Catalysts,
Год журнала:
2024,
Номер
14(12), С. 874 - 874
Опубликована: Ноя. 29, 2024
In
this
study,
biochar-loaded
E3+:BiOCl
(C/3E3+:BiOCl)
was
synthesized
with
varying
levels
of
E3+
doping
using
a
one-step
solvothermal
method
and
used
for
tetracycline
hydrochloride
(TC-HCl)
degradation.
Their
structure,
shape
morphology
were
not
only
characterized
by
power
X-ray
diffraction
(XRD),
scanning
electron
microscope
(SEM)
transmission
microscopy
(TEM)
but
also
UV-vis
diffuse
reflectance
spectra
upconversion
(UC).
The
results
indicated
significant
enhancement
in
the
photocatalytic
activity
catalyst
following
introduction
Er3+.
composite
material
C/3E3+:BiOCl,
concentration
3
mol%,
demonstrated
highest
activity,
achieving
an
impressive
visible
light
degradation
efficiency
89.2%
TC
HCl
within
90
min.
This
marks
increase
33.5%
compared
to
BiOCl
monomer
17.4%
C/BiOCl.
Additionally,
when
exposed
wavelengths
exceeding
600
nm,
C/3E3+:BiOCl
maintained
photodegradation
44.3%,
while
C/BiOCl
showed
no
under
same
conditions.
finding
highlights
effectiveness
as
matrix,
which
enhances
performance
through
effect
transfer
mechanisms
associated
biochar.
ACS Applied Materials & Interfaces,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 24, 2025
Single-atom
catalysts
(SACs)
are
prone
to
agglomeration
or
migration
during
catalytic
processes,
making
the
development
of
highly
dispersible
SACs
greatly
essential
for
performance
photocatalytic
CO2
reduction.
Herein,
cobalt-containing
keto-enamine
covalent
organic
frameworks
(COFs)
(Co/TpPa-1)
successfully
in
situ
synthesized
by
utilizing
interlayer
nitrogen
atom
coordinated
with
metallic
cobalt,
which
is
used
effectively
prevent
monometallic
atoms
ensure
homogeneous
dispersion
resulting
metalized
COFs.
In
reduction,
Co/TpPa-1
composite
exhibits
significantly
enhanced
compared
TpPa-1
The
CO
yield
0.05
mM
approximately
414.5
μmol
g-1
h-1,
representing
a
two-order-of-magnitude
improvement
over
COF
catalyst
(approximately
4.15
h-1).
Moreover,
shows
99.45%
selectivity
and
good
stability,
maintaining
97%
reduction
rate
after
four
cycles.
reason
lies
fact
that
interaction
between
monatomic
Co
COFs
enhances
visible
light
absorption
extends
lifetime
photogenerated
carriers
promoting
electron
transfer
through
loaded
Co.
This
work
provides
new
idea
synthesis
high
selectivity.
Advanced
oxidation
processes
have
been
increasingly
applied
to
degrade
organic
pollutants
through
the
generation
of
strong
oxidizing
radicals
by
catalyst
activation
reactions.
In
this
study,
Co3O4/g-C3N4
van
der
Waals
heterojunction
(CCN)
was
successfully
prepared
calcining
a
mixture
Co3O4
and
g-C3N4
(BCN)
in
order
improve
performance
elucidate
mechanism
CCN-activated
peroxymonosulfate
(PMS)
catalytic
degradation
tetracycline
(TC)
under
visible
light.
This
unique
nanostructure
possesses
an
abundance
active
sites,
thus
significantly
facilitating
transport
charge.
The
TC
removal
rate
optimized
reaches
300.1
×
10-3
min-1
within
10
min
light,
nearly
46.2
times
that
BCN.
dominated
h+
1O2.
pathways
were
analyzed
detail.
reduced
toxicity
intermediates
reveals
potential
risk
environment
posed
CCN-3/PMS
system.
Finally,
preliminary
economic
analysis
process
carried
out.
study
provides
simple
promising
route
for
efficient
PMS
CCN
photocatalytic
remediation
water
pollution.
Catalysts,
Год журнала:
2024,
Номер
14(12), С. 874 - 874
Опубликована: Ноя. 29, 2024
In
this
study,
biochar-loaded
E3+:BiOCl
(C/3E3+:BiOCl)
was
synthesized
with
varying
levels
of
E3+
doping
using
a
one-step
solvothermal
method
and
used
for
tetracycline
hydrochloride
(TC-HCl)
degradation.
Their
structure,
shape
morphology
were
not
only
characterized
by
power
X-ray
diffraction
(XRD),
scanning
electron
microscope
(SEM)
transmission
microscopy
(TEM)
but
also
UV-vis
diffuse
reflectance
spectra
upconversion
(UC).
The
results
indicated
significant
enhancement
in
the
photocatalytic
activity
catalyst
following
introduction
Er3+.
composite
material
C/3E3+:BiOCl,
concentration
3
mol%,
demonstrated
highest
activity,
achieving
an
impressive
visible
light
degradation
efficiency
89.2%
TC
HCl
within
90
min.
This
marks
increase
33.5%
compared
to
BiOCl
monomer
17.4%
C/BiOCl.
Additionally,
when
exposed
wavelengths
exceeding
600
nm,
C/3E3+:BiOCl
maintained
photodegradation
44.3%,
while
C/BiOCl
showed
no
under
same
conditions.
finding
highlights
effectiveness
as
matrix,
which
enhances
performance
through
effect
transfer
mechanisms
associated
biochar.