Nature Communications,
Год журнала:
2021,
Номер
12(1)
Опубликована: Янв. 12, 2021
Abstract
The
active
layer
morphology
transition
of
organic
photovoltaics
under
non-equilibrium
conditions
are
vital
importance
in
determining
the
device
power
conversion
efficiency
and
stability;
however,
a
general
unified
picture
on
this
issue
has
not
been
well
addressed.
Using
combined
situ
ex
characterizations,
morphological
parameters
relating
to
kinetics
thermodynamics
evolution
extracted
studied
model
systems
thermal
annealing.
coupling
competition
crystallization
demixing
found
be
critical
evolution,
phase
purification
interfacial
orientation.
A
summarizing
different
diagrams
all
possible
kinetic
routes
is
proposed.
current
observations
address
fundamental
issues
underlying
formation
complex
multi-length
scale
bulk
heterojunction
blends
provide
useful
optimization
guidelines
for
processing
devices
with
higher
stability.
Advanced Materials,
Год журнала:
2021,
Номер
33(41)
Опубликована: Авг. 31, 2021
Abstract
Improving
power
conversion
efficiency
(PCE)
is
important
for
broadening
the
applications
of
organic
photovoltaic
(OPV)
cells.
Here,
a
maximum
PCE
19.0%
(certified
value
18.7%)
achieved
in
single‐junction
OPV
cells
by
combining
material
design
with
ternary
blending
strategy.
An
active
layer
comprising
new
wide‐bandgap
polymer
donor
named
PBQx‐TF
and
low‐bandgap
non‐fullerene
acceptor
(NFA)
eC9‐2Cl
rationally
designed.
With
optimized
light
utilization,
resulting
binary
cell
exhibits
good
17.7%.
NFA
F‐BTA3
then
added
to
as
third
component
simultaneously
improve
parameters.
The
improved
unitization,
cascaded
energy
level
alignment,
enhanced
intermolecular
packing
result
open‐circuit
voltage
0.879
V,
short‐circuit
current
density
26.7
mA
cm
−2
,
fill
factor
0.809.
This
study
demonstrates
that
further
improvement
PCEs
high‐performance
requires
fine
tuning
electronic
structures
morphologies
layers.
Chemical Reviews,
Год журнала:
2022,
Номер
122(18), С. 14180 - 14274
Опубликована: Авг. 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.
Nature Communications,
Год журнала:
2021,
Номер
12(1)
Опубликована: Янв. 12, 2021
Abstract
The
chemical
structure
of
donors
and
acceptors
limit
the
power
conversion
efficiencies
achievable
with
active
layers
binary
donor-acceptor
mixtures.
Here,
using
quaternary
blends,
double
cascading
energy
level
alignment
in
bulk
heterojunction
organic
photovoltaic
are
realized,
enabling
efficient
carrier
splitting
transport.
Numerous
avenues
to
optimize
light
absorption,
transport,
charge-transfer
state
levels
opened
by
constitution
components.
Record-breaking
PCEs
18.07%
achieved
where,
electronic
morphology
optimization,
simultaneous
improvements
open-circuit
voltage,
short-circuit
current
fill
factor
occur.
donor
acceptor
structures
afford
control
over
levels,
manipulation
hole-transfer
rates,
non-radiative
recombination
losses.
Nature Communications,
Год журнала:
2020,
Номер
11(1)
Опубликована: Авг. 7, 2020
Abstract
A
major
challenge
for
organic
solar
cell
(OSC)
research
is
how
to
minimize
the
tradeoff
between
voltage
loss
and
charge
generation.
In
early
2019,
we
reported
a
non-fullerene
acceptor
(named
Y6)
that
can
simultaneously
achieve
high
external
quantum
efficiency
low
OSC.
Here,
use
combination
of
experimental
theoretical
modeling
reveal
structure-property-performance
relationships
this
state-of-the-art
OSC
system.
We
find
distinctive
π–π
molecular
packing
Y6
not
only
exists
in
single
crystals
but
also
thin
films.
