Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
34(24)
Published: Feb. 19, 2024
Abstract
Photosynthesis
of
hydrogen
peroxide
(H
2
O
)
is
regarded
as
an
economically
efficient
and
environmentally
friendly
synthesis
method.
However,
the
scalability
photocatalytic
H
production
(PHP)
hindered
by
sluggish
reaction
kinetics
rapid
recombination
photogenerated
charge
carriers.
In
this
study,
organic
amine‐constrained
ions
intercalated
carbon
nitride/CdSe‐diethylenetriamine
(K
+
/I
−
‐CN/CdSe‐D)
S‐scheme
heterojunction
synthesized
using
organic–inorganic
hybrid
approach
employed
for
PHP
first
time.
The
optimization
interface
I
K
contributed
to
enhanced
light
absorption
capabilities
reduced
interlayer
transfer
distance.
Concurrently,
synergy
C─Se
bonds
at
effectively
modulated
electron
pathways.
coordination
environment
mechanism
are
thoroughly
investigated
extended
X‐ray
fine
structure
in
situ
irradiated
photoelectron
spectroscopy.
rate
40%K
‐CN/CdSe‐D
reached
2240.23
µmol
h
−1
g
pure
water.
This
study
highlights
significance
dual
tuning
chemical
ionic
intercalation
effective
strategy
enhancing
,
paving
way
further
advancements
technology.
Nature Communications,
Journal Year:
2023,
Volume and Issue:
14(1)
Published: Nov. 6, 2023
Photocatalytic
two-electron
oxygen
reduction
to
produce
high-value
hydrogen
peroxide
(H2O2)
is
gaining
popularity
as
a
promising
avenue
of
research.
However,
structural
evolution
mechanisms
catalytically
active
sites
in
the
entire
photosynthetic
H2O2
system
remains
unclear
and
seriously
hinders
development
highly-active
stable
photocatalysts.
Herein,
we
report
high-loading
Ni
single-atom
photocatalyst
for
efficient
synthesis
pure
water,
achieving
an
apparent
quantum
yield
10.9%
at
420
nm
solar-to-chemical
conversion
efficiency
0.82%.
Importantly,
using
situ
synchrotron
X-ray
absorption
spectroscopy
Raman
directly
observe
that
initial
Ni-N3
dynamically
transform
into
high-valent
O1-Ni-N2
after
O2
adsorption
further
evolve
form
key
*OOH
intermediate
before
finally
forming
HOO-Ni-N2.
Theoretical
calculations
experiments
reveal
structure
reduces
formation
energy
barrier
suppresses
O=O
bond
dissociation,
leading
improved
production
activity
selectivity.
Journal of the American Chemical Society,
Journal Year:
2023,
Volume and Issue:
145(5), P. 2975 - 2984
Published: Jan. 25, 2023
Multicomponent
reactions
(MCRs)
can
be
used
to
introduce
different
functionalities
into
highly
stable
covalent
organic
frameworks
(COFs).
In
this
work,
the
irreversible
three-component
Doebner
reaction
is
utilized
synthesize
four
chemically
quinoline-4-carboxylic
acid
DMCR-COFs
(DMCR-1-3
and
DMCR-1NH)
equipped
with
an
acid-base
bifunctionality.
These
show
superior
photocatalytic
H2O2
evolution
(one
of
most
important
industrial
oxidants)
compared
imine
COF
analogue
(Imine-1).
This
achieved
sacrificial
oxidants
but
also
in
pure
water
under
oxygen
or
air
atmosphere.
Furthermore,
high
photostability,
durability,
recyclability.
MCR-COFs
thus
provide
a
viable
materials'
platform
for
solar
chemical
energy
conversion.
Angewandte Chemie International Edition,
Journal Year:
2023,
Volume and Issue:
62(26)
Published: April 25, 2023
Abstract
Photocatalytic
oxygen
reduction
reaction
(ORR)
offers
a
promising
hydrogen
peroxide
(H
2
O
)
synthetic
strategy,
especially
the
one‐step
two‐electron
(2e
−
ORR
route
holds
great
potential
in
achieving
highly
efficient
and
selectivity.
However,
2e
is
rarely
harvested
underlying
mechanism
for
regulating
pathways
remains
greatly
obscure.
