Advanced Materials,
Journal Year:
2022,
Volume and Issue:
35(7)
Published: Nov. 22, 2022
Abstract
Achieving
a
finely
tuned
active
layer
morphology
with
suitable
vertical
phase
to
facilitate
both
charge
generation
and
transport
has
long
been
the
main
goal
for
pursuing
highly
efficient
bulk
heterojunction
all‐polymer
solar
cells
(all‐PSCs).
Herein,
solution
address
above
challenge
via
synergistically
combining
ternary
blend
strategy
layer‐by‐layer
(LbL)
procedure
is
proposed.
By
introducing
synthesized
polymer
acceptor
(
P
A
),
PY‐Cl,
higher
crystallinity
into
designed
host
PY‐SSe‐V,
distribution
molecular
ordering
of
LbL‐type
all‐PSCs
can
be
improved
in
comparison
PM6/PY‐SSe‐V
binary
all‐PSCs.
The
formation
superior
microstructure
not
only
promote
extraction
properties
but
also
reduce
energetic
disorder
non‐radiative
recombination
loss,
thus
improving
all
three
photovoltaic
parameters
simultaneously.
Consequently,
PM6/(PY‐SSe‐V:PY‐Cl)
show
best
efficiency
18.14%,
which
among
highest
values
reported
date
This
work
provides
facile
effective
obtaining
high‐efficiency
Chemical Reviews,
Journal Year:
2022,
Volume and Issue:
122(18), P. 14180 - 14274
Published: Aug. 5, 2022
Organic
photovoltaics
(OPVs)
have
progressed
steadily
through
three
stages
of
photoactive
materials
development:
(i)
use
poly(3-hexylthiophene)
and
fullerene-based
acceptors
(FAs)
for
optimizing
bulk
heterojunctions;
(ii)
development
new
donors
to
better
match
with
FAs;
(iii)
non-fullerene
(NFAs).
The
application
NFAs
an
A–D–A
configuration
(where
A
=
acceptor
D
donor)
has
enabled
devices
efficient
charge
generation
small
energy
losses
(Eloss
<
0.6
eV),
resulting
in
substantially
higher
power
conversion
efficiencies
(PCEs)
than
FA-based
devices.
discovery
Y6-type
(Y6
2,2′-((2Z,2′Z)-((12,13-bis(2-ethylhexyl)-3,9-diundecyl-12,13-dihydro-[1,2,5]-thiadiazolo[3,4-e]-thieno[2″,3″:4′,5′]thieno-[2′,3′:4,5]pyrrolo-[3,2-g]thieno-[2′,3′:4,5]thieno-[3,2-b]indole-2,10-diyl)bis(methanylylidene))bis(5,6-difluoro-3-oxo-2,3-dihydro-1H-indene-2,1-diylidene))dimalononitrile)
A–DA′
D–A
further
propelled
the
PCEs
go
beyond
15%
due
smaller
Eloss
values
(∼0.5
eV)
external
quantum
efficiencies.
Subsequently,
Y6-series
single-junction
increased
>19%
may
soon
approach
20%.
This
review
provides
update
recent
progress
OPV
following
aspects:
developments
novel
donors,
understanding
structure–property
relationships
underlying
mechanisms
state-of-the-art
OPVs,
tasks
underpinning
commercialization
such
as
device
stability,
module
development,
potential
applications,
high-throughput
manufacturing.
Finally,
outlook
prospects
section
summarizes
remaining
challenges
technology.
Journal of the American Chemical Society,
Journal Year:
2021,
Volume and Issue:
143(7), P. 2665 - 2670
Published: Feb. 10, 2021
Despite
the
significant
progresses
made
in
all-polymer
solar
cells
(all-PSCs)
recently,
relatively
low
short-circuit
current
density
(Jsc)
and
large
energy
loss
are
still
quite
difficult
to
overcome
for
further
development.
To
address
these
challenges,
we
developed
a
new
class
of
narrow-bandgap
polymer
acceptors
incorporating
benzotriazole
(BTz)-core
fused-ring
segment,
named
PZT
series.
Compared
commonly
used
benzothiadiazole
(BT)-containing
PYT,
less
electron-deficient
BTz
renders
derivatives
with
significantly
red-shifted
optical
absorption
up-shifted
levels,
leading
simultaneously
improved
Jsc
open-circuit
voltage
resultant
all-PSCs.
More
importantly,
regioregular
(PZT-γ)
has
been
achieve
higher
regiospecificity
avoiding
formation
isomers
during
polymerization.
Benefiting
from
more
extended
absorption,
better
backbone
ordering,
optimal
blend
morphology
donor
component,
PZT-γ-based
all-PSCs
exhibit
record-high
power
conversion
efficiency
15.8%
greatly
enhanced
24.7
mA/cm2
0.51
eV.
Nature Communications,
Journal Year:
2021,
Volume and Issue:
12(1)
Published: Sept. 6, 2021
Abstract
All-polymer
solar
cells
(all-PSCs)
based
on
polymerized
small
molecular
acceptors
(PSMAs)
have
made
significant
progress
recently.
Here,
we
synthesize
two
A-DA’D-A
molecule
acceptor
PSMAs
of
PS-Se
with
benzo[c][1,2,5]thiadiazole
A’-core
and
PN-Se
benzotriazole
A’-core,
for
the
studies
effect
structure
photovoltaic
performance
PSMAs.
The
possess
broad
absorption
showing
more
red-shifted
than
suitable
electronic
energy
levels
application
as
polymer
in
all-PSCs
PBDB-T
donor.
Cryogenic
transmission
electron
microscopy
visualizes
aggregation
behavior
donor
PSMA
their
solutions.
