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Testing of carbon supported PdePt electrocatalysts for methanol electrooxidation in direct methanol fuel cells
lvarez a, Pere L. Cabot b, Hans-Ju Francisco Alcaide a,*, Garbin e A rgen Grande a, Oscar Miguel a, Amaia Querejeta a
n, 196, 20009 San Sebastia n, Spain Dpto. de Energ a, CIDETEC-IK4, P Miramo `s, 1-11, Laboratori dElectroqu mica de Materials i del Medi Ambient, Dept. Qu mica F sica, Universitat de Barcelona, Mart i Franque 08028 Barcelona, Spain
a b

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Article history: Received 2 November 2010 Received in revised form 31 December 2010 Accepted 5 January 2011 Available online 4 February 2011 Keywords: PdePt Methanol electrooxidation CO tolerance Direct methanol fuel cell

In the present work, a detailed characterization of the electrochemical behavior of carbon supported PdePt electrocatalysts toward CO and methanol electrooxidation in direct methanol fuel cells is reported. Technical electrodes containing an ionomer in their catalyst layer were prepared for this purpose. CO and methanol electrooxidation reactions were used as test reactions to compare the electrocatalytic behavior of bimetallic supported nanoparticles in acidic liquid electrolyte and in solid polymer electrolyte (real fuel cell operating conditions). Experimental results in both environments are consistent and show that the electrochemical behavior of carbon supported PdePt depends on their composition, giving the best performance in direct methanol single fuel cell with a Pd:Pt atomic ratio of 25:75 in the catalyst. Copyright 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.



The use of direct methanol fuel cells (DMFCs) as auxiliary power source for portable applications has been recently increased [1]. Methanol is easy handled, distributed, and stored. DMFCs are low-temperature devices with simple design, they do not need reformer or humidication, refueling is easy and fast, having high energy density compared to pressurized hydrogen (w6.1 vs. 1.0 kWh kg1, respectively). They nd applications in leisure (mobile homes, cabins, boats), trafc regulation, security, and remote sensors, between others. However, some issues concerning the performance of the anode electrocatalyst, cost and system durability persist and must be solved to guarantee their commercialization on a large-scale [2].

The activity of the anode electrocatalyst at temperatures below 60  C should be improved to gain in the fuel cell performance. It has been recognized that platinum shows the highest activity among single metals for methanol electrooxidation in acidic medium [3], but it is readily poisoned by the CO intermediates formed in this reaction [4]. Furthermore, the high cost and low availability of Pt limits its use in DMFCs [5]. The main strategies to enhance the catalyst activity are dispersing Pt on high surface area carbonaceous materials, the optimization of the catalyst layer structure in technical electrodes (the practical electrodes used in fuel cells), used in membrane electrode assemblies (MEAs), and the use of Ptbased alloys [6]. In this sense, PteRu alloys are nowadays the catalysts of choice for methanol oxidation [7], because of their high tolerance for CO poisoning, which is generally explained

* Corresponding author. Tel.: 34 943 309 022; fax: 34 943 309 136. E-mail address: (F. Alcaide). 0360-3199/$ e see front matter Copyright 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved. doi:10.1016/j.ijhydene.2011.01.015

