Effect of cathode gas diffusion layer on water transport and cell performance in direct methanol fuel cells

The optimal design of the cathode gas diffusion layer (GDL) for direct methanol fuel cells (DMFCs) is not only to attain better cell performance, but also to achieve better water management for the DMFC system. In this work, the effects of both the PTFE loading in the cathode backing layer (BL) as well as in the micro-porous layer (MPL) and the carbon loading in the MPL on both water transport and cell performance were investigated experimentally. The experimental data showed that with the presence of a hydrophobic MPL in the GDL, the water-crossover flux through the membrane decreased slightly with increasing the PTFE loading in the BL. However, a higher PTFE loading in the BL not only lowered cell performance, but also resulted in an unstable discharging process. It was also found that the PTFE loading in the MPL had little effect on the water-crossover flux, but its effect on cell performance was substantial: the 40-wt% PTFE loading in the MPL was found to be the optimal value to achieve the best performance. The experimental results further showed that increasing the carbon loading in the MPL significantly lowered the water-crossover flux, but a too high carbon loading would decrease the cell performance as the result of the increased oxygen transport resistance; the 2.0-mg C cm⁻² carbon loading was found to exhibit the best performance.     

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.     

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

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

Effect of variation of hydrophobicity of anode diffusion media along the through-plane direction in direct methanol fuel cells

Reducing methanol crossover from the anode to cathode in direct methanol fuel cells (DMFCs) is critical for attaining high cell performance and fuel utilization, particularly when highly concentrated methanol fuel is fed into DMFCs. In this study, we present a novel design of anode diffusion media (DM) wherein spatial variation of hydrophobicity along the through-plane direction is realized by special polytetrafluoroethylene (PTFE) coating procedure. According to the capillary transport theory for porous media, the anode DM design can significantly affect both methanol and water transport processes in DMFCs. To examine its influence, three different membrane-electrode assemblies are fabricated and tested for various methanol feed concentrations. Polarization curves show that cell performance at high methanol feed concentration conditions is greatly improved with the anode DM design with increasing hydrophobicity toward the anode catalyst layer. In addition, we investigate the influence of the wettability of the anode microporous layer (MPL) on cell performance and show that for DMFC operation at high methanol feed concentration, the hydrophilic anode MPL fabricated with an ionomer binder is more beneficial than conventional hydrophobic MPLs fabricated with PTFE. This paper highlights that controlling wetting characteristics of the anode DM and MPL is of paramount importance for mitigating methanol crossover in DMFCs.     

Measurement of water transport rates across the gas diffusion layer in a proton exchange membrane fuel cell,and the influence of polytetrafluoroethylene content and micro-porous layer

Water management in a proton exchange membrane (PEM) fuel cell is one of the critical issues for improving fuel cell performance and durability, and water transport across the gas diffusion layer plays a key role in PEM fuel cell water management. In this work, we investigated the effects of polytetrafluoroethylene (PTFE) content and the application of a micro-porous layer (MPL) in the gas diffusion layer (GDL) on the water transport rate across the GDL. The results show that both PTFE and the MPL play a similar role of restraining water transport. The effects of different carbon loadings in the MPL on water transport were also investigated. The results demonstrate that the higher the carbon loading in the MPL, the more it reduces the water transport rate. Using the given cell hardware and components, the optimized operation conditions can be obtained based on a water balance analysis.     

The influence of anode diffusion layer on the performance of direct dimethyl ether fuel cell

The effects of the parameters of the anode gas diffusion layer (GDL), including the PTFE content in the backing layer (BL), the PTFE content in the microporous layer (MPL), and the carbon black loading on the performance of a liquid‐feed direct dimethyl ether fuel cell (DDFC), were experimentally investigated. The results indicated that increase in the PTFE content can produce more cracks across the whole surface of the MPL. These cracks were benefit to the anode two‐phase mass transport. The optimal PTFE content in anode BL and MPL was 18 and 40 wt%, respectively. The performances of the DDFCs tended to decline with the increase in the carbon black loading in the anode GDLs due to the difficult long path of mass transport. The maximum power density was obtained with 18 wt% PTFE in BL and 0 mg cm^?2 carbon black loading, the optimal result, was 76.6 mW cm^?2 at ambient pressure. Copyright © 2011 John Wiley & Sons, Ltd.     

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.     

