Editing Benzotrithiophene-Based Covalent Organic Frameworks for Developing New Sonosensitizers
Chunyuan Hou,
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Nan Han,
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Bin Zhu
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et al.
ACS Applied Materials & Interfaces,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 2, 2025
Recent
insights
into
covalent
organic
frameworks
(COFs)
provide
an
opportunity
for
developing
new
sonosensitizers
with
the
advantages
of
both
small
molecules
and
inorganic
nanoagents.
Herein,
we
synthesize
two
benzotrithiophene-based
imine-linked
COFs
(BTT-DPh-COF
BTT-DPy-COF)
through
density-functional-theory-guided
structure
editing.
The
tailored
donor-acceptor
(D-A)
structures
optimize
band
position
endow
them
good
intrinsic
sonodynamic
activity,
which
can
efficiently
kill
cancer
cells,
showing
excellent
therapeutic
effect.
Particularly,
because
enhanced
D-A
effect
that
promotes
charge
separation
transfer
behavior,
BTT-DPy-COF
exhibits
superior
ultrasound-triggered
reactive
oxygen
species
(ROS)
generation
capability
than
BTT-DPh-COF.
Therefore,
these
studies
highlight
great
potential
elaborate
editing
configurations
as
suitable
candidates
advanced
sonosensitizers.
Language: Английский
Targeted Electron‐Hole Separation to Decoupled Redox‐Active Sites Over a PEA2PbBr4/CeO2 P‐N Heterojunction for Enhanced Photocatalytic Oxidation
Ying Chen,
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Sunzai Ke,
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Xuhui Yang
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et al.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 1, 2024
Abstract
Photocatalytic
selective
oxidation
of
C(sp
3
)─H
bonds
into
valuable
carbonyl
compounds
offers
a
promising
approach
to
advance
green
organic
synthesis
and
contribute
more
sustainable
chemical
industry.
However,
significant
challenges
remain
due
the
low
efficiency
photocatalysts,
primarily
caused
by
insufficient
charge
separation
limited
ability
intermixed
surface
redox‐active
sites
precisely
capture
photoinduced
carriers.
Here,
PEA
2
PbBr
4
/CeO
(PPB/CeO
)
p‐n
heterojunction
is
designed
fabricated.
Experimental
characterizations
theoretical
calculations
reveal
that
strong
internal
electric
field
(IEF)
formed
at
interface
within
heterojunction,
which
drives
targeted
accumulation
holes
on
PPB
electrons
CeO
.
Importantly,
displays
superior
oxygen
affinity
facilitating
O
reduction,
while
validates
stronger
adsorption
activation
capability
toluene
molecule
promoting
C─H
bond
dissociation.
In
this
context,
are
directionally
separated
transported
decoupled
reduction
in
PPB/CeO
,
thereby
significantly
accelerating
aerobic
bonds.
Toward
photocatalytic
model
substrate
toluene,
optimized
‐5%
composite
exhibits
conversion
rate
10
050
µmol
g
−1
h
nine
times
enhanced
comparison
with
blank
(1160
).
Language: Английский