Mass balance research for high electrochemical performance direct methanol fuel cells with reduced methanol crossover at various operating conditions

Mass balance research in direct methanol fuel cells (DMFCs) provides a more practical method in characterizing the mass transport phenomena in a membrane electrode assembly (MEA). This method can be used to measure methanol utilization efficiency, water transport coefficient (WTC), and methanol to electricity conversion rate of a MEA in DMFCs. First, the vital design parameters of a MEA are recognized for achieving high methanol utilization efficiency with increased power density. In particular, the structural adjustment of anode diffusion layer by adding microporous layer (MPL) is a very effective way to decrease WTC with reduced methanol crossover due to the mass transfer limitation in the anode. On the other hand, the cathode MPL in the MEA design can contribute in decreasing methanol crossover. The change of structure of cathode diffusion layer is also found to be a very effective way in improving power density. In contrast, the WTC of DMFC MEAs remains virtually constant in the range of 3.4 and 3.6 irrespective of the change of the cathode GDL. The influence of operating condition on the methanol utilization efficiency, WTC, and methanol to electricity conversion rate is also presented and it is found that these mass balance properties are strongly affected by temperature, current density, methanol concentration, and the stoichiometry of fuel and air.     

Methanol and water crossover in a passive liquid-feed direct methanol fuel cell

Methanol crossover, water crossover, and fuel efficiency for a passive liquid-feed direct methanol fuel cell (DMFC) were all experimentally determined based on the mass balance of the cell discharged under different current loads. The effects of different operating conditions such as current density and methanol concentration, as well as the addition of a hydrophobic water management layer, on the methanol and water crossover were investigated. Different from the active DMFC, the cell temperature of the passive DMFC increased with the current density, and the changes of methanol and water crossover with current density were inherently coupled with the temperature rise. When feeding with 2–4 M methanol solution, with an increase in current density, both the methanol crossover and the water crossover increased, while the fuel efficiency first increased but then decreased slightly. The results also showed that a reduction of water crossover from the anode to the cathode was always accompanied with a reduction of methanol crossover. Not only did the water management layer result in lower water crossover or achieve neutral or reverse water transport, but it also lowered the methanol crossover and increased the fuel efficiency.     

Basic model for membrane electrode assembly design for direct methanol fuel cells

This research proposes a model that predicts the effect of the anode diffusion layer and membrane properties on the electrochemical performance and methanol crossover of a direct methanol fuel cell (DMFC) membrane electrode assembly (MEA). It is an easily extensible, lumped DMFC model. Parameters used in this design model are experimentally obtainable, and some of the parameters are indicative of material characteristics. The quantification of these material parameters builds up a material database. Model parameters for various membranes and diffusion layers are determined by using various techniques such as polarization, mass balance, electrochemical impedance spectroscopy (EIS), and interpretation of the response of the cell to step changes in current. Since the investigation techniques cover different response times of the DMFC, processes in the cell such as transport, reaction and charge processes can be investigated separately. Properties of single layers of the MEA are systematically varied, and subsequent analysis enables identification of the influence of the layer's properties on the electrochemical performance and methanol crossover. Finally, a case study indicates that the use of a membrane with lower methanol diffusivity and a thicker anode micro-porous layer (MPL) yields MEAs with lower methanol crossover but similar power density.     

Water management in a passive direct methanol fuel cell

Passive direct methanol fuel cells (DMFCs) are under development for use in portable applications because of their enhanced energy density in comparison with other fuel cell types. The most significant obstacles for DMFC development are methanol and water crossover because methanol diffuses through the membrane generating heat but no power. The presence of a large amount of water floods the cathode and reduces cell performance. The present study was carried out to understand the performance of passive DMFCs, focused on the water crossover through the membrane from the anode to the cathode side. The water crossover behaviour in passive DMFCs was studied analytically with the results of a developed model for passive DMFCs. The model was validated with an in‐house designed passive DMFC. The effect of methanol concentration, membrane thickness, gas diffusion layer material and thickness and catalyst loading on fuel cell performance and water crossover is presented. Water crossover was lowered with reduction on methanol concentration, reduction of membrane thickness and increase on anode diffusion layer thickness and anode and cathode catalyst layer thickness. It was found that these conditions also reduced methanol crossover rate. A membrane electrode assembly was proposed to achieve low methanol and water crossover and high power density, operating at high methanol concentrations. The results presented provide very useful and actual information for future passive DMFC systems using high concentration or pure methanol. Copyright © 2012 John Wiley & Sons, Ltd.     

