BI-NANO PT/HYDRO CNF

“New Bi-Functional Catalyst and Meso-porous Layer for PEM Fuel Cells: Low Loading of Pt Nanoparticles on One Side of a Hydrophobic CNF Layer”

 Coordinatore THE UNIVERSITY OF BIRMINGHAM 

 Organization address address: Edgbaston
city: BIRMINGHAM
postcode: B15 2TT

contact info
Titolo: Ms.
Nome: May
Cognome: Chung
Email: send email
Telefono: 441214000000
Fax: 441214000000

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 200˙371 €
 EC contributo 200˙371 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2011-IEF
 Funding Scheme MC-IEF
 Anno di inizio 0
 Periodo (anno-mese-giorno) 0000-00-00   -   0000-00-00

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    THE UNIVERSITY OF BIRMINGHAM

 Organization address address: Edgbaston
city: BIRMINGHAM
postcode: B15 2TT

contact info
Titolo: Ms.
Nome: May
Cognome: Chung
Email: send email
Telefono: 441214000000
Fax: 441214000000

UK (BIRMINGHAM) coordinator 200˙371.80

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

first    vulcan    membrane    commercial    hydrophobicity    xc    particles    electrode    cell    certain    performance    proton    cnf    cathode    orr    carbon    stability    fuel    layer    pt   

 Obiettivo del progetto (Objective)

'Proton exchange membrane fuel cells (PEMFCs) in combination with hydrogen are considered one of the best candidates to help to mitigate the climate change. However, there are still some challenges to release this technology to the market. One of the main costly issues for its commercialization is the amount of the platinum (Pt) that is used as catalyst, especially in the cathode where the oxygen reduction reaction (ORR) takes place. Even though progress has been made during the past years decreasing the Pt loading, the utilization and stability of Pt must be increased to meet the application demands by changing the current commercial carbon support (mainly Vulcan XC-72). Here it is proposed the use of a hydrophobic carbon nanofiber (CNF) layer as Pt support that combine high stability to oxidation, high specific surface area without micropores and large pore volume.

The first part of the project consists of the growth of a CNF layer, which is directly grown on one side of a carbon paper substrate. The first objective of the project is the direct deposition of Pt nanoparticles on only one side of the CNF layer while avoiding a deep penetration of the Pt particles and maintaining certain hydrophobicity. The external location of the Pt particles, close to the central membrane, is crucial for a high fuel cell performance. On the other hand, certain hydrophobicity is needed to improve the evacuation of water formed in the cathode eliminating, or at least reducing, the use of PTFE. The second objective is the study of the influence of the addition of proton conductive polymers in the electrocatalytic ORR of the electrode. Finally, the last objective is the fuel cell electrochemical characterization of the electrodes by preparing membrane electrode assemblies (MEAs) by using commercial and/or in-house prepared anodes and membranes, so that the fuel cell performance can be measured and compared with a commercial MEA based on Pt/Vulcan XC-72.'

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