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Covalently, Non-Covalently and Non Functionalized Networked Graphitic Structures as robust catalyst support in PEM electrodes (abstract)

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Covalently, Non-Covalently and Non Functionalized Networked Graphitic Structures as robust catalyst

support in PEM electrodes

Emanuela Negro, Marnix de Vries, Roman Latsuzbaia, Ger Koper

Advanced Soft Matter, Faculty of Applied Science, TU Delft

Julianalaan 136, 2628BL, Delft (NL)

Networked Carbon Graphitic structures, here called Carbon Nano Networks (CNNs), result a robust catalyst support in PEM fuel cells electrodes. This special class of nanostructures, Figure 1, is synthetized by Chemical Vapor Deposition of ethylene on various metallic catalyst nanoparticles, e.g Ni, Pt, Co [1]. The networked carbon structure is obtained from the graphitization of the large amount of ligand stabilizing nanoparticles, that can be produced at exceptionally high yield [2,3]. CNNs show remarkably high thermal stability, thermal and electric conductivity and mechanical strength.

Platinum nanoparticles are attached to covalently, non covalently and non functionalized CNNs [4,5]. The obtained catalyst activity and electrochemically active surface area (ECSA) are tested by rotating disk electrode. ECSA decrease is tested by accelerated durability tests, cycling the potential between 0.6 and 1.2 V vs RHE. Oxidation resistance is tested by termogravimetric analysis.

Pt/CNNs result more active and more durable than commercial catalyst, Figure 2. CNNs have higher oxidation resistance than other carbon supports, resulting in catalyst higher durability under fuel cell operating conditions. Additionally, a networked structure allow for an even electrical conductivity thus reducing potential gradients in the electrode responsible of Ostwald ripening. Platinum deposited over non-covalently functionalized CNNs result the most durable catalyst, due to the even distribution of monodisperse nanoparticles, efficiently bound to the graphitic surface via π-π interaction with pyrene carboxylic acid , Figure 3.

The relatively low cost of the synthesis procedure and their good performance make CNNs a potential substitute of actual catalyst support for Fuel Cell applications.

REFERENCES

1. Kowlgi, K., et al., Controlling the Structure and Degree of Branching of Graphitic Nanorod Networks. Carbon, 2012. Submitted.

2. Kowlgi, K., et al., Uniform metal nanoparticles produced at high yield in dense microemulsions. Journal of Colloid and Interface Science, 2012. 372(1): p. 16-23.

3. Negro, E; Latsuzbaia, R; Koper, G; High Yield wet synthesis of Ultrafine Nanoparticles: Kinetics and Control. 2012. In Preparation. 4. Oh, H.-S.; Kim, H., Efficient Synthesis of Pt

Nanoparticles Supported on Hydrophobic Graphitized Carbon Nanofibers for Electrocatalysts Using Noncovalent

Functionalization. Advanced Functional Materials, 2011. 21(20): p. 3954-3960.

5. He, D.; Mu, S.; and Pan, M. , Perfluorosulfonic acid-functionalized Pt/carbon nanotube catalysts with enhanced stability and performance for use in proton exchange membrane fuel cells. Carbon, 2011. 49(1): p. 82-88.

Figure 1 SEM image of Carbon-Nano-Networks

Figure 2 Accelerated durability tests

Figure 3 Platinum nanoparticles over non-covalently functyionalized CNNs

--- 200 nm

--- 100 nm

Abstract #1610, 224th ECS Meeting, © 2013 The Electrochemical Society

ecsdl.org/site/terms_use address. Redistribution subject to ECS license or copyright; see

131.180.131.94 Downloaded on 2013-10-28 to IP

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