Bio-inspired flow field designs for polymer electrolyte membrane fuel cells

The branching structures found in biological systems have evolved to an optimum arrangement that distributes nutrients efficiently in the system. Since the flow fields of polymer electrolyte membrane (PEM) fuel cells serve similar functions to the nutrient transport systems in plants and animals, it is expected that flow fields with a similar hierarchical structure could optimize the transport efficiency of reactants and improve the performance of fuel cells. In this paper, a series of bio-inspired flow field designs inspired by the venation structure of a tree leaf is developed. Two different configurations, interdigitated and non-interdigitated, are considered in implementing the hierarchical structures. Murray's law, which describes the optimum configuration found in biological circulatory systems, is used to determine the flow channel widths of different generations. The bio-inspired design using Murray's law is compared to a design with constant channel width. Both numerical and experimental studies are carried out to investigate these bio-inspired designs. The mass, velocity, and pressure distributions within the channels and the gas diffusion layers, as well as the fuel cell performance, are studied for different flow field designs. The results show that the bio-inspired interdigitated designs substantially improve the fuel cell performance by 20–25% compared to the conventional designs.     

Development of flow field design of polymer electrolyte membrane fuel cell using in-situ impedance spectroscopy

The design of a flow field channel of a polymer electrolyte membrane fuel cell (PEMFC) was investigated by computational fluid dynamic (CFD) simulation and in-situ three-channel impedance spectroscopy. To investigate the efficiency of the in-situ three-channel impedance spectroscopy method, it was adopted with a heterogeneous stack, which was composed according to three different types of flow field design. The in-situ three-channel method proved its validity by showing corresponding result with that obtained from the experiments and CFD simulation at the same experimental condition. This study demonstrates that a heterogeneous stack and in-situ three-channel impedance spectroscopy are powerful tools for predicting and analyzing the performance of a fuel cell stack.     

Network based optimization model for pin-type flow field of polymer electrolyte membrane fuel cell

The flow field of a bipolar plate distributes reactants for polymer electrolyte membrane (PEM) fuel cells and removes the produced water from the fuel cells. It greatly influences the performance of fuel cells, especially the concentration losses. Pin-type design, as one of the widely utilized flow field configurations, has the advantage of low pressure drop but the disadvantage of uneven flow distribution and stagnant areas. In this paper, a network-based optimization model was developed to optimize the pin-type flow field configuration. Two optimization cases, uniform flow distribution with and without considering reactant consumption along flow channels, were investigated and the corresponding optimized designs were developed. Three-dimensional numerical simulations of PEM fuel cell were conducted to validate the proposed optimization model and also to compare the performance of the fuel cells using the optimized designs and the regular pin-type design. The numerical results verified the designs generated with the present optimization model. Both the optimized designs exhibited substantially higher fuel cell performance compared to the regular pin-type configuration. Moreover, the optimized design with considering reactant consumption performed even better than the one without considering the consumption, emphasizing the significance of reactant consumption in the flow field optimization model.     

Characterization of flooding and two-phase flow in polymer electrolyte membrane fuel cell stacks

A partially flooded gas diffusion layer (GDL) model is proposed and solved simultaneously with a stack flow network model to estimate the operating conditions under which water flooding could be initiated in a polymer electrolyte membrane (PEM) fuel cell stack. The models were applied to the cathode side of a stack, which is more sensitive to the inception of GDL flooding and/or flow channel two-phase flow. The model can predict the stack performance in terms of pressure, species concentrations, GDL flooding and quality distributions in the flow fields as well as the geometrical specifications of the PEM fuel cell stack. The simulation results have revealed that under certain operating conditions, the GDL is fully flooded and the quality is lower than one for parts of the stack flow fields. Effects of current density, operating pressure, and level of inlet humidity on flooding are investigated.     

Development of polymer electrolyte membrane fuel cell stack

The proton exchange membrane fuel cell (PEMFC) is one of the strongest contenders as a power source for space, electric vehicle and domestic applications. Since 1988 intensive research is being carried out at our centre to develop PEMFCs. The main RandD activities are: (i) to develop a method for the electrode preparation (ii) to enhance platinum utilisation using low platinum loading and (iii) to design multicell stacks. The results of RandD development of the above activities are discussed in this paper.     

