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Synthesis and characterization of Pt-Co/carbon xerogel electrocatalysts for Proton Exchange Membrane Fuel Cells (PEMFC)

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Synthesis and characterization of Pt-Co/carbon xerogel electrocatalysts for Proton Exchange

Membrane Fuel Cells (PEMFC)

A. Zubiaur,a* T. Asset,a,b,c P.-Y. Olu,a,b,c L. Dubau,b,c F. Maillard b,c and N. Job a

a Laboratory of Chemical Engineering – Nanomaterials, Catalysis, Electrochemistry, University of Liège, B6a, 4000 Liège,

Belgium

b CNRS, LEPMI, F-38000 Grenoble, France c Univ. Grenoble Alpes, LEPMI, F-38000 Grenoble, France

* Corresponding author email address: A.Zubiaur@ulg.ac.be

Proton exchange membrane fuel cell (PEMFC) catalysts are generally made of carbon black (CB)-supported platinum-based nanoparticles. However, the properties of CBs, as described by Rodríguez-Reinoso [1], are not optimal for electrocatalysis. A possible solution to the drawbacks of CBs is the use of synthetic nanostructured materials with a controllable and reproducible texture and with a pure, known and constant chemical composition; carbon xerogels (CX) exhibit such properties [2].

Recently, various highly dispersed CX-supported Pt nanoparticles catalysts (Pt/CX) have been synthesized via several methods, such as the strong electrostatic adsorption (SEA) [3] or the charge-enhanced dry impregnation (CEDI) [4].

However, the decrease of the Pt mass contained in the PEMFC electrodes, in particular at the cathode where the oxygen reduction reaction (ORR) is processed, remains a major challenge. Improving the ORR mass activity is currently best achieved by alloying Pt with 3d-transition metal atoms such as cobalt (Co). These alloys perform better than the ORR because the substitution of some Pt atoms by 3d-metal atoms with smaller radius leads to a modified Pt electronic structure [5]. Several pathways are currently being studied to synthesize Pt-Co alloy particles/CX, Co-Pt core-shell particles/CX and Pt-Co hollow particles/CX (Fig. 1) in our groups. The first results indicate that the specific and mass activity of the bimetallic hollow particles dispersed on CX is 2 to 5-fold higher than that of pure Pt/CB.

Figure 1: a) TEM micrograph of Pt-Co hollow particles/CX, and b) EDX line-scan of a single Pt–Co hollow particle, the profiles show Pt (red profile) and Co (green profile) over the entire particle. The obtained image corresponds to the

projection of a hollow shell as indicated by the lack of signal in the centre of the particle.

References

[1] F. Rodríguez-Reinoso, Carbon as a catalyst support in Porosity in carbons, J.W. Patrick, Ed.(Wiley, UK, 1995), p. 253 [2] N. Job, A. Théry, R. Pirard, et al., Carbon, 2005, 43, 2481-2494

[3] A. Zubiaur, M. Chatenet, F. Maillard, et al., Fuel cells, 2014, 14, 343-349

[4] C. Cao, G. Yang, L. Dubau, et al., Applied Catalysis B : Environmental, 2014, 150-151, 101-106

[5] J. R. Kitchin, J. K. Nørskov, M. A. Barteau, et al., Journal of Chemical Physics, 2004, Vol. 120, No. 21, 10240-10246

Electrolysis & Fuel Cell Discussions

Challenges towards zero platinum for oxygen

13-16 September 2015, La Grande Motte, France

Figure

Figure 1: a) TEM micrograph of Pt-Co hollow particles/CX, and b) EDX line-scan of a single Pt–Co hollow particle, the profiles show Pt (red profile) and Co (green profile) over the entire particle

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