A Precise Preparation Strategy for 2D Nanoporous Thulium-Organic Framework: High Catalytic Performance in CO2-Epoxide Cycloaddition and Knoevenagel Condensation
Inorganic Chemistry,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 22, 2025
Efficient
conversion
of
carbon
dioxide
(CO2)
into
high-value
chemicals
is
viewed
as
one
the
most
promising
approaches
for
solving
problem
an
energy
shortage
and
serious
environment
pollution.
However,
design
synthesis
confined
multifunctional
catalysts
with
in
situ
engineered
task-specific
sites
nanoporous
environments
remain
a
complex
challenging
task
due
to
lack
in-depth
understanding
their
structure
reaction
mechanism.
Herein,
we
report
highly
robust
2D
framework
{[Tm(HFPDC)(DMF)2]·DMF·H2O}n
(NUC-120)
(H4FPDC
=
4,4′-(4-(4-fluorophenyl)pyridine-2,6-diyl)diisophthalic
acid).
The
thermally
activated
host
[Tm(HFPDC)]n
(NUC-120a)
has
following
two
merits:
(i)
structure,
(ii)
massive
quantity
functional
sites.
Moreover,
NUC-120
NUC-120a
display
high
thermal
chemical
stability,
which
have
been
proved
by
TGA
soaking
experiments
acid–base
water
organic
solvents.
Catalytic
that
NUC-120a,
presence
n-Bu4NBr
cocatalyst
could
efficiently
catalyze
coupling
CO2
epoxides
under
comparatively
mild
conditions.
Furthermore,
also
displays
catalytic
performance
Knoevenagel
condensation
reactions
aldehydes
malononitrile,
should
be
because
coexisting
Lewis
acidic
basic
can
separately
activate
aldehyde
malononitrile
molecules.
Thereby,
this
work
further
provides
insight
desired
materials
generated
using
existing
suitable
secondary
building
units
(SBUs)
meticulously
regulating
growth
environments.
Язык: Английский
Directionally induced hydrogen bonding interactions of heteroatom-incorporated amine adsorbents for promoting steady CO2 capture
Journal of Materials Chemistry A,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 1, 2025
Novel
strategy
to
improve
cyclic
stabilities
of
solid
amine
adsorbents
utilizes
the
directional
induction
hydrogen
bonds
via
heteroatom
incorporation.
Язык: Английский
Electrocatalytic CO2 Reduction toward C2 Products on a Bimetallic CuZn-DAT Catalyst: Enhancement Mechanism of Zn and DAT on Ethanol Formation
Energy & Fuels,
Год журнала:
2025,
Номер
unknown
Опубликована: Май 8, 2025
Язык: Английский
Advances in CO2 Capture and Separation Materials: Emerging Trends, Challenges, and Prospects for Sustainable Applications
Carbon Capture Science & Technology,
Год журнала:
2025,
Номер
unknown, С. 100441 - 100441
Опубликована: Май 1, 2025
Язык: Английский
Synthesis of cyclic carbonates by addition of CO2 to epoxides at atmospheric pressure
Journal of CO2 Utilization,
Год журнала:
2025,
Номер
97, С. 103120 - 103120
Опубликована: Май 20, 2025
Язык: Английский
Oxygen Defect Engineering Boosts Photocatalytic CO2 Cycloaddition Reaction With a Solar-to-Chemical Conversion Efficiency of 0.6%
ACS Applied Materials & Interfaces,
Год журнала:
2025,
Номер
unknown
Опубликована: Май 29, 2025
Solar-driven
conversion
of
CO2
into
high-value
cyclic
carbonates
is
considered
an
ideal
carbon
emission
reduction
strategy
but
synchronously
faces
the
challenges
a
low
reaction
rate
and
unclear
catalytic
mechanism.
Herein,
oxygen
vacancy-rich
Bi4NbO8Cl
(BNOC-OVs)
are
fabricated
as
cycloaddition
photocatalysts
via
facile
calcination
in
CO
atmosphere.
The
introduction
OVs
creates
high
density
lattice
disorder
defects,
which
offers
abundant
Lewis
acidic-basic
active
sites
to
efficiently
drive
reaction.
Crucially,
both
experimental
data
functional
theory
(DFT)
computations
demonstrate
that
enhance
adsorption
energies
substrate
molecules
reduce
barriers
regulating
surface
properties
electronic
structure.
As
result,
BNOC-OVs2
exhibits
outstanding
photocatalytic
performance
for
1,2-epoxybutane,
with
1,2-butylene
carbonate
formation
9224.5
μmol·g-1·h-1,
much
superior
other
bismuth-based
state-of-the-art
catalyst
system
same
substrates.
For
first
time,
solar
chemical
(STC)
efficiency
determined,
up
0.6%.
This
study
innovative
pathway
toward
fabricating
high-performance
by
modulating
engineering
creative
insight
mechanism
reactions.
Язык: Английский