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by a bifunctional mechanism, in which CO is oxidized by the oxygenated species formed on the Ru surface atoms [8]. However, there is much discussion about the effect of the Ru content in the literature, but in general the optimum Ru content in PteRu alloys for anodic methanol oxidation varies from 10% at room temperature to 50% at 60  C [9]. Furthermore, other systems than PteRu have been investigated for their suitability as methanol electrooxidation catalysts, including PteRh [10e12], PteSn [13e16], PteMo [17e19], PdeAg [20], PdeNi [21e23] and PtePd [24e28]. Good results have been reported for PtePd under some conditions, due to the synergistic effect between Pt and Pd, which has been explained by an electronic effect of Pd on Pt or the improvement of the reaction rate by decreasing the electrode poisoning. The use of palladium in fuel cell catalysts [29] is interesting, because it is more widespread in the Earth crust than platinum (abundance of 1.5 102 vs. 5 103 parts per million by mass, respectively [30]), and it is less expensive than Pt. Replacing Pt by Pd, if the electrocatalysis demands are satised, would then decrease the cost of the electrodes [31,32]. In addition, it is very stable in the acidic fuel cell environment [33] and it also exhibits interesting electrocatalytic properties for CO electrooxidation [34e37]. These properties have lead to consider Pd as a possible catalyst for those reactions in which CO appears as a poisoning intermediate, such as in the methanol or, more recently, in the ethanol [24,38e40], and formic acid [41e44] electrooxidation. The electrochemical properties of PtePd unsupported nanoparticles have been widely studied in terms of CO tolerance, methanol and formic acid oxidation [45e47]. However, a detailed study of the electrochemical behavior of carbon supported PtePd nanoparticles in a real DMFC environment has not been yet performed. The aim of this work is to study the electrochemical behavior of carbon supported PdePt electrocatalysts in the complete range of Pd content to approach the conditions for the best operation, which has not been previously done in such a wide range of compositions. A comparison between measurements in liquid and solid polymer electrolyte was made to experimentally conrm whether the conclusions achieved in previous studies using three-electrode cells could be extrapolated to real fuel cell operating conditions. In this sense, methanol oxidation has been selected as the probe reaction. Thus, technical electrodes, made of a diffusion layer and a catalysts layer, were prepared, and CO stripping and methanol electrooxidation experiments were performed in three-electrode cell and in single DMFC under practical conditions.

) and 2q scan from operating with Cu Ka radiation (l 1.5406 A 30 to 100 (at 0.02 min1). Diffraction peaks were assigned according to the International Center for Diffraction Data (ICDD) cards in PDF-2 database. The XRD data were used to determine the lattice parameter (from the interplanar distances), by rening the unit cell dimensions using WinPLOTR software, and the average crystallite size (from Scherrer equation) [48]. The instrumental and the microstrain broadening were accounted for in the calculation of the crystallite sizes by the given software, which allowed importing directly the experimental diffractograms without the need of the introduction of the parameters corresponding to the XRD instrumentation. The mass ratio of metal to carbon in the electrocatalysts and Pd:Pt atomic ratios were analyzed by the energy dispersive X-ray (EDX) technique. The EDX measurements were performed by means of an INCA-300 energy analyzer coupled to a JSM5910-LV JEOL scanning electron microscope (SEM). The compositions detailed in Table 1 show the average of ve different measurements on the same sample, with relative error less than 1%.

2.2. MEAs

Preparation and testing of technical electrodes and

Porous diffusion electrodes for three-electrode cell experiments were prepared by the spraying method [49]. The diffusion layers were LT1400W ELAT GDL (E-TEK, Inc.). For each electrode, appropriate amounts of the supported catalyst and 5 wt. % Naon ionomer dispersion (Aldrich) were ultrasonically dispersed in a mixture of isopropanol (Acros Organics, pur.) and ultrapure water (k  0.054 mS cm1, Millipore). Then, the ink was sprayed onto the diffusion layer by an air-brush gun fed with pure nitrogen. The metal loading in the electrode was 0.20 mg cm2 and the Naon content was 20 wt. % (dry weight). Square shape MEAs (active geometric area of 16 cm2) were catalyst coated membranes, that is, the catalyst layers were sprayed directly onto both sides of a Naon NR212 membrane. The composition of the anode catalyst layer was the same as the porous electrodes for the three-electrode cell explained above. The oxygen cathode catalyst layer contained 0.2 mgPt cm2 and a 30 wt. % (dry weight) of Naon. Finally, gas diffusion layers ELAT GDL (E-TEK, Inc.) were placed beside the cathode and the anode electrodes, respectively. Electrochemical measurements in a conventional thermostatted three-electrode cell were performed with a



Table 1 e Composition from EDX and physical parameters from XRD analysis of PdLPt catalysts. Catalyst Metal loading (wt. %)
18.9 19.3 20.0 20.0 19.1

Pd:Pta (a/o)
100 73:27 44:56 30:70 100

Crystallite size (nm)

3.4 5.6 4.1 2.3 2.1 0.31 0.43 0.61 0.57 0.24

Lattice parameter (nm)

0.3881 0.3902 0.3914 0.3902 0.3930 0.0015 0.0008 0.0003 0.0008 0.0019

The catalysts used in this work were commercial Pd, Pd75ePt25, Pd50ePt50, Pd25ePt75 (where subscripts indicate atomic percent, a/o), and Pt, all supported at 20 wt. % on carbon black Vulcan XC-72, from Premetek Co. They were characterized by X-Ray diffraction (XRD). The XRD diffractograms were obtained by a Bruker D8 Advance diffractometer

Pd/C Pd75Pt25/C Pd50Pt50/C Pd25Pt75/C Pt/C

a Pd:Pt atomic ratio determined by EDX measurements.


