalyst layer. The present investigation provides further important information on the critical role of the MPL in the PEMFC.     

Effects of porosity distribution variation on the liquid water flux through gas diffusion layers of PEM fuel cells

Flooding of the membrane electrode assembly (MEA) and dehydrating of the polymer electrolyte membrane have been the key problems to be solved for polymer electrolyte membrane fuel cells (PEMFCs). So far, almost no papers published have focused on studies of the liquid water flux through differently structured gas diffusion layers (GDLs). For gas diffusion layers including structures of uniform porosity, changes in porosity (GDL with microporous layer (MPL)) and gradient change porosity, using a one-dimensional model, the liquid saturation distribution is analyzed based on the assumption of a fixed liquid water flux through the GDL. And then the liquid water flux through the GDL is calculated based on the assumption of a fixed liquid saturation difference between the interfaces of the catalyst layer/GDL and the GDL/gas channel. Our results show that under steady-state conditions, the liquid water flux through the GDL increases as contact angle and porosity increase and as the GDL thickness decreases. When a MPL is placed between the catalyst layer and the GDL, the liquid saturation is redistributed across the MPL and GDL. This improves the liquid water draining performance. The liquid water flux through the GDL increases as the MPL porosity increases and the MPL thickness decreases. When the total thickness of the GDL and MPL is kept constant and when the MPL is thinned to 3 μm, the liquid water flux increases considerably, i.e. flooding of MEA is difficult. A GDL with a gradient of porosity is more favorable for liquid water discharge from catalyst layer into the gas channel; for the GDLs with the same equivalent porosity, the larger the gradient is, the more easily the liquid water is discharged. Of the computed cases, a GDL with a linear porosity 0.4x + 0.4 is the best.     

Experimental investigation of the role of a microporous layer on the water transport and performance of a PEM fuel cell

A highly reliable experimental system that consistently closed the overall water balance to within 5% was developed to study the role of a microporous layer (MPL), attached to carbon paper porous transport layer (PTL), on the water transport and performance of a standard 100 cm² active area PEM fuel cell. Various combinations of cells were built and tested with PTLs at the electrodes using either carbon fibre paper with a MPL (SGL 10BB) or carbon fibre paper without a MPL (SGL 10BA). The net water drag coefficient at three current densities (0.3, 0.5 and 0.7 A cm⁻²) for two combinations of anode/cathode relative humidity (60/100% and 100/60%) and stoichiometric ratios of H₂/air (1.4/3 and 1.4/2) was determined from water balance measurements. The addition of a MPL to the carbon fibre paper PTL at the cathode did not cause a statistically significant change to the overall drag coefficient although there was a significant improvement to the fuel cell performance and durability when a MPL was used at the cathode. The presence of a MPL on either electrode or on both electrodes also exhibited similar performance compared to when the MPL was placed at the cathode. These results indicate that the presence of MPL indeed improves the cell performance although it does not affect the net water drag coefficient. The correlation between cell performance and global water transport cannot be ascertained and warrants further experimental investigation.     

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.     

Improvement of PEMFC water management by employing water transport plate as bipolar plate

In this study, a porous hydrophilic water transport plate (WTP) has been employed as a bipolar plate to improve water management in proton exchange membrane fuel cells (PEMFCs). The electric conductivity, gas blocking property, water permeability and wettability of the WTP were characterized. The performance, electrochemical impedance spectroscopy (EIS) and water balance of fuel cells with WTPs and solid plates were evaluated. Benefiting from the humidification and drainage functions of the WTP, the performance of fuel cells with WTPs significantly improved compared with fuel cells with traditional solid plates. As indicated from the experiments, a WTP that was placed on the cathode side is favorable for cell performance and system complexity. Additionally, hydrogen stoichiometry hardly affects the water transport, whereas a decrease in air stoichiometry can switch the main function of the WTP from humidification to water drainage. The results show that the use of WTP technology is promising for water management improvement in PEMFCs.     

An impedance study for the anode micro-porous layer in an operating direct methanol fuel cell

This study presents the benefit to an operating direct methanol fuel cell (DMFC) by coating a micro-porous layer (MPL) on the surface of anode gas diffusion layer (GDL). Taking the membrane electrode assembly (MEA) with and without the anodic MPL structure into account, the performances of the two types of MEA are evaluated by measuring the polarization curves together with the specific power density at a constant current density. Regarding the cell performances, the comparisons between the average power performances of the two different MEAs at low and high current density, various methanol concentrations and air flow rates are carried out by using the electrochemical impedance spectroscopy (EIS) technique. In contrast to conventional half cell EIS measurements, both the anode and cathode impedance spectra are measured in real-time during the discharge regime of the DMFC. As comparing each anode and cathode EIS between the two different MEAs, the influences of the anodic MPL on the anode and cathode reactions are systematically discussed and analyzed. Furthermore, the results are used to infer complete and reasonable interpretations of the combined effects caused by the anodic MPL on the full cell impedance, which correspond with the practical cell performance.     

