| 1. |
- Cai, Shengyun, et al.
(författare)
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Photo-stable substituted dihydroindolo[2,3-b]carbazole-based organic dyes : tuning the photovoltaic properties by optimizing the pi structure for panchromatic DSSCs
- 2014
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Ingår i: Tetrahedron. - : Elsevier BV. - 0040-4020 .- 1464-5416. ; 70:43, s. 8122-8128
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Tidskriftsartikel (refereegranskat)abstract
- Three dihydroindolo[2,3-b]carbazole (DDC) donor based organic dyes (DDC6-DDC8) with long conjugated systems were successfully synthesized and characterized by optical, electrochemical, computational analysis, and photovoltaic methods. It was found that the elongated pi system as well as the high molar extinction coefficients (4.2-5.3 M-1 cm(-1)) sufficiently reinforced the light harvesting ability with the IPCE response of one dye DDC8 extended to 850 nm, which resulted in large J(sc) of these dyes based devices (high as 16.41 mA cm(-2)). The attached alkyl chains suppress the dark current to some extent, resulting the DDC6 and DDC7 devices in high V-oc, while DDC8 displayed low V-oc, because BTD in DDC8 could attract the iodine ion, which could accelerate the charge recombination. Among the three dyes, DDC7 displayed the best performance with an eta value 6.53% under 4 mu m thick scattering layer (condition 1+1), which was boosted to 7.49% under 8 mu m thick scattering layer (condition 1+2). The photo-stability measurements indicated that all the three dyes are fairly photo-stable.
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| 2. |
- Tian, Guojian, et al.
(författare)
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A new D-A-pi-A type organic sensitizer based on substituted dihydroindolo [2,3-b] carbazole and DPP unit with a bulky branched alkyl chain for highly efficient DSCs
- 2015
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Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry (RSC). - 2050-7488 .- 2050-7496. ; 3:7, s. 3777-3784
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Tidskriftsartikel (refereegranskat)abstract
- Two new D-A-pi-A configuration metal-free organic sensitizers (T1-T2) based on 5,7-dihexyl-6,12-diphenyl-5,7-dihydroindolo[2,3-b]carbazole and a DPP unit with a bulky branched alkyl chain have been synthesized for dye-sensitized solar cells. Due to a bulky branched alkyl chain being attached to the donor and DPP unit, both compounds obtain high V-oc values. Under standard global AM 1.5 solar light conditions, the T1 based-device gives a high conversion efficiency of 8.24% with a J(sc) of 15.72 mA cm(-2), a V-oc of 0.74 V and a FF of 0.71. These excellent performances make the donor dihydroindolo[2,3-b] carbazole and DPP unit promising candidates for further application in DSCs.
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| 3. |
- Wu, Panpan, et al.
(författare)
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Highly efficient fluorene/indole-based hole transport materials for green PhOLEDs
- 2019
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Ingår i: Dyes and Pigments. - : Elsevier BV. - 0143-7208 .- 1873-3743. ; 162, s. 153-159
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Tidskriftsartikel (refereegranskat)abstract
- Three hole transport materials, FIPN-p-PCz, FIPN-p-TPA and FIPN-DPCz, incorporating fluorene/indole core with carbazole or triphenylamine unit were synthesized and fully characterized. The photophysical properties, thermal properties and electrochemical properties of these three compounds were fully investigated. The FIPN-based hole transport materials show high thermal stability(Td > 420 °C) and appropriate highest occupied molecular orbital (HOMO) level (∼-5.2 eV). Green phosphorescent organic light-emitting diodes (PhOLEDs) using these FIPN-based derivatives were fabricated to investigate the device performance, compared with NPB as the reference hole transport material. It turned out that the devices using these three compounds exhibited superior performance than that of the NPB-based PhOLED device. Especially, the FIPN-p-PCz based device showed outstanding electroluminescence performance with the maximum current efficiency and external quantum efficiency of 53.7 cd/A and 17.3%, respectively, which was almost twice that of the NPB based device.
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