Carbon-supported membrane electrode

Fig. 1 COj concentration (solid symbols) and accumulative carbon weight loss (open symbols, integrated from the CO flux at the exit of the working electrode) as a function of time over a commercial conventional-carbon-supported membrane electrode assembly (MEA). The N -fed working electrode (50 cm min" ) was held at a potential of 1.2 V versus the H -fed counter/reference electrode (200 cm min" ) at 95°C and 80% inlet relative humidity (RHj i j). RHE reversible hydrogen electrode...

The methanol permeability in perfluorosulfonate proton exchange membranes at elevated temperature has been also investigated by other electrochemical techniques. One technique involves using carbon supported Pt electrodes placed to both sides of the membrane to serve as concentration sensors. By adding methanol to one or both sides of the membrane, one can calculate the methanol permeability from the time responses of anodic peak currents on the two working electrodes. Experiments have been performed on a Nafion -117 membrane in 2.0 M H2SO4 at 60 and 70 C. 

Finally, a simple method for a rapid evaluation of the activity of high surface area electrocatalysts is to observe the electrocatalytic response of a dispersion of carbon-supported catalyst in a thin layer of a recast proton exchange membrane.This type of electrode can be easily obtained from a solution of Nafion. As an example. Fig. 11 gives the comparative... 

The function of the electrolyte membrane is to facilitate transport of protons from anode to cathode and to serve as an effective barrier to reactant crossover. The electrodes host the electrochemical reactions within the catalyst layer and provide electronic conductivity, and pathways for reactant supply to the catalyst and removal of products from the catalyst [96], The GDL is a carbon paper of 0.2 0.5 mm thickness that provides rigidity and support to the membrane electrode assembly (MEA). It incorporates hydrophobic material that facilitates the product water drainage and prevents... 

Modeling of Membrane-Electrode-Assembly Degradation in Proton-Exchange-Membrane Fuel Cells - Local H2 Starvation and Start-Stop Induced Carbon-Support Corrosion... 

As COR and OER occur simultaneously in the cathode, their kinetics are particularly important in evaluating carbon-support corrosion. The kinetics of OER is material-specific, dependent on catalyst composition and electrode fabrication.35,37 -39 A number of OER kinetics studies were done on Pt metal electrodes.37-39 However, there is a lack of OER kinetics data on electrodes made of Pt nano-particles dispersed on carbon supports. Figure 2 shows the measured OER current density with respect to the overpotential defined by Eq. (6).35 The 02 concentration was measured at the exit of a 50-cm2 cell using a gas chromatograph (GC). The 02 evolution rate (= 02 concentration x cathode flow rate) was then converted to the OER current density, assuming 4e /02 molecule. Diluted H2 (10%) and a thicker membrane (50 p,m) were used in the measurement to minimize H2 crossover from anode to cathode, because H2 would react with 02 evolved at the cathode and incur inaccuracy in the measured OER current density. Figure 2 indicates that the OER... 

Fig. 13.27. Potential vs. current density plots for state-of-the-art fuel cells, o, proton exchange membrane fuel cell , solid oxide fuel cell , pressurized phosphonic acid fuel cell (PAFC) a, direct methanol fuel cell, direct methanol PAFC , alkaline fuel cell. (Reprinted from M. A. Parthasarathy, S. Srinivasan, and A. J. Appleby, Electrode Kinetics of Oxygen Reduction at Carbon-Supported and Un-supported Platinum Microcrystal-lite/Nafion Interfaces, J. Electroanalytical Chem. 339 101-121, copyright 1992, p. 103, Fig. 1, with permission from Elsevier Science.)...

The SPE HDH reactor is flexible in terms of structural materials and functions, e.g. electrode materials could be mesh- or carbon-supported gas diffusion ones the SPE could be a cation or anion exchange membrane (e.g. Nafion 117 or Fu-MATech FT-FKE-S) and the reactor can treat either aqueous or non-aqueous (e.g. a paraffin oil) wastes with or without supporting electrolytes. 

As shown in Figure 1.6, the optimized cathode and anode structures in PEMFCs include carbon paper or carbon cloth coated with a carbon-PTFE (polytetrafluoroethylene) sub-layer (or diffusion layer) and a catalyst layer containing carbon-supported catalyst and Nafion ionomer. The two electrodes are hot pressed with the Nafion membrane in between to form a membrane electrode assembly (MEA), which is the core of the PEMFC. Other methods, such as catalyst coated membranes, have also been used in the preparation of MEAs. 

Liu, D.-J. and Yang, J., Method of Fabricating Electrode Catalyst Layers with Directionally Oriented Carbon Support for Proton Exchange Membrane Fuel Cell, U.S. Patent Application 20060269827, November 30, 2006. 

Adjacent the ionomeric membrane on both sides are the catalyst layers (Fig. 1). As described above, these are platinum black/PTFE composites with high platinum loadings (typically 4 mg Pt/cm on each electrode) or composites of carbon-supported platinum and recast ionomer, with or without added PTFE, of much lower platinum loading (as low as 0.1 mg Pt/cm on each electrode). The electrochemical processes in the fuel cell take place at these electrocatalysts. In the hydrogen (or methanol reformate)/air fuel cell, the processes at the anode and cathode, respectively, are ... 

In Section 3, the slow rate of the ORR at the Pt/ionomer interface was described as a central performance limitation in PEFCs. The most effective solution to this limitation is to employ dispersed platinum catalysts and to maximize catalyst utilization by an effective design of the cathode catalyst layer and by the effective mode of incorporation of the catalyst layer between the polymeric membrane electrolyte and the gas distributor/current collector. The combination of catalyst layer and polymeric membrane has been referred to as the membrane/electrode (M E) assembly. However, in several recent modes of preparation of the catalyst layer in PEFCs, the catalyst layer is deposited onto the carbon cloth, or paper, in much the same way as in phosphoric acid fuel cell electrodes, and this catalyzed carbon paper is hot-pressed, in turn, to the polymeric membrane. Thus, two modes of application of the catalyst layer - to the polymeric membrane or to a carbon support - can be distinguished and the specific mode of preparation of the catalyst layer could further vary within these two general application approaches, as summarized in Table 4. 

Taylor et al.8 were the first to report an electrochemical method for preparation of MEAs for PEMFCs. In their technique, Pt was electrochemically reduced and deposited at the electrode membrane interface, where it was actually utilized as an electrocatalyst. Nation, which is an ion exchange polymer membrane, is first coated on a noncatalyzed carbon support. The Nafion-coated carbon support is then immersed into a commercial acidic Pt plating solution for electrodeposition. Application of a cathodic potential results in diffusion of platinum cations through the active Nation layer. The migrated platinum species are reduced and form Pt particle at the electrode/membrane interface only on the sites which are both electronically and ionically conductive. The deposition of Pt particles merely at the electrode/membrane interface maximizes the Pt utilization. The Pt particles of 2-3.5 nm and a Pt loading of less than 0.05 mg cm-2 were obtained employing this technique.8 The limitation of this method is the difficulty of the diffusion of platinum... 

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