Chemical programming for micro- and nanoarchitectonics of 3D/4D-printed thermoelectric materials
Nano Today,
Journal Year:
2025,
Volume and Issue:
61, P. 102658 - 102658
Published: Feb. 11, 2025
Language: Английский
Advancements in metal-iodine batteries: progress and perspectives
Zhigang Shen,
No information about this author
Dianheng Yu,
No information about this author
Hongye Ding
No information about this author
et al.
Rare Metals,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 17, 2025
Language: Английский
Point-of-use upcycling of 3D printing waste for developing 3D-printed Zn–I2 batteries
Journal of Materials Chemistry A,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
This
study
reveals
a
mechanical
upcycling
approach
combined
with
electrode
engineering
to
transform
carbon
nanofiber
and
polylactic
acid-based
3D
printing
waste
into
functional
components
for
sustainable
zinc–iodine
batteries.
Language: Английский
A novel water-reducer-based hydrogel electrolyte for robust and flexible Zn-I2 battery
Energy storage materials,
Journal Year:
2024,
Volume and Issue:
unknown, P. 103981 - 103981
Published: Dec. 1, 2024
Language: Английский
Iodine/Chlorine Multi‐Electron Conversion Realizes High Energy Density Zinc‐Iodine Batteries
Jiajin Zhao,
No information about this author
Yan Chen,
No information about this author
Mengyan Zhang
No information about this author
et al.
Advanced Science,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 5, 2024
Abstract
Aqueous
zinc‐iodine
(Zn‐I
2
)
batteries
are
promising
energy
storage
devices;
however,
the
conventional
single‐electron
reaction
potential
and
density
of
iodine
cathode
inadequate
for
practical
applications.
Activation
high‐valence
reactions
has
evoked
a
compelling
direction
to
developing
high‐voltage
batteries.
Herein,
ethylene
glycol
(EG)
is
proposed
as
co‐solvent
in
water‐in‐deep
eutectic
solvent
(WiDES)
electrolyte,
enabling
significant
utilization
two‐electron‐transfer
I
+
/I
0
−
facilitating
an
additional
reversibility
Cl
/Cl
redox
reaction.
Spectroscopic
characterizations
calculations
analyses
reveal
that
EG
integrates
into
Zn
2+
solvation
structure
hydrogen‐bond
donor,
competitively
binding
O
atoms
H
O,
which
triggers
transition
from
water‐rich
water‐poor
clusters
,
effectively
disrupting
network.
Consequently,
aqueous
Zn‐I
cell
achieves
exceptional
capacity
987
mAh
g
I2
−1
with
1278
Wh
kg
marking
enhancement
≈300
compared
electrolyte
devoid
EG,
enhancing
Coulombic
efficiency
(CE)
68.2%
98.7%.
Moreover,
pouch
exhibits
3.72
cm
−2
4.52
mWh
exhibiting
robust
cycling
stability.
Overall,
this
work
contributes
further
development
high‐capacity
Language: Английский