Ionic
liquids (ILs) modification, following the concept of “solid
catalyst with ionic liquid layer (SCILL)”, has been demonstrated
to be an effective approach to improving both activity and stability
of Pt-based catalysts for the oxygen reduction reaction. In this work,
the SCILL concept has been applied to a trimetallic PtNiMo/C system,
which has been documented recently to be significantly advantageous
over the benchmark PtNi-based catalysts for oxygen reduction. To achieve
this, two hydrophobic ILs ([BMIM][NTF2] and [MTBD][BETI]) were used
to modify PtNiMo/C with four IL-loading amounts between 7 and 38 wt
%. We found that the Pt mass activity (@0.9 V) could be improved by
up to 50% with [BMIM][NTF2] and even 70% when [MTBD][BETI] is used.
Exceeding a specific IL loading amount, however, leads to a mass transport
related activity drop. Moreover, it is also disclosed that both ILs
can effectively suppress the formation of nonreactive oxygenated species,
while at the same time imposing little effect on the electrochemical
active surface area. For a deeper understanding of the degradation
mechanism of pristine and IL modified PtNiMo/C, we applied identical
location transmission electron microscopy and in situ scanning flow cell coupled to inductively coupled plasma mass spectrometry
techniques. It is disclosed that the presence of ILs has selectively
accelerated the dissolution of Mo and eventually results in a more
severe degradation of PtNiMo/C. This shows that future research needs
to identify ILs that prevent the Mo dissolution to leverage the potential
of the IL modification of PtNiMo catalysts.