Here,
by
loading
sulfone
units
into
covalent
organic
frameworks
(FS‐COFs),
we
present
an
photocatalyst
H
generation
via
from
pure
water
air.
Under
visible
light
irradiation,
FS‐COFs
exert
superb
yield
of
3904.2
μmol
h
−1
g
,
outperforming
most
reported
metal‐free
catalysts
under
similar
conditions.
Experimental
theoretical
investigation
reveals
that
accelerate
separation
photoinduced
electron‐hole
(e
‐h
+
pairs,
enhance
protonation
COFs,
promote
adsorption
Yeager‐type,
which
jointly
alters
process
two‐step
to
one,
thereby
with
high
Angewandte Chemie International Edition,
Journal Year:
2023,
Volume and Issue:
62(49)
Published: Aug. 14, 2023
Abstract
Benefiting
from
the
excellent
structural
tunability,
robust
framework,
ultrahigh
porosity,
and
rich
active
sites,
covalent
organic
frameworks
(COFs)
are
widely
recognized
as
promising
photocatalysts
in
chemical
conversions,
emerged
hydrogen
peroxide
(H
2
O
)
photosynthesis
2020.
H
,
serving
an
environmental‐friendly
oxidant
a
liquid
fuel,
has
attracted
increasing
researchers
to
explore
its
potential.
Over
past
few
years,
numerous
COFs‐based
developed
with
encouraging
achievements
production,
whereas
no
comprehensive
review
articles
exist
summarize
this
specific
significant
area.
Herein
we
provide
systematic
overview
of
advances
challenges
COFs
photocatalytic
production.
We
first
introduce
priorities
photosynthesis.
Then,
various
strategies
improve
efficiency
discussed.
The
perspective
outlook
for
future
emerging
field
finally
offered.
This
timely
will
pave
way
development
highly
efficient
practical
production
value‐added
chemicals
not
limited
.
Angewandte Chemie International Edition,
Journal Year:
2022,
Volume and Issue:
62(9)
Published: Dec. 30, 2022
The
full
reaction
photosynthesis
of
H2
O2
that
can
combine
water-oxidation
and
oxygen-reduction
without
sacrificial
agents
is
highly
demanded
to
maximize
the
light-utilization
overcome
complex
reaction-process
anthraquinone-oxidation.
Here,
a
kind
oxidation-reduction
molecular
junction
covalent-organic-framework
(TTF-BT-COF)
has
been
synthesized
through
covalent-coupling
tetrathiafulvalene
(photo-oxidation
site)
benzothiazole
(photo-reduction
site),
which
presents
visible-light-adsorption
region,
effective
electron-hole
separation-efficiency
photo-redox
sites
enables
generation
.
Specifically,
record-high
yield
(TTF-BT-COF,
≈276
000
μM
h-1
g-1
)
for
achieved
among
porous
crystalline
photocatalysts.
This
first
work
design
COFs
,
might
extend
scope
in
production.
Angewandte Chemie International Edition,
Journal Year:
2023,
Volume and Issue:
62(38)
Published: Aug. 1, 2023
H2
O2
is
a
significant
chemical
widely
utilized
in
the
environmental
and
industrial
fields,
with
growing
global
demand.
Without
sacrificial
agents,
simultaneous
photocatalyzed
synthesis
through
oxygen
reduction
reaction
(ORR)
water
oxidation
(WOR)
dual
channels
from
seawater
green
sustainable
but
still
challenging.
Herein,
two
novel
thiophene-containing
covalent
organic
frameworks
(TD-COF
TT-COF)
were
first
constructed
served
as
catalysts
for
via
indirect
2e-
ORR
direct
WOR
channels.
The
photocatalytic
production
performance
can
be
regulated
by
adjusting
N-heterocycle
modules
(pyridine
triazine)
COFs.
Notably,
no
just
using
air
raw
materials,
TD-COF
exhibited
high
yields
of
4060
μmol
h-1
g-1
3364
deionized
natural
seawater,
respectively.
Further
computational
mechanism
studies
revealed
that
thiophene
was
primary
photoreduction
unit
ORR,
while
benzene
ring
(linked
to
imine
bond)
central
photooxidation
WOR.
current
work
exploits
COFs
overall
provides
fresh
insight
into
creating
innovative
photocatalyzing
synthesis.
