2013
DOI: 10.3144/expresspolymlett.2013.6
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Photovoltaic properties and annealing effects of a low bandgap copolymer containing dithienothiophene and benzothiadiazole units

Abstract: Abstract.A conjugated alternating copolymer as the donor material of the active layer in polymer solar cells has been designed and synthesized via Stille coupling reaction. The alternating structure consisted of 3,5-didecanyldithieno[3,2-b:2!,3!-d]thiophene (DDTT) donor unit and 5,6-bis(tetradecyloxy)benzo-2,1,3-thiadiazole (BT) acceptor unit. Since both units have been attached pendant chains, the polymer was soluble in common organic solvents. UV-vis spectrum exhibited a broad absorption band in the range of… Show more

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Cited by 8 publications
(8 citation statements)
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“…Semiconducting polymers represent a class of electronic materials which have been applied in the development of a large variety of new electronic and optoelectronic devices, including organic light emitting diodes (OLEDs) [1][2][3], organic photovoltaic cells (OPVs) [4][5][6][7], organic field effect transistors (OFETs) [8], transducers for chemical or biochemical analysis [9,10] and many other applications [11,12]. Depending on the device functionality, a different semiconducting property of the active material is more relevant: charge-carrier recombination efficiency for OLEDs, energy conversion efficiency for OPVs and charge-carrier mobility for OFETs, for example.…”
Section: Introductionmentioning
confidence: 99%
“…Semiconducting polymers represent a class of electronic materials which have been applied in the development of a large variety of new electronic and optoelectronic devices, including organic light emitting diodes (OLEDs) [1][2][3], organic photovoltaic cells (OPVs) [4][5][6][7], organic field effect transistors (OFETs) [8], transducers for chemical or biochemical analysis [9,10] and many other applications [11,12]. Depending on the device functionality, a different semiconducting property of the active material is more relevant: charge-carrier recombination efficiency for OLEDs, energy conversion efficiency for OPVs and charge-carrier mobility for OFETs, for example.…”
Section: Introductionmentioning
confidence: 99%
“…After cooled to room temperature, the mixture was poured into water (100 mL) and extracted with dichloromethane. The organic phase was washed with water and dried over anhydrous MgSO 4 . After concentration, the crude product was purified on silica gel chromatography using a petroleum ether/dichloromethane mixture (1/1 by volume) as eluent to afford a yellow liquid (4.49 g, 73.2%).…”
Section: [22!:5!2"-terthiophene]-3!-carbaldehyde (3)mentioning
confidence: 99%
“…Then the mixture was heated to 70°C for 24 h. After cooled to room temperature, the mixture was extracted with CH 2 Cl 2 and washed with water. The organic phase was dried over anhydrous MgSO 4 and the solvent was removed by rotary evaporation. The crude product was purified on silica gel chromatography using petroleum ether as eluent to afford a yellow-green solid (1.03 g, 39.1%).…”
Section: 5!-dibromo-3"-(chloromethyl)-mentioning
confidence: 99%
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