Construction and Embedding of Oxygen Vacancies in Organic-Inorganic S-scheme Heterojunctions for Optimizing the Photocatalytic Degradation Performance of PDI-Nb/BiVO4 towards Antibiotics
Applied Catalysis B Environment and Energy,
Год журнала:
2025,
Номер
unknown, С. 125141 - 125141
Опубликована: Фев. 1, 2025
Язык: Английский
Advancements and challenges of industrial‐level acidic CO2 electrolysis
MetalMat,
Год журнала:
2024,
Номер
unknown
Опубликована: Сен. 1, 2024
Abstract
The
use
of
green
renewable
energy
to
convert
carbon
dioxide
(CO
2
)
into
valuable
chemicals
and
fuels
through
CO
electrolysis
technology
(also
known
as
electrochemical
reduction
reaction,
eCO
RR)
is
an
advantageous
technology,
which
could
greatly
aid
the
global
carbon‐neutral
goal.
Although
progress
has
been
made
in
alkaline/neutral
media,
low
conversion
efficiency
target
products,
carbonate/bicarbonate
salt
precipitation,
blockage
electrode
holes
caused
by
are
not
conducive
industrial
applications.
Acidic
media
address
these
issues;
however,
conditions,
there
other
challenges
that
need
be
addressed,
such
hydrogen
evolution,
poor
tolerance
electrocatalysts,
electrolysers.
This
review
discusses
recent
advances
industrial‐level
acidic
electrolysis,
including
reaction
mechanisms,
device
design,
aiming
promote
its
commercialization.
In
addition,
a
comprehensive
evaluation
strategy
RR
system
proposed,
perspectives
provided
based
on
related
discussion.
Язык: Английский
Progress in Catalysts for Formic Acid Production by Electrochemical Reduction of Carbon Dioxide
Topics in Current Chemistry,
Год журнала:
2024,
Номер
383(1)
Опубликована: Дек. 3, 2024
Язык: Английский
Directional Transport of Photogenerated Electrons to Reduction Sites in Covalent Organic Frameworks by Microenvironment Modulation for CO2 Photoreduction
Junxian Bai,
Mengke Zhang,
Fangyuan Si
и другие.
Advanced Functional Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Дек. 8, 2024
Abstract
As
the
transfer
of
photogenerated
electrons
to
CO
2
directly
determines
its
reduction
performance,
it
is
important
boost
local
electron
density
at
reaction
site.
Herein,
a
new
strategy
demonstrated
evaluate
site
by
modulating
microenvironment
molecular
level
based
on
3
rationally
designed
relatively
electron‐deficient
(ED)
and
electron‐rich
(ER)
type
COFs.
Expectedly,
En‐COF‐TAPB‐TDOEB
exhibits
high
due
presence
an
additional
electric
field,
whose
polarization
direction
consistent
with
that
basic
unit
comparison,
in
Am‐COF‐TAPB‐TFB
Pr‐COF‐TFPB‐TAB
mostly
distribute
benzene
triphenylene,
respectively,
delay
exciton
dissociation
field
inverse
compared
Consequently,
shows
superior
photoreduction
efficiency
Pr‐COF‐TFPB‐TAB.
Further
mechanism
investigation
demonstrates
influence
polar
excited
state
charge
separation
pathways
π‐system
En‐COF‐TAPB‐TDOEB,
which
convincingly
confirms
ability
directional
transport
sites
photocatalysts
correlated
their
activity
reduction.
Язык: Английский