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PGSTAT 30 (Eco Chemie) potentiostat driven by the GPES software. The working electrode was located inside a cylindrical holder, which had an inlet and an outlet that allowed the circulation of gases. The geometrical area exposed to the solution was 0.79 cm2. The counter electrode was a platinum wire, which was introduced in a compartment separated from the main solution by a glass frit. The reference electrode was a reversible hydrogen electrode, RHE (Gaskatel, GmbH) immersed in a glass tube connected with the main compartment of the cell by a LuggineHaber capillary. The electrolyte was 0.5 mol dm3 H2SO4 (Merck, Suprapur) aqueous solution deaerated by N2 bubbling for 20 min. Cyclic voltammograms were recorded under inert N2 atmosphere at 25.0  C and 20 mV s1 up to obtain reproducible voltammograms. CO voltammetric stripping experiments were performed at 25.0  C feeding the working electrode with a mixture of 0.1% CO in N2 at 0.250 cm3 min1 and atmospheric pressure for 50 min, while holding the electrode potential at 0.100 V vs. RHE. After adsorption and still holding the admission potential, CO was removed from the solution by N2 bubbling and the electrode gas feed was switched to N2 for 20 min. Then, two consecutive CO stripping voltammograms were recorded in the positive direction at 20 mV s1. Single cell experiments were performed placing a MEA in a commercial fuel cell hardware FCT 16SCH (Fuel Cell Technologies, Inc.), which was assembled using a uniform torque of 5 Nm. The MEA performance was evaluated by measuring the currentevoltage curves (potentiostatic polarization plots in steady-state conditions), using a home-made DMFC test station. Polarization curves were recorded after the MEA was activated following a procedure based on that reported in ref. [50]. Deionized water at 60  C was circulated for 12 h through the anodic and cathodic compartments of the single cell, each time that a fresh MEA was installed into the single cell hardware. Afterward, the cell temperature was set at 60  C. The anode feed was 2.0 mol dm3 aqueous solution of methanol at 1.5 mL min1 and zero backpressure, preheated at the cell temperature. The cathode feed was dry O2 (99.999%, Praxair) at 100 standard cm3 min1 and zero backpressure. Furthermore, the electrochemical characterization of the catalysts was performed in the MEA. In cyclic voltammetry measurements, the working electrode was the anode fed with humidied nitrogen at 50 standard cm3 min1, and the counter electrode and the reference electrode (DHE) was the cathode fed with humidied hydrogen at 50 standard cm3 min1 [51]. Cyclic voltammograms were recorded at a scan rate of 20 mV s1 and 60.0  C. CO stripping experiments were performed feeding the working electrode with a mixture of 0.1 vol. % CO in N2 at 250 standard cm3 min1 at atmospheric pressure for 50 min, while holding the electrode potential at 0.100 V vs. RHE. After adsorption and still holding the admission potential, the electrode gas feed was switched to N2 for 20 min at 250 standard cm3 min1. Then, two consecutive CO stripping voltammograms were recorded in the positive direction at 20 mV s1. The methanol oxidation activity was also measured in the MEA, feeding the working electrodes a with 2.0 mol dm3 aqueous methanol solution at 1.5 mL min1, and the reference/counter electrode with humidied hydrogen at 50 standard cm3 min1.