Comparison of numerical simulation results with experimental current density and methanol-crossover data for direct methanol fuel cells

The simulation results of a one-dimensional (1D) direct methanol fuel cell (DMFC) model are compared with the current density and methanol-crossover data that are experimentally measured under several different cell designs and operating conditions. No fitting parameters are employed for the comparison and model input parameters obtained from the literature are consistently used for all the cases of comparison. The numerical predictions agree well with the experimental data and the 1D DMFC model successfully captures key experimental trends that are observed in the cell current density and methanol-crossover data. This clearly illustrates that the present DMFC model can be applicable for optimizing DMFC component designs and operating conditions. In addition, the model simulations further indicate that the reduction of the methanol concentration in the anode catalyst layer is critical to simultaneously suppress both the electro-osmotic drag (EOD) and the diffusion aspects of methanol crossover.     

Modeling and simulation of a direct methanol fuel cell anode

A mathematical model for the anode of a direct methanol fuel cell (DMFC) is presented. This model considers the mass transport in the whole anode compartment and the proton exchange membrane (PEM), together with the kinetic and ohmic resistance effects through the catalyst layer. The influence of key parameters on methanol crossover and anode performance is investigated. Our results indicate that, at low current density and high methanol concentration, the methanol crossover poses a serious problem for a DMFC. The anodic overpotential and reaction-rate distributions throughout the catalyst layer are more sensitive to the protonic conductivity than to the diffusion coefficient of methanol. Increasing the protonic conductivity can effectively enhance the performance of a DMFC.     

Power management of a direct methanol fuel cell system

The effect of discharge rate of direct methanol fuel cell (DMFC) on fuel efficiency was comparatively investigated using a DMFC single cell and a DMFC system. The results obtained from the single cell were used to model the DMFC system. Several semi-empirical equations were derived that relate discharge current, voltage, power output, energy density and fuel consumption for a nominal 25 W DMFC system. The decrease in fuel efficiency with decreased power output that is observed for the DMFC system is attributable to the increase of methanol crossover that can be observed for an individual cell. A DMFC system can achieve maximum energy density and fuel efficiency at an appropriately high level of power output.     

Transient behavior analysis of a new designed passive direct methanol fuel cell fed with highly concentrated methanol

A new structure of passive direct methanol fuel cell (DMFC) with two methanol reservoirs separated by a porous medium layer is designed and a corresponding mathematical model is presented. The new designed passive DMFC can be directly fed with highly concentrated methanol solution or neat methanol. The porosity (?_pr) of the porous medium layer is optimized using the proposed model. Some operation parameters are also optimized by both the numerical calculation and experimental measurement. The new designed DMFC can be continuously operated for about 4.5 times longer than a conventional passive DMFC with the optimum parameters. The methanol crossover during the same discharging is only about 50% higher.     

In situ measurements of water crossover through the membrane for direct methanol fuel cells

We show analytically that the water-crossover flux through the membrane used for direct methanol fuel cells (DMFCs) can be in situ determined by measuring the water flow rate at the exit of the cathode flow field. This measurement method enables investigating the effects of various design and geometric parameters as well as operating conditions, such as properties of cathode gas diffusion layer (GDL), membrane thickness, cell current density, cell temperature, methanol solution concentration, oxygen flow rate, etc., on water crossover through the membrane in situ in a DMFC. Water crossover through the membrane is generally due to electro-osmotic drag, diffusion and back convection. The experimental data showed that diffusion dominated the total water-crossover flux at low current densities due to the high water concentration difference across the membrane. With the increase in current density, the water flux by diffusion decreased, but the flux by back convection increased. The corresponding net water-transport coefficient was also found to decrease with current density. The experimental results also showed that the use of a hydrophobic cathode GDL with a hydrophobic MPL could substantially reduce water crossover through the membrane, and thereby significantly increasing the limiting current as the result of the improved oxygen transport. It was found that the cell operating temperature, oxygen flow rate and membrane thickness all had significant influences on water crossover, but the influence of methanol concentration was negligibly small.     

