Journal of Materials Chemistry A,
Год журнала:
2024,
Номер
12(43), С. 29814 - 29825
Опубликована: Янв. 1, 2024
DQHBA-COF
with
bipolar
redox-active
centers
was
grown
in
situ
on
the
conductive
graphene
surface,
endowing
symmetric
supercapacitors
and
capacitive
deionization
systems
a
high
ion
storage
capacity
excellent
cycling
durability.
Abstract
Covalent
organic
framework
(COF)
materials,
known
for
their
robust
porous
character,
sustainability,
and
abundance,
have
great
potential
as
cathodes
aqueous
Zn‐ion
batteries
(ZIBs).
However,
application
is
hindered
by
low
reversible
capacity
discharge
voltage.
Herein,
a
donor–acceptor
configuration
COF
(NT‐COF)
utilized
the
cathode
ZIBs.
The
cell
exhibits
high
voltage
plateau
of
≈1.4
V
214
mAh
g
−1
at
0.2
A
when
utilizing
Mn
2+
electrolyte
additive
in
ZnSO
4
electrolyte.
synergistic
combination
mechanism
proposed,
involving
deposition/dissolution
reactions
Zn
SO
(OH)
6
·4H
2
O
co‐(de)insertion
H
+
2−
NT‐COF.
Meanwhile,
NT‐COF
with
facilitates
efficient
generation
separation
electron‐hole
pairs
upon
light
exposure,
thereby
enhancing
electrochemical
within
battery.
This
leads
to
reduction
charging
internal
overvoltage,
ultimately
minimizing
electricity
consumption.
Under
ambient
weather
conditions,
an
average
430
on
sunny
days
maintains
consistent
cycling
stability
duration
200
cycles
(≈19
days)
.
research
inspires
advancement
Zn‐organic
high‐energy‐density
energy
storage
systems
or
photo‐electrochemical
batteries.
Advanced Energy Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Окт. 13, 2024
Abstract
Zinc
(Zn)
emerges
as
an
ideal
anode
for
aqueous‐based
energy
storage
devices
because
of
its
safety,
non‐toxicity,
and
cost‐effectiveness.
However,
the
reversibility
zinc
anodes
is
constrained
by
unchecked
dendrite
proliferation
parasitic
side
reactions.
To
minimize
these
adverse
effects,
a
highly
oriented,
crystalline
2D
porous
fluorinated
covalent
organic
framework
(denoted
TpBD‐2F)
thin
film
in
situ
synthesized
on
Zn
protective
layer.
The
zincophilic
hydrophobic
TpBD‐2F
provides
numerous
1D
nanochannels,
which
facilitate
hopping/transfer
2+
repel
H
2
O
infiltration,
thus
regulating
flux
inhibiting
interfacial
corrosion.
resulting
enabled
stable
plating/stripping
symmetric
cells
over
1200
h
at
mA
cm
−2
.
Furthermore,
assembled
full
(Zn‐ion
capacitors)
deliver
ultra‐long
cycling
life
100
000
cycles
current
density
5
A
g
−1
,
outperforming
nearly
all
reported
materials.
Advanced Functional Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 17, 2025
Abstract
Aqueous
zinc‐ion
batteries
(AZIBs),
candidates
for
large‐scale
energy
storage,
face
limitations
due
to
the
poor
reversibility
of
zinc
anodes.
It
reports
on
pyridine
derivatives
with
high
donor
characteristics,
including
2‐chloro‐1‐methylpyridinium
iodide
(CMPI)
and
pyridine‐2‐acetaldoxime
methyl
(PAMI),
as
effective
additives.
At
lower
concentrations,
these
additives
markedly
curtail
dendrites
formation
evolution
hydrogen
anode,
thereby
prolonging
AZIBs
life.
Through
a
combination
theory
experiments,
impact
side‐chain
groups
kinetic
process
depositioni
is
elucidated.
In
contrast
PAM
+
,
CMPI
demonstrates
enhanced
adsorption
self‐assembles
at
anode‐electrolyte
interface,
forming
barrier
free
water
protective
ZnI
layer
via
I
−
ion
integration.
This
dual‐layer
strategy
boosts
plating/stripping
by
100‐fold
achieves
coulombic
efficiency
99.7%
in
zinc–copper
half‐
batteries.
The
findings
advance
understanding
electrolyte
additive
structures
deposition,
providing
molecular
framework
screening
aqueous
metal‐ion
Abstract
Aqueous
Zn‐metal
batteries
(AZBs)
are
thought
as
highly
prospective
candidates
for
large‐scale
energy‐storage
systems
because
of
their
abundant
natural
resources,
low
cost,
high
safety,
and
environmentally
friendly.
Nevertheless,
the
key
problems
AZBs
uncontrollable
zinc
dendrites
growth
water‐induced
erosion
faced
by
anodes.
Therefore,
reducing
hydrophilicity
anode
introducing
zincophilic
sites
availably
strategy.
Herein,
3D
highly‐conductive
host
is
developed
to
inhibit
Zn
growth,
which
have
a
porous
structure
consisting
graphene
carbon
nanotubes
embedded
with
nucleation
Prussian
blue
analogs
(ZnHCF@3D‐GC).
The
inner
ZnHCF
possess
minimized
barriers,
can
serve
favorable
sites,
provide
buffer
interspace
allow
even
more
high‐capacity
plating.
Additionally,
density
functional
theory
results
show
that
exhibits
strong
binding
energy
adsorption
(002)
plane,
guide
horizontal
deposition
in
host.
As
result,
assembled
symmetrical
cell
able
stabilize
900
cycles
at
an
ultrahigh
current
100
mA
cm
−2
.
Zn‐ZnHCF@3D‐GC//MnO
2
Zn‐ZnHCF@3D‐GC//ZnHCF
full
cells
be
stably
cycled
1000
2.0
A
g
−1
Advanced Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 25, 2025
Abstract
Aqueous
ammonium‐ion
(NH
4
+
)
batteries
(AAIBs)
have
recently
been
considered
as
attractive
alternatives
for
next‐generation
large‐scale
energy
storage
systems,
on
account
of
their
cost‐effectiveness,
nonflammability,
less
corrosive,
small
hydrated
ionic
radius,
and
rapid
NH
diffusion
kinetics.
In
addition,
the
tetrahedral
structure
exhibits
preferential
orientation
characteristics,
resulting
in
a
different
electrochemical
mechanism
from
spherical
charge
carriers
such
Li
,
Na
K
.
Therefore,
unlocking
‐ion
mechanisms
host
electrode
materials
is
pivotal
to
advancing
design
high‐performance
AAIBs.
Organic
materials,
with
customizable,
flexible,
stable
molecular
structures,
along
ease
recycling
disposal,
offer
tremendous
potential.
However,
development
cutting‐edge
organic
specifically
AAIBs
remains
an
exciting,
yet
largely
untapped,
frontier.
This
review
systematically
explores
interaction
between
ions
electrostatic
interactions
including
hydrogen
bonding.
It
also
highlights
application
diverse
molecules,
conducting
polymers,
covalent
frameworks
(COFs),
organic‐inorganic
hybrids
Lastly,
addresses
key
challenges
future
perspectives
organic‐material‐based
AAIBs,
aiming
push
boundaries
aqueous
systems.