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.     

Humidification studies on polymer electrolyte membrane fuel cell

Two methods of humidifying the anode gas, namely, external and membrane humidification, for a polymer electrolyte membrane fuel (PEMFC) cell are explained. It is found that the water of solvation of protons decreases with increase in the current density and the electrode area. This is due to insufficient external humidification. In a membrane-based humidification, an optimum set of parameters, such as gas flow rate, area and type of the membrane, must be chosen to achieve effective humidification. The present study examines the dependence of water pick-up by hydrogen on the temperature, area and thickness of the membrane in membrane humidification. Since the performance of the fuel cell is dependent more on hydrogen humidification than on oxygen humidification, the scope of the work is restricted to the humidification of hydrogen using Nafion^® membrane. An examination is made on the dependence of water pick-up by hydrogen in membrane humidification on the temperature, area and thickness of the membrane. The dependence of fuel cell performance on membrane humidification and external humidification in the anode gas is also considered.     

Optimization of polymer electrolyte membrane fuel cell flow channels using a genetic algorithm

The design of the flow channels in PEM fuel cells directly impacts the transport of reactant gases to the electrodes and affects cell performance. This paper presents results from a study to optimize the geometry of the flow channels in a PEM fuel cell. The optimization process implements a genetic algorithm to rapidly converge on the channel geometry that provides the highest net power output from the cell. In addition, this work implements a method for the automatic generation of parameterized channel domains that are evaluated for performance using a commercial computational fluid dynamics package from ANSYS. The software package includes GAMBIT as the solid modeling and meshing software, the solver FLUENT, and a PEMFC Add-on Module capable of modeling the relevant physical and electrochemical mechanisms that describe PEM fuel cell operation. The result of the optimization process is a set of optimal channel geometry values for the single-serpentine channel configuration. The performance of the optimal geometry is contrasted with a sub-optimal one by comparing contour plots of current density, oxygen and hydrogen concentration. In addition, the role of convective bypass in bringing fresh reactant to the catalyst layer is examined in detail. The convergence to the optimal geometry is confirmed by a bracketing study which compares the performance of the best individual to those of its neighbors with adjacent parameter values.     

Modeling the phenomena of dehydration and flooding of a polymer electrolyte membrane fuel cell

A one-dimensional, two-phase, transient PEM fuel cell model including gas diffusion layer, cathode catalyst layer and membrane is developed. The electrode is assumed to consist of a network of dispersed Pt/C forming spherically shaped agglomerated zones that are filled with electrolyte. Water is modeled in all three phases: vapor, liquid and dissolved in the ionomer to capture the effect of dehydration of the ionomer as well as flooding of the porous media. The anode is modeled as a sophisticated spatially reduced interface. Motivated by environmental scanning electron microscope (ESEM) images of contact angles for microscopic water droplets on fibers of the gas diffusion layer, we introduce the feature of immobile saturation. A step change of the saturation between the catalyst layer and the gas diffusion layer is modeled based on the assumption of a continuous capillary pressure at the interface. The model is validated against voltammetry experiments under various humidification conditions which all show hysteresis effects in the mass transport limited region. The transient saturation profiles clearly show that insufficient liquid water removal causes pore flooding, which is responsible for the oxygen mass transport limitation at high current density values. The simulated and measured current responses from chronoamperometry experiments are compared and analyzed.     

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.     

Enhanced diffusion in polymer electrolyte membrane fuel cells using oscillating flow

This study investigates the enhancement of the oxygen diffusion rate at the cathode of a proton exchange membrane fuel cell (PEMFC) due to pure oscillating flow. A unit cell of PEMFC using hydrogen fuel and oscillating air was tested. The experimental results show that the non-dimensional effective diffusivity varies linearly with the square of the Womersley number, when the Womersley number is close to unity. The non-dimensional effective diffusivity varies linearly with the Womersley number itself when the Womersley number is much larger than unity. Similar trend has been confirmed from the theoretical approach. Under the experimental conditions in this study, the reaction rate of oxygen increased linearly with respect to the sweep distance. The experimental results showed that a power density of 115.4 mW/cm² was obtained from the unit cell with oscillating flow, which is comparable to that obtained with forced flow. Therefore, an oscillating flow is found to be able to increase the concentration of the oxygen in the channel of PEMFCs, and consequently enhances mass-transfer, similarly to the use of forced flow using blowers or compressors.     