In
addition,
a
bicontinuous-interpenetrating
network
PBDB-T:PN-Se
blend
film
size
10~20
nm
is
clearly
observed
by
photoinduced
force
microscopy.
desirable
morphology
active
layer
leads
its
all-PSC
higher
power
conversion
efficiency
16.16%.
Advanced Materials,
Journal Year:
2022,
Volume and Issue:
34(27)
Published: March 22, 2022
State-of-art
Y-series
polymer
acceptors
are
typically
based
on
a
mono-thiophene
linker,
which
can
cause
some
twisted
molecular
conformations
and
thus
limit
the
performance
of
all-polymer
solar
cells
(all-PSCs).
Here,
high-performance
acceptor
vinylene
linkers
is
reported,
leads
to
surprising
changes
in
polymers'
conformations,
optoelectronic
properties,
enhanced
photovoltaic
performance.
It
found
that
thiophene
or
bithiophene
(PY-T-γ
PY-2T-γ)
display
significant
twisting
between
end-groups
linker
units,
while
vinylene-based
(PY-V-γ)
exhibits
more
coplanar
rigid
conformation.
As
result,
PY-V-γ
demonstrates
better
conjugation
tighter
interchain
stacking,
results
higher
mobility
reduced
energetic
disorder.
Furthermore,
detailed
morphology
investigations
reveal
PY-V-γ-based
blend
high
domain
purity
fill
factor
its
all-PSCs.
With
these,
efficiency
17.1%
achieved
all-PSCs,
highest
reported
for
binary
all-PSCs
date.
This
work
vinylene-linker
superior
unit
build
with
chain
conformation,
beneficial
aggregation
efficient
Angewandte Chemie International Edition,
Journal Year:
2021,
Volume and Issue:
60(18), P. 10137 - 10146
Published: Jan. 27, 2021
Abstract
Polymerization
sites
of
small
molecule
acceptors
(SMAs)
play
vital
roles
in
determining
device
performance
all‐polymer
solar
cells
(all‐PSCs).
Different
from
our
recent
work
about
fluoro‐
and
bromo‐
co‐modified
end
group
IC‐FBr
(a
mixture
IC‐FBr1
IC‐FBr2),
this
paper,
we
synthesized
purified
two
regiospecific
substituted
groups
(IC‐FBr‐
o
&
IC‐FBr‐
m
),
which
were
then
employed
to
construct
regio‐regular
polymer
named
PYF‐T‐
,
respectively
.
In
comparison
with
its
isomeric
counterparts
different
conjugated
coupling
sites,
exhibits
stronger
bathochromic
absorption
achieve
better
photon
harvesting.
Meanwhile,
adopts
more
ordered
inter‐chain
packing
suitable
phase
separation
after
blending
the
donor
PM6,
resulted
suppressed
charge
recombination
efficient
transport.
Strikingly,
observed
a
dramatic
difference
between
While
devices
based
on
PM6:PYF‐T‐
can
yield
power
conversion
efficiency
(PCE)
15.2
%,
only
show
poor
efficiencies
1.4
%.
This
demonstrates
success
configuration‐unique
fluorinated
designing
high‐performance
regular
acceptors,
provides
guidelines
towards
developing
all‐PSCs
efficiencies.
ChemSusChem,
Journal Year:
2021,
Volume and Issue:
14(17), P. 3569 - 3578
Published: April 30, 2021
Abstract
Self‐assembled
monolayers
(SAMs)
based
on
Br‐2PACz
([2‐(3,6‐dibromo‐9
H
‐carbazol‐9‐yl)ethyl]phosphonic
acid)
2PACz
([2‐(9H‐Carbazol‐9‐yl)ethyl]phosphonic
and
MeO‐2PACz
([2‐(3,6‐dimethoxy‐9H‐carbazol‐9‐yl)ethyl]phosphonic
molecules
were
investigated
as
hole‐extracting
interlayers
in
organic
photovoltaics
(OPVs).
The
highest
occupied
molecular
orbital
(HOMO)
energies
of
these
SAMs
measured
at
−6.01
−5.30
eV
for
MeO‐2PACz,
respectively,
found
to
induce
significant
changes
the
work
function
(WF)
indium‐tin‐oxide
(ITO)
electrodes
upon
chemical
functionalization.
OPV
cells
PM6
(poly[(2,6‐(4,8‐bis(5‐(2‐ethylhexyl‐3‐fluoro)thiophen‐2‐yl)‐benzo[1,2‐b:4,5‐b’]dithiophene))‐alt‐(5,5‐(1’,3’‐di‐2‐thienyl‐5’,7’‐bis(2‐ethylhexyl)benzo[1’,2’‐c:4’,5’‐c’]dithiophene‐4,8‐dione)])
:
BTP‐eC9
PC
71
BM
([6,6]‐phenyl‐C71‐butyric
acid
methyl
ester)
using
ITO/Br‐2PACz
anodes
exhibited
a
maximum
power
conversion
efficiency
(PCE)
18.4
%,
outperforming
devices
with
ITO/MeO‐2PACz
(14.5
%)
ITO/poly(3,4‐ethylenedioxythiophene):poly(styrene
sulfonate)
(PEDOT
PSS)
(17.5
%).
higher
PCE
was
originate
from
much
WF
(−5.81
eV)
compared
(4.58
ITO/PEDOT
PSS
(4.9
eV),
resulting
lower
interface
resistance,
improved
hole
transport/extraction,
trap‐assisted
recombination,
longer
carrier
lifetimes.
Importantly,
electrode
chemically
stable,
after
removal
SAM
it
could
be
recycled
reused
construct
fresh
OPVs
equally
impressive
performance.