Direct Laser Scribing of All‐Solid‐State In‐Plane Proton Microsupercapacitors on Ionic Covalent Organic Framework Films
X Li,
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Dong‐Dong Han,
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Ye‐Can Zhang
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et al.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 10, 2025
Abstract
Proton
microsupercapacitors
(MSCs)
are
promising
energy
storage
devices
for
cutting‐edge
applications.
However,
all‐solid‐state
designs
face
challenges
due
to
the
need
synergistic
innovations
in
electrolytes,
electrodes,
and
interface
engineering.
Herein,
direct
laser
scribing
of
metal‐free
in‐plane
proton
MSCs
reported
on
ionic
covalent
organic
framework
(iCOF)
films.
The
solid‐state
AA‐stacked
iCOF
electrolytes
with
perfect
2D
channels
(
d
=
0.33
nm)
prepared
by
vacuum
filtration,
exhibiting
conductivities
from
0.23
4.7
mS
cm
−1
depending
humidity.
Furthermore,
patterned
carbon
electrodes
fabricated
via
situ
carbonization
iCOFs,
forming
a
seamless
electrolyte‒electrode
interface.
To
reveal
photophysical
features
insulating
iCOFs
conductive
laser‐treated
femtosecond
transient
absorption
experiments
carried
out.
multiphysics
simulation
indicates
that
electric
field
is
uniformly
distributed
at
electrode−electrolyte
Notably,
resulting
MSC
exhibits
an
ultrahigh
specific
capacitance
(≈10.13
mF
−2
101.3
F
−3
),
high
volumetric
density
(2.52
mWh
rapid
scan
rate
(1000
mV
s
excellent
cycling
stability
(no
degradation
after
50
000
cycles).
This
approach
provides
high‐performance
MSCs,
revealing
great
potential
applications
intelligent
microsystems.
Language: Английский
Covalent organic frameworks and their composites as enhanced energy storage materials
Divya Divya,
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H K Mishra,
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Ritambhara Jangir
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et al.
Chemical Communications,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
Fabrication,
and
preparation
methods
of
COFs
along
with
a
complete
review
the
last
one
decade's
progress
in
field
energy
storage
conversion
devices,
notably
batteries,
capacitors
fuel
cells,
has
been
presented.
Language: Английский
Geomimetic Interfacial Hydrothermal Synthesis of Crystalline Ionic Vinylene‐Linked Covalent Organic Frameworks
Small,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 5, 2025
Abstract
Ionic
vinylene‐linked
covalent
organic
frameworks
(ivCOFs)
with
ionic
characteristics
and
highly
conjugated
structures
have
been
promising
functional
materials.
However,
both
the
number
of
reported
COFs
its
synthetic
methodologies
still
be
limited.
Herein,
two
new
kinds
(named
as
COF‐NUC‐1
COF‐NUC‐2)
are
synthesized
by
novel
geomimetic
interfacial
hydrothermal
synthesis
for
first
time.
Due
to
insolubility
aldehyde
monomers
in
water,
a
molecule/water
interface
is
created,
where
water‐soluble
N‐ethyl‐2,4,6‐trimethylpyridinium
bromide
(ETMP‐Br)
can
react
via
interface‐confined
Knoevenagel
condensation
reaction.
The
resultant
show
high
crystallinity,
chemical
stability,
hydrophilic
nature.
Benefiting
from
electron‐withdrawing
redox
properties
pyridinium
salts,
as‐fabricated
memristor
based
on
film
shows
stable
nonvolatile
memory
effects,
featuring
ON/OFF
current
ratio
0.66
×
10
3
small
switch‐on
voltage
−0.68
V.
This
work
expands
realm
ivCOFs
deepens
understanding
synthesis.
Language: Английский
Membranes constructing with excellent performances for aqueous zinc-ion battery: A review
Juan Wu,
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Mengyao Li,
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Haoyu Li
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et al.
Coordination Chemistry Reviews,
Journal Year:
2025,
Volume and Issue:
531, P. 216478 - 216478
Published: Feb. 8, 2025
Language: Английский
Anion-Exchange Strategy for Ru/RuO2-Embedded N/S-Co-Doped Porous Carbon Composites for Electrochemical Nitrogen Fixation
Shahzeb Ali Samad,
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Xuanzi Ye,
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Zhiya Han
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et al.
