2011
DOI: 10.1002/adma.201101274
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Improving Device Efficiency of Polymer/Fullerene Bulk Heterojunction Solar Cells Through Enhanced Crystallinity and Reduced Grain Boundaries Induced by Solvent Additives

Abstract: The power conversion efficiency of a device incorporating a crystalline polymer/fullerene thin film improves from 5% to 7.3% – a relative increase of 45% – when an additive, diiodohexane (DIH), is present during processing. The DIH‐processed active layer exhibits substantially enhanced polymer crystallinity and smaller fractal‐like fullerene clusters.

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Cited by 467 publications
(232 citation statements)
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References 26 publications
(11 reference statements)
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“…Shown in Figure 4 a, for the TMB film, dark irregularly shaped structures with a size up to ≈500 nm were observed, which are attributed to PC 71 BM‐rich domains 38, 39. For the CB film, PC 71 BM‐rich domains with size scales from ≈200 to ≈400 nm were also observed.…”
mentioning
confidence: 89%
“…Shown in Figure 4 a, for the TMB film, dark irregularly shaped structures with a size up to ≈500 nm were observed, which are attributed to PC 71 BM‐rich domains 38, 39. For the CB film, PC 71 BM‐rich domains with size scales from ≈200 to ≈400 nm were also observed.…”
mentioning
confidence: 89%
“…Stille polymerisation whilst versatile and reliable affords number-average molecular weights (M n ) below 10 kDa (Table 1), as has been observed with those reported for similar copolymers. [26,29] It may be possible to achieve higher molecular weights by direct heteroarylation polymerisations. [28] Optical properties.…”
Section: Resultsmentioning
confidence: 99%
“…Use of a bi(alkyl)thiophene aids solubility, though the tail-totail configuration of the alkyl chains is vital in preserving crystallinity. [21] Such alkylated TPD-2T polymers have achieved efficiencies as high as 7.3% in BHJ photovoltaic cells and field-effect transistors exhibit hole mobilities as high as 0.6 cm 2 /V s. [22][23][24][25][26][27] In addition, these polymers have recently been reported with both economic and green syntheses. [28,29] Here, we report a novel and efficient synthesis of the TPD unit facilitating late-stage alkylation by haloalkanes and direct C-H activation polymerisation.…”
Section: Introductionmentioning
confidence: 99%
“…To promote solubility, the branched -EH chain of the TPD unit was used. M n of P32 was 9.7 kDa with a PDI of 1.4 ( [80] reported [82]. To increase the coplanarity of the conjugated backbone and enhance crystalline, Wei et al further incorporated the TT unit into the Th/TPD based copolymer.…”
Section: Polythiophene-based Polymers Containing 23-diarylquinoxalinmentioning
confidence: 97%