Results and discussion

3.1. Structural and electrochemical characterization of PdePt catalysts

Fig. 1 depicts the XRD diffractograms of the Pd/C, Pd75ePt25/C, Pd50ePt50/C, Pd25ePt75/C and Pt/C catalysts. Typical peaks characteristic of the face-centered cubic (FCC) lattice structure of Pd and Pt are also indicated in this gure. Although the atomic size of Pd and Pt is similar and their crystal structures are the same, explaining their similar diffraction peaks, the slight shift of the PdePt characteristic diffraction peaks toward lower 2q values when compared to those of Pd strongly indicates the incorporation of Pt and Pd atoms in the same lattice. Table 1 shows the lattice parameter of the PdePt catalysts as well as their mean crystallite sizes, determined as the mean values obtained for each reection (the overlap f (100) and (200) reections were deconvoluted with the help of the software). The values corresponding to Pd/C and Pt/C have been included for comparison. The lattice parameters of PdePt/C catalysts are higher than that for Pd/C, but lower than de value for Pt/C, which is indicative of alloy formation. Furthermore, the mean crystallite size of PdePt carbon supported catalysts increases with the Pd content. Both results are in agreement with those previously reported in the literature [29]. It is well known that the PtePd system shows complete solid solubility based on a FCC lattice. It has been recently demonstrated that this also applies to nanocrystalline materials and that Vegards rule applies [52]. A careful examination of the data presented in Table 1, including plotting the lattice parameter vs. at.% Pt, shows signicant deviations from Vegards rule, particularly for the 75 at.% Pt sample, which could be attributed to differences in crystallite size in the nanosize range, which is known to affect the lattice parameter. The electrochemical characterization of the catalysts studied in this work was performed by cyclic voltammetry at 25  C in 0.5 M H2SO4 to simulate the proton exchange membrane electrolyte in the MEA. Reliable results were obtained after activation of the working electrodes by means of cyclic scans between 0.050 and 0.750 V at 0.100 V s1 until a stationary prole was obtained. Fig. 2 presents the steady

Fig. 1 e X-ray diffractograms for Pd/C, PdePt/C and Pt/C catalysts (in parenthesis planes corresponding to characteristic diffraction signals of FCC Pd).

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cyclic voltammograms at 20 mV s1, when the technical electrodes were prepared with Pd/C, PdePt/C, and Pt/C. The cyclic voltammogram corresponding to the Pd/C catalyst, curve a in Fig. 2, is similar to those reported in the literature in acidic electrolyte for Pd dispersed on graphite [53] and for unsupported Pd nanoparticles [54]. The two peaks observed before 0.250 V correspond to adsorption/desorption of hydrogen [55]. When going toward more positive potentials, the oxide region appears between 0.700 and 0.800 V. The shape of the cyclic voltammogram of the Pt/C catalyst, curve e in Fig. 2, displays the typical features found for smooth polycrystalline platinum in liquid electrolyte [56], slightly modied because of the contribution of the carbon support and the ionomer present in the catalyst layer. It can be seen that the adsorption/desorption hydrogen peaks were slightly less well resolved than those observed on polycrystalline Pt. There is also some contribution of the carbon support, as suggested by the slight curvature in the double layer region. As in the case

of Pd/C catalyst, a dominant hydrous oxide peak was observed. Finally, for the PdePt/C catalysts, curves b, c and d in Fig. 2, the hydrogen desorption only appears as a broad peak in the positive scan, in good agreement with the literature [37]. The oxide formation and reduction takes place at about the same potentials as for the Pt/C catalyst (ca. 0.700e0.800 V). Furthermore, CO stripping voltammograms were registered to gain more understanding about the CO electrooxidation characteristics on the catalysts. Fig. 3 shows the corresponding stripping voltammograms on Pd/C, PdePt/C, and Pt/C. All stripping voltammograms show a main CO oxidation peak, which moves toward less positive potentials as Pd is replaced by Pt in the catalysts. This indicates the easier oxidation of adsorbed CO on Pt/C when compared to Pd/ C. It is worth to note that each PdePt/C catalyst only originates one CO oxidation peak, showing the synergistic effect of both metals, as previously pointed out by Papageorgopoulos et al. [37]. The intermediate position of these peaks between those corresponding to Pd/C and Pt/C suggests an electronic modication affecting the CO adsorption characteristics on PdePt when compared to pure Pd and Pt metals [57]. This suggestion is supported by the fact that in the cyclic voltammograms of Fig. 2, the oxide formation occurs at about the same potential when all the catalysts are compared. Therefore, an easier CO oxidation on PdePt catalyst owing to the formation of oxides at lower potentials than those observed for pure Pt can be discarded. In addition, a close inspection of the CO oxidation peak potentials of PdePt/C catalysts reveals that the electrochemical CO adsorption behavior depends clearly on their bulk composition. This is shown in Fig. 4, in which one can see a linear dependence between the CO oxidation peak and the Pd content. This observation suggests that the surface and bulk composition of PdePt supported catalysts changes in a similar way. A similar result was previously reported for unsupported PdePt nanoparticles in ref. [47]. Note in addition the different cathodic reduction peaks of the oxides formed at the end of the anodic scan. The cathodic peaks are shifted to more negative values and wider when the Pd content decreases. In particular, the cathodic currents for Pt/C in the potential region of 0.4e0.6 V in Fig. 3 are quite high but not very different from that shown in Fig. 2e. This can be

