Self-Supported α-MoB/β-MoB2 Ceramic Electrodes for Efficient High-Current-Density Hydrogen Evolution in Acidic, Neutral, and Alkaline pH-Values
Sishi Huang,
Anding Huang,
Haisen Huang
и другие.
ACS Applied Materials & Interfaces,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 27, 2025
This
paper
describes
the
production
and
high-current-density
hydrogen
evolution
reaction
(HER)
performance
in
whole
pH
range
(from
acidic
to
basic
values)
of
self-supported
α-MoB/β-MoB2
ceramic
electrodes,
aiming
for
use
industrial
electrocatalytic
water
splitting.
Tape-casting
phase-inversion
process,
followed
by
sintering,
were
employed
synthesize
β-MoB2
which
exhibited
well
arranged
large
finger-like
pores,
providing
numerous
active
sites
channels
electrolyte
entry
release.
The
between
sintering
aid
MoO3
situ
produces
heterojunctions,
significantly
improve
performance.
At
a
current
density
1000
mA·cm-2,
electrode
manifested
an
overpotential
289
mV
294
alkaline
aqueous
solutions,
respectively,
stable
operation
over
time
(>100
h).
also
performed
neutral
solution,
with
354
at
100
mA·cm-2.
Theoretical
(DFT)
calculations
demonstrated
that
heterojunction
alters
electronic
configuration
β-MoB2,
favoring
effective
electron
transfer
mechanism;
thereby,
adsorption
free
energy
ions
is
close
zero,
dissociation
molecules
under
conditions
are
enhanced.
Язык: Английский
Free water releases hydrogen
Nature Reviews Chemistry,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 5, 2025
Язык: Английский
Interfacial-Free-Water-Enhanced Mass Transfer to Boost Current Density of Hydrogen Evolution
Nano Letters,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 14, 2025
The
advancement
of
water
electrolysis
highlights
the
growing
importance
electrolyzers
capable
operating
at
high
current
densities,
where
mass
transfer
dynamics
plays
a
crucial
role.
In
electrode
reactions,
interfacial
is
key
factor
in
regulating
these
dynamics.
However,
potential
utilizing
interfacial-free
(IFW)
to
modulate
behavior
remains
underexplored.
Herein,
we
investigate
effect
structure
on
hydrogen
evolution
reaction
(HER)
performance
across
different
density
ranges,
using
designed
platinum-coated
nickel
hydroxide
foam
(Pt@Ni(OH)2-NF)
electrodes.
We
reveal
that
with
increasing
density,
changes
alter
rate-determining
step
HER.
Pt@Ni(OH)2-NF
exhibited
excellent
alkaline
electrolytes,
achieving
1000
mA
cm-2
114
mV
overpotential.
This
study
provides
novel
approach
optimizing
by
enhancing
transfer,
further
paving
way
for
more
efficient
and
energy-saving
production.
Язык: Английский
Unraveling Side Reactions in Paired CO2 Electrolysis at Operando Conditions: A Case Study of Ethylene Glycol Oxidation
Journal of the American Chemical Society,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 11, 2025
Replacing
the
oxygen
evolution
reaction
(OER)
in
CO2
electrolysis
with
an
energetically
and
economically
favorable
alternative
is
very
promising.
Yet,
understanding
paired
organic
oxidation
environment
for
reduction
particularly
challenging,
as
monitoring
multiple
side
reactions
problematic.
Herein,
we
examined
of
ethylene
glycol
(EG),
one
simplest
polyols,
a
model
on
series
nickel
oxyhydroxide
catalysts
(β-NiMxOOH,
M
=
Ni,
Co,
Fe,
Cu).
Using
situ
techniques,
including
surface-enhanced
infrared
absorption
spectroscopy
(SEIRAS)
differential
electrochemical
mass
spectrometry
(DEMS),
together
various
ex
approaches,
obtained
potential-resolved
quantitative
information
comprising
OER,
overoxidation
to
CO/CO2,
catalyst
dissolution,
from
electrolyte
decarbonation.
Many
factors
impurity
cations,
pH,
potential
can
substantially
influence
product
distribution
reactions.
Such
influences
are
nearly
identical
both
electrocatalytic
chemical-electrochemical
pathways.
The
optimized
system
achieve
stable
high
Faradaic
efficiencies
formate
(∼100%),
glycolaldehyde
(∼86%),
glycolate
(∼66%),
respectively.
Importantly,
easily
suffer
higher
energy
consumption
than
conventional
counterpart,
provided
unregulated.
Yet
modulated
consumed
21.1%
less
even
when
separation
was
considered.
This
work
reveals
unique
electrolysis,
opening
up
opportunities
designing
efficient
systems
real-life
applications.
Язык: Английский
Structure and Dissociation of Water at the Electrode–Solution Interface Studied by In Situ Vibrational Spectroscopic Techniques
Shanshan Li,
R. S. Shi,
Jiaru Song
и другие.
Analytical Chemistry,
Год журнала:
2025,
Номер
unknown
Опубликована: Май 13, 2025
In
aqueous
electrochemistry,
water
in
contact
with
charged
surfaces
is
ubiquitous
and
indispensable,
dictating
the
binding
of
solutes
to
electrode
as
well
transport
process
protons
electrons
interfacial
region.
A
comprehensive
understanding
structure
dissociation
at
molecular
level
extremely
important
yet
challenging,
given
its
critical
role
various
physical,
chemical,
biological
processes.
situ
vibrational
spectroscopic
techniques
serve
a
powerful
tool
for
acquiring
probing
reaction
mechanisms
real
time.
this
review,
we
briefly
summarize
latest
advances
electric
double
layer
model
experimental
methods
employed
electrode-solution
interface.
Particular
emphasis
placed
on
that
have
unveiled
new
insights
into
across
diverse
under
ambient
conditions.
And
then,
it
also
provides
an
overview
recent
progress
subtle
relationship
between
activity,
aiming
provide
novel
fields
energy
catalysis.
Язык: Английский
Unraveling Mechanism of Hydrogen Evolution Reactions in Alkaline media: Recent Advances in In-situ Raman Spectroscopy
Chemical Communications,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 1, 2025
In
situ
Raman
spectroscopy
used
for
monitoring
the
electrocatalytic
process
reveals
hydrogen
evolution
reaction
mechanism,
providing
theoretical
guidance
fabricating
efficient
catalysts.
Язык: Английский