AVS 62nd International Symposium & Exhibition | |
Plasma Science and Technology | Monday Sessions |
Session PS+EM-MoA |
Session: | Directed Self Assembly and Plasma Synthesis of Novel Materials |
Presenter: | Joffrey Baneton, ULB, Belgium |
Authors: | J. Baneton, ULB, Belgium D. Merche, ULB, Belgium M. Raes, VUB, Belgium V. Debaille, ULB, Belgium G. Caldarella, ULg, Belgium V. Stergiopoulos, ULg, Belgium H. Terryn, VUB, Belgium N. Job, ULg, Belgium F.A.B. Reniers, ULB, Belgium |
Correspondent: | Click to Email |
Catalytic layers are one of the most important components of proton exchange membrane fuel cells (PEMFC) because they directly influence the transport of matter and the reactivity of the electrodes [1]. In many cases, platinum associated with carbon black forms the most interesting material because of its very high catalytic activity [2]. Unfortunately, some limitations remain due to the cost of platinum and the difficulty to control the structure of the carbon support.
In this study, we propose a new promising technique using platinum (II) acetylacetonate [Pt(acac)2] powder mixed with porous carbon and nebulized in a RF atmospheric plasma torch directly on commercial gas diffusion layer (GDL). This fast and “one-pot” methodology leads to the formation of homogeneous and reproducible samples with a variable and controlled content of metallic platinum on the surface, as analyzed by X-ray Photoelectron Spectroscopy (XPS) and Scanning Electron Microscopy (SEM). The catalytic activity per mass unit can be studied by a combination of Inductively Coupled Plasma Mass Spectrometry (ICP-MS) and electrochemical measurements.
We demonstrate that the plasma treatment and mostly the reactive oxygen species play a critical role in the activation of the support surface and the binding of the platinum nanoparticles on it, reinforcing previous observations [3,4]. In the case of an argon-oxygen plasma pretreatment of the GDL, a significant increase of the platinum content on the surface can be observed.
The influence of different process parameters on the synthesis of the platinum nanoparticles was studied. We show that the carrier gas flow rate, the power injected in the discharge and the treatment time do not have a significant impact on the surface composition. On the other hand, some nebulizer parameters such as the number of pulses or the loading of Pt-C allow the tuning of the amount of Pt grafted on the surface without altering its metallic nature.
Finally, the influence of the type of carbon powder (e.g. CB, CX or CNTs) was investigated. It appears that it can modify the surface organization and consequently also the intrinsic characteristics of the material. It reveals that the distribution of platinum nanoparticles and the access to the catalytic sites can be optimized depending of the porosity and the active surface of the carbon support.
[1] Gasteiger et al. Handbook of Fuel Cells – Fundamentals, Technology and Applications. 2003, 3, 593
[2] Chatenet et al. New and Future Developments in Catalysis. 2013, 401-423
[3] Pireaux et al. Method for Depositing Nanoparticles on Substrates, 2002 (Patent)
[4] Claessens et al. Nanotechnology, 2010, 21, 38, 385603