Importantly,
such
leads
(i)
formation
delocalized
emissive
excitons
enable
small
non-radiative
loss,
(ii)
delocalization
electron
wavefunctions
at
donor/acceptor
interfaces
significantly
reduces
Coulomb
attraction
interfacial
electron-hole
pairs.
These
properties
are
critical
enabling
highly
efficient
generation
systems
with
negligible
donor-acceptor
energy
offset.
ACS Energy Letters,
Год журнала:
2020,
Номер
5(5), С. 1554 - 1567
Опубликована: Апрель 7, 2020
With
the
recent
emergence
of
a
new
class
high-performance
nonfullerene
acceptors
(NFAs),
organic
solar
cells
(OSCs)
have
entered
phase
research
featuring
high
power
conversion
efficiencies
(PCEs).
In
this
Perspective,
we
summarize
progress
made
from
Y-series
NFAs
and
matched
polymer
donors
analyze
molecular
design
strategies
for
boosting
device
performance.
We
also
perform
PCE
prediction
OSCs
propose
requirements
NFAs,
aiming
at
20%,
which
is
comparable
to
those
Si
perovskite-based
counterparts.
Finally,
assess
three
factors
efficiency,
stability,
cost
outline
challenges
facing
future
development
directions
OSCs.
This
work
expected
provide
valuable
suggestions
with
comprehensive
view
advance
practical
application
Advanced Energy Materials,
Год журнала:
2021,
Номер
11(15)
Опубликована: Янв. 14, 2021
Abstract
Organic
solar
cells
are
composed
of
electron
donating
and
accepting
organic
semiconductors.
Whilst
a
significant
palette
donors
has
been
developed
over
three
decades,
until
recently
only
small
number
acceptors
have
proven
capable
delivering
high
power
conversion
efficiencies.
In
particular
the
fullerenes
dominated
landscape.
this
perspective,
emergence
family
materials–the
non‐fullerene
(NFAs)
is
described.
These
delivered
discontinuous
advance
in
cell
efficiencies,
with
milestone
20%
now
sight.
Intensive
international
efforts
synthetic
chemistry
established
clear
design
rules
for
molecular
engineering
enabling
an
ever‐expanding
efficiency
candidates.
However,
these
materials
challenge
accepted
wisdom
how
work
force
new
thinking
areas
such
as
morphology,
charge
generation
recombination.
This
perspective
provides
historical
context
development
NFAs,
also
addresses
current
plus
considers
important
manufacturability
criteria.
There
no
doubt
that
NFAs
propelled
technology
to
efficiencies
necessary
viable
commercial
technology–but
far
can
they
be
pushed,
will
deliver
on
equally
metrics
stability?
Journal of the American Chemical Society,
Год журнала:
2020,
Номер
142(29), С. 12751 - 12759
Опубликована: Июнь 30, 2020
Bulk-heterojunction
organic
photovoltaic
devices
with
nonfullerene
acceptors
(NFAs)
exhibit
efficient
hole
transfer
small
interfacial
energy
offset,
which
results
in
power
conversion
efficiencies
above
17%
single
junction
using
the
high-performance
NFA
of
Y6.
However,
underlying
mechanism
responsible
for
channel
polymer/Y6
blends
remains
poorly
understood.
Herein,
we
report
that
photocharge
generation
is
mediated
by
an
intra-moiety
excited
state
a
blend
donor
polymer
PM6
and
Y6
broadband
transient
absorption
(TA)
spectroscopy.
By
comparing
TA
data
recorded
from
solution
film
samples,
identify
ultrafast
formation
excimer
together
primary
local
excitation
on
time
scale
∼0.2
ps
film.
The
acts
as
intermediate
channel,
dissociates
into
free
polarons
∼15
PM6/Y6
at
room
temperature.
state,
arising
intermolecular
coupling
domains,
markedly
different
charge
commonly
accepted
electron
channel.
These
findings
suggest
manipulating
interplay
between
species
can
provide
promising
route
further
improving
device
performance.