Abstract
Aqueous
zinc‐ion
batteries
(AZIBs)
have
garnered
significant
attention
as
next‐generation
energy
storage
systems.
However,
developing
high‐energy‐density
cathode
materials
remains
a
critical
challenge.
Organic
compounds
with
multi‐electron
transfer
processes
offer
promising
solution
to
this
issue.
In
concept,
we
outline
the
fundamental
structural
principles
and
mechanisms
underlying
of
redox‐active
organic
compounds.
We
categorize
various
into
n‐type
,
p‐type
bipolar
compounds,
discuss
their
features,
redox
chemistry,
capacity
performance
in
AZIBs
by
analyzing
cyclic
voltammetry
profiles
charge
mechanisms.
Our
goal
is
valuable
insights
molecular
design
chemistry
achieve
high‐performance
AZIBs.
Advanced Functional Materials,
Год журнала:
2024,
Номер
34(45)
Опубликована: Май 28, 2024
Abstract
Designing
multiple
redox
sites
in
electroactive
organic
cathodes
that
allow
more
electron
transfer
is
a
permanent
target
for
energy
storage.
Here,
six‐electron
zinc–organic
batteries
are
reported
accessed
by
duodecuple
H‐bonded
NH
4
+
storage
N‐heterocyclic
dipyrazino[2,3‐f:2′,3′‐h]quinoxaline‐2,3,6,7,10,11‐hexacarbonitrile
(DQH)
cathode.
DQH
features
an
extended
π‐conjugated
aromatic
planarity
enriched
with
super
delocalization
routes
and
dodecahedral‐active
imine/cyano
motifs,
achieving
high
capacity
up
to
385
mAh
g
−1
at
0.5
A
.
Besides,
cathode
redox‐exclusively
couples
small‐hydration‐size
low‐desolvation‐energy‐barrier
ions
(0.33
nm
0.19
eV
vs
0.86
0.36
of
Zn
2+
)
via
flexible
H‐bonding
interactions.
topo‐coordination
enables
anti‐dissolution
aqueous
electrolytes
avoid
common
decay
small
molecules,
solves
the
instability
low
interfacial
reaction
kinetics
issues
caused
rigidly
sluggishly
repeated
insertion
ions.
This
gives
battery
high‐rate
ability
(30
lifespan
000
cycles
10
).
Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 5, 2024
Abstract
Multiple
redox‐active
amphoteric
organics
with
more
n‐p
fused
electron
transfer
is
an
ongoing
pursuit
for
superior
zinc–organic
batteries
(ZOBs).
Here
we
report
multi‐heterocycle‐site
donor‐acceptor
conjugated
organic
superstructures
(AOSs)
by
integrating
three‐electron‐accepting
n‐type
triazine
motifs
and
dual‐electron‐donating
p‐type
piperazine
units
via
H‐bonding
π–π
stacking.
AOSs
expose
flower‐shaped
N‐heteromacrocyclic
delocalization
topologies
to
promise
full
accessibility
of
built‐in
ultralow
activation
energy,
thus
liberating
capacity
(465
mAh
g
−1
)
Zn||AOSs
battery.
More
importantly,
the
extended
multiple
donor‐acceptor‐fused
feature
satisfied
discharge
voltage
anti‐dissolution
in
electrolytes,
pushing
both
energy
density
cycle
life
ZOBs
a
new
level
(412
Wh
kg
70,000
cycles@10
A
).
An
anion–cation
hybrid
18
e
−
charge
storage
mechanism
rationalized
heteromacrocyclic
modules
cathode,
entailing
six
tert‐N
coupling
CF
3
SO
ions
at
high
potential
twelve
imine
sites
coordinating
Zn
2+
low
potential.
These
findings
constitute
major
advance
multielectron
materials
stand
good
starting
point
advanced
ZOBs.
Aqueous
zinc-sulfur
batteries
(AZSBs)
have
emerged
as
promising
candidates
for
high-energy
density,
cost-effective,
and
environmentally
sustainable
energy
storage
systems.
Despite
their
potential,
several
challenges
hinder
the
realization
of
high-performance
AZSBs,
including
sluggish
reaction
kinetics,
disproportionation
reactions
ZnS
in
water,
low
conductivity
volume
expansion
sulfur
cathode,
poor
wetting
properties,
dendrite
growth
issues
zinc
anode.
This
review
comprehensively
summarizes
optimization
strategies
overcoming
these
challenges.
We
discuss
cathode
modification
approaches,
such
sulfur/carbon
composites,
sulfide
catalytic
matrices,
which
address
while
enhancing
conversion
kinetics.
Additionally,
electrolyte
engineering
strategies,
use
iodide-based
additives
co-solvent
modifications,
are
examined
effectiveness
improving
kinetics
properties.
advancements,
AZSBs
still
face
with
long-cycle
stability.
Therefore,
this
proposes
future
perspectives
development
AZSBs.
aim
to
provide
valuable
insights
into
sulfur-based
materials
advance
achievement
Aqueous
zinc
ion
batteries
(AZIBs)
stand
out
among
various
battery
technologies
for
their
advantages,
including
low
cost,
high
safety,
and
green
credentials.
We
chemically
polymerized
anthraquinone
triphenylamine
derivatives
to
prepare
the
π-conjugated
polymers
poly
2-((4-(diphenylamine)benzylidene)amino)anthracene-9,10-dione
(PDAH)
2-((4-((4-bromophenyl)(phenyl)amino)benzylidene)amino)anthracene-9,10-dione
(PDABr),
as
cathode
materials
AZIBs.
