EES Catalysis,
Год журнала:
2024,
Номер
2(4), С. 932 - 940
Опубликована: Янв. 1, 2024
Ru
nanocluster-anchored
sulfur
and
nitrogen
co-doped
carbon
hollow
spheres
exhibit
high
hydrogen
evolution
reaction
performance
in
alkaline
real
seawater.
Green Chemistry,
Год журнала:
2023,
Номер
25(23), С. 9818 - 9825
Опубликована: Янв. 1, 2023
A
CuIn
5
S
8
nanosheet
photocatalyst
with
oxygen
incorporation
was
developed,
the
aim
of
converting
PET
plastic
into
commodity
chemicals
paired
water
splitting
hydrogen.
Nano Letters,
Год журнала:
2024,
Номер
24(31), С. 9768 - 9775
Опубликована: Июль 26, 2024
Excessive
production
of
waste
polyethylene
terephthalate
(PET)
poses
an
ecological
challenge,
which
necessitates
developing
technologies
to
extract
the
values
from
end-of-life
PET.
Upcycling
has
proven
effective
in
addressing
low
profitability
current
recycling
strategies,
yet
existing
upcycling
operate
under
energy-intensive
conditions.
Here
we
report
a
cascade
strategy
steer
transformation
PET
into
glycolate
overall
yield
92.6%
ambient
The
approach
involves
setting
up
robust
hydrolase
with
95.6%
depolymerization
ethylene
glycol
(EG)
monomer
within
12
h,
followed
by
electrochemical
process
initiated
CO-tolerant
Pd/Ni(OH)
Abstract
Electrochemical
upcycling
of
end‐of‐life
polyethylene
terephthalate
(PET)
using
renewable
electricity
offers
a
route
to
generate
valuable
chemicals
while
processing
plastic
wastes.
However,
it
remains
huge
challenge
design
an
electrocatalyst
with
reliable
structure‐property
relationships
for
PET
valorization.
Herein,
spinel
Co
3
O
4
rich
oxygen
vacancies
improved
activity
toward
formic
acid
(FA)
production
from
hydrolysate
is
reported.
Experimental
investigations
combined
theoretical
calculations
reveal
that
incorporation
V
into
not
only
promotes
the
generation
reactive
hydroxyl
species
(OH
*
)
at
adjacent
tetrahedral
2+
(Co2+
Td),
but
also
induces
electronic
structure
transition
octahedral
3+
(Co3+
Oh)
Oh),
which
typically
functions
as
highly‐active
catalytic
sites
ethylene
glycol
(EG)
chemisorption.
Moreover,
enlarged
Co‐O
covalency
induced
by
facilitates
electron
transfer
EG
OH
via
Co2+
Oh‐O‐Co2+
Td
interaction
and
following
C─C
bond
cleavage
direct
oxidation
glyoxal
intermediate
pathway.
As
result,
‐Co
catalyst
exhibits
high
half‐cell
oxidation,
Faradaic
efficiency
(91%)
productivity
(1.02
mmol
cm
−2
h
−1
FA.
Lastly,
demonstrated
hundred
gram‐scale
formate
crystals
can
be
produced
real‐world
bottles
two‐electrode
electroreforming,
yield
82%.