Photovoltaic properties and annealing effects of a low bandgap copolymer containing dithienothiophene and benzothiadiazole units

• Main Authors: T. L. Wang, Y. T. Shieh, C. H. Yang, T. H. Ho, C. H. Chen
• Format: Article
• Language: English
• Published: Budapest University of Technology 2013-01-01
• Series: eXPRESS Polymer Letters
• Subjects: Nanomaterials; polymer solar cells; low bandgap; annealing
• Online Access: http://www.expresspolymlett.com/letolt.php?file=EPL-0003799&mi=cd

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 270–780 nm and a low bandgap of 1.83 eV. The highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) energy levels of the polymer were estimated to be –5.10 and –3.27 eV, respectively. Based on the ITO/PEDOT:PSS/PDDTTBT:PCBM/Al device structure, the power conversion efficiency (PCE) under the illumination of AM 1.5 (100 mW/cm2) was 0.127%. The effects of annealing temperature (50–150°C) for 30 min on the device performance were studied. It was found that PCE of 0.292% could be acquired under the annealing condition at 50°C for 30 min. The improved device efficiency under the optimal condition was confirmed by the higher light harvest in UV-vis spectra, the enhanced quenching of photoluminescence (PL) emission, and the improved nanoscale morphology by atomic force microscopy (AFM) examination.