Development of an advanced MEA to use high-concentration methanol fuel in a direct methanol fuel cell system

Despite serious methanol crossover issues in Direct Methanol Fuel Cells (DMFCs), the use of high-concentration methanol fuel is highly demanded to improve the energy density of passive fuel DMFC systems for portable applications. In this paper, the effects of a hydrophobic anode micro-porous layer (MPL) and cathode air humidification are experimentally studied as a function of the methanol-feed concentration. It is found in polarization tests that the anode MPL dramatically influences cell performance, positively under high-concentration methanol-feed but negatively under low-concentration methanol-feed, which indicates that methanol transport in the anode is considerably altered by the presence of the anode MPL. In addition, the experimental data show that cathode air humidification has a beneficial effect on cell performance due to the enhanced backflow of water from the cathode to the anode and the subsequent dilution of the methanol concentration in the anode catalyst layer. Using an advanced membrane electrode assembly (MEA) with the anode MPL and cathode air humidification, we report that the maximum power density of 78 mW/cm² is achieved at a methanol-feed concentration of 8 M and cell operating temperature of 60 °C. This paper illustrates that the anode MPL and cathode air humidification are key factors to successfully operate a DMFC with high-concentration methanol fuel.     

Numerical study of the effect of the GDL structure on water crossover in a direct methanol fuel cell

A two-dimensional two-phase non-isothermal mass transport model is developed to numerically investigate the behavior of water transport through the membrane electrode assembly (MEA) of a direct methanol fuel cell. The model enables the visualization of the distribution of the liquid saturation through the MEA and the analysis of the distinct effects of the three water transport mechanisms: diffusion, convection and electro-osmotic drag, on the water-crossover flux through the membrane. A parametric study is then performed to examine the effects of the structure design of the gas diffusion layer (GDL) on water crossover. The results indicate that the flow-channel rib coverage on the GDL surface and the deformation of the GDL can cause an uneven distribution of the water-crossover flux along the in-plane direction, especially at higher current densities. It is also found that both the contact angle and the permeability of the cathode GDL can significantly influence the water-crossover flux. The water-crossover flux can be reduced by improving the hydrophobicity of the cathode GDL.     

Effects of the microstructure and powder compositions of a micro-porous layer for the anode on the performance of high concentration methanol fuel cell

To investigate the effects of the microstructure and powder compositions for the micro-porous layer (MPL) of an anode on the cell performance of a direct methanol fuel cell (DMFC) using a highly concentrated methanol solution up to 7 M, various powders and their compositions were applied as a filler of the MPL in the membrane electrode assembly (MEA). Several nano- and microstructured carbons such as commercial carbon black (CB), spherical activated carbon (AC), multi-walled carbon nanotube (MWCNT), and platelet carbon nanofiber (PCNF) were selected with different morphology and surface properties, and a meso-porous silica (one of SBA series) was also included for its porous and hydrophilic properties. The coating morphology and physical properties such as porosity and gas permeability were measured, and electrochemical properties of MEA with the MPL were examined by using current–voltage polarization, electrochemical impedance spectroscopy, and voltammetric analyses. A mixture of different carbons was found to be effective for lowering methanol crossover with sustaining electrical conductivity and gas permeability. A MEA with modified-anode MPLs made of CB (50 vol%) and PCNF (50 vol%) powders showed a maximum power density of 67.7 mW cm⁻² under operation with a 7 M concentration of methanol.     

Application of hyperdispersant to the cathode diffusion layer for direct methanol fuel cell

In this study, Nafion ionomer, as a kind of hyperdispersant, was added to polytetrafluoroethylene (PTFE) water dispersion system to suppress the size of PTFE particles in the ink of microporous layer (MPL). The agglomeration behavior of PTFE in ethanol and MPL were investigated by laser diffraction, dynamic light scattering (DLS) and metallurgical microscopes. The electronic resistance, pore size distribution, gas permeability and surface hydrophobic/hydrophilic properties were also characterized for prepared gas diffusion layers (GDLs). It was shown that PTFE water dispersion system suffered flocculating when dispersed in ethanol and this agglomeration behavior was reduced by employing Nafion ionomer. With the increase in the Nafion ionomer adopted in the MPL, not only the decreased hydrophobic property was shown in the MPL, but the decreased PTFE particle size was also achieved, which results in improved crosslink of carbon and pores themselves as well as the volume loss of pores in micron scale. The increased gas permeability and electronic conductivity of the GDL made the one employing the PTFE dispersion system with 1% Nafion content own its advantages as the cathode diffusion layer for a direct methanol fuel cell (DMFC) under near-ambient conditions.     

