Hydroxide-Oxide-Sulfur-Stabilized Bismuth Nanorod Conversion: Selective Induction of the Electrochemical Reduction of CO2 to Formate
Naveenkumar Palanimuthu,
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Ramasamy Santhosh Kumar,
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Saleem Sidra
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et al.
ACS Applied Nano Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 14, 2025
The
electrochemical
CO2
reduction
reaction
(e-CO2RR)
converts
value-added
chemicals
into
formate.
Bismuth-based
resources
exhibit
promising
potential
in
the
of
to
formate
due
their
low
toxicity
and
ability
enhance
*OCHO
intermediate
pathway.
However,
there
are
numerous
hurdles
optimizing
activity
applicability.
Here,
we
describe
assembly
structurally
stable
bismuth
hydroxide,
oxide,
sulfide
nanorods
supported
by
a
reduced
graphene
oxide
(rGO)
nanosheet
through
simple
hydrothermal
method.
obtained
optimized
rGO-Bi2S3
improved
e-CO2RR
conversions
H-cell
systems
compared
hydroxide
electrocatalysts.
maintain
high
within
wide
window
(−0.76
−1.26
V
vs
RHE)
obtain
overall
Faradaic
efficiency
±84%
at
−1.16
RHE,
current
density
±41.50
mA
cm–2,
stability
for
longer
than
12
h,
with
greater
±86%
an
system.
Theoretical
calculations
reveal
that
strong
interaction
between
rGO
Bi2S3
stabilizes
adsorption
e-CO2RR.
resulting
structural
transformation
based
on
sulfur,
provides
encouraging
avenue
future
energy
conversion.
Language: Английский
Synergistic Acceleration of CO2 Electroreduction Kinetics by Oxygen Vacancy and Heterogeneous Interface for Efficient HCOOH Production
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 7, 2025
Abstract
Constructing
highly
efficient
bismuth
(Bi)‐based
catalysts
to
accelerate
the
sluggish
kinetic
process
of
CO
2
electroreduction
HCOOH
is
crucial
for
promoting
its
practical
application
but
also
challenging.
Herein,
cerium
oxide
catalyst
integrated
with
dual
active
centers
oxygen
vacancy
and
heterogeneous
interface
fabricated
facilitate
reduction
enhance
performance.
It
revealed
that
introduction
endows
a
remarkably
enhanced
adsorption
capacity
facilitates
transfer
more
electrons
*
.
Furthermore,
it
even
steers
reaction
pathway
favorably
toward
production.
The
optimization
adsorption,
activation,
energy
barriers
expedited
HCOOH.
As
expected,
this
exhibits
catalytic
performance
Faradaic
efficiency
97%
at
current
density
300
mA
cm
−2
This
work
highlights
significant
synergistic
advantages
vacancies
interfaces
in
optimizing
molecular
process.
Language: Английский
Research progress on the reaction mechanism, metal-based catalysts, and reactors for CO2 electroreduction to formic acid/formate
Huichang Liang,
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Yankun Li,
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Zhichao Miao
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et al.
Journal of environmental chemical engineering,
Journal Year:
2025,
Volume and Issue:
unknown, P. 116547 - 116547
Published: April 1, 2025
Language: Английский
Advances and challenges in the electroreduction of carbon dioxide in acidic electrolyte
Chenglong Wang,
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Wangjiang Gao,
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Hexing Yang
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et al.
Journal of Energy Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 1, 2025
Language: Английский
Pulsed Electrocatalysis on SnO2 Electrodes for Boosting Formate Selectivity and Activity during CO2 Electroreduction
Yihang Yang,
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Jieshu Zhou,
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Zhouhang Li
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et al.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 13, 2025
Abstract
Tin
oxide
(SnO
2
)
is
considered
a
candidate
catalyst
for
the
electrocatalytic
CO
reduction
(CO
R)
to
formate
conversion.
However,
self‐reduction
of
SnO
metallic
Sn
at
high
current
densities
leads
an
unavoidable
sharp
decrease
in
selectivity.
Herein,
‐based
(Pul‐SnO
synthesized
via
pulsed
electrocatalysis
precursors.
Due
ability
maintain
oxidation
valence
states
and
promote
formation
oxygen
vacancies,
Pul‐SnO
exhibited
selectivity
90%
density
600
mA
cm
−2
,
significantly
higher
than
that
conventional
Sn‐based
(81%
100
obtained
constant
potential
electrocatalysis.
The
situ
Raman
spectra,
kinetic
isotope
effect,
cyclic
voltammetry,
theoretical
calculations
demonstrated
molecules
activation
vacancies
enhance
water
dissociation,
thereby
accelerating
proton‐coupled
electron
transfer
process
reduce
free
energy
*OCHO
intermediate
generation.
Moreover,
identified
adsorbed
hydroxyls
(*OH)
with
suitable
coverage
during
R
also
further
make
more
energy‐favorable.
As
result,
showed
super
formate,
while
maintaining
excellent
activity
stability.
Language: Английский
Bi Doped In2O3 Nanofiber for Efficient Electrocatalytic CO2 Reduction
Yuanxiang Zhao,
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Xinchun Lv,
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Zifan Zhu
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et al.
ChemCatChem,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 9, 2024
Abstract
Electrocatalytic
carbon
dioxide
reduction
reaction
(CO
2
RR)
to
formic
acid
(HCOOH)
is
attracted
for
superfluous
CO
removal
and
HCOOH
production
under
ambient
conditions.
Indium‐based
catalysts
has
considered
as
a
good
candidate
material
RR
due
their
environmentally
friendly
features.
However,
the
catalytic
efficiency
limited
by
poor
Faradaic
(FE)
high
overpotential
of
electrocatalyst,
activity
stability
indium‐based
are
unsatisfactory,
especially
in
industrial
current
density
that
critical
commercialization.
Herein,
fiber
Bi‐doped
In
O
3
was
synthesized
through
electrospinning
method,
it
demonstrate
FE
88.2%
at
−1.5
V
versus
RHE
(reversible
hydrogen
electrode)
with
partial
−21.8
mA
cm
−2
H
type
cell.
Specially,
Bi‐In
electrocatalyst
also
reach
standard,
which
can
work
−400
92.7%
(yield
6.9
mmol
h
−1
)
home‐made
Flow
Importantly,
shows
24
long‐term
test
−300
.
The
improvement
catalyst
ascribed
optimized
electronic
structure
site,
reduced
function
value
beneficial
reducing
formation
energy
key
*OCHO
intermediates.
Language: Английский