Passive direct methanol fuel cells fed with methanol vapor

A vapor fed passive direct methanol fuel cell (DMFC) is proposed to achieve a high energy density by using pure methanol for mobile applications. Vapor is provided from a methanol reservoir to the membrane electrode assembly (MEA) through a vaporizer, barrier and buffer layer. With a composite membrane of lower methanol cross-over and diffusion layers of hydrophilic nanomaterials, the humidity of the MEA was enhanced by water back diffusion from the cathode to the anode through the membrane in these passive DMFCs. The humidity in the MEA due to water back diffusion results in the supply of water for an anodic electrochemical reaction with a low membrane resistance. The vapor fed passive DMFC with humidified MEA maintained 20–25 mW cm⁻² power density for 360 h and performed with a 70% higher fuel efficiency and 1.5 times higher energy density when compared with a liquid fed passive DMFC.     

Effect of the cathode open ratios on the water management of a passive vapor-feed direct methanol fuel cell fed with neat methanol

A novel approach has been proposed to improve the water management of a passive direct methanol fuel cell (DMFC) fed with neat methanol without increasing its volume or weight. By adopting perforated covers with different open ratios at the cathode, the water management has been significantly improved in a DMFC fed with neat methanol. An optimized cathode open ratio could ensure both the sufficient supply of oxygen and low water loss. While changing the open ratio of anode vaporizer can adjust the methanol crossover rate in a DMFC. Furthermore, the gas mixing layer, added between the anode vaporizer and the anode current collector to increase the mass transfer resistance, can improve the cell performance, decrease the methanol crossover, and increase the fuel efficiency. For the case of a DMFC fed with neat methanol, an anode vaporizer with the open ratio of 12% and a cathode open ratio of 20% produced the highest peak power density, 22.7 mW cm⁻², and high fuel efficiency, 70.1%, at room temperature of 25 ± 1 °C and ambient humidity of 25-50%.     

Design and simulation of a liquid electrolyte passive direct methanol fuel cell with low methanol crossover

This study investigates an aqueous solution of sulfuric acid that serves as the liquid electrolyte (LE) in a passive direct methanol fuel cell (DMFC). The addition of an LE can reduce methanol crossover and increase the fuel utilization significantly. To improve the performance of an LE-DMFC, a mathematical model is developed to optimize the thicknesses of both the LE layer and the Nafion membrane. The maximum power density of the LE-DMFC is improved by approximately 30% compared with a conventional DMFC (C-DMFC) when each is fed by methanol solutions of the same concentration. Due to the low methanol crossover of the LE-DMFC, a highly concentrated methanol solution can be directly fed into the LE-DMFC. The discharge time and volume energy density of the LE-DMFC are two times longer and three times greater than those of the C-DMFC, respectively. In addition, fuel utilization increases by approximately 100%.     

Operational characteristics of the direct methanol fuel cell stack on fuel and energy efficiency with performance and stability

This paper is presented to investigate operational characteristics of a direct methanol fuel cell (DMFC) stack with regard to fuel and energy efficiency, including its performance and stability under various operating conditions. Fuel efficiency of the DMFC stack is strongly dependent on fuel concentration, working temperature, current density, and anode channel configuration in the bipolar plates and noticeably increases due to the reduced methanol crossover through the membrane, as the current density increases and the methanol concentration, anode channel depth, and temperature decreases. It is, however, revealed that the energy efficiency of the DMFC stack is not always improved with increased fuel efficiency, since the reduced methanol crossover does not always indicate an increase in the power of the DMFC stack. Further, a lower methanol concentration and temperature sacrifice the power and operational stability of the stack with the large difference of cell voltages, even though the stack shows more than 90% of fuel efficiency in this operating condition. The energy efficiency is therefore a more important characteristic to find optimal operating conditions in the DMFC stack than fuel efficiency based on the methanol utilization and crossover, since it considers both fuel efficiency and cell electrical power. These efforts may contribute to commercialization of the highly efficient DMFC system, through reduction of the loss of energy and fuel.     

