Recent advances in potassium metal batteries: electrodes, interfaces and electrolytes
Chemical Society Reviews,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 1, 2025
This
review
explores
the
latest
advancements
in
potassium
metal
batteries,
including
electrode
design,
interface
engineering,
and
electrolyte
optimization
to
suppress
dendrite
formation
enhance
cycling
stability.
Язык: Английский
Unraveling the Diversity of the Storage Mechanism in Carbonyl Materials toward Different Metal Ions
ACS Applied Materials & Interfaces,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 15, 2025
Due
to
their
structural
diversity,
environmental
friendliness,
and
resource
renewability,
organic
electroactive
compounds
are
versatile
hosts
for
the
energy
storage
of
different
metal
ions.
However,
consistency
variety
performance
mechanism
designed
electrode
materials
in
aqueous
electrolytes
toward
ions
have
rarely
been
researched.
Here,
one
type
material
integrated
with
anhydride
imide
groups
was
studied
detail.
Among
two
functional
groups,
carbonyl
were
found
be
dominant
contributors
during
initial
discharge
step
due
higher
binding
ions,
while
imides
responsible
second-step
coordination
monovalent
With
increment
valence
guest
activity
decreased
became
nearly
inactive
aluminum
On
contrary,
always
active
various
capacity
when
increased.
Moreover,
similar
behaviors
close
potentials
detected
first
these
Язык: Английский
Cyclable Micron‐Sized Silicon‐Based Lithium‐Ion Batteries at −40 °C Enabled by Temperature‐Dependent Solvation Regulation
Advanced Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Май 15, 2025
Abstract
Micron‐sized
silicon
(µSi)
anodes
hold
great
promise
for
high‐energy
lithium‐ion
batteries
(LIBs).
However,
the
rechargeable
cyclability
of
µSi
at
sub‐zero
Celsius,
especially
below
−20
°C
remains
challenging,
caused
by
severe
volume
change
and
cracking
solid
electrolyte
interphase
(SEI)
during
cycling.
Here,
low‐temperature
µSi‐based
LIBs
is
realized
using
an
featured
with
temperature‐adaptive
ion‐dipole
interactions.
The
synergistic
effect
methyl
group
as
a
weak
electron
donor
electronegative
fluorine
atoms
endows
difluoroacetate
(MDFA)
binding
affinity
Li
+
.
Moreover,
between
oxygen
in
both
MDFA
fluoroethylene
carbonate
(FEC)
decreases
lower
temperatures,
accompanied
temperature‐responsive
enhancement
‐anion
coordination.
Thus,
MDFA/FEC
exhibits
extraordinary
contact
ion
pairs‐dominated
solvation
structure
subzero
which
facilitates
desolvation
formation
thin,
robust
inorganic‐rich
SEI.
As
expected,
show
record‐breaking
capacity
786
mAh
g
−1
after
100
cycles
−40
under
0.1
A
,
full
cells
display
impressive
rechargeability
°C.
This
work
paves
way
extending
applications
to
extreme
cold
conditions.
Язык: Английский