Molecules,
Journal Year:
2024,
Volume and Issue:
29(10), P. 2217 - 2217
Published: May 9, 2024
A
series
of
MOF-derived
ZrO2-supported
Pd-Ni
bimetallic
catalysts
(PdNi/UiO-67-CTAB(n)-A500)
were
prepared
by
co-impregnation
and
pyrolysis
at
500
°C
under
air
atmosphere
using
UiO-67-CTAB(n)
(CTAB:
cetyltrimethylammonium
bromide;
n:
the
concentration
CTAB;
n
=
0,
3,
8,
13,
18)
as
a
sacrificial
template.
The
catalytic
activity
PdNi/UiO-66-CTAB(n)-A500
in
1,3-butadiene
hydrogenation
was
found
to
be
dependent
on
crystal
morphology
UiO-67
highest
observed
over
PdNi/UiO-67-CTAB(3)-A500
catalyst
which
synthesized
UiO-67-CTAB(3)
with
uniform
octahedral
template
for
selective
hydrogenation.
conversion
total
butene
selectivity
98.4%
44.8%
40
within
1
h
catalyst,
respectively.
can
regenerated
flowing
N2
200
°C.
Carbon
deposited
surface
main
reason
its
deactivation.
This
work
is
valuable
high-efficiency
catalyst’s
development
1,3-butadiene.
Materials,
Journal Year:
2025,
Volume and Issue:
18(10), P. 2251 - 2251
Published: May 13, 2025
Developing
efficient
and
durable
non-precious
metal
catalysts
for
oxygen
electrocatalysis
in
fuel
cells
zinc–air
batteries
remains
an
urgent
issue
to
be
addressed.
Herein,
a
bimetallic
CoCe-NC
catalyst
is
synthesized
through
pyrolysis
of
Co/Ce
co-doped
metal–organic
frameworks
(MOFs),
retaining
the
inherently
high
surface
area
MOFs
maximize
exposure
Co-N
Ce-N
active
sites.
The
electronic
interaction
between
Co
Ce
atoms
effectively
modulates
adsorption/desorption
behavior
oxygen-containing
intermediates,
thereby
enhancing
intrinsic
catalytic
activity.
In
alkaline
media,
exhibits
E1/2
=
0.854
V
electrocatalytic
capability
comparable
commercial
Pt/C,
along
with
superior
methanol
resistance
durability.
Notably,
demonstrates
overpotential
84
mV
lower
than
Pt/C
at
300
mA
cm−2
GDE
half-cell.
When
employed
as
cathode
batteries,
it
open-circuit
voltage
1.47
V,
peak
power
density
202
mW
cm−2,
exceptional
cycling
Molecules,
Journal Year:
2024,
Volume and Issue:
29(10), P. 2217 - 2217
Published: May 9, 2024
A
series
of
MOF-derived
ZrO2-supported
Pd-Ni
bimetallic
catalysts
(PdNi/UiO-67-CTAB(n)-A500)
were
prepared
by
co-impregnation
and
pyrolysis
at
500
°C
under
air
atmosphere
using
UiO-67-CTAB(n)
(CTAB:
cetyltrimethylammonium
bromide;
n:
the
concentration
CTAB;
n
=
0,
3,
8,
13,
18)
as
a
sacrificial
template.
The
catalytic
activity
PdNi/UiO-66-CTAB(n)-A500
in
1,3-butadiene
hydrogenation
was
found
to
be
dependent
on
crystal
morphology
UiO-67
highest
observed
over
PdNi/UiO-67-CTAB(3)-A500
catalyst
which
synthesized
UiO-67-CTAB(3)
with
uniform
octahedral
template
for
selective
hydrogenation.
conversion
total
butene
selectivity
98.4%
44.8%
40
within
1
h
catalyst,
respectively.
can
regenerated
flowing
N2
200
°C.
Carbon
deposited
surface
main
reason
its
deactivation.
This
work
is
valuable
high-efficiency
catalyst’s
development
1,3-butadiene.