A three-dimensional two-phase flow model for a liquid-fed direct methanol fuel cell

A three-dimensional, two-phase, multi-component model has been developed for a liquid-fed DMFC. The modeling domain consists of the membrane, two catalyst layers, two diffusion layers, and two channels. Both liquid and gas phases are considered in the entire anode, including the channel, the diffusion layer and the catalyst layer; while at the cathode, two phases are considered in the gas diffusion layer and the catalyst layer but only single gas phase is considered in the channels. For electrochemical kinetics, the Tafel equation incorporating the effects of two phases is used at both the cathode and anode sides. At the anode side the presence of gas phase reduces the active catalyst areas, while at the cathode side the presence of liquid water reduces the active catalyst areas. The mixed potential effects due to methanol crossover are also included in the model. The results from the two-phase flow mode fit the experimental results better than those from the single-phase model. The modeling results show that the single-phase models over-predict methanol crossover. The modeling results also show that the porosity of the anode diffusion layer plays an important role in the DMFC performance. With low diffusion layer porosity, the produced carbon dioxide cannot be removed effectively from the catalyst layer, thus reducing the active catalyst area as well as blocking methanol from reaching the reaction zone. A similar effect exits in the cathode for the liquid water.     

Design of a MEA with multi-layer electrodes for high concentration methanol DMFCs

According to the conventional MEA test, methanol and water crossover are the main factors to determine performance of a passive DMFC. Thus, to ensure the high cell performance of a passive DMFC using high concentration methanol of 50–95 vol%, the MEA in this study introduces the barrier layer to limit the crossover of high concentration methanol, a hydrophobic layer to reduce water crossover, and a hydrophilic layer to enhance the water recovery from the cathode to the anode. The functional layers of the MEA have the effect of improving the performance of the passive DMFC by decreasing the methanol and water crossover. In spite of the operation with 95 vol% methanol, the MEA with multi-layer electrodes for high concentration methanol DMFCs shows a maximum power density of 35.1 mW cm⁻² and maintains a high power density of 30 mW cm⁻² (0.405 V) under constant current operation.     

Real time measurements of methanol crossover in a DMFC

Methanol crossover is a serious problem in a direct methanol fuel cell (DMFC), which causes significant voltage loss and waste of fuel. Due to methanol crossover, most DMFCs must operate on a fuel with a very low methanol concentration; yet very low methanol concentration also causes a poor cell performance. Thus, it is very important to find the optimal operating conditions of methanol concentration and other operating parameters. In this research, methanol crossover rate in a DMFC is determined by measuring the carbon dioxide concentration at the cathode exit in real time. By measuring methanol crossover and cell performances at different inlet methanol concentrations and various operating conditions three types of characteristics are identified in the relationships between methanol crossover and cell current density. Further analysis of these relationships between methanol crossover and cell performances reveals the optimal methanol concentration and other operating parameters, at which the cell reaches optimal performance without incurring excessive methanol crossover. Furthermore, transient peaks of methanol crossover have been identified when the cell voltage suddenly changes. Analyses of these peaks show that they are caused by the hysteresis of methanol concentration at the interface between the anode catalyst layer and the membrane.     