Computational study of water transport in proton exchange membrane fuel cells

A computational fuel cell dynamics framework is used to develop a unified water transport equation for a proton exchange membrane fuel cell (PEMFC). Various modes of water transport, i.e., diffusion, convection and electro-osmotic drag, are incorporated in the unified water transport equation. The water transport model is then applied to elucidate water management in three-dimensional fuel cells with dry-to-low humidified inlet gases after its validation against available experimental data for dry oxidant and fuel streams. An internal circulation of water with the aid of counter-flow design is found to be of vital importance for low-humidity operation, for example, in the portable application of a PEMFC without an external humidifier. The general features of water transport in PEMFCs are discussed to show various water transport regimes of practical interest, such as anode water loss, cathode flooding, and the equilibrium condition of water at the channel outlets, particularly for limiting situations where anode and cathode water profiles acquire an equilibrium state. From the practical point of view, the effects of the flow arrangement, membrane thickness, and inlet gas humidity as important determinants of fuel cell performance are also analyzed to elucidate fuel cell water transport characteristics.     

Effect of catalyst layer with zeolite on the performance of a proton exchange membrane fuel cell operated under low-humidity conditions

Proton exchange membrane fuel cells (PEMFCs) employ a proton conductive membrane as the separator to transport a hydrogen proton from the anode to the cathode. The membrane's proton conductivity depends on the water content in the membrane, which is affected by the operating conditions. A membrane electrode assembly (MEA) that can self-sustain water is the key component for developing a light-weight and compact PEMFC system without humidifiers. Hence, zeolite is employed to the anode catalyst layer in this study. The effect of the gas diffusion layer (GDL) materials, catalyst loading, binder loading, and zeolite loading on the MEA performance is investigated. The MEA durability is also investigated through the electrochemical impedance spectroscopy (EIS) method. The results suggest that the MEA with the SGL28BCE carbon paper, Pt loadings of 0.1 and 0.7 mg cm^?2 in the anode and cathode, respectively, Nafion-to-carbon weight ratio of 0.5, and zeolite-to-carbon weight ratio of 0.3 showed the best performance when the cell temperature is 60 °C and supplies with dry hydrogen and air from the environment. According to the impedance variation measured by EIS, the MEA with zeolite in the anode catalyst layer shows higher and more stable performance than those without zeolite.     

Experimental study on dual recirculation of polymer electrolyte membrane fuel cell

Durability and start-up ability in sub-zero environment are two technical bottlenecks of vehicular polymer electrolyte membrane (PEM) fuel cell systems. With exhaust gas recirculation on the anode and cathode side, the cell voltage at low current density can be reduced, and the membrane can be humidified without external humidifier. They may be helpful to prolong the working lifetime and to promote the start-up ability. This paper presents an experimental study on a PEM fuel cell system with anodic and cathodic recirculation. The system is built up based on a 10 kW fuel cell stack, which consists of 50 cells and has an active area of 261 cm². A cathodic recirculation pump and a hydrogen recirculation pump are utilized on the cathode and anode side, respectively. Key parameters, e.g., stack current, stack voltage, cell voltage, air flow, relative humidity on the cathode side, oxygen concentration at the inlet and outlet of the cathode side, are measured. Results show that: 1) with a cathodic recirculation the system gets good self-humidification effect, which is similar to that with an external humidifier; 2) with a cathodic recirculation and a reduction of fresh air flux, the cell voltage can be obviously reduced; 3) with an anodic recirculation the cell voltage can also be reduced due to a reduction in the hydrogen partial pressure, the relative humidity on the cathode side is a little smaller than the case with only cathode recirculation. It indicates that, for our stack the cathodic recirculation is effective to clamp cell voltage at low current density, and a self-humidification system is possible with cathodic recirculation. Further study will focus on the dynamic model and control of the dual recirculation fuel cell system.     

Water balance for the design of a PEM fuel cell system

The design of a proton exchange membrane (PEM) fuel cell system is important for the optimization of the function of supporting parameters in the fuel cell. The water balance in a PEM fuel cell is investigated based on the water transport phenomena. In this investigation, the diffusion of water from the cathode side to the anode side of the cell is observed to not occur at 20% relative humidity at the cathode (RHC) and 58% relative humidity at the anode (RHA). The minimum concentration of condensed water at the cathode side is observed at a cathode gas inlet relative humidity of 40% RHC–92% RHC and at temperatures between 343 K and 363 K. RHC operating conditions that are greater than 90% and at a temperature of 363 K increased the concentration of condensed water and occurred quickly, which result in a water balance that became difficult to control. On the anode side, the condensation of water is observed at operating temperatures of 353 K and 363 K.     

Understanding the role of cathode structure and property on water management and electrochemical performance of a PEM fuel cell

Water management is vital for the successful development of PEM fuel cells. Water should be carefully balanced within a PEM fuel cell to meet the conflicting requirements of membrane hydration and cathode anti-flooding. In order to understand the key factors that can improve water management and fuel cell performance, the cathodes with different structures and properties are prepared and tested in this study. The experimental results show that even though no micro-porous layer (MPL) is placed between the cathode catalyst layer (CCL) and macro-porous substrate (MaPS), a hydrophobic CCL is effective to prevent cathode flooding and keep membrane hydrated. The impedance study and the analysis of the polarization curves indicate that the optimized hydrophobic micro-porous structure in the MPL or the hydrophobic CCL could be mainly responsible for the improved water management in PEM fuel cells, which functions as a watershed to provide wicking of liquid water to the MaPS and increase the membrane hydration by enhancing the back-diffusion of water from the cathode side to the anode side through the membrane.     

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.     

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。