Angewandte Chemie International Edition,
Journal Year:
2023,
Volume and Issue:
62(41)
Published: Aug. 26, 2023
Nitrogen-heterocycle-based
covalent
organic
frameworks
(COFs)
are
considered
promising
candidates
for
the
overall
photosynthesis
of
hydrogen
peroxide
(H2
O2
).
However,
effects
relative
nitrogen
locations
remain
obscured
and
photocatalytic
performances
COFs
need
to
be
further
improved.
Herein,
a
collection
functionalized
by
various
diazines
including
pyridazine,
pyrimidine,
pyrazine
have
been
judiciously
designed
synthesized
photogeneration
H2
without
sacrificial
agents.
Compared
with
pyrimidine
pyrazine,
pyridazine
embedded
in
TpDz
tends
stabilize
endoperoxide
intermediate
species,
leading
toward
more
efficient
direct
2e-
oxygen
reduction
reaction
(ORR)
pathway.
Benefiting
from
effective
electron-hole
separation,
low
charge
transfer
resistance,
high-efficiency
ORR
pathway,
an
excellent
production
rate
7327
μmol
g-1
h-1
solar-to-chemical
conversion
(SCC)
value
0.62
%
has
achieved
TpDz,
which
ranks
one
best
COF-based
photocatalysts.
This
work
might
shed
fresh
light
on
rational
design
functional
targeting
photocatalysts
production.
Nature Communications,
Journal Year:
2023,
Volume and Issue:
14(1)
Published: Oct. 28, 2023
Developing
efficient
artificial
photocatalysts
for
the
biomimetic
photocatalytic
production
of
molecular
materials,
including
medicines
and
clean
energy
carriers,
remains
a
fundamentally
technologically
essential
challenge.
Hydrogen
peroxide
is
widely
used
in
chemical
synthesis,
medical
disinfection,
energy.
However,
current
industrial
production,
predominantly
by
anthraquinone
oxidation,
suffers
from
hefty
penalties
toxic
byproducts.
Herein,
we
report
hydrogen
protonation-induced
dispersible
porous
polymers
with
good
charge-carrier
transport
properties.
Significant
generation
occurs
under
ambient
conditions
at
an
unprecedented
rate
23.7
mmol
g-1
h-1
apparent
quantum
efficiency
11.3%
450
nm.
Combined
simulations
spectroscopies
indicate
that
sub-picosecond
ultrafast
electron
"localization"
both
free
carriers
exciton
states
catalytic
reaction
centers
underlie
remarkable
performance
polymers.
Angewandte Chemie International Edition,
Journal Year:
2023,
Volume and Issue:
62(43)
Published: Sept. 5, 2023
Singlet
oxygen
(1
O2
)
is
an
excellent
reactive
species
(ROSs)
for
the
selective
conversion
of
organic
matter,
especially
in
advanced
oxidation
processes
(AOPs).
However,
due
to
huge
dilemma
synthesizing
single-site
type
catalysts,
control
and
regulation
1
generation
AOPs
still
challenging
underlying
mechanism
remains
largely
obscure.
Here,
taking
advantage
well-defined
flexibly
tunable
sites
covalent
frameworks
(COFs),
we
report
first
achievement
precisely
regulating
ROSs
peroxymonosulfate
(PMS)-based
by
site
engineering
COFs.
Remarkably,
COFs
with
bipyridine
units
(BPY-COFs)
facilitate
PMS
activation
via
a
nonradical
pathway
100
%
,
whereas
biphenyl-based
(BPD-COFs)
almost
identical
structures
activate
produce
radicals
(⋅OH
SO4.-
).
The
BPY-COFs/PMS
system
delivers
boosted
performance
degradation
target
pollutants
from
water,
which
ca.
9.4
times
that
its
BPD-COFs
counterpart,
surpassing
most
reported
PMS-based
systems.
Mechanism
analysis
indicated
highly
electronegative
pyridine-N
atoms
on
BPY-COFs
provide
extra
adsorb
terminal
H
PMS,
resulting
simultaneous
adsorption
O
one
pyridine
ring,
facilitates
cleavage
S-O
bond
generate
.