Free vibration analysis of a polymer electrolyte membrane fuel cell

A free vibration analysis of a polymer electrolyte membrane fuel cell (PEMFC) is performed by modelling the PEMFC as a 20 cm × 20 cm composite plate structure. The membrane, gas diffusion electrodes, and bi-polar plates are modelled as composite material plies. Energy equations are derived based on Mindlin's plate theory, and natural frequencies and mode shapes of the PEMFC are calculated using finite element modelling. A parametric study is conducted to investigate how the natural frequency varies as a function of thickness, Young's modulus, and density for each component layer. It is observed that increasing the thickness of the bi-polar plates has the most significant effect on the lowest natural frequency, with a 25% increase in thickness resulting in a 17% increase in the natural frequency. The mode shapes of the PEMFC provide insight into the maximum displacement exhibited as well as the stresses experienced by the single cell under vibration conditions that should be considered for transportation and stationary applications. This work provides insight into how the natural frequencies of the PEMFC should be tuned to avoid high amplitude oscillations by modifying the material and geometric properties of individual components.     

Development of porous carbon foam polymer electrolyte membrane fuel cell

In order to prove the feasibility of using porous carbon foam material in a polymer electrolyte membrane fuel cell (PEMFC), a single PEMFC is constructed with a piece of 80PPI (pores per linear inch) Reticulated Vitreous Carbon (RVC) foam at a thickness of 3.5 mm employed in the cathode flow-field. The cell performance of such design is compared with that of a conventional fuel cell with serpentine channel design in the cathode and anode flow-fields. Experimental results show that the RVC foam fuel cell not only produces comparative power density to, but also offers interesting benefits over the conventional fuel cell. A 250 h long term test conducted on a RVC foam fuel cell shows that the durability and performance stability of the material is deemed to be acceptable. Furthermore, a parametric study is conducted on single RVC foam fuel cells. Effect of geometrical and material parameters of the RVC foam such as PPI and thickness and operating conditions such as pressure, temperature, and stoichiometric ratio of the reactant gases on the cell performance is experimentally investigated in detail. The single cell with the 80PPI RVC foam exhibits the best performance, especially if the thinnest foam (3.5 mm) is used. The cell performance improves with increasing the operating gauge pressure from 0 kPa to 80 kPa and the operating temperature from 40 °C to 60 °C, but deteriorates as it further increases to 80 °C. The cell performance improves as the stoichiometric ratio of air increases from 1.5 to 4.5; however, the improvement becomes marginal when it is raised above 3.0. On the other hand, changing the stoichiometric ratio of hydrogen does not have a significant impact on the cell performance.     

A review of polymer electrolyte membrane fuel cell stack testing

This paper presents an overview of polymer electrolyte membrane fuel cell (PEMFC) stack testing. Stack testing is critical for evaluating and demonstrating the viability and durability required for commercial applications. Single cell performance cannot be employed alone to fully derive the expected performance of PEMFC stacks, due to the non-uniformity in potential, temperature, and reactant and product flow distributions observed in stacks. In this paper, we provide a comprehensive review of the state-of-the art in PEMFC testing. We discuss the main topics of investigation, including single cell vs. stack-level performance, cell voltage uniformity, influence of operating conditions, durability and degradation, dynamic operation, and stack demonstrations. We also present opportunities for future work, including the need to verify the impact of stack size and cell voltage uniformity on performance, determine operating conditions for achieving a balance between electrical efficiency and flooding/dry-out, meet lifetime requirements through endurance testing, and develop a stronger understanding of degradation.     

Detailed thermodynamic analysis of polymer electrolyte membrane fuel cell efficiency

It is common knowledge that efficiency of fuel cells is highest when no electric current is produced while when the fuel cell is really working, the efficiency is reduced by dissipation. In this paper the relation between efficiency and dissipation inside the fuel cell is formulated within the framework of classical irreversible thermodynamics of mixtures. It is shown that not only dissipation influences the efficiency but that there are also some other terms which become important if there are steep temperature gradients inside the fuel cell. Indeed, we show that the new terms are negligible in polymer-electrolyte membrane fuel cells while they become important in solid oxide fuel cells. In summary, this paper presents a formulation of non-equilibrium thermodynamics of fuel cells and provides analysis of efficiency in terms of processes inside the fuel cells, revealing some new terms affecting the efficiency.     