The
anthraquinone-based
structure's
charge
storage
capacity,
coupled
with
strong
transfer
capability,
enabled
these
electrode
exhibit
excellent
electrochemical
performance.
Among
them,
electron-withdrawing
group
-introduced
in
PDABr
induces
a
p-π
interaction
adjacent
benzene
ring,
optimizing
electron
migration
within
battery.
This
enhancement
improves
material's
stability
activity,
leading
superior
performance,
especially
rate
cycle
life,
stability.
Comparative
experiments
revealed
that
PDABr//Zn
exhibited
higher
specific
capacity
(0.1
A
g-1,
210.57
mA
h
g-1)
than
PDAH//Zn
145.7
g-1).
At
same
current
density,
also
showed
better
cycling
(capacity
retention
of
93%
after
6000
cycles
at
5
Additionally,
exceptional
maintaining
its
upon
returning
initial
density.
By
comparing
physical
properties
PDABr//Zn,
relationship
between
conjugation
effect
performance
is
elucidated.
study
provides
strategy
fine-tuned,
molecular
design
organic
materials,
specifically
aimed
enhancing
high-energy
zinc-ion
batteries.
International Journal of Molecular Sciences,
Год журнала:
2025,
Номер
26(8), С. 3838 - 3838
Опубликована: Апрель 18, 2025
Aqueous
zinc-ion
batteries
(AZIBs)
have
attracted
interest
for
their
low
cost
and
environmental
friendliness.
Two
bipolar
organic
materials
with
different
degrees
of
conjugation,
pPMQT
pNTQT,
were
rationally
designed
synthesized
as
cathode
candidates
AZIBs
based
on
4,4′-diaminotriphenylamine
(TPA),
2,7-diaminoanthraquinone
(AQ),
two
anhydrides.
This
molecular
design
features
an
increased
conjugation
electron
cloud
density,
thereby
improving
charge
transport
kinetics,
specific
capacity,
cycling
stability.
In
comparison
pPMQ
pNTQ
(n-type),
pNTQT
demonstrate
better
electrochemical
characteristics.
this
work,
shows
outstanding
performance.
It
exhibits
initial
capacity
349.79
mAh
g−1
at
0.1
A
retains
a
190.25
(87.6%)
after
5000
cycles
5
g−1.
comparison,
demonstrates
only
207.55
g−1,
its
retention
rate
is
81.2%.
At
the
same
time,
both
polymer
films
attractive
electrochromic
(EC)
properties,
displaying
reversible
color
transitions
from
yellow
to
dark
blue
in
UV–visible
spectrum.
work
lays
foundation
further
development
triphenylamine-based
polyimide
application
electrochromism.
Stretchable
supercapacitors
are
essential
components
in
wearable
electronics
due
to
their
low
heat
generation
and
seamless
integration
capabilities.
Thermoplastic
polyurethane
elastomers,
recognized
for
dynamic
hydrogen-bonding
structure,
exhibit
excellent
stretchability,
making
them
well-suited
these
applications.
This
study
introduces
fluorine-based
interactions
the
hard
segments
of
thermoplastic
polyurethanes,
resulting
polyurethanes
with
a
elastic
modulus,
high
fracture
strength,
exceptional
fatigue
resistance,
self-healing
properties.
By
utilizing
as
binders
meshed
fabric
scaffolds,
we
developed
highly
stretchable
conductors.
These
conductors
maintain
resistance
(∼26
ohms)
under
biaxial
stretching
stable
bidirectional
conductivity
after
1600
cycles.
The
fabricated
supercapacitor
electrode,
incorporating
current
collectors,
polyurethane,
MXene,
achieves
an
ultrahigh
areal
specific
capacitance
7200
mF
cm
ACS Applied Energy Materials,
Год журнала:
2024,
Номер
7(22), С. 10230 - 10237
Опубликована: Ноя. 6, 2024
Aqueous
zinc–sulfur
batteries
(AZSBs)
are
emerging
as
high-energy-density
due
to
the
high
capacity
of
sulfur-based
cathodes.
However,
sulfur
suffers
from
poor
conductivity
and
sluggish
reaction
kinetics.
Therefore,
conductive
carbons
were
employed
additives
enhance
hosts
encapsulate
sulfur,
thereby
improving
kinetics
cycle
stability.
This
work
reveals
critical
role
carbon
in
crystallization
its
impact
on
AZSBs'
performance.
Amorphous
with
uniform
distribution
S@Ketjen
black
(S@KB),
unlike
crystallinity
aggregation
others,
results
best
electrochemical
performance,
demonstrating
higher
capacity,
enhanced
kinetics,
long-cycle
Abstract
Phenoxazine
is
a
commonly
used
molecular
building
block,
for
example
in
optoelectronic
applications
and
pharmaceuticals.
However,
it
highly
susceptible
to
rapid
photodegradation,
especially
halogenated
solvents.
In
the
present
study,
we
identify
degradation
products
both
non‐halogenated
solvents
by
UV/Vis
absorption,
NMR
spectroscopy
mass
spectrometry.
We
also
propose
substitution
strategy
aimed
at
effectively
suppressing
high
photoreactivity.
Kinetic
studies
show
that
quantum
yield
of
photodegradation
φ
differs
factor
more
than
1000
between
trisubstituted
derivatives
N‐substituted
phenoxazine.