posted on 2020-07-16, 16:37authored byMichael
J. Dzara, Kateryna Artyushkova, Moulay Tahar Sougrati, Chilan Ngo, Margaret A. Fitzgerald, Alexey Serov, Barr Zulevi, Plamen Atanassov, Frédéric Jaouen, Svitlana Pylypenko
Electrocatalysts
for the oxygen reduction reaction within polymer
electrolyte membrane fuel cells based on iron, nitrogen, and carbon
elements (Fe–N–C) have received significant research
attention as they offer an inexpensive alternative to catalysts based
on platinum-group metals. Although both the performance and the fundamental
understanding of Fe–N–C catalysts have improved over
the past decade, there remains a need to differentiate the relative
activity of different active sites. Toward this goal, our study is
focused on characterizing the interactions between O2 and
a set of five structurally different Fe–N–C materials.
Detailed characterization of the Fe speciation was performed with 57Fe Mössbauer spectroscopy and soft X-ray absorption
spectroscopy of the Fe L3,2-edge, whereas nitrogen chemical
states were investigated with X-ray photoelectron spectroscopy (XPS).
In addition to initial sXAS and XPS measurements performed in ultra-high
vacuum (UHV), measurements were also performed (at the identical location)
in an atmosphere of 100 mTorr of O2 at 80 °C (O2-rich). XPS and sXAS results reveal the presence of several
types of FeNxCy adsorption sites. FeNxCy sites that are proposed as the most active ones
do not show significant change (based on the techniques used in this
study) when their environment is changed from UHV to O2-rich. Correlation with Mössbauer and sXAS results suggests
that this is most likely due to the persistence of strongly adsorbed
O2 molecules from their previous exposure to air. However,
other species do show spectroscopic changes from UHV conditions to
O2-rich. This implies that these sites have a weaker interaction
with O2 that results in their desorption in vacuum conditions
and re-adsorption when exposed to the O2-rich environment.
The nature of these weakly and strongly O2-adsorbing FeNxCy sites is discussed
in the context of different synthetic and processing parameters employed
to fabricate each of these five Fe–N–C materials.