Effects of basic gas diffusion layer components on PEMFC performance with capillary pressure gradient

The gas diffusion layer (GDL) is composed of a substrate and a micro-porous layer (MPL), and is treated with polytetrafluoroethylene (PTFE) to promote water discharge. Additionally, the MPL mainly consists of carbon black and PTFE. In other words, the optimal design of these elements has a dominant effect on the polymer electrolyte membrane fuel cell (PEMFC) performance. For the GDL, it is crucial to prevent water flooding, and the water flux within the GDL is strongly affected by the capillary pressure gradient. In this study, the PEMFC performance was systematically investigated by varying the substrate PTFE content, MPL PTFE content, and MPL carbon loading per unit area. The effects of each experimental variable on the PEMFC performance and especially on the capillary pressure gradient were quantitatively analyzed when the GDLs were manufactured by the doctor blade manufacturing method. The experimental results indicated that as the PTFE content of the anode and cathode GDL increased, the PEMFC performance deteriorated due to the deformation of the porosity and tortuosity of the GDL. Additionally, the PEMFC performance improved as the MPL PTFE content of the cathode GDL increased at low relative humidity (RH), but the PEMFC performance tendency was reversed at high RH. Further, the MPL carbon loading of 2 mg/${\text{cm}}^2$ demonstrated the best performance, and the advantages and disadvantages of the MPL carbon loading were identified. In addition, the effects of each experimental variable on liquid water, water vapor, and gas permeability were investigated.     

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.     

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.     

Double microporous layer cathode for membrane electrode assembly of passive direct methanol fuel cells

A novel membrane electrode assembly (MEA) is described that utilizes a double microporous layer (MPL) structure in the cathode of a passive direct methanol fuel cell (DMFC). The double MPL cathode uses Ketjen Black carbon as an inner-MPL and Vulcan XC-72R carbon as an outer-MPL. Experimental results indicate that this double MPL structure at the cathode provides not only a higher oxygen transfer rate, but enables more effective back diffusion of water; thus, leading to an improved power density and stability of the passive DMFC. The maximum power density of an MEA with a double MPL cathode was observed to be ca. 33.0 mW cm⁻², which is found to be a substantial improvement over that for a passive DMFC with a conventional MEA. A. C. impedance analysis suggests that the increased performance of a DMFC with the double MPL cathode might be attributable to a decreased charge transfer resistance for the cathode oxygen reduction reaction.     

Effect of PTFE loading of gas diffusion layers on the performance of proton exchange membrane fuel cells running at high‐efficiency operating conditions

In this paper, the effects of microporous layer (MPL) addition and polytetrafluoroethylene (PTFE) loading of gas diffusion layers (GDLs) on the overall performance of the proton exchange membrane fuel cell have been investigated. The focus was on fuel cells that operate at relatively low current densities where the power demand is low, but the efficiency is of concern. The results show that, in the activation loss‐controlled region, the performance of the fuel cell operating with moderately PTFE‐treated carbon substrates is superior over that operating with coated GDLs. This is due to the addition of the MPL which lengthens the diffusion paths and significantly reduces the mass transport properties. Conversely, in the ohmic loss‐controlled region, the fuel cell with coated GDLs performs better than those with carbon substrates. This is explained by the enhanced contact of the GDL with the adjacent components after the MPL addition, which outweighs the negative effects associated with the activation loss‐controlled region. Also, it was found that the fuel cell performance becomes lower if the GDL is treated with a relatively high PTFE loading in either the carbon substrate (due to the decrease in the porosity of the GDL) or the MPL. Copyright © 2012 John Wiley & Sons, Ltd.     

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.     

Reaction analysis of a direct methanol fuel cell employing a porous carbon plate operated at high methanol concentrations

It is known that a small amount of intermediate products, i.e., formaldehyde, formic acid and so on, is exhausted from a direct methanol fuel cell (DMFC). The production rates of such intermediates are affected by the methanol and water concentrations at the anode, and also the distribution of these products is variable. We investigated the production of the intermediates from a passive DMFC containing a porous carbon plate (PCP), which allows the use of methanol at high concentrations up to 100% due to the high resistivity to the methanol transport through the PCP. The production rates of each intermediate and their distribution were measured not only for a DMFC employing various PCPs with different transportation resistivities, but also for a DMFC without PCP. The results were analyzed in terms of the rate of methanol crossover (MCO) and water flux through the membrane. The detected intermediates were formaldehyde, formic acid, and methylformate, in accordance with previous reports. The production rates of the intermediates were strongly dependent on the flux of the MCO rather than the apparent methanol concentration. When the DMFC was operated under the rate limiting conditions of the methanol transport by the PCP, the production rates of the intermediates were low. However, when it was operated outside of the rate limiting conditions, the production rate increased with the increasing rate of methanol crossover.     

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.