A–π–D–π–A based porphyrin for solution processed small molecule bulk heterojunction solar cells
In this article, we have designed and synthesized a porphyrin with the following molecular architecture A–π–D–π–A in which ethyl rhodanine end capping groups were linked to the core porphyrin donor via an octyl thiophene-ethynylene π bridge denoted as VC117 and used it as an electron donor along wit...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2015-01, Vol.3 (31), p.16287-16301 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | In this article, we have designed and synthesized a porphyrin with the following molecular architecture A–π–D–π–A in which ethyl rhodanine end capping groups were linked to the core porphyrin donor
via
an octyl thiophene-ethynylene π bridge denoted as
VC117
and used it as an electron donor along with ([6,6]-phenyl C
71
butyric acid methyl ester) (PC
71
BM) as an electron acceptor for the fabrication of solution processed organic solar cells. The solution processed BHJ organic solar cell with an optimized weight ratio of 1 : 1
VC117
: PC
71
BM in THF (tetrahydrofuran) showed an overall power conversion efficiency (PCE) of 2.95% with short circuit current
J
sc
= 8.34 mA cm
−2
, open circuit voltage
V
oc
= 0.82 V and fill factor FF = 0.43. Nonetheless, when the active layer of the solar cell was processed from a mixture of 4% v/v of pyridine in THF solvent, it achieved a PCE value of 4.46% and further improved up to 5.50% after thermal annealing. This is ascribed to the enhancement of both the
J
sc
and FF values. The higher value of
J
sc
is explained by the increased absorption profile of the blend, the higher incident photon to current efficiency (IPCE) response and the better crystallinity of the active layer when processed with solvent additives and thermal annealing while the enhancement of FF is due to the better charge transport capability and the charge collection efficiency of the latter device. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/C5TA03463A |