The surface coverage of PEM fuel cell electrodes
F. Dundar
a,b,*
, A. Pilenga
b
, G. Tsotridis
b
a
Department of Mechanical Engineering, Meliksah University, 38280, Kayseri, Turkey
b
Institute for Energy and Transport, Joint Research Centre, European Commission, Postbus 2, 1755 ZG Petten,
The Netherlands
article info
Article history:
Received 4 June 2015
Received in revised form
8 September 2015
Accepted 22 October 2015
Available online 12 November 2015
Keywords:
Fuel cells
Carbon monoxide
Coverage
Desorption
Impurity
Bond strength
abstract
A quantitative study was conducted on Hydrogen (H
2
), water (H
2
O) and carbon monoxide
(CO) molecule concentration on a PteRu catalyst surface used for PEM fuel cells. Strongly
bonded hydrogen molecules which can withstand 100 ppm CO exposure at 50
C were
calculated as 54% of the total hydrogen bonds present on catalyst surface during pure H
2
purge. The very weakly bonded hydrogen molecules that could be removed with pure inert
gasses were not taken into account. Additionally, the water and hydrogen molecule con-
tent on the surface of the catalyst layer was compared and bonded hydrogen molecule
ratios of 33e63% were obtained for different temperatures (25
C, 50
C and 75
C) and
relative humidity values (Dew Point Temperatures of 25
C, 35
C and 45
C). Furthermore,
10 ppm CO exposure time at dry conditions was varied from 30 s to 1 h at 50
C. The
majority of the weakly adsorbed hydrogen molecules desorbed in the first 10 min with
300 sccm gas flow over PteRu catalyst layer. The desorption process stopped after 10 min.
The hydrogen molecules were bonded strong enough to stick to the surface under 10 ppm
CO exposure at 50
C. The bonded hydrogen molecule ratio of 66e67% was calculated for 10
e60 min of 10 ppm CO exposure.
Copyright © 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights
reserved.
Introduction
Polymer Electrolyte Membrane (PEM) fuel cells are promising
energy converters for the coming decade. The high energy
density and continuous power generation capability puts
them ahead of other energy deposition technologies as the
primary electricity supplier for portable and stationary appli-
cations. However, their positive features are yet to be devel-
oped to commercialize particularly for automotive industry.
High cost, infrastructure and durability problems are among
the severe barriers to overcome [1].
A huge improvement was accomplished during the last
decade on PEM fuel cells. The cost of a typical 80 kW auto-
motive PEM fuel cell system declined from 275 $/kW to 47 $/
kW within 10 years (2002e2012) [2]. This was accomplished by
intensive research efforts. Catalyst research is the highest
funded research category for fuel cells according to United
States (US) Department of Energy (DOE) [2] followed by sys-
tems and balance of plant, durability, analysis and testing,
mass transport, MEA integration, impurities and membrane
studies. The increasing interest on catalyst, durability and
impurity studies shows the importance of durability on cata-
lyst surfaces as a major cost item.
* Corresponding author. Department of Mechanical Engineering, Meliksah University, 38280, Kayseri, Turkey. Tel.: þ90 533 578 9251.
E-mail address: fdundar@meliksah.edu.tr (F. Dundar).
Available online at www.sciencedirect.com
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journal homepage: www.elsevier.com/locate/he
international journal of hydrogen energy 41 (2016) 497 e504
http://dx.doi.org/10.1016/j.ijhydene.2015.10.088
0360-3199/Copyright © 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.