Fig. 2 e Cyclic voltammograms for electrodes catalyzed with (a) Pd/C, (b) Pd50ePt50/C (c) Pd75ePt25/C, (d) Pd25ePt75/C, and (e) and Pt/C in 0.5 mol dmL3 H2SO4. T [ 25.0 0.1  C. Scan rate of 20 mV sL1.

Fig. 3 e CO stripping cyclic voltammograms for Pd/C (B), Pd75ePt25/C (,), Pd50ePt50/C (>), Pd25ePt75/C (D), and Pt/C (3) catalysts in 0.5 mol dmL3 H2SO4. T [ 25.0 0.1  C. Scan rate of 20 mV sL1.


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Fig. 4 e CO oxidation peak potential values vs. Pd content in catalysts (experiments performed using aqueous H2SO4 as electrolyte).

due to the higher anodic limit in Fig. 3, which allows a greater production of Pt oxides.

3.2. Performance of Pd/C, PdePt/C and Pt/C catalyzed anodes in MEAs

To compare the electrochemical behavior of Pd/C, PdePt/C and Pt/C in three-electrode cell with that observed in real fuel cell operating conditions, we prepared MEAs containing these catalysts in their anodes and Pt/C in their cathodes. As the main object of this work is such a comparison, the metal loadings of the electrodes were lower than those usually used in DMFC, and therefore, not so high performances are expected. Fig. 5 shows the effect of the type of catalyst on CO electrooxidation in the MEAs. These experiments were performed at 60  C, because those given at room temperature have a limited validity regarding the catalyst behavior under practical conditions. It can be seen that CO stripping voltammograms follow the same trend observed in the three-electrode cell with liquid electrolyte

(see Fig. 3): the CO peak is shifted toward more negative potentials when decreasing the amount of Pd in the catalyst. In addition, a linear variation of the CO oxidation peak potential with the Pd content is also found, as illustrated in Fig. 6, in good agreement with the results obtained in the three-electrode cell (Fig. 4). So in spite of the different conditions, the results of both types of experiments are consistent. Fig. 7 shows the linear sweep voltammograms of the anodes made of PdePt/C and Pt/C in 2.0 mol dm3 methanol at 60  C. The plotted current densities are referred to the real surface area for each working electrode, which was measured by determining the CO stripping charge and assuming that 420 mC cm2 corresponds to a monolayer of adsorbed CO [46,58,59]. As can be seen, the general shape of the curve is similar for all PdePt/C catalysts. The current density slowly increases with the applied potential. The best activity toward methanol electrooxidation is shown by the electrode catalyzed with Pd25ePt75/C. At 0.600 V, potential which gives an acceptable cell voltage in a DMFC, the currents decrease following the order: Pd25ePt75/C > Pd50ePt50/C z Pt/ C > Pd75ePt25/C, i.e. there is a maximum value of the catalyst activity for Pd contents around 25 at.%. On the other hand, it is shown that the electrocatalytic activity of pure Pd for methanol oxidation in acidic media in the low anodic potential region, when compared to Pt, is insignicant (see Fig. 5), in agreement with previous results in the literature [60]. The increase of the catalytic activity when Pd is added to Pt and its decrease when the Pd content is further increased can be explained considering two different reaction mechanisms for methanol oxidation on Pt and PdePt, in which different adsorbed intermediates are involved, as previously suggested [29]. According to this hypothesis, Platinum nanoparticles become covered by intermediates produced from methanol dehydrogenation, such as (:COH)ads, which require three neighboring platinum sites to be adsorbed. Thus, the Pt surface becomes slowly covered with this poison, according to reaction (1) of the following sequence:

Pt CH3OH / Pte(COH)ads 3H 3e


Pte(COH)ads H2O / Pt CO2 3H 3e


Fig. 5 e In situ CO stripping cyclic voltammograms for Pd/C (B), Pd75ePt25/C (,), Pd50ePt50/C (>), Pd25ePt75/C (D) and Pt/C (3) catalysts, after the adsorption of CO at 0.100 V vs. RHE. Working electrodes fed with N2; reference/counter electrode fed with H2. Both gases humidied by bubbling through water at the cell temperature of 60 1  C. Only the positive scan at 20 mV sL1 is shown. MEA made of Naon NR212.

