All-polymer
solar cells (all-PSCs) can offer unique merits of high
morphological stability to thermal and mechanical stress. To realize
their full potential as flexible or wearable devices, it is highly
desirable that the all-PSCs can be fabricated from a green solvent
with simple post-treatment to avoid thermal annealing on the flexible
substrate. This posed a severe challenge on material design to tune
their properties with suitable solubility, aggregation, and morphology.
To address this challenge, here, a simple bicomponent random approach
on a D–A-type polymer donor was developed by just varying the
D–A molar ratio. Under this approach, a series of new random
polymers PBDT
a
–TPD
b
with different molar ratios of the D component of
2D-benzo[1,2-b:4,5-b′]dithiophene
(BDT) and A component of thieno[3,4-c]pyrrole-4,6-dione
(TPD) were designed and synthesized. The energy levels, light absorption,
solubility, and packing structure of random donors PBDT
a
–TPD
b
were found
to vary substantially with the various D–A molar ratios. The
devices based on PBDT
a
–TPD
b
/P(NDI2HD-T) were fabricated to explore the
synergistic effects of the processing solvent and composition of D–A-type
random polymers. The results show that nanoscale morphology, balanced
miscibility/crystallinity of blend, and photovoltaic properties could
be rationally optimized by tuning the composition of random donors.
As a result, as-cast all-PSC-based optimal donor PBDT5–TPD4 achieves the best power conversion efficiency (PCE) of 8.20%
processed from a green solvent, which performs better than that the
reference polymer (PCE: 6.41%). This efficiency is the highest value
for all-PSCs from BDT–TPD-based donors. Moreover, the optimized
devices were relatively insensitive to the thickness of the active
layer and exhibited good stability.