Polymers,
Journal Year:
2025,
Volume and Issue:
17(4), P. 543 - 543
Published: Feb. 19, 2025
Ionic
porous
polymers
have
been
widely
utilized
efficiently
to
anchor
various
metal
atoms
for
the
preparation
of
metal-embedded
heteroatom-doped
carbon
composites
as
active
materials
electrocatalytic
applications.
However,
rational
design
heteroatom
and
elements
in
HPC-based
remains
a
significant
challenge,
due
tendency
aggregation
nanoparticles
during
pyrolysis.
In
this
study,
nitrogen
(N)-
sulfur
(S)-enriched
ionic
covalent
organic
framework
(iCOF)
incorporating
viologen
thieno[3,4-b]
thiophene
(TbT)
was
constructed
via
Zincke-type
polycondensation.
The
synthesized
iCOF
possesses
crystalline
structure
with
pore
size
3.05
nm,
low
optical
band
gap
1.88
eV,
superior
conductivity
10-2.672
S
cm-1
at
333
K,
confirming
conjugated
nature
our
novel
iCOF.
By
applying
precursor,
ruthenium
ruthenium(IV)
oxide
(Ru/RuO2)
nanoparticle-embedded
N/S-co-doped
composite
(NSPC-Ru)
prepared
by
using
two-step
sequence
anion-exchange
pyrolysis
processes.
electrochemical
reduction
reaction
(eNRR)
application,
NSPC-Ru
achieves
an
impressive
NH3
yield
rate
32.0
μg
h-1
mg-1
Faradaic
efficiency
13.2%
-0.34
V
vs.
RHE.
Thus,
innovative
approach
proposes
new
route
iCOF-derived
enhanced
NRR
performance.
Language: Английский
Mass Transport Based on Covalent Organic Frameworks
Accounts of Chemical Research,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 11, 2025
ConspectusMass
transport
is
fundamental
to
biological
systems
and
industrial
processes,
governing
chemical
reactions,
substance
exchange,
energy
conversion
across
various
material
scales.
In
systems,
ion
transport,
such
as
proton
migration
through
voltage-gated
channels,
regulates
cellular
potential,
signaling,
metabolic
balance.
transporting
molecules
solid,
liquid,
or
gas
phases
dictates
reactant
contact
diffusion
rates,
directly
impacting
reaction
efficiency
conversion.
Optimizing
these
processes
necessitates
the
design
of
efficient
interfaces
channels
enhance
mass
transport.Crystalline
porous
materials,
particularly
covalent
organic
frameworks
(COFs),
offer
an
excellent
platform
for
investigating
optimizing
transport.
With
ordered,
pre-engineered
nano-
subnanometer
pores,
COFs
enable
confined
garnered
significant
attention
conversion,
catalysis,
drug
delivery,
adsorption,
separation
applications.
Deeper
investigations
into
mechanism
in
at
molecular
level
are
crucial
advancing
materials
science,
chemistry,
engineering.Our
group
focuses
on
explore
multisubstance
cooperative
mechanisms
structure-activity
relationships
ions,
water,
gases.
We
have
expanded
linker
chemistry
by
developing
irreversible
α-aminoketone-linked
introducing
Suzuki
coupling
COF
preparation.
proposed
strategies
side-chain-induced
dipole-facilitated
stacking
prenucleation
slow
growth
achieve
record
large
pore
sizes
highly
oriented
nanochannels.
implemented
exfoliation
interwoven
strategy
accelerate
complex
interfaces,
refined
permeability
sieve-based
membranes
precise
size
engineering,
elucidated
effects
hydrophobicity/hydrophilicity
water
phase
transition
diffusion.
Building
insights,
we
designed
novel
open
framework
ionomers
tailor
microenvironment
electrocatalytic
uncovered
multiple
mechanisms.
