Annealing-free efficient organic solar cells via an alkylbenzene side-chain strategy of small-molecule electron acceptors
Research on alkylbenzene side-chain engineering of acceptors, which can affect the crystallinity of molecules and packing orientations of blend films, has deeply promoted the development of organic solar cells (OSCs). In this contribution, we developed two novel small-molecule electron acceptors C4...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2020-01, Vol.8 (42), p.22155-22162 |
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Sprache: | eng |
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Zusammenfassung: | Research on alkylbenzene side-chain engineering of acceptors, which can affect the crystallinity of molecules and packing orientations of blend films, has deeply promoted the development of organic solar cells (OSCs). In this contribution, we developed two novel small-molecule electron acceptors
C4
and
C6
. They exhibit similar optical (an absorption edge reaching 900 nm) and electrochemical properties (narrow band gap,
E
g
≈ 1.55 eV), but their photovoltaic properties are quite different. The power conversion efficiency (PCE) of
C6
-based OSCs is 14.54% (
V
OC
= 0.84 V,
J
SC
= 23.82 mA cm
−2
, and FF = 72.68%), which is much higher than that of the
C4
-based control device (7.28%). The difference of PCE is because
C6
shows excellent compatibility with the polymer donor
PM6
. The subtle change of the alkylbenzene side chain is found to have a great impact on the blend film morphology. Compared to
PM6
:
C4
blend films,
PM6
:
C6
blend films exhibit a smaller π–π stacking
d
-spacing (3.61 Å) and larger coherence length (CCL = 17.7 Å), which is beneficial to promote charge transfer, further affecting the PCE of OSCs. Notably, devices based on
PM6
:
C6
can achieve 14.54% efficiency, which is one of the best efficiencies of annealing-free OSCs (AF-OSCs). In reality, AF-OSCs relatively simplify the device manufacturing process compared to annealed cells, manifesting remarkable application potential in the future. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/D0TA05787H |