A Roadmap of Sustainable Hydrogen Production and Storage: Innovations and Challenges
Small,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 9, 2025
The
present
review
offers
a
strategic
roadmap
for
overcoming
conventional
photocatalyst
limitations
and
emphasizes
recent
advancements
in
hybrid
photocatalysts,
thereby
addressing
electrode
topology-associated
challenges
sustainable
hydrogen
(H₂)
production
storage.
Unlike
traditional
reviews,
this
paper
explores
the
latest
developments
photocatalysts
provides
thorough
analysis
of
H₂
fuel
technology,
including
water
splitting,
photocatalytic
reactions,
storage
issues.
A
detailed
photoelectrochemical
(PEC)
which
mimics
photosynthesis,
to
produce
carbon-neutral
importance
optimizing
PEC
devices
with
co-catalysts
are
highlighted.
Advanced
designs,
Z-scheme
S-scheme
heterojunctions,
doping,
surface
modifications,
copolymerization,
discussed
impact
various
materials,
such
as
conjugated
microporous
polymers
(CMPs),
covalent
organic
frameworks
(COFs),
graphdiyne,
MBene,
TiO₂-based
compounds,
metal
sulfides,
group
III-V
on
activity
is
examined.
Furthermore,
highlights
strategies
improving
performance,
targeted
vacancy
creation,
composite
formation.
Recommendations
include
designing
cost-effective
efficient
photoelectrodes,
maximizing
light
utilization,
simplifying
cell
design.
By
storage,
transport,
conversion
challenges,
not
only
covers
critical
aspects
but
also
towards
achieving
future.
Language: Английский
Covalent Organic Frameworks Enhance Photocatalytic Hydrogen Peroxide Production through Synergistic Effects
Lin Wang,
No information about this author
Changzhi Han,
No information about this author
Shiyong Gao
No information about this author
et al.
ACS Catalysis,
Journal Year:
2025,
Volume and Issue:
unknown, P. 5683 - 5693
Published: March 24, 2025
Language: Английский
Impact of Interfaces on the Performance of Covalent Organic Frameworks for Photocatalytic Hydrogen Production
Small,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 18, 2024
The
rise
in
global
temperatures
and
environmental
contamination
resulting
from
traditional
fossil
fuel
usage
has
prompted
a
search
for
alternative
energy
sources.
Utilizing
solar
to
drive
the
direct
splitting
of
water
hydrogen
production
emerged
as
promising
solution
these
challenges.
Covalent
organic
frameworks
(COFs)
are
ordered,
crystalline
materials
made
up
molecules
linked
by
covalent
bonds,
featuring
permanent
porosity
wide
range
structural
topologies.
COFs
serve
suitable
platforms
solar-driven
produce
hydrogen,
their
building
blocks
can
be
tailored
possess
adjustable
band
gaps,
charge
separation
capabilities,
porosity,
wettability,
chemical
stability.
Here,
impact
interface
context
photocatalytic
reaction
is
focused
propose
strategies
enhance
performance
photocatalysis.
In
particular,
how
hybrid
interfaces
affect
focused.
Language: Английский
Aqueous-Phase Synthesis of Cyclic Trinuclear Cluster-Based Metal–Organic Frameworks
Kun Wu,
No information about this author
Wei Zhao,
No information about this author
Ling Huang
No information about this author
et al.
Journal of the American Chemical Society,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 10, 2025
The
synthesis
of
metal-organic
frameworks
(MOFs)
often
involves
high-boiling-point
organic
solvents,
which
can
have
extensive
environmental
impact
and
limit
their
large-scale
applications.
Here,
we
present
a
one-pot
aqueous-phase
approach
for
the
rapid
preparation
33
trinuclear-copper-cluster-based
MOFs
(1
to
33)
with
different
pyrazoles
under
ultrasonic
irradiation.
To
address
water-solubility
challenge
linkers,
employ
aromatic
amines/aldehydes
pyrazole
aldehydes/amines
in
situ
generate
imine-based
pyrazoles.
This
linker
dismantling
strategy
enables
formation
low-concentration
pyrazoles,
are
essential
assembly
aqueous
phase.
use
preassembled
trinuclear
gold
complexes
instead
amines
affords
an
Au-Cu-based
MOF
(34)
alternating
copper
clusters,
rare
example
mixed
yet
precise
arrangement
metal
compositions.
Additionally,
direct
addition
pyruvic
acid
reaction
mixture
results
facile
carboxylic-acid-functionalized
(35),
eliminating
need
preinstallation
or
postmodification
steps
traditional
synthesis.
Furthermore,
demonstrate
11-AA
as
efficient
photocatalyst
cross-dehydrogenative
coupling
(CDC)
reactions,
exploiting
synergetic
effect
substrate
activation
on
sites
subsequent
initiated
by
photosensitive
linkers.
work
offers
simple
solution
making
minimal
impact;
it
also
opens
up
possibilities
developing
multifunctional
diverse
Language: Английский
Incorporating atomic-level center into porphyrin-based COF for photocatalytic H2 evolution
Guo‐Wei Guan,
No information about this author
Su‐Tao Zheng,
No information about this author
Liping Zhang
No information about this author
et al.
Chemical Engineering Journal,
Journal Year:
2025,
Volume and Issue:
unknown, P. 163127 - 163127
Published: April 1, 2025
Language: Английский
Microfluidic synthesis of MOFs, COFs, and HOFs: Insights and advances
Materials Science and Engineering R Reports,
Journal Year:
2025,
Volume and Issue:
165, P. 101005 - 101005
Published: April 29, 2025
Language: Английский
Functionalization of Covalent Organic Frameworks with Thiazole Rings and Hydroxyl Groups for Improved Photocatalytic Water Splitting Performance
Yuxiang Chen,
No information about this author
Feng Duan,
No information about this author
Jiejie Zhang
No information about this author
et al.
ACS Applied Materials & Interfaces,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 6, 2025
Photocatalytic
water
splitting
for
hydrogen
production
holds
considerable
potential
simultaneously
addressing
fuel
and
carbon
neutrality,
although
increasing
photocatalyst
activity
enhancing
exciton
dissociation
continue
to
be
very
difficult
tasks.
Covalent
organic
frameworks
(COFs)
with
predesignable
structures
customizable
functionalities
are
promising
candidates
photocatalysis.
In
this
study,
we
present
the
design
synthesis
of
these
COFs
using
thiazole
rings
as
linkage
units.
Three
(denoted
COF-S-OH-1,
COF-S-OH-2,
COF-S-OH-3)
were
prepared
based
on
aldehyde
ligands
varying
numbers
hydroxyl
groups
(2-hydroxybenzene-1,3,5-tricarbaldehyde,
2,4-dihydroxybenzene-1,3,5-tricarbaldehyde,
2,4,6-trihydroxybenzene-1,3,5-tricarbaldehyde,
respectively).
The
results
demonstrate
that
constructed
linkages
exhibit
superior
stability
conjugation
compared
those
linked
solely
by
imine
bonds,
ultimately
achieving
enhanced
electronic
conductivity.
tight
interaction
between
donor
acceptor
in
donor-acceptor
(D-A)
system
facilitates
an
improved
photocatalytic
evolution
performance.
Furthermore,
number
(electron-donating
groups)
significantly
enhances
efficiency
resulting
COFs.
Language: Английский