Optimal catalyst layer structure of polymer electrolyte membrane fuel cell

In a membrane electrode assembly (MEA) of polymer electrolyte membrane fuel cells, the structure and morphology of catalyst layers are important to reduce electrochemical resistance and thus obtain high single cell performance. In this study, the catalyst layers fabricated by two catalyst coating methods, spraying method and screen printing method, were characterized by the microscopic images of catalyst layer surface, pore distributions, and electrochemical performances to study the effective MEA fabrication process. For this purpose, a micro-porous layer (MPL) was applied to two different coating methods intending to increase single cell performances by enhancing mass transport. Here, the morphology and structure of catalyst layers were controlled by different catalyst coating methods without varying the ionomer ratio. In particular, MEA fabricated by a screen printing method in a catalyst coated substrate showed uniformly dispersed pores for maximum mass transport. This catalyst layer on micro porous layer resulted in lower ohmic resistance of 0.087 Ω cm² and low mass transport resistance because of enhanced adhesion between catalyst layers and a membrane and improved mass transport of fuel and vapors. Consequently, higher electrochemical performance of current density of 1000 mA cm^-2 at 0.6 V and 1600 mAcm⁻² under 0.5 V came from these low electrochemical resistances comparing the catalyst layer fabricated by a spraying method on membranes because adhesion between catalyst layers and a membrane was much enhanced by screen printing method.     

The effect of baffle shape on the performance of a polymer electrolyte membrane fuel cell with a biometric flow field

Flow field design on the cathode side, inspired by leaf shapes, leads to a high performance, as it achieves a good distribution of reactants. Furthermore, the addition of baffles to the cathode channel also increases the supply of reactants in the cathode catalyst. However, research on the addition of baffles to the cathode channel has still been limited to straight channels and conventional flow fields. Therefore, in this work, a numerical study was conducted to investigate the effect of baffles on the leaf flow field on the performance of a polymer electrolyte membrane fuel cell. The generated 3D model is composed of nine layers with a 25-cm² active area. The beam and chevron shapes of the baffles, which were inserted into the mother channel, were compared. The simulation results revealed that the addition of beam-shaped baffles that are close to each other can increase the current and power densities by up to 18% due to the more uniform distribution of the oxygen mass fraction.     

Experimental analysis of internal gas flow configurations for a polymer electrolyte membrane fuel cell stack

The internal gas distribution system utilised for supplying fresh reactants and removing reaction products from the individual cells of a fuel cell stack can be designed in a parallel, a serial or a mixture of parallel and serial gas flow configuration. In order to investigate the interdependence between the internal stack gas distribution configuration and single cell as well as overall stack performance, a small laboratory-scale fuel cell stack consisting of identical unit cells was subject to operation with different gas distribution configurations and different operating parameters. The current/voltage characteristics measured with the different gas distribution configurations are analysed and compared on unit cell- as well as on stack-level. The results show the significant impact of the internal stack gas distribution system on operation and performance of the individual unit cells and the overall stack.     

Externally cooled high temperature polymer electrolyte membrane fuel cell stack

One key issue in high temperature polymer electrolyte membrane fuel cell (HT-PEMFC) stack development is heat removal at the operating temperature of 140–180 °C. Conventionally, this process is done using coolants such as thermooil, steam or pressurized water. In this contribution, external liquid cooling designs are described, which are avoiding two constraints. First, in the cell active area, no liquid coolant is present avoiding any sealing problems with respect to the electrode. Secondly, the external positioning allows high temperature gradients between the heat removal zone and the active area resulting in a good adjustability of appropriate reformate conversion temperatures (e.g. 160 °C) and a more compact cell design. Different design concepts were investigated using modeling techniques and a selection of them has also been investigated experimentally. The experiments proved the feasibility of the external cooling design and showed that the temperature gradients within the active area are below 15 K under typical operating conditions.