Exergy flow and energy utilization of direct methanol fuel cells based on a mathematic model

An exergetic analysis model for direct methanol fuel cell (DMFC) is established in the present paper. Expressions of electrical, thermal and total exergetic efficiencies have been deduced with consideration of methanol crossover and over potential in operation. Furthermore, energy utilization of a DMFC system is quantitatively calculated and changes of electrical efficiency and thermal efficiency at various current density, methanol concentration, operating temperature, and cathode pressure have been investigated. Some suggestions of optimal operating conditions of direct methanol fuel cell based on our findings are put forward. Results show that the thermal energy generated in a DMFC takes up a significant amount of exergy in total energy and should be sufficiently used to obtain high total efficiency in a DMFC, high methanol crossover rate is the predominant cause of energy loss when the fuel cell operates at low current density, and total exergetic efficiency of a DMFC reaches its peak value at relatively high current density.     

Effect of design of multilayer electrodes in direct methanol fuel cells (DMFCs)

In a direct methanol fuel cell (DMFC), optimized multilayer electrode design is critical to mitigate methanol crossover and improve cell performance. In this paper, we present a one-dimensional (1-D) two-phase model based on the saturation jump theory in order to explore the methanol and water transport characteristics using various multilayer electrode configurations. To experimentally validate the 1-D model, two different membrane electrode assemblies (MEAs) with and without an anode microporous layer (MPL) are fabricated and tested under various cell current density and methanol feed concentration conditions. Then, 1-D DMFC simulations are performed and the results compared to the experimental data. In general, the numerical predictions are in good agreement with the experimental data; thus, the 1-D DMFC simulations successfully model the effects of the anode MPL that were observed experimentally. In addition to the comparison study, additional numerical simulations are carried out to precisely examine the role of the anode and cathode MPLs and the effect of the hydrophobicity of the anode catalyst layer on the water and liquid saturation distributions inside the DMFCs. This paper demonstrates the quantitative accuracy of the saturation jump model for simulating multilayer DMFC MEAs and also provides greater insight into the operational characteristics of DMFCs incorporating multilayer electrodes.     

Effects of structural aspects on the performance of a passive air-breathing direct methanol fuel cell

This study systematically investigates the effects of structural aspects on the performance of a passive air-breathing direct methanol fuel cell (DMFC). Three factors are selected in this study: (1) two different open ratios of the current collector; (2) two different assembly methods of the diffusion layer; and (3) three membrane types with different thicknesses. The interrelations and interactions among these factors have been taken into account. The results demonstrate that these structural factors combine to significantly affect the cell performance of DMFCs. The higher open ratio not only provides a larger area for mass transfer passage and facilitates removal of the products, but also promotes higher methanol crossover. The hot-pressed diffusion layer (DL) can mitigate methanol permeation while the non-bonded variant is able to enhance product removal. The increase of membrane thickness helps obtain a lower methanol crossover rate and higher methanol utilisation efficiency, but also depresses cell performance under certain conditions. In this research, the maximum power density of 10.7 mW cm⁻² is obtained by selecting the current collector with a lower open ratio, the non-bonded DL, and the Nafion 117 membrane. The effect of methanol concentration on the performance of DMFCs is also explored.     

Effects of anode microporous layers made of carbon powder and nanotubes on water transport in direct methanol fuel cells

The effects of the design parameters of the anode diffusion layer (DL), including the PTFE loading in the backing layer (BL), and the carbon and PTFE loading in the microporous layer (MPL), on water transport through the membrane and the performance of a liquid-feed direct methanol fuel cell (DMFC) are experimentally investigated. The results indicate that increasing the PTFE loading in the BL and introducing a MPL could decrease water crossover through the membrane without sacrificing cell performance when the feed methanol concentration is increased. It is also found that changing the PTFE loading in the MPL has little effect on water crossover, whereas increasing the carbon loading in the MPL could noticeably decrease the water-crossover flux. Nevertheless, the ability of the MPL to reduce water crossover is limited by the presence of a number of mud cracks. To reduce further the water-crossover flux, a crack-free MPL made of multi-walled carbon nanotubes (MWCNTs) and PTFE is proposed. Tests indicate that the DMFC with the nanotube MPL results in a much lower water-crossover flux than a conventional carbon-powder MPL. More importantly, the use of the nanotube MPL allows the DMFC to be operated with a higher methanol concentration, and thereby increases the fuel cell system energy density.