The
synergistically
enhanced
three-phase
effectively
modulates
electrochemical
CO2
reduction
pathway
significantly
boosts
power
density
proton-exchange
membrane
fuel
cells
(PEMFCs).In
this
Account,
summarize
recent
advances
COF-based
emphasizing
nanochannel
construction
strategies,
including
linkage,
size,
orientation,
function
gradient
modulations.
discuss
functional
COFs,
correlations
between
structure
properties,
their
applications
separation,
storage,
catalysis.
Finally,
outline
current
challenges
future
opportunities
synthetic
mechanisms,
By
understanding
phenomena
from
microscopic
particles
macroscopic
scales,
Account
aims
provide
aligning
with
offering
insights
catalytic
performance.
Language: Английский
An Alkynyl-Based Olefin-linked Covalent Organic Framework as an Anode Material for Potassium-ion Batteries
Bertha Lotsi,
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Luke Schkeryantz,
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Cuong Dang
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et al.
Polymer,
Journal Year:
2025,
Volume and Issue:
unknown, P. 128453 - 128453
Published: April 1, 2025
Language: Английский
Processable and Recyclable Covalent Organic Framework Gel Electrolytes
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 25, 2025
Abstract
Covalent
organic
framework
(COF)‐based
electrolytes
with
abundant
ordered
channels
and
accessible
interaction
sites
have
shown
great
potential
in
energy
storage
transformation,
although
their
practical
applications
are
strongly
impeded
by
inherent
insolubility
non‐melt
processability.
Developing
processable
COF
gel
recycling
them
remains
a
formidable
challenge.
In
this
study,
the
processing
of
to
gels
demonstrated
through
interlayer
manipulation
enable
solution‐reconstruction
for
first
time,
inspired
working
principle
wedges.
Good
solution‐processability
powders
strong
acid
mediums
is
achieved
inserting
oxygen
atoms
into
its
promote
charge
repulsion.
This
modification
enabled
readily
dispersable
as
colloidal
nanosheets
an
aqueous
solution
trifluoroacetic
(TFA).
Starting
from
here,
modulated
competitive
interactions
among
TFA,
COF,
water
molecules,
reconfigure
materials
between
gelified
colloidally
dispersed
states.
The
reconfigured
maintains
mechanical
properties
long
cycle
life
electrolyte
battery
(>800
h).
approach
realizes
can
recycle
out
repeated
use,
offering
new
insights
strategies
preparation
sustainable
recycling.
Language: Английский
Quasi-Solid-State Electrolytes: Bridging the gap between solid and liquid electrolytes for Zinc-Ion batteries
Tao Xue,
No information about this author
Jinpeng Guan,
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Yongbiao Mu
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et al.
Chemical Engineering Journal,
Journal Year:
2025,
Volume and Issue:
unknown, P. 162994 - 162994
Published: April 1, 2025
Language: Английский
Another Way to Realize LiMn2O4 as a Solid Electrolyte
Jingzhen Du,
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Zewen Sun,
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Bohao Peng
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et al.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 19, 2024
Abstract
The
development
and
application
of
solid‐state
electrolytes
(SSEs)
play
a
crucial
role
in
advancing
lithium
metal
batteries
(LMBs).
Consequently,
the
search
for
high‐performance,
economic,
easily
fabricated
SSEs
has
become
prevailing
trend.
In
this
work,
we
explore
an
alternative
approach
to
design
traditional
commercial
lithium‐ion
cathode
material,
spinel‐type
LiMn
2
O
4
(LMO)
as
SSE.
By
blending
LMO
with
poly(vinylidene
difluoride)
combining
two
layers
polyethylene
(PE)
film
on
top
bottom,
effectively
reduce
its
high
electronic
conductivity,
thereby
creating
PE/LMO/PE
SSE
demonstrates
ionic
conductivity
(3.15
×
10
−4
S
cm
−1
at
35°C),
low
(7.31
−11
),
good
interfacial
contact
stability
both
anode,
LiFePO
nickel‐rich
Li[Ni
0.8
Co
0.1
Mn
]O
cathodes.
This
study
offers
new
direction
electrochemically
active
material
LMO,
while
providing
simple
feasible
solution
SSEs.
Additionally,
it
opens
up
perspectives
selecting
high‐performance
use
LMBs,
paving
economic
path
toward
commercialization
batteries.
Language: Английский