Platinum-modified
first-row transition-metal catalyst (M = Ni,
Co, and Cu) nanoparticles on a carbon black Vulcan XC-72R (CBV) support
were synthesized using rotating disk slurry electrodeposition (RoDSE)
followed by spontaneous galvanic displacement (SGD) reactions. These
RoDSE–SGD catalysts were evaluated for the oxygen reduction
reaction (ORR) in 0.1 M KOH using rotating disk electrode techniques.
The Ni and Co RoDSEs were done by using an electrochemical applied
potential of −0.75 V versus the RHE and for Cu, −0.80
V versus the RHE using a CBV slurry solution containing 0.1 M KClO4. These metal nanoparticles on CBV (M/CBV) catalysts were
modified with a Pt precursor via a spontaneous galvanic displacement
(SGD) reaction, producing a Pt-M/CBV material to catalyze the ORR
in an alkaline medium. High-resolution scanning transmission electron
microscopy (HR-STEM) analysis indicates that the PtM/CBV samples include
M clusters and Pt single atoms. The ORR characterization measurements
were done under a controlled temperature (25.0 °C) and with a
mass loading of 100 μg/cm2 on a glassy carbon (GC)
rotating disk electrode at 1600 rpm. The PtCo/CBV showed the highest
ORR mass activity of 0.741 A/mgPt at 0.90 V versus the
reversible hydrogen electrode (RHE) compared with commercial Pt/CBV.
The M/CBV RoDSE catalysts were also tested for the oxygen evolution
reaction (OER), and Ni/CBV provided the lowest overpotential of 450
mV at 10 mA/cm2
disk in 0.1 M KOH.
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