Recycling of Spent Lithium Iron Phosphate Cathodes: Challenges and Progress
ACS Applied Materials & Interfaces,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 16, 2024
The
number
of
spent
lithium
iron
phosphate
(LiFePO
Language: Английский
In situ growth and interfacial reconstruction of Mo-doped Ni3S2/VO2 as anti-corrosion electrocatalyst for long-term durable seawater splitting
Huyen Dao,
No information about this author
Saleem Sidra,
No information about this author
Van Hien Hoa
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et al.
Applied Catalysis B Environment and Energy,
Journal Year:
2024,
Volume and Issue:
365, P. 124925 - 124925
Published: Dec. 10, 2024
Language: Английский
A hierarchical NiPOx@NiFe LDH nanoarray for durable seawater oxidation
Yuchun Ren,
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Jiayun Song,
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Shengjun Sun
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et al.
Journal of Colloid and Interface Science,
Journal Year:
2025,
Volume and Issue:
687, P. 708 - 714
Published: Feb. 17, 2025
Language: Английский
Improved Activity and Corrosion Resistance in Seawater Oxidation: Harnessing the Synergy between the Phosphide Layer and Nickel–Iron Hydroxide
Lianmei Kang,
No information about this author
Dandan Cai,
No information about this author
Shipeng Geng
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et al.
Energy & Fuels,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 23, 2025
Language: Английский
High Catalytic Selectivity of Electron/Proton Dual‐Conductive Sulfonated Polyaniline Micropore Encased IrO2 Electrocatalyst by Screening Effect for Oxygen Evolution of Seawater Electrolysis
Yuhan Shen,
No information about this author
Shengqiu Zhao,
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Fanglin Wu
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et al.
Advanced Science,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 4, 2024
Abstract
Acidic
seawater
electrolysis
offers
significant
advantages
in
high
efficiency
and
sustainable
hydrogen
production.
However,
situ
of
acidic
remains
a
challenge.
Herein,
stable
efficient
catalyst
(SPTTPAB/IrO
2
)
is
developed
by
coating
iridium
oxide
(IrO
with
microporous
conjugated
organic
framework
functionalized
sulfonate
groups
(‐SO
3
H)
to
tackle
these
challenges.
The
SPTTPAB/IrO
presents
‐SO
H
concentration
5.62
×
10
−4
mol
g
−1
micropore
below
nm
numbering
1.026
16
.
Molecular
dynamics
simulations
demonstrate
that
the
blocked
98.62%
Cl
−
from
reaching
catalyst.
This
structure
combines
electron
conductivity
proton
H,
weakens
adsorption,
suppresses
metal‐chlorine
coupling,
thus
enhancing
catalytic
activity
selectivity.
As
result,
overpotential
for
oxygen
evolution
reaction
(OER)
only
283
mV@10
mA
cm
−2
,
Tafel
slope
16.33
mV
dec
which
reduces
13.8%
37.8%
compared
commercial
IrO
respectively.
Impressively,
exhibits
outstanding
performance,
35.3%
improvement
over
69
@1.9
V,
while
degradation
rate
(0.018
h
24.6%
study
an
innovative
solution
designing
high‐performance
electrocatalysts.
Language: Английский