Fig. 6 e In situ CO oxidation peak potential values vs. Pd content in catalysts (experiments carried out using Naon NR212 proton exchange membrane as electrolyte).

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Fig. 7 e In situ j-E curves corresponding to the methanol electrooxidation on electrodes catalyzed with: Pd25ePt75/C (,), Pd50ePt50/C (>), Pd75ePt25/C (D), and Pt/C (B) at 60  C. Working electrodes fed with 2.0 mol dmL3 MeOH at 1.5 mL minL1. Reference/counter electrode fed with humidied H2 at the cell temperature. Scan rate of 1 mV sL1. MEA made of Naon NR212.

The adsorbed intermediate is removed in the further oxidation, reaction (2), which appears to be slow to explain the accumulation of the poisoning adsorbed species. Nevertheless, when adding Pd to form PdePt nanoparticles, the presence of palladium has a diluting effect and limits the presence of three adjacent Pt sites that are necessary for the adsorption of the poisoning species. In this case, the presence of only two neighboring platinum sites would be more common, the methanol adsorption on two Pt sites probably favoring the adsorption of (:CO)ads species, as indicated by reaction (3) of the following sequence:

To further remove the now different poisoning adsorbed species, reaction (4) should take place. If we assume that the rate of reaction (4) is higher than that of reaction (2), the poisoning effect of the (CO)ads adsorbed species should be smaller than that of (COH)ads ones. As this is the result of the Pd addition, the catalyst should have better electroactivity than pure Pt, as depicted in Fig. 7 for a Pd content of 25 at.%. However, when the Pd content increases, the amount of couples of neighboring Pt sites becomes smaller, with the concomitant decrease of the catalytic activity, and when it is too high, it further decreases due to the insignicant catalytic activity of pure Pd. Fig. 8 shows the voltage-current density, V-j, and the power density-current density, P-j, characteristics obtained in the single DMFC operating with a 2 mol dm3 aqueous methanol at 60  C and atmospheric pressure. The cathode was fed with pure O2 at atmospheric pressure, to maximize its activity and to minimize cathode effects on the relative activities of the cells. It is apparent that there are differences in performance for the different catalysts. In fact, the best performance was obtained when the anode was made of Pd25ePt75/C. Furthermore, the behavior of the catalysts in the single DMFC reects the results of anode polarization experiments found in MEAs. Therefore, the results obtained in single cell experiments are consistent with those published carried out in electrochemical cells. This could be tentatively extended to previous results in the literature obtained in three-electrode cells to predict a good approach when applied to real fuel cells [27e29].



Pt CH3OH / Pte(CO)ads 4H 4e


Pte(CO)ads H2O / Pt CO2 2H 2e


In this work we have reported a detailed characterization of the electrochemical behavior of PdePt/C catalysts toward methanol electrooxidation in technical electrodes. The results obtained in three-electrode cell with liquid electrolyte and in single cell with solid electrolyte (real fuel cell operating conditions) are consistent, showing that, between the specimens studied, the electrocatalytic oxidation of methanol is more effective in the case of the bimetallic system Pd25ePt75/ C. The electrochemical measurements in three-electrode cell using technical electrodes can then be applied as a simple tool for characterizing the activity of the electrocatalysts. The positive electrocatalytic effect of small amounts of Pd can be explained by a decrease in the poisoning rate of Pt by CO species resulting from the electronic effect of Pd on Pt.

The authors thank the Spanish Government MCINN and FEDER for nancial support (MAT2008-06631-C03-03/MAT).

Fig. 8 e V-j and P-j curves for liquid-DMFCs with Pd25ePt75/ C (,), Pd50ePt50/C (>), Pd75ePt25/C (D), and Pt/C (B) catalyzed anodes fed with 2.0 mol dmL3 MeOH at 1.5 mL minL1. Cathode: 0.2 mgPt cmL2 of Pt/Vulcan catalyst fed with dry O2 at 50 mL minL1. Cell temperature of 60  C.


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