Inorganic Chemistry,
Год журнала:
2024,
Номер
63(17), С. 7571 - 7588
Опубликована: Апрель 18, 2024
Recently,
global-scale
efforts
have
been
conducted
for
the
electroreduction
of
CO2
as
a
potentially
beneficial
pathway
conversion
greenhouse
gases
to
useful
chemicals
and
renewable
fuels.
This
study
focuses
on
development
selective
sustainable
electrocatalysts
reduction
aqueous
CO.
A
RuIIcomplex
[Ru(tptz)(ACN)Cl2]
(RCMP)
(tptz
=
2,4,6-tris(2-pyridyl)-1,3,5-triazine,
ACN
acetonitrile)
was
prepared
molecular
electrocatalyst
reaction
in
an
solution.
Density
functional
theory-calculated
frontier
orbitals
suggested
that
tptz
ligand
plays
key
role
dictating
electrocatalytic
reactions.
The
RCMP
grafted
onto
graphene
oxide
(GO)
surface
both
noncovalently
(GO/RCMP)
covalently
(GO-RCMP).
field
emission
scanning
electron
microscopy
elemental
distribution
analyses
revealed
homogeneous
complex
GO
sheet.
photoluminescence
spectra
confirmed
accelerated
charge-transfer
nanohybrids.
Compared
bare
complex,
GO-RCMP
GO/RCMP
nanohybrids
showed
enhanced
activity,
achieving
>95%
90%
Faradaic
efficiencies
CO
production
at
more
positive
onset
potentials,
respectively.
nanohybrid
demonstrated
outstanding
activity
with
current
∼84
μA.
offers
perspective
outer-
inner-sphere
electron-transfer
mechanisms
electrochemical
energy
systems.
Inorganic Chemistry,
Год журнала:
2024,
Номер
unknown
Опубликована: Дек. 17, 2024
Developing
a
multi-site
Pd-based
electrocatalyst
for
CO2-to-C1
conversion
with
high
performance
and
selectivity
in
the
hydrogenation
pathway
CO2
electroreduction
reaction
is
both
desirable
challenging.
Here,
we
develop
triple-site
metallene
(Pd82Bi11In7),
which
can
achieve
an
unprecedented
Faraday
efficiency
of
72.6
±
1%
methanol
production.
X-ray
photoelectron
spectroscopy
analysis
indicates
that
some
electrons
transfer
from
In
Bi
to
Pd
inside
Pd82Bi11In7,
forming
local
electron-rich
Pd-site,
primary
electron-deficient
center
In-site,
secondary
Bi-site.
Meanwhile,
Pd82Bi11In7
has
stronger
adsorption
*COOH
*CO,
avoids
generation
formic
acid
CO.
Moreover,
reduces
potential
determining
step
energy
barrier
controls
path
direct
The
synergistic
effect
triple-sites
enables
efficient
methanol.
Inorganic Chemistry Frontiers,
Год журнала:
2024,
Номер
11(15), С. 4770 - 4779
Опубликована: Янв. 1, 2024
In
situ
Raman
spectroscopy
reveals
that
Mg
and
B
synergistically
stabilize
Cu
+
across
a
wide
potential
range
on
Cu-based
catalyst,
facilitating
the
conversion
of
CO
2
to
C
2+
products.
ACS Materials Letters,
Год журнала:
2024,
Номер
6(11), С. 5112 - 5119
Опубликована: Окт. 16, 2024
Two-dimensional
metal–organic
frameworks
(2D
MOF)
have
attracted
great
attention
in
the
electrocatalytic
reduction
of
CO2
owing
to
their
well-defined
structure
and
high
surface
area.
Nevertheless,
how
combine
accessible
metal
active
sites
with
electron
transfer
still
poses
challenges
structural
assembly.
Herein,
two-dimensional
AgCe-MOFs
intralayer
π–π
stacking
interactions
were
assembled
by
linking
one-dimensional
Ce–O
chains
Ag(I).
Its
nanosheet
can
be
facilely
prepared
via
self-exfoliation
upon
loss
uncoordinated
interlayer
acetonitrile.
The
2D
AgCe-MOF
nanosheets'
merits
more
exposed
efficient
channels
displayed
outstanding
electrochemical
performance
99.5%
selectivity
CO.
establishment
electrical
transport
exposure
catalytic
a
framework
through
designed
supramolecular
is
expected
potential
strategy
for
construction
electrocatalysts.
Inorganic Chemistry Frontiers,
Год журнала:
2023,
Номер
10(24), С. 7146 - 7154
Опубликована: Янв. 1, 2023
We
demonstrate
an
environment-friendly
universal
methodology
to
control
MOF
crystal
dimensions
from
nanometres
micrometres
only
by
introducing
oil-in-water
microemulsion.
Inorganic Chemistry,
Год журнала:
2024,
Номер
63(17), С. 7571 - 7588
Опубликована: Апрель 18, 2024
Recently,
global-scale
efforts
have
been
conducted
for
the
electroreduction
of
CO2
as
a
potentially
beneficial
pathway
conversion
greenhouse
gases
to
useful
chemicals
and
renewable
fuels.
This
study
focuses
on
development
selective
sustainable
electrocatalysts
reduction
aqueous
CO.
A
RuIIcomplex
[Ru(tptz)(ACN)Cl2]
(RCMP)
(tptz
=
2,4,6-tris(2-pyridyl)-1,3,5-triazine,
ACN
acetonitrile)
was
prepared
molecular
electrocatalyst
reaction
in
an
solution.
Density
functional
theory-calculated
frontier
orbitals
suggested
that
tptz
ligand
plays
key
role
dictating
electrocatalytic
reactions.
The
RCMP
grafted
onto
graphene
oxide
(GO)
surface
both
noncovalently
(GO/RCMP)
covalently
(GO-RCMP).
field
emission
scanning
electron
microscopy
elemental
distribution
analyses
revealed
homogeneous
complex
GO
sheet.
photoluminescence
spectra
confirmed
accelerated
charge-transfer
nanohybrids.
Compared
bare
complex,
GO-RCMP
GO/RCMP
nanohybrids
showed
enhanced
activity,
achieving
>95%
90%
Faradaic
efficiencies
CO
production
at
more
positive
onset
potentials,
respectively.
nanohybrid
demonstrated
outstanding
activity
with
current
∼84
μA.
offers
perspective
outer-
inner-sphere
electron-transfer
